Array
(
[blok] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
[groups] => Array
(
[18] => Array
(
[id] => 18
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[sort] => 1
[status_code] => active
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[materials] => Array
(
[128] => Array
(
[id] => 128
[name] => RASopatie – diagnostyka molekularna wrodzonych zaburzeń rozwojowych
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/128/posterw_erze.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
[linked] => Array
(
[129] => Array
(
[id] => 129
[site_id] => 1
[status_id] => 5
[name] => Zastosowanie metod cytogenetycznych w diagnostyce zaburzeń wieku rozwojowego
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/129/posterw_erze.png
[video] => resources/data/material/129/wisniowiecka_zastosowanie_cytogenetyki.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Barbara Wiśniowiecka-Kowalnik
)
[authors_data] => Array
(
[0] => Array
(
[id] => 7
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Barbara Wiśniowiecka-Kowalnik
[firstname] => Barbara
[lastname] => Wiśniowiecka-Kowalnik
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 7-barbara_wisniowiecka_kowalnik
[url] => eksperci/7-barbara_wisniowiecka_kowalnik
)
)
[authors_ids] => Array
(
[0] => 7
)
[topics] => Array
(
[0] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 129-zastosowanie_metod_cytogenetycznych_w_diagnostyce_zaburzen_wieku_rozwojowego
[url] => wideo/129-zastosowanie_metod_cytogenetycznych_w_diagnostyce_zaburzen_wieku_rozwojowego
[short_name] => Zastosowanie metod cytogenetycznych w diagnostyce ...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[131] => Array
(
[id] => 131
[site_id] => 1
[status_id] => 5
[name] => Typy dziedziczenia chorób genetycznych i poradnictwo genetyczne
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/131/posterw_erze.png
[video] => resources/data/material/131/kutkowska_typy_dziedziczenia.mp4
[content] =>
[ext] => Array
(
[linked] => Array
(
[0] => Array
(
[id] =>
)
)
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n.med. Anna Kutkowska-Kaźmierczak
)
[authors_data] => Array
(
[0] => Array
(
[id] => 64
[site_id] => 1
[status_id] => 5
[name] => dr n.med. Anna Kutkowska-Kaźmierczak
[firstname] => Anna
[lastname] => Kutkowska-Kaźmierczak
[title] => dr n.med.
[affiliation] => Zakład Genetyki Klinicznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 64-anna_kutkowska_kazmierczak
[url] => eksperci/64-anna_kutkowska_kazmierczak
)
)
[authors_ids] => Array
(
[0] => 64
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 131-typy_dziedziczenia_chorob_genetycznych_i_poradnictwo_genetyczne
[url] => wideo/131-typy_dziedziczenia_chorob_genetycznych_i_poradnictwo_genetyczne
[short_name] => Typy dziedziczenia chorób genetycznych i poradnict...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[132] => Array
(
[id] => 132
[site_id] => 1
[status_id] => 5
[name] => Diagnostyka wrodzonych wad metabolizmu
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/132/posterw_erze.png
[video] => resources/data/material/132/rygiel_diagnostyka_wrodzonych_wad_metabolizmu.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab. n. med., prof. IMID Agnieszka Rygiel
)
[authors_data] => Array
(
[0] => Array
(
[id] => 65
[site_id] => 1
[status_id] => 5
[name] => dr hab. n. med., prof. IMID Agnieszka Rygiel
[firstname] => Agnieszka
[lastname] => Rygiel
[title] => dr hab. n. med., prof. IMID
[affiliation] => Zakład Genetyki Medycznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 65-agnieszka_rygiel
[url] => eksperci/65-agnieszka_rygiel
)
)
[authors_ids] => Array
(
[0] => 65
)
[topics] => Array
(
[0] => 2
[1] => 4
[2] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 132-diagnostyka_wrodzonych_wad_metabolizmu
[url] => wideo/132-diagnostyka_wrodzonych_wad_metabolizmu
[short_name] => Diagnostyka wrodzonych wad metabolizmu
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[2] => Array
(
[id] => 2
[site_id] => 1
[status_id] => 5
[name] => metabolizm
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 2-metabolizm
[url] => /2-metabolizm
)
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[133] => Array
(
[id] => 133
[site_id] => 1
[status_id] => 5
[name] => Diagnostyka molekularna genetycznie uwarunkowanego zapalenia trzustki
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/133/posterw_erze.png
[video] => resources/data/material/133/rygiel_diagn_molek_genet_uwarunk_zapalenia_trzustki.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab. n. med., prof. IMID Agnieszka Rygiel
)
[authors_data] => Array
(
[0] => Array
(
[id] => 65
[site_id] => 1
[status_id] => 5
[name] => dr hab. n. med., prof. IMID Agnieszka Rygiel
[firstname] => Agnieszka
[lastname] => Rygiel
[title] => dr hab. n. med., prof. IMID
[affiliation] => Zakład Genetyki Medycznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 65-agnieszka_rygiel
[url] => eksperci/65-agnieszka_rygiel
)
)
[authors_ids] => Array
(
[0] => 65
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 133-diagnostyka_molekularna_genetycznie_uwarunkowanego_zapalenia_trzustki
[url] => wideo/133-diagnostyka_molekularna_genetycznie_uwarunkowanego_zapalenia_trzustki
[short_name] => Diagnostyka molekularna genetycznie uwarunkowanego...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[134] => Array
(
[id] => 134
[site_id] => 1
[status_id] => 5
[name] => Postępowanie diagnostyczne w niepełnosprawności intelektualnej
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/134/posterw_erze.png
[video] => resources/data/material/134/postepowanie_diagnostyczne_w_niepelnosprawnosci_intelektualnej_brak_nazwy_kursu.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Magdalena Bartnik-Głaska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 66
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Magdalena Bartnik-Głaska
[firstname] => Magdalena
[lastname] => Bartnik-Głaska
[title] => dr n. med.
[affiliation] => Zakład Genetyki Medycznej, Instytut Matki i Dziecka, Warszawa
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 66-magdalena_bartnik_glaska
[url] => eksperci/66-magdalena_bartnik_glaska
)
)
[authors_ids] => Array
(
[0] => 66
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 134-postepowanie_diagnostyczne_w_niepelnosprawnosci_intelektualnej
[url] => wideo/134-postepowanie_diagnostyczne_w_niepelnosprawnosci_intelektualnej
[short_name] => Postępowanie diagnostyczne w niepełnosprawności in...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[135] => Array
(
[id] => 135
[site_id] => 1
[status_id] => 5
[name] => Zespoły mikrodelecyjne i mikroduplikacyjne
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/135/posterw_erze.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n.med. Anna Kutkowska-Kaźmierczak
)
[authors_data] => Array
(
[0] => Array
(
[id] => 64
[site_id] => 1
[status_id] => 5
[name] => dr n.med. Anna Kutkowska-Kaźmierczak
[firstname] => Anna
[lastname] => Kutkowska-Kaźmierczak
[title] => dr n.med.
[affiliation] => Zakład Genetyki Klinicznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 64-anna_kutkowska_kazmierczak
[url] => eksperci/64-anna_kutkowska_kazmierczak
)
)
[authors_ids] => Array
(
[0] => 64
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 9
[3] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 135-zespoly_mikrodelecyjne_i_mikroduplikacyjne
[url] => wideo/135-zespoly_mikrodelecyjne_i_mikroduplikacyjne
[short_name] => Zespoły mikrodelecyjne i mikroduplikacyjne
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[9] => Array
(
[id] => 9
[site_id] => 1
[status_id] => 5
[name] => zespół delecji
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 9-zespol_delecji
[url] => /9-zespol_delecji
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[136] => Array
(
[id] => 136
[site_id] => 1
[status_id] => 5
[name] => „Już” znane zespoły mikrodelecji/mikroduplikacji w diagnostyce zaburzeń wieku rozwojowego
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/136/posterw_erze.png
[video] => resources/data/material/136/kedzior_juz_znane_zespoly_mikrodelecji.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr Marta Kędzior
)
[authors_data] => Array
(
[0] => Array
(
[id] => 67
[site_id] => 1
[status_id] => 5
[name] => dr Marta Kędzior
[firstname] => Marta
[lastname] => Kędzior
[title] => dr
[affiliation] => Zakład Genetyki Medycznej, IMiD
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 67-marta_kedzior
[url] => eksperci/67-marta_kedzior
)
)
[authors_ids] => Array
(
[0] => 67
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 9
[3] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 136-juz_znane_zespoly_mikrodelecjimikroduplikacji_w_diagnostyce_zaburzen_wieku_rozwojowego
[url] => wideo/136-juz_znane_zespoly_mikrodelecjimikroduplikacji_w_diagnostyce_zaburzen_wieku_rozwojowego
[short_name] => „Już” znane zespoły mikrodelecji/mikroduplikacji w...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[9] => Array
(
[id] => 9
[site_id] => 1
[status_id] => 5
[name] => zespół delecji
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 9-zespol_delecji
[url] => /9-zespol_delecji
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[137] => Array
(
[id] => 137
[site_id] => 1
[status_id] => 5
[name] => Genetyczne uwarunkowania kraniostenoz
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/137/posterw_erze.png
[video] => resources/data/material/137/kutkowska_genetycz_uwarunkow_kraniostenoz.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n.med. Anna Kutkowska-Kaźmierczak
)
[authors_data] => Array
(
[0] => Array
(
[id] => 64
[site_id] => 1
[status_id] => 5
[name] => dr n.med. Anna Kutkowska-Kaźmierczak
[firstname] => Anna
[lastname] => Kutkowska-Kaźmierczak
[title] => dr n.med.
[affiliation] => Zakład Genetyki Klinicznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 64-anna_kutkowska_kazmierczak
[url] => eksperci/64-anna_kutkowska_kazmierczak
)
)
[authors_ids] => Array
(
[0] => 64
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 137-genetyczne_uwarunkowania_kraniostenoz
[url] => wideo/137-genetyczne_uwarunkowania_kraniostenoz
[short_name] => Genetyczne uwarunkowania kraniostenoz
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[138] => Array
(
[id] => 138
[site_id] => 1
[status_id] => 5
[name] => Niepełnosprawność intelektualna – podłoże genetyczne
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/138/posterw_erze.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n.med. Anna Kutkowska-Kaźmierczak
)
[authors_data] => Array
(
[0] => Array
(
[id] => 64
[site_id] => 1
[status_id] => 5
[name] => dr n.med. Anna Kutkowska-Kaźmierczak
[firstname] => Anna
[lastname] => Kutkowska-Kaźmierczak
[title] => dr n.med.
[affiliation] => Zakład Genetyki Klinicznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 64-anna_kutkowska_kazmierczak
[url] => eksperci/64-anna_kutkowska_kazmierczak
)
)
[authors_ids] => Array
(
[0] => 64
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 138-niepelnosprawnosc_intelektualna__podloze_genetyczne
[url] => wideo/138-niepelnosprawnosc_intelektualna__podloze_genetyczne
[short_name] => Niepełnosprawność intelektualna – podłoże genetycz...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[139] => Array
(
[id] => 139
[site_id] => 1
[status_id] => 5
[name] => Niedosłuch w erze genomowej - możliwości diagnostyczne
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/139/posterw_erze.png
[video] => resources/data/material/139/niepokoj_niedosluch.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Niepokój
)
[authors_data] => Array
(
[0] => Array
(
[id] => 68
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Niepokój
[firstname] => Katarzyna
[lastname] => Niepokój
[title] => dr n. med.
[affiliation] => Zakład Genetyki Medycznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 68-katarzyna_niepokoj
[url] => eksperci/68-katarzyna_niepokoj
)
)
[authors_ids] => Array
(
[0] => 68
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 139-niedosluch_w_erze_genomowej___mozliwosci_diagnostyczne
[url] => wideo/139-niedosluch_w_erze_genomowej___mozliwosci_diagnostyczne
[short_name] => Niedosłuch w erze genomowej - możliwości diagnosty...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[140] => Array
(
[id] => 140
[site_id] => 1
[status_id] => 5
[name] => Zastosowanie sekwencjonowania w diagnostyce molekularnej
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/140/posterw_erze.png
[video] => resources/data/material/140/wertheim_zastosowanie_sekwencjonowania_w_diagnostyce_molekularnej.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 140-zastosowanie_sekwencjonowania_w_diagnostyce_molekularnej
[url] => wideo/140-zastosowanie_sekwencjonowania_w_diagnostyce_molekularnej
[short_name] => Zastosowanie sekwencjonowania w diagnostyce moleku...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[141] => Array
(
[id] => 141
[site_id] => 1
[status_id] => 5
[name] => Interpretacja wyników badań molekularnych na przykładzie genetycznie uwarunkowanych chorób skóry
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/141/posterw_erze.png
[video] => resources/data/material/141/interpretacja_wynikow_badan_molekularnych_na_przykladzie_genetycznie_uwarunkowanych_chorob_skory_wertheimtyssarowska_12_min_uciety_poczatek_zdania.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 141-interpretacja_wynikow_badan_molekularnych_na_przykladzie_genetycznie_uwarunkowanych_chorob_skory
[url] => wideo/141-interpretacja_wynikow_badan_molekularnych_na_przykladzie_genetycznie_uwarunkowanych_chorob_skory
[short_name] => Interpretacja wyników badań molekularnych na przyk...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[142] => Array
(
[id] => 142
[site_id] => 1
[status_id] => 5
[name] => Diagnostyka mukowiscydozy i chorób CFTR zależnych 30 lat po odkryciu genu CFTR
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/142/posterw_erze.png
[video] => resources/data/material/142/wertheim_diagnostyka_mukowiscydzy.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 142-diagnostyka_mukowiscydozy_i_chorob_cftr_zaleznych_30_lat_po_odkryciu_genu_cftr
[url] => wideo/142-diagnostyka_mukowiscydozy_i_chorob_cftr_zaleznych_30_lat_po_odkryciu_genu_cftr
[short_name] => Diagnostyka mukowiscydozy i chorób CFTR zależnych ...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[143] => Array
(
[id] => 143
[site_id] => 1
[status_id] => 5
[name] => Badania molekularne w diagnostyce galaktozemii
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/143/posterw_erze.png
[video] => resources/data/material/143/wertheim_bad_molek_w_diagnost_galaktozemii.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 143-badania_molekularne_w_diagnostyce_galaktozemii
[url] => wideo/143-badania_molekularne_w_diagnostyce_galaktozemii
[short_name] => Badania molekularne w diagnostyce galaktozemii
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
)
)
[sort] => 1
[status_code] => active
[authors] => Array
(
[0] => dr n. med., prof IMiD Monika Gos
)
[authors_data] => Array
(
[0] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => dr n. med., prof IMiD Monika Gos
[firstname] => Monika
[lastname] => Gos
[title] => dr n. med., prof IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-monika_gos
[url] => eksperci/13-monika_gos
)
)
[authors_ids] => Array
(
[0] => 13
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 128-rasopatie__diagnostyka_molekularna_wrodzonych_zaburzen_rozwojowych
[url] => wideo/128-rasopatie__diagnostyka_molekularna_wrodzonych_zaburzen_rozwojowych
[short_name] => RASopatie – diagnostyka molekularna wrodzonych zab...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
[logotypy] => Array
(
)
[pliki] => Array
(
[97] => Array
(
[id] => 97
[site_id] => 1
[status_id] => 5
[entity_key] => material
[entity_id] => 128
[name] => RASopatie – diagnostyka molekularna wrodzonych zaburzeń rozwojowych
[file] => resources/data/pliki/material/128/rasopatie_diagnostyka_molekularna_wrodzonych_zaburzen_rozwojowych.pdf
[sort] => 94
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
[129] => Array
(
[id] => 129
[name] => Zastosowanie metod cytogenetycznych w diagnostyce zaburzeń wieku rozwojowego
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/129/posterw_erze.png
[video] => resources/data/material/129/wisniowiecka_zastosowanie_cytogenetyki.mp4
[content] =>
[ext] => Array
(
[files_header] =>
[linked] => Array
(
[128] => Array
(
[id] => 128
[site_id] => 1
[status_id] => 5
[name] => RASopatie – diagnostyka molekularna wrodzonych zaburzeń rozwojowych
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/128/posterw_erze.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med., prof IMiD Monika Gos
)
[authors_data] => Array
(
[0] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => dr n. med., prof IMiD Monika Gos
[firstname] => Monika
[lastname] => Gos
[title] => dr n. med., prof IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-monika_gos
[url] => eksperci/13-monika_gos
)
)
[authors_ids] => Array
(
[0] => 13
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 128-rasopatie__diagnostyka_molekularna_wrodzonych_zaburzen_rozwojowych
[url] => wideo/128-rasopatie__diagnostyka_molekularna_wrodzonych_zaburzen_rozwojowych
[short_name] => RASopatie – diagnostyka molekularna wrodzonych zab...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[131] => Array
(
[id] => 131
[site_id] => 1
[status_id] => 5
[name] => Typy dziedziczenia chorób genetycznych i poradnictwo genetyczne
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/131/posterw_erze.png
[video] => resources/data/material/131/kutkowska_typy_dziedziczenia.mp4
[content] =>
[ext] => Array
(
[linked] => Array
(
[0] => Array
(
[id] =>
)
)
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n.med. Anna Kutkowska-Kaźmierczak
)
[authors_data] => Array
(
[0] => Array
(
[id] => 64
[site_id] => 1
[status_id] => 5
[name] => dr n.med. Anna Kutkowska-Kaźmierczak
[firstname] => Anna
[lastname] => Kutkowska-Kaźmierczak
[title] => dr n.med.
[affiliation] => Zakład Genetyki Klinicznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 64-anna_kutkowska_kazmierczak
[url] => eksperci/64-anna_kutkowska_kazmierczak
)
)
[authors_ids] => Array
(
[0] => 64
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 131-typy_dziedziczenia_chorob_genetycznych_i_poradnictwo_genetyczne
[url] => wideo/131-typy_dziedziczenia_chorob_genetycznych_i_poradnictwo_genetyczne
[short_name] => Typy dziedziczenia chorób genetycznych i poradnict...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[132] => Array
(
[id] => 132
[site_id] => 1
[status_id] => 5
[name] => Diagnostyka wrodzonych wad metabolizmu
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/132/posterw_erze.png
[video] => resources/data/material/132/rygiel_diagnostyka_wrodzonych_wad_metabolizmu.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab. n. med., prof. IMID Agnieszka Rygiel
)
[authors_data] => Array
(
[0] => Array
(
[id] => 65
[site_id] => 1
[status_id] => 5
[name] => dr hab. n. med., prof. IMID Agnieszka Rygiel
[firstname] => Agnieszka
[lastname] => Rygiel
[title] => dr hab. n. med., prof. IMID
[affiliation] => Zakład Genetyki Medycznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 65-agnieszka_rygiel
[url] => eksperci/65-agnieszka_rygiel
)
)
[authors_ids] => Array
(
[0] => 65
)
[topics] => Array
(
[0] => 2
[1] => 4
[2] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 132-diagnostyka_wrodzonych_wad_metabolizmu
[url] => wideo/132-diagnostyka_wrodzonych_wad_metabolizmu
[short_name] => Diagnostyka wrodzonych wad metabolizmu
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[2] => Array
(
[id] => 2
[site_id] => 1
[status_id] => 5
[name] => metabolizm
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 2-metabolizm
[url] => /2-metabolizm
)
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[133] => Array
(
[id] => 133
[site_id] => 1
[status_id] => 5
[name] => Diagnostyka molekularna genetycznie uwarunkowanego zapalenia trzustki
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/133/posterw_erze.png
[video] => resources/data/material/133/rygiel_diagn_molek_genet_uwarunk_zapalenia_trzustki.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab. n. med., prof. IMID Agnieszka Rygiel
)
[authors_data] => Array
(
[0] => Array
(
[id] => 65
[site_id] => 1
[status_id] => 5
[name] => dr hab. n. med., prof. IMID Agnieszka Rygiel
[firstname] => Agnieszka
[lastname] => Rygiel
[title] => dr hab. n. med., prof. IMID
[affiliation] => Zakład Genetyki Medycznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 65-agnieszka_rygiel
[url] => eksperci/65-agnieszka_rygiel
)
)
[authors_ids] => Array
(
[0] => 65
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 133-diagnostyka_molekularna_genetycznie_uwarunkowanego_zapalenia_trzustki
[url] => wideo/133-diagnostyka_molekularna_genetycznie_uwarunkowanego_zapalenia_trzustki
[short_name] => Diagnostyka molekularna genetycznie uwarunkowanego...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[134] => Array
(
[id] => 134
[site_id] => 1
[status_id] => 5
[name] => Postępowanie diagnostyczne w niepełnosprawności intelektualnej
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/134/posterw_erze.png
[video] => resources/data/material/134/postepowanie_diagnostyczne_w_niepelnosprawnosci_intelektualnej_brak_nazwy_kursu.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Magdalena Bartnik-Głaska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 66
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Magdalena Bartnik-Głaska
[firstname] => Magdalena
[lastname] => Bartnik-Głaska
[title] => dr n. med.
[affiliation] => Zakład Genetyki Medycznej, Instytut Matki i Dziecka, Warszawa
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 66-magdalena_bartnik_glaska
[url] => eksperci/66-magdalena_bartnik_glaska
)
)
[authors_ids] => Array
(
[0] => 66
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 134-postepowanie_diagnostyczne_w_niepelnosprawnosci_intelektualnej
[url] => wideo/134-postepowanie_diagnostyczne_w_niepelnosprawnosci_intelektualnej
[short_name] => Postępowanie diagnostyczne w niepełnosprawności in...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[135] => Array
(
[id] => 135
[site_id] => 1
[status_id] => 5
[name] => Zespoły mikrodelecyjne i mikroduplikacyjne
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/135/posterw_erze.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n.med. Anna Kutkowska-Kaźmierczak
)
[authors_data] => Array
(
[0] => Array
(
[id] => 64
[site_id] => 1
[status_id] => 5
[name] => dr n.med. Anna Kutkowska-Kaźmierczak
[firstname] => Anna
[lastname] => Kutkowska-Kaźmierczak
[title] => dr n.med.
[affiliation] => Zakład Genetyki Klinicznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 64-anna_kutkowska_kazmierczak
[url] => eksperci/64-anna_kutkowska_kazmierczak
)
)
[authors_ids] => Array
(
[0] => 64
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 9
[3] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 135-zespoly_mikrodelecyjne_i_mikroduplikacyjne
[url] => wideo/135-zespoly_mikrodelecyjne_i_mikroduplikacyjne
[short_name] => Zespoły mikrodelecyjne i mikroduplikacyjne
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[9] => Array
(
[id] => 9
[site_id] => 1
[status_id] => 5
[name] => zespół delecji
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 9-zespol_delecji
[url] => /9-zespol_delecji
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[136] => Array
(
[id] => 136
[site_id] => 1
[status_id] => 5
[name] => „Już” znane zespoły mikrodelecji/mikroduplikacji w diagnostyce zaburzeń wieku rozwojowego
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/136/posterw_erze.png
[video] => resources/data/material/136/kedzior_juz_znane_zespoly_mikrodelecji.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr Marta Kędzior
)
[authors_data] => Array
(
[0] => Array
(
[id] => 67
[site_id] => 1
[status_id] => 5
[name] => dr Marta Kędzior
[firstname] => Marta
[lastname] => Kędzior
[title] => dr
[affiliation] => Zakład Genetyki Medycznej, IMiD
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 67-marta_kedzior
[url] => eksperci/67-marta_kedzior
)
)
[authors_ids] => Array
(
[0] => 67
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 9
[3] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 136-juz_znane_zespoly_mikrodelecjimikroduplikacji_w_diagnostyce_zaburzen_wieku_rozwojowego
[url] => wideo/136-juz_znane_zespoly_mikrodelecjimikroduplikacji_w_diagnostyce_zaburzen_wieku_rozwojowego
[short_name] => „Już” znane zespoły mikrodelecji/mikroduplikacji w...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[9] => Array
(
[id] => 9
[site_id] => 1
[status_id] => 5
[name] => zespół delecji
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 9-zespol_delecji
[url] => /9-zespol_delecji
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[137] => Array
(
[id] => 137
[site_id] => 1
[status_id] => 5
[name] => Genetyczne uwarunkowania kraniostenoz
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/137/posterw_erze.png
[video] => resources/data/material/137/kutkowska_genetycz_uwarunkow_kraniostenoz.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n.med. Anna Kutkowska-Kaźmierczak
)
[authors_data] => Array
(
[0] => Array
(
[id] => 64
[site_id] => 1
[status_id] => 5
[name] => dr n.med. Anna Kutkowska-Kaźmierczak
[firstname] => Anna
[lastname] => Kutkowska-Kaźmierczak
[title] => dr n.med.
[affiliation] => Zakład Genetyki Klinicznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 64-anna_kutkowska_kazmierczak
[url] => eksperci/64-anna_kutkowska_kazmierczak
)
)
[authors_ids] => Array
(
[0] => 64
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 137-genetyczne_uwarunkowania_kraniostenoz
[url] => wideo/137-genetyczne_uwarunkowania_kraniostenoz
[short_name] => Genetyczne uwarunkowania kraniostenoz
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[138] => Array
(
[id] => 138
[site_id] => 1
[status_id] => 5
[name] => Niepełnosprawność intelektualna – podłoże genetyczne
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/138/posterw_erze.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n.med. Anna Kutkowska-Kaźmierczak
)
[authors_data] => Array
(
[0] => Array
(
[id] => 64
[site_id] => 1
[status_id] => 5
[name] => dr n.med. Anna Kutkowska-Kaźmierczak
[firstname] => Anna
[lastname] => Kutkowska-Kaźmierczak
[title] => dr n.med.
[affiliation] => Zakład Genetyki Klinicznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 64-anna_kutkowska_kazmierczak
[url] => eksperci/64-anna_kutkowska_kazmierczak
)
)
[authors_ids] => Array
(
[0] => 64
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 138-niepelnosprawnosc_intelektualna__podloze_genetyczne
[url] => wideo/138-niepelnosprawnosc_intelektualna__podloze_genetyczne
[short_name] => Niepełnosprawność intelektualna – podłoże genetycz...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[139] => Array
(
[id] => 139
[site_id] => 1
[status_id] => 5
[name] => Niedosłuch w erze genomowej - możliwości diagnostyczne
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/139/posterw_erze.png
[video] => resources/data/material/139/niepokoj_niedosluch.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Niepokój
)
[authors_data] => Array
(
[0] => Array
(
[id] => 68
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Niepokój
[firstname] => Katarzyna
[lastname] => Niepokój
[title] => dr n. med.
[affiliation] => Zakład Genetyki Medycznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 68-katarzyna_niepokoj
[url] => eksperci/68-katarzyna_niepokoj
)
)
[authors_ids] => Array
(
[0] => 68
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 139-niedosluch_w_erze_genomowej___mozliwosci_diagnostyczne
[url] => wideo/139-niedosluch_w_erze_genomowej___mozliwosci_diagnostyczne
[short_name] => Niedosłuch w erze genomowej - możliwości diagnosty...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[140] => Array
(
[id] => 140
[site_id] => 1
[status_id] => 5
[name] => Zastosowanie sekwencjonowania w diagnostyce molekularnej
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/140/posterw_erze.png
[video] => resources/data/material/140/wertheim_zastosowanie_sekwencjonowania_w_diagnostyce_molekularnej.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 140-zastosowanie_sekwencjonowania_w_diagnostyce_molekularnej
[url] => wideo/140-zastosowanie_sekwencjonowania_w_diagnostyce_molekularnej
[short_name] => Zastosowanie sekwencjonowania w diagnostyce moleku...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[141] => Array
(
[id] => 141
[site_id] => 1
[status_id] => 5
[name] => Interpretacja wyników badań molekularnych na przykładzie genetycznie uwarunkowanych chorób skóry
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/141/posterw_erze.png
[video] => resources/data/material/141/interpretacja_wynikow_badan_molekularnych_na_przykladzie_genetycznie_uwarunkowanych_chorob_skory_wertheimtyssarowska_12_min_uciety_poczatek_zdania.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 141-interpretacja_wynikow_badan_molekularnych_na_przykladzie_genetycznie_uwarunkowanych_chorob_skory
[url] => wideo/141-interpretacja_wynikow_badan_molekularnych_na_przykladzie_genetycznie_uwarunkowanych_chorob_skory
[short_name] => Interpretacja wyników badań molekularnych na przyk...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[142] => Array
(
[id] => 142
[site_id] => 1
[status_id] => 5
[name] => Diagnostyka mukowiscydozy i chorób CFTR zależnych 30 lat po odkryciu genu CFTR
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/142/posterw_erze.png
[video] => resources/data/material/142/wertheim_diagnostyka_mukowiscydzy.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 142-diagnostyka_mukowiscydozy_i_chorob_cftr_zaleznych_30_lat_po_odkryciu_genu_cftr
[url] => wideo/142-diagnostyka_mukowiscydozy_i_chorob_cftr_zaleznych_30_lat_po_odkryciu_genu_cftr
[short_name] => Diagnostyka mukowiscydozy i chorób CFTR zależnych ...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[143] => Array
(
[id] => 143
[site_id] => 1
[status_id] => 5
[name] => Badania molekularne w diagnostyce galaktozemii
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/143/posterw_erze.png
[video] => resources/data/material/143/wertheim_bad_molek_w_diagnost_galaktozemii.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 143-badania_molekularne_w_diagnostyce_galaktozemii
[url] => wideo/143-badania_molekularne_w_diagnostyce_galaktozemii
[short_name] => Badania molekularne w diagnostyce galaktozemii
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
)
)
[sort] => 1
[status_code] => active
[authors] => Array
(
[0] => dr n. med. Barbara Wiśniowiecka-Kowalnik
)
[authors_data] => Array
(
[0] => Array
(
[id] => 7
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Barbara Wiśniowiecka-Kowalnik
[firstname] => Barbara
[lastname] => Wiśniowiecka-Kowalnik
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 7-barbara_wisniowiecka_kowalnik
[url] => eksperci/7-barbara_wisniowiecka_kowalnik
)
)
[authors_ids] => Array
(
[0] => 7
)
[topics] => Array
(
[0] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 129-zastosowanie_metod_cytogenetycznych_w_diagnostyce_zaburzen_wieku_rozwojowego
[url] => wideo/129-zastosowanie_metod_cytogenetycznych_w_diagnostyce_zaburzen_wieku_rozwojowego
[short_name] => Zastosowanie metod cytogenetycznych w diagnostyce ...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
[logotypy] => Array
(
)
[pliki] => Array
(
[98] => Array
(
[id] => 98
[site_id] => 1
[status_id] => 5
[entity_key] => material
[entity_id] => 129
[name] => Zastosowanie metod cytogenetycznych w diagnostyce zaburzeń wieku rozwojowego
[file] => resources/data/pliki/material/129/zastosowanie_metod_cytogenetycznych_w_diagnostyce_wieku_rozowjowego.pdf
[sort] => 95
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
[131] => Array
(
[id] => 131
[name] => Typy dziedziczenia chorób genetycznych i poradnictwo genetyczne
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/131/posterw_erze.png
[video] => resources/data/material/131/kutkowska_typy_dziedziczenia.mp4
[content] =>
[ext] => Array
(
[linked] => Array
(
[0] =>
)
[files_header] =>
)
[sort] => 1
[status_code] => active
[authors] => Array
(
[0] => dr n.med. Anna Kutkowska-Kaźmierczak
)
[authors_data] => Array
(
[0] => Array
(
[id] => 64
[site_id] => 1
[status_id] => 5
[name] => dr n.med. Anna Kutkowska-Kaźmierczak
[firstname] => Anna
[lastname] => Kutkowska-Kaźmierczak
[title] => dr n.med.
[affiliation] => Zakład Genetyki Klinicznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 64-anna_kutkowska_kazmierczak
[url] => eksperci/64-anna_kutkowska_kazmierczak
)
)
[authors_ids] => Array
(
[0] => 64
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 131-typy_dziedziczenia_chorob_genetycznych_i_poradnictwo_genetyczne
[url] => wideo/131-typy_dziedziczenia_chorob_genetycznych_i_poradnictwo_genetyczne
[short_name] => Typy dziedziczenia chorób genetycznych i poradnict...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
[logotypy] => Array
(
)
[pliki] => Array
(
[100] => Array
(
[id] => 100
[site_id] => 1
[status_id] => 5
[entity_key] => material
[entity_id] => 131
[name] => Typy dziedziczenia chorób genetycznych i poradnictwo genetyczne
[file] => resources/data/pliki/material/131/typy_dziedziczenia_chorob_genetycznych_i_poradnictwo_genetyczne.pdf
[sort] => 97
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
[132] => Array
(
[id] => 132
[name] => Diagnostyka wrodzonych wad metabolizmu
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/132/posterw_erze.png
[video] => resources/data/material/132/rygiel_diagnostyka_wrodzonych_wad_metabolizmu.mp4
[content] =>
[ext] => Array
(
[files_header] =>
[linked] => Array
(
[128] => Array
(
[id] => 128
[site_id] => 1
[status_id] => 5
[name] => RASopatie – diagnostyka molekularna wrodzonych zaburzeń rozwojowych
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/128/posterw_erze.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med., prof IMiD Monika Gos
)
[authors_data] => Array
(
[0] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => dr n. med., prof IMiD Monika Gos
[firstname] => Monika
[lastname] => Gos
[title] => dr n. med., prof IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-monika_gos
[url] => eksperci/13-monika_gos
)
)
[authors_ids] => Array
(
[0] => 13
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 128-rasopatie__diagnostyka_molekularna_wrodzonych_zaburzen_rozwojowych
[url] => wideo/128-rasopatie__diagnostyka_molekularna_wrodzonych_zaburzen_rozwojowych
[short_name] => RASopatie – diagnostyka molekularna wrodzonych zab...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[129] => Array
(
[id] => 129
[site_id] => 1
[status_id] => 5
[name] => Zastosowanie metod cytogenetycznych w diagnostyce zaburzeń wieku rozwojowego
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/129/posterw_erze.png
[video] => resources/data/material/129/wisniowiecka_zastosowanie_cytogenetyki.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Barbara Wiśniowiecka-Kowalnik
)
[authors_data] => Array
(
[0] => Array
(
[id] => 7
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Barbara Wiśniowiecka-Kowalnik
[firstname] => Barbara
[lastname] => Wiśniowiecka-Kowalnik
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 7-barbara_wisniowiecka_kowalnik
[url] => eksperci/7-barbara_wisniowiecka_kowalnik
)
)
[authors_ids] => Array
(
[0] => 7
)
[topics] => Array
(
[0] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 129-zastosowanie_metod_cytogenetycznych_w_diagnostyce_zaburzen_wieku_rozwojowego
[url] => wideo/129-zastosowanie_metod_cytogenetycznych_w_diagnostyce_zaburzen_wieku_rozwojowego
[short_name] => Zastosowanie metod cytogenetycznych w diagnostyce ...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[131] => Array
(
[id] => 131
[site_id] => 1
[status_id] => 5
[name] => Typy dziedziczenia chorób genetycznych i poradnictwo genetyczne
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/131/posterw_erze.png
[video] => resources/data/material/131/kutkowska_typy_dziedziczenia.mp4
[content] =>
[ext] => Array
(
[linked] => Array
(
[0] => Array
(
[id] =>
)
)
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n.med. Anna Kutkowska-Kaźmierczak
)
[authors_data] => Array
(
[0] => Array
(
[id] => 64
[site_id] => 1
[status_id] => 5
[name] => dr n.med. Anna Kutkowska-Kaźmierczak
[firstname] => Anna
[lastname] => Kutkowska-Kaźmierczak
[title] => dr n.med.
[affiliation] => Zakład Genetyki Klinicznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 64-anna_kutkowska_kazmierczak
[url] => eksperci/64-anna_kutkowska_kazmierczak
)
)
[authors_ids] => Array
(
[0] => 64
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 131-typy_dziedziczenia_chorob_genetycznych_i_poradnictwo_genetyczne
[url] => wideo/131-typy_dziedziczenia_chorob_genetycznych_i_poradnictwo_genetyczne
[short_name] => Typy dziedziczenia chorób genetycznych i poradnict...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[133] => Array
(
[id] => 133
[site_id] => 1
[status_id] => 5
[name] => Diagnostyka molekularna genetycznie uwarunkowanego zapalenia trzustki
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/133/posterw_erze.png
[video] => resources/data/material/133/rygiel_diagn_molek_genet_uwarunk_zapalenia_trzustki.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab. n. med., prof. IMID Agnieszka Rygiel
)
[authors_data] => Array
(
[0] => Array
(
[id] => 65
[site_id] => 1
[status_id] => 5
[name] => dr hab. n. med., prof. IMID Agnieszka Rygiel
[firstname] => Agnieszka
[lastname] => Rygiel
[title] => dr hab. n. med., prof. IMID
[affiliation] => Zakład Genetyki Medycznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 65-agnieszka_rygiel
[url] => eksperci/65-agnieszka_rygiel
)
)
[authors_ids] => Array
(
[0] => 65
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 133-diagnostyka_molekularna_genetycznie_uwarunkowanego_zapalenia_trzustki
[url] => wideo/133-diagnostyka_molekularna_genetycznie_uwarunkowanego_zapalenia_trzustki
[short_name] => Diagnostyka molekularna genetycznie uwarunkowanego...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[134] => Array
(
[id] => 134
[site_id] => 1
[status_id] => 5
[name] => Postępowanie diagnostyczne w niepełnosprawności intelektualnej
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/134/posterw_erze.png
[video] => resources/data/material/134/postepowanie_diagnostyczne_w_niepelnosprawnosci_intelektualnej_brak_nazwy_kursu.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Magdalena Bartnik-Głaska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 66
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Magdalena Bartnik-Głaska
[firstname] => Magdalena
[lastname] => Bartnik-Głaska
[title] => dr n. med.
[affiliation] => Zakład Genetyki Medycznej, Instytut Matki i Dziecka, Warszawa
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 66-magdalena_bartnik_glaska
[url] => eksperci/66-magdalena_bartnik_glaska
)
)
[authors_ids] => Array
(
[0] => 66
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 134-postepowanie_diagnostyczne_w_niepelnosprawnosci_intelektualnej
[url] => wideo/134-postepowanie_diagnostyczne_w_niepelnosprawnosci_intelektualnej
[short_name] => Postępowanie diagnostyczne w niepełnosprawności in...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[135] => Array
(
[id] => 135
[site_id] => 1
[status_id] => 5
[name] => Zespoły mikrodelecyjne i mikroduplikacyjne
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/135/posterw_erze.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n.med. Anna Kutkowska-Kaźmierczak
)
[authors_data] => Array
(
[0] => Array
(
[id] => 64
[site_id] => 1
[status_id] => 5
[name] => dr n.med. Anna Kutkowska-Kaźmierczak
[firstname] => Anna
[lastname] => Kutkowska-Kaźmierczak
[title] => dr n.med.
[affiliation] => Zakład Genetyki Klinicznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 64-anna_kutkowska_kazmierczak
[url] => eksperci/64-anna_kutkowska_kazmierczak
)
)
[authors_ids] => Array
(
[0] => 64
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 9
[3] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 135-zespoly_mikrodelecyjne_i_mikroduplikacyjne
[url] => wideo/135-zespoly_mikrodelecyjne_i_mikroduplikacyjne
[short_name] => Zespoły mikrodelecyjne i mikroduplikacyjne
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[9] => Array
(
[id] => 9
[site_id] => 1
[status_id] => 5
[name] => zespół delecji
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 9-zespol_delecji
[url] => /9-zespol_delecji
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[136] => Array
(
[id] => 136
[site_id] => 1
[status_id] => 5
[name] => „Już” znane zespoły mikrodelecji/mikroduplikacji w diagnostyce zaburzeń wieku rozwojowego
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/136/posterw_erze.png
[video] => resources/data/material/136/kedzior_juz_znane_zespoly_mikrodelecji.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr Marta Kędzior
)
[authors_data] => Array
(
[0] => Array
(
[id] => 67
[site_id] => 1
[status_id] => 5
[name] => dr Marta Kędzior
[firstname] => Marta
[lastname] => Kędzior
[title] => dr
[affiliation] => Zakład Genetyki Medycznej, IMiD
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 67-marta_kedzior
[url] => eksperci/67-marta_kedzior
)
)
[authors_ids] => Array
(
[0] => 67
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 9
[3] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 136-juz_znane_zespoly_mikrodelecjimikroduplikacji_w_diagnostyce_zaburzen_wieku_rozwojowego
[url] => wideo/136-juz_znane_zespoly_mikrodelecjimikroduplikacji_w_diagnostyce_zaburzen_wieku_rozwojowego
[short_name] => „Już” znane zespoły mikrodelecji/mikroduplikacji w...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[9] => Array
(
[id] => 9
[site_id] => 1
[status_id] => 5
[name] => zespół delecji
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 9-zespol_delecji
[url] => /9-zespol_delecji
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[137] => Array
(
[id] => 137
[site_id] => 1
[status_id] => 5
[name] => Genetyczne uwarunkowania kraniostenoz
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/137/posterw_erze.png
[video] => resources/data/material/137/kutkowska_genetycz_uwarunkow_kraniostenoz.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n.med. Anna Kutkowska-Kaźmierczak
)
[authors_data] => Array
(
[0] => Array
(
[id] => 64
[site_id] => 1
[status_id] => 5
[name] => dr n.med. Anna Kutkowska-Kaźmierczak
[firstname] => Anna
[lastname] => Kutkowska-Kaźmierczak
[title] => dr n.med.
[affiliation] => Zakład Genetyki Klinicznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 64-anna_kutkowska_kazmierczak
[url] => eksperci/64-anna_kutkowska_kazmierczak
)
)
[authors_ids] => Array
(
[0] => 64
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 137-genetyczne_uwarunkowania_kraniostenoz
[url] => wideo/137-genetyczne_uwarunkowania_kraniostenoz
[short_name] => Genetyczne uwarunkowania kraniostenoz
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[138] => Array
(
[id] => 138
[site_id] => 1
[status_id] => 5
[name] => Niepełnosprawność intelektualna – podłoże genetyczne
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/138/posterw_erze.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n.med. Anna Kutkowska-Kaźmierczak
)
[authors_data] => Array
(
[0] => Array
(
[id] => 64
[site_id] => 1
[status_id] => 5
[name] => dr n.med. Anna Kutkowska-Kaźmierczak
[firstname] => Anna
[lastname] => Kutkowska-Kaźmierczak
[title] => dr n.med.
[affiliation] => Zakład Genetyki Klinicznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 64-anna_kutkowska_kazmierczak
[url] => eksperci/64-anna_kutkowska_kazmierczak
)
)
[authors_ids] => Array
(
[0] => 64
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 138-niepelnosprawnosc_intelektualna__podloze_genetyczne
[url] => wideo/138-niepelnosprawnosc_intelektualna__podloze_genetyczne
[short_name] => Niepełnosprawność intelektualna – podłoże genetycz...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[139] => Array
(
[id] => 139
[site_id] => 1
[status_id] => 5
[name] => Niedosłuch w erze genomowej - możliwości diagnostyczne
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/139/posterw_erze.png
[video] => resources/data/material/139/niepokoj_niedosluch.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Niepokój
)
[authors_data] => Array
(
[0] => Array
(
[id] => 68
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Niepokój
[firstname] => Katarzyna
[lastname] => Niepokój
[title] => dr n. med.
[affiliation] => Zakład Genetyki Medycznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 68-katarzyna_niepokoj
[url] => eksperci/68-katarzyna_niepokoj
)
)
[authors_ids] => Array
(
[0] => 68
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 139-niedosluch_w_erze_genomowej___mozliwosci_diagnostyczne
[url] => wideo/139-niedosluch_w_erze_genomowej___mozliwosci_diagnostyczne
[short_name] => Niedosłuch w erze genomowej - możliwości diagnosty...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[140] => Array
(
[id] => 140
[site_id] => 1
[status_id] => 5
[name] => Zastosowanie sekwencjonowania w diagnostyce molekularnej
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/140/posterw_erze.png
[video] => resources/data/material/140/wertheim_zastosowanie_sekwencjonowania_w_diagnostyce_molekularnej.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 140-zastosowanie_sekwencjonowania_w_diagnostyce_molekularnej
[url] => wideo/140-zastosowanie_sekwencjonowania_w_diagnostyce_molekularnej
[short_name] => Zastosowanie sekwencjonowania w diagnostyce moleku...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[141] => Array
(
[id] => 141
[site_id] => 1
[status_id] => 5
[name] => Interpretacja wyników badań molekularnych na przykładzie genetycznie uwarunkowanych chorób skóry
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/141/posterw_erze.png
[video] => resources/data/material/141/interpretacja_wynikow_badan_molekularnych_na_przykladzie_genetycznie_uwarunkowanych_chorob_skory_wertheimtyssarowska_12_min_uciety_poczatek_zdania.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 141-interpretacja_wynikow_badan_molekularnych_na_przykladzie_genetycznie_uwarunkowanych_chorob_skory
[url] => wideo/141-interpretacja_wynikow_badan_molekularnych_na_przykladzie_genetycznie_uwarunkowanych_chorob_skory
[short_name] => Interpretacja wyników badań molekularnych na przyk...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[142] => Array
(
[id] => 142
[site_id] => 1
[status_id] => 5
[name] => Diagnostyka mukowiscydozy i chorób CFTR zależnych 30 lat po odkryciu genu CFTR
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/142/posterw_erze.png
[video] => resources/data/material/142/wertheim_diagnostyka_mukowiscydzy.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 142-diagnostyka_mukowiscydozy_i_chorob_cftr_zaleznych_30_lat_po_odkryciu_genu_cftr
[url] => wideo/142-diagnostyka_mukowiscydozy_i_chorob_cftr_zaleznych_30_lat_po_odkryciu_genu_cftr
[short_name] => Diagnostyka mukowiscydozy i chorób CFTR zależnych ...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[143] => Array
(
[id] => 143
[site_id] => 1
[status_id] => 5
[name] => Badania molekularne w diagnostyce galaktozemii
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/143/posterw_erze.png
[video] => resources/data/material/143/wertheim_bad_molek_w_diagnost_galaktozemii.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 143-badania_molekularne_w_diagnostyce_galaktozemii
[url] => wideo/143-badania_molekularne_w_diagnostyce_galaktozemii
[short_name] => Badania molekularne w diagnostyce galaktozemii
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
)
)
[sort] => 1
[status_code] => active
[authors] => Array
(
[0] => dr hab. n. med., prof. IMID Agnieszka Rygiel
)
[authors_data] => Array
(
[0] => Array
(
[id] => 65
[site_id] => 1
[status_id] => 5
[name] => dr hab. n. med., prof. IMID Agnieszka Rygiel
[firstname] => Agnieszka
[lastname] => Rygiel
[title] => dr hab. n. med., prof. IMID
[affiliation] => Zakład Genetyki Medycznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 65-agnieszka_rygiel
[url] => eksperci/65-agnieszka_rygiel
)
)
[authors_ids] => Array
(
[0] => 65
)
[topics] => Array
(
[0] => 2
[1] => 4
[2] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 132-diagnostyka_wrodzonych_wad_metabolizmu
[url] => wideo/132-diagnostyka_wrodzonych_wad_metabolizmu
[short_name] => Diagnostyka wrodzonych wad metabolizmu
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[2] => Array
(
[id] => 2
[site_id] => 1
[status_id] => 5
[name] => metabolizm
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 2-metabolizm
[url] => /2-metabolizm
)
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
[logotypy] => Array
(
)
[pliki] => Array
(
[101] => Array
(
[id] => 101
[site_id] => 1
[status_id] => 5
[entity_key] => material
[entity_id] => 132
[name] => Diagnostyka wrodzonych wad metabolizmu
[file] => resources/data/pliki/material/132/diagnostyka_molekularna_chorob_metabolicznych.pdf
[sort] => 98
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
[133] => Array
(
[id] => 133
[name] => Diagnostyka molekularna genetycznie uwarunkowanego zapalenia trzustki
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/133/posterw_erze.png
[video] => resources/data/material/133/rygiel_diagn_molek_genet_uwarunk_zapalenia_trzustki.mp4
[content] =>
[ext] => Array
(
[files_header] =>
[linked] => Array
(
[128] => Array
(
[id] => 128
[site_id] => 1
[status_id] => 5
[name] => RASopatie – diagnostyka molekularna wrodzonych zaburzeń rozwojowych
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/128/posterw_erze.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med., prof IMiD Monika Gos
)
[authors_data] => Array
(
[0] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => dr n. med., prof IMiD Monika Gos
[firstname] => Monika
[lastname] => Gos
[title] => dr n. med., prof IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-monika_gos
[url] => eksperci/13-monika_gos
)
)
[authors_ids] => Array
(
[0] => 13
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 128-rasopatie__diagnostyka_molekularna_wrodzonych_zaburzen_rozwojowych
[url] => wideo/128-rasopatie__diagnostyka_molekularna_wrodzonych_zaburzen_rozwojowych
[short_name] => RASopatie – diagnostyka molekularna wrodzonych zab...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[129] => Array
(
[id] => 129
[site_id] => 1
[status_id] => 5
[name] => Zastosowanie metod cytogenetycznych w diagnostyce zaburzeń wieku rozwojowego
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/129/posterw_erze.png
[video] => resources/data/material/129/wisniowiecka_zastosowanie_cytogenetyki.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Barbara Wiśniowiecka-Kowalnik
)
[authors_data] => Array
(
[0] => Array
(
[id] => 7
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Barbara Wiśniowiecka-Kowalnik
[firstname] => Barbara
[lastname] => Wiśniowiecka-Kowalnik
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 7-barbara_wisniowiecka_kowalnik
[url] => eksperci/7-barbara_wisniowiecka_kowalnik
)
)
[authors_ids] => Array
(
[0] => 7
)
[topics] => Array
(
[0] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 129-zastosowanie_metod_cytogenetycznych_w_diagnostyce_zaburzen_wieku_rozwojowego
[url] => wideo/129-zastosowanie_metod_cytogenetycznych_w_diagnostyce_zaburzen_wieku_rozwojowego
[short_name] => Zastosowanie metod cytogenetycznych w diagnostyce ...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[131] => Array
(
[id] => 131
[site_id] => 1
[status_id] => 5
[name] => Typy dziedziczenia chorób genetycznych i poradnictwo genetyczne
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/131/posterw_erze.png
[video] => resources/data/material/131/kutkowska_typy_dziedziczenia.mp4
[content] =>
[ext] => Array
(
[linked] => Array
(
[0] => Array
(
[id] =>
)
)
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n.med. Anna Kutkowska-Kaźmierczak
)
[authors_data] => Array
(
[0] => Array
(
[id] => 64
[site_id] => 1
[status_id] => 5
[name] => dr n.med. Anna Kutkowska-Kaźmierczak
[firstname] => Anna
[lastname] => Kutkowska-Kaźmierczak
[title] => dr n.med.
[affiliation] => Zakład Genetyki Klinicznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 64-anna_kutkowska_kazmierczak
[url] => eksperci/64-anna_kutkowska_kazmierczak
)
)
[authors_ids] => Array
(
[0] => 64
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 131-typy_dziedziczenia_chorob_genetycznych_i_poradnictwo_genetyczne
[url] => wideo/131-typy_dziedziczenia_chorob_genetycznych_i_poradnictwo_genetyczne
[short_name] => Typy dziedziczenia chorób genetycznych i poradnict...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[132] => Array
(
[id] => 132
[site_id] => 1
[status_id] => 5
[name] => Diagnostyka wrodzonych wad metabolizmu
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/132/posterw_erze.png
[video] => resources/data/material/132/rygiel_diagnostyka_wrodzonych_wad_metabolizmu.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab. n. med., prof. IMID Agnieszka Rygiel
)
[authors_data] => Array
(
[0] => Array
(
[id] => 65
[site_id] => 1
[status_id] => 5
[name] => dr hab. n. med., prof. IMID Agnieszka Rygiel
[firstname] => Agnieszka
[lastname] => Rygiel
[title] => dr hab. n. med., prof. IMID
[affiliation] => Zakład Genetyki Medycznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 65-agnieszka_rygiel
[url] => eksperci/65-agnieszka_rygiel
)
)
[authors_ids] => Array
(
[0] => 65
)
[topics] => Array
(
[0] => 2
[1] => 4
[2] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 132-diagnostyka_wrodzonych_wad_metabolizmu
[url] => wideo/132-diagnostyka_wrodzonych_wad_metabolizmu
[short_name] => Diagnostyka wrodzonych wad metabolizmu
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[2] => Array
(
[id] => 2
[site_id] => 1
[status_id] => 5
[name] => metabolizm
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 2-metabolizm
[url] => /2-metabolizm
)
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[134] => Array
(
[id] => 134
[site_id] => 1
[status_id] => 5
[name] => Postępowanie diagnostyczne w niepełnosprawności intelektualnej
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/134/posterw_erze.png
[video] => resources/data/material/134/postepowanie_diagnostyczne_w_niepelnosprawnosci_intelektualnej_brak_nazwy_kursu.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Magdalena Bartnik-Głaska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 66
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Magdalena Bartnik-Głaska
[firstname] => Magdalena
[lastname] => Bartnik-Głaska
[title] => dr n. med.
[affiliation] => Zakład Genetyki Medycznej, Instytut Matki i Dziecka, Warszawa
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 66-magdalena_bartnik_glaska
[url] => eksperci/66-magdalena_bartnik_glaska
)
)
[authors_ids] => Array
(
[0] => 66
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 134-postepowanie_diagnostyczne_w_niepelnosprawnosci_intelektualnej
[url] => wideo/134-postepowanie_diagnostyczne_w_niepelnosprawnosci_intelektualnej
[short_name] => Postępowanie diagnostyczne w niepełnosprawności in...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[135] => Array
(
[id] => 135
[site_id] => 1
[status_id] => 5
[name] => Zespoły mikrodelecyjne i mikroduplikacyjne
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/135/posterw_erze.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n.med. Anna Kutkowska-Kaźmierczak
)
[authors_data] => Array
(
[0] => Array
(
[id] => 64
[site_id] => 1
[status_id] => 5
[name] => dr n.med. Anna Kutkowska-Kaźmierczak
[firstname] => Anna
[lastname] => Kutkowska-Kaźmierczak
[title] => dr n.med.
[affiliation] => Zakład Genetyki Klinicznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 64-anna_kutkowska_kazmierczak
[url] => eksperci/64-anna_kutkowska_kazmierczak
)
)
[authors_ids] => Array
(
[0] => 64
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 9
[3] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 135-zespoly_mikrodelecyjne_i_mikroduplikacyjne
[url] => wideo/135-zespoly_mikrodelecyjne_i_mikroduplikacyjne
[short_name] => Zespoły mikrodelecyjne i mikroduplikacyjne
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[9] => Array
(
[id] => 9
[site_id] => 1
[status_id] => 5
[name] => zespół delecji
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 9-zespol_delecji
[url] => /9-zespol_delecji
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[136] => Array
(
[id] => 136
[site_id] => 1
[status_id] => 5
[name] => „Już” znane zespoły mikrodelecji/mikroduplikacji w diagnostyce zaburzeń wieku rozwojowego
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/136/posterw_erze.png
[video] => resources/data/material/136/kedzior_juz_znane_zespoly_mikrodelecji.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr Marta Kędzior
)
[authors_data] => Array
(
[0] => Array
(
[id] => 67
[site_id] => 1
[status_id] => 5
[name] => dr Marta Kędzior
[firstname] => Marta
[lastname] => Kędzior
[title] => dr
[affiliation] => Zakład Genetyki Medycznej, IMiD
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 67-marta_kedzior
[url] => eksperci/67-marta_kedzior
)
)
[authors_ids] => Array
(
[0] => 67
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 9
[3] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 136-juz_znane_zespoly_mikrodelecjimikroduplikacji_w_diagnostyce_zaburzen_wieku_rozwojowego
[url] => wideo/136-juz_znane_zespoly_mikrodelecjimikroduplikacji_w_diagnostyce_zaburzen_wieku_rozwojowego
[short_name] => „Już” znane zespoły mikrodelecji/mikroduplikacji w...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[9] => Array
(
[id] => 9
[site_id] => 1
[status_id] => 5
[name] => zespół delecji
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 9-zespol_delecji
[url] => /9-zespol_delecji
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[137] => Array
(
[id] => 137
[site_id] => 1
[status_id] => 5
[name] => Genetyczne uwarunkowania kraniostenoz
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/137/posterw_erze.png
[video] => resources/data/material/137/kutkowska_genetycz_uwarunkow_kraniostenoz.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n.med. Anna Kutkowska-Kaźmierczak
)
[authors_data] => Array
(
[0] => Array
(
[id] => 64
[site_id] => 1
[status_id] => 5
[name] => dr n.med. Anna Kutkowska-Kaźmierczak
[firstname] => Anna
[lastname] => Kutkowska-Kaźmierczak
[title] => dr n.med.
[affiliation] => Zakład Genetyki Klinicznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 64-anna_kutkowska_kazmierczak
[url] => eksperci/64-anna_kutkowska_kazmierczak
)
)
[authors_ids] => Array
(
[0] => 64
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 137-genetyczne_uwarunkowania_kraniostenoz
[url] => wideo/137-genetyczne_uwarunkowania_kraniostenoz
[short_name] => Genetyczne uwarunkowania kraniostenoz
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[138] => Array
(
[id] => 138
[site_id] => 1
[status_id] => 5
[name] => Niepełnosprawność intelektualna – podłoże genetyczne
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/138/posterw_erze.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n.med. Anna Kutkowska-Kaźmierczak
)
[authors_data] => Array
(
[0] => Array
(
[id] => 64
[site_id] => 1
[status_id] => 5
[name] => dr n.med. Anna Kutkowska-Kaźmierczak
[firstname] => Anna
[lastname] => Kutkowska-Kaźmierczak
[title] => dr n.med.
[affiliation] => Zakład Genetyki Klinicznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 64-anna_kutkowska_kazmierczak
[url] => eksperci/64-anna_kutkowska_kazmierczak
)
)
[authors_ids] => Array
(
[0] => 64
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 138-niepelnosprawnosc_intelektualna__podloze_genetyczne
[url] => wideo/138-niepelnosprawnosc_intelektualna__podloze_genetyczne
[short_name] => Niepełnosprawność intelektualna – podłoże genetycz...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[139] => Array
(
[id] => 139
[site_id] => 1
[status_id] => 5
[name] => Niedosłuch w erze genomowej - możliwości diagnostyczne
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/139/posterw_erze.png
[video] => resources/data/material/139/niepokoj_niedosluch.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Niepokój
)
[authors_data] => Array
(
[0] => Array
(
[id] => 68
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Niepokój
[firstname] => Katarzyna
[lastname] => Niepokój
[title] => dr n. med.
[affiliation] => Zakład Genetyki Medycznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 68-katarzyna_niepokoj
[url] => eksperci/68-katarzyna_niepokoj
)
)
[authors_ids] => Array
(
[0] => 68
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 139-niedosluch_w_erze_genomowej___mozliwosci_diagnostyczne
[url] => wideo/139-niedosluch_w_erze_genomowej___mozliwosci_diagnostyczne
[short_name] => Niedosłuch w erze genomowej - możliwości diagnosty...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[140] => Array
(
[id] => 140
[site_id] => 1
[status_id] => 5
[name] => Zastosowanie sekwencjonowania w diagnostyce molekularnej
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/140/posterw_erze.png
[video] => resources/data/material/140/wertheim_zastosowanie_sekwencjonowania_w_diagnostyce_molekularnej.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 140-zastosowanie_sekwencjonowania_w_diagnostyce_molekularnej
[url] => wideo/140-zastosowanie_sekwencjonowania_w_diagnostyce_molekularnej
[short_name] => Zastosowanie sekwencjonowania w diagnostyce moleku...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[141] => Array
(
[id] => 141
[site_id] => 1
[status_id] => 5
[name] => Interpretacja wyników badań molekularnych na przykładzie genetycznie uwarunkowanych chorób skóry
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/141/posterw_erze.png
[video] => resources/data/material/141/interpretacja_wynikow_badan_molekularnych_na_przykladzie_genetycznie_uwarunkowanych_chorob_skory_wertheimtyssarowska_12_min_uciety_poczatek_zdania.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 141-interpretacja_wynikow_badan_molekularnych_na_przykladzie_genetycznie_uwarunkowanych_chorob_skory
[url] => wideo/141-interpretacja_wynikow_badan_molekularnych_na_przykladzie_genetycznie_uwarunkowanych_chorob_skory
[short_name] => Interpretacja wyników badań molekularnych na przyk...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[142] => Array
(
[id] => 142
[site_id] => 1
[status_id] => 5
[name] => Diagnostyka mukowiscydozy i chorób CFTR zależnych 30 lat po odkryciu genu CFTR
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/142/posterw_erze.png
[video] => resources/data/material/142/wertheim_diagnostyka_mukowiscydzy.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 142-diagnostyka_mukowiscydozy_i_chorob_cftr_zaleznych_30_lat_po_odkryciu_genu_cftr
[url] => wideo/142-diagnostyka_mukowiscydozy_i_chorob_cftr_zaleznych_30_lat_po_odkryciu_genu_cftr
[short_name] => Diagnostyka mukowiscydozy i chorób CFTR zależnych ...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[143] => Array
(
[id] => 143
[site_id] => 1
[status_id] => 5
[name] => Badania molekularne w diagnostyce galaktozemii
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/143/posterw_erze.png
[video] => resources/data/material/143/wertheim_bad_molek_w_diagnost_galaktozemii.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 143-badania_molekularne_w_diagnostyce_galaktozemii
[url] => wideo/143-badania_molekularne_w_diagnostyce_galaktozemii
[short_name] => Badania molekularne w diagnostyce galaktozemii
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
)
)
[sort] => 1
[status_code] => active
[authors] => Array
(
[0] => dr hab. n. med., prof. IMID Agnieszka Rygiel
)
[authors_data] => Array
(
[0] => Array
(
[id] => 65
[site_id] => 1
[status_id] => 5
[name] => dr hab. n. med., prof. IMID Agnieszka Rygiel
[firstname] => Agnieszka
[lastname] => Rygiel
[title] => dr hab. n. med., prof. IMID
[affiliation] => Zakład Genetyki Medycznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 65-agnieszka_rygiel
[url] => eksperci/65-agnieszka_rygiel
)
)
[authors_ids] => Array
(
[0] => 65
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 133-diagnostyka_molekularna_genetycznie_uwarunkowanego_zapalenia_trzustki
[url] => wideo/133-diagnostyka_molekularna_genetycznie_uwarunkowanego_zapalenia_trzustki
[short_name] => Diagnostyka molekularna genetycznie uwarunkowanego...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
[logotypy] => Array
(
)
[pliki] => Array
(
[102] => Array
(
[id] => 102
[site_id] => 1
[status_id] => 5
[entity_key] => material
[entity_id] => 133
[name] => Diagnostyka molekularna genetycznie uwarunkowanego zapalenia trzustki
[file] => resources/data/pliki/material/133/diagnostyka_molekularna_genetycznie_uwarunkowanego_zapalenia_trzustki.pdf
[sort] => 99
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
[134] => Array
(
[id] => 134
[name] => Postępowanie diagnostyczne w niepełnosprawności intelektualnej
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/134/posterw_erze.png
[video] => resources/data/material/134/postepowanie_diagnostyczne_w_niepelnosprawnosci_intelektualnej_brak_nazwy_kursu.mp4
[content] =>
[ext] => Array
(
[files_header] =>
[linked] => Array
(
[128] => Array
(
[id] => 128
[site_id] => 1
[status_id] => 5
[name] => RASopatie – diagnostyka molekularna wrodzonych zaburzeń rozwojowych
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/128/posterw_erze.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med., prof IMiD Monika Gos
)
[authors_data] => Array
(
[0] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => dr n. med., prof IMiD Monika Gos
[firstname] => Monika
[lastname] => Gos
[title] => dr n. med., prof IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-monika_gos
[url] => eksperci/13-monika_gos
)
)
[authors_ids] => Array
(
[0] => 13
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 128-rasopatie__diagnostyka_molekularna_wrodzonych_zaburzen_rozwojowych
[url] => wideo/128-rasopatie__diagnostyka_molekularna_wrodzonych_zaburzen_rozwojowych
[short_name] => RASopatie – diagnostyka molekularna wrodzonych zab...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[129] => Array
(
[id] => 129
[site_id] => 1
[status_id] => 5
[name] => Zastosowanie metod cytogenetycznych w diagnostyce zaburzeń wieku rozwojowego
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/129/posterw_erze.png
[video] => resources/data/material/129/wisniowiecka_zastosowanie_cytogenetyki.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Barbara Wiśniowiecka-Kowalnik
)
[authors_data] => Array
(
[0] => Array
(
[id] => 7
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Barbara Wiśniowiecka-Kowalnik
[firstname] => Barbara
[lastname] => Wiśniowiecka-Kowalnik
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 7-barbara_wisniowiecka_kowalnik
[url] => eksperci/7-barbara_wisniowiecka_kowalnik
)
)
[authors_ids] => Array
(
[0] => 7
)
[topics] => Array
(
[0] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 129-zastosowanie_metod_cytogenetycznych_w_diagnostyce_zaburzen_wieku_rozwojowego
[url] => wideo/129-zastosowanie_metod_cytogenetycznych_w_diagnostyce_zaburzen_wieku_rozwojowego
[short_name] => Zastosowanie metod cytogenetycznych w diagnostyce ...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[131] => Array
(
[id] => 131
[site_id] => 1
[status_id] => 5
[name] => Typy dziedziczenia chorób genetycznych i poradnictwo genetyczne
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/131/posterw_erze.png
[video] => resources/data/material/131/kutkowska_typy_dziedziczenia.mp4
[content] =>
[ext] => Array
(
[linked] => Array
(
[0] => Array
(
[id] =>
)
)
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n.med. Anna Kutkowska-Kaźmierczak
)
[authors_data] => Array
(
[0] => Array
(
[id] => 64
[site_id] => 1
[status_id] => 5
[name] => dr n.med. Anna Kutkowska-Kaźmierczak
[firstname] => Anna
[lastname] => Kutkowska-Kaźmierczak
[title] => dr n.med.
[affiliation] => Zakład Genetyki Klinicznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 64-anna_kutkowska_kazmierczak
[url] => eksperci/64-anna_kutkowska_kazmierczak
)
)
[authors_ids] => Array
(
[0] => 64
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 131-typy_dziedziczenia_chorob_genetycznych_i_poradnictwo_genetyczne
[url] => wideo/131-typy_dziedziczenia_chorob_genetycznych_i_poradnictwo_genetyczne
[short_name] => Typy dziedziczenia chorób genetycznych i poradnict...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[132] => Array
(
[id] => 132
[site_id] => 1
[status_id] => 5
[name] => Diagnostyka wrodzonych wad metabolizmu
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/132/posterw_erze.png
[video] => resources/data/material/132/rygiel_diagnostyka_wrodzonych_wad_metabolizmu.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab. n. med., prof. IMID Agnieszka Rygiel
)
[authors_data] => Array
(
[0] => Array
(
[id] => 65
[site_id] => 1
[status_id] => 5
[name] => dr hab. n. med., prof. IMID Agnieszka Rygiel
[firstname] => Agnieszka
[lastname] => Rygiel
[title] => dr hab. n. med., prof. IMID
[affiliation] => Zakład Genetyki Medycznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 65-agnieszka_rygiel
[url] => eksperci/65-agnieszka_rygiel
)
)
[authors_ids] => Array
(
[0] => 65
)
[topics] => Array
(
[0] => 2
[1] => 4
[2] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 132-diagnostyka_wrodzonych_wad_metabolizmu
[url] => wideo/132-diagnostyka_wrodzonych_wad_metabolizmu
[short_name] => Diagnostyka wrodzonych wad metabolizmu
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[2] => Array
(
[id] => 2
[site_id] => 1
[status_id] => 5
[name] => metabolizm
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 2-metabolizm
[url] => /2-metabolizm
)
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[133] => Array
(
[id] => 133
[site_id] => 1
[status_id] => 5
[name] => Diagnostyka molekularna genetycznie uwarunkowanego zapalenia trzustki
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/133/posterw_erze.png
[video] => resources/data/material/133/rygiel_diagn_molek_genet_uwarunk_zapalenia_trzustki.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab. n. med., prof. IMID Agnieszka Rygiel
)
[authors_data] => Array
(
[0] => Array
(
[id] => 65
[site_id] => 1
[status_id] => 5
[name] => dr hab. n. med., prof. IMID Agnieszka Rygiel
[firstname] => Agnieszka
[lastname] => Rygiel
[title] => dr hab. n. med., prof. IMID
[affiliation] => Zakład Genetyki Medycznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 65-agnieszka_rygiel
[url] => eksperci/65-agnieszka_rygiel
)
)
[authors_ids] => Array
(
[0] => 65
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 133-diagnostyka_molekularna_genetycznie_uwarunkowanego_zapalenia_trzustki
[url] => wideo/133-diagnostyka_molekularna_genetycznie_uwarunkowanego_zapalenia_trzustki
[short_name] => Diagnostyka molekularna genetycznie uwarunkowanego...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[135] => Array
(
[id] => 135
[site_id] => 1
[status_id] => 5
[name] => Zespoły mikrodelecyjne i mikroduplikacyjne
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/135/posterw_erze.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n.med. Anna Kutkowska-Kaźmierczak
)
[authors_data] => Array
(
[0] => Array
(
[id] => 64
[site_id] => 1
[status_id] => 5
[name] => dr n.med. Anna Kutkowska-Kaźmierczak
[firstname] => Anna
[lastname] => Kutkowska-Kaźmierczak
[title] => dr n.med.
[affiliation] => Zakład Genetyki Klinicznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 64-anna_kutkowska_kazmierczak
[url] => eksperci/64-anna_kutkowska_kazmierczak
)
)
[authors_ids] => Array
(
[0] => 64
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 9
[3] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 135-zespoly_mikrodelecyjne_i_mikroduplikacyjne
[url] => wideo/135-zespoly_mikrodelecyjne_i_mikroduplikacyjne
[short_name] => Zespoły mikrodelecyjne i mikroduplikacyjne
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[9] => Array
(
[id] => 9
[site_id] => 1
[status_id] => 5
[name] => zespół delecji
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 9-zespol_delecji
[url] => /9-zespol_delecji
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[136] => Array
(
[id] => 136
[site_id] => 1
[status_id] => 5
[name] => „Już” znane zespoły mikrodelecji/mikroduplikacji w diagnostyce zaburzeń wieku rozwojowego
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/136/posterw_erze.png
[video] => resources/data/material/136/kedzior_juz_znane_zespoly_mikrodelecji.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr Marta Kędzior
)
[authors_data] => Array
(
[0] => Array
(
[id] => 67
[site_id] => 1
[status_id] => 5
[name] => dr Marta Kędzior
[firstname] => Marta
[lastname] => Kędzior
[title] => dr
[affiliation] => Zakład Genetyki Medycznej, IMiD
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 67-marta_kedzior
[url] => eksperci/67-marta_kedzior
)
)
[authors_ids] => Array
(
[0] => 67
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 9
[3] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 136-juz_znane_zespoly_mikrodelecjimikroduplikacji_w_diagnostyce_zaburzen_wieku_rozwojowego
[url] => wideo/136-juz_znane_zespoly_mikrodelecjimikroduplikacji_w_diagnostyce_zaburzen_wieku_rozwojowego
[short_name] => „Już” znane zespoły mikrodelecji/mikroduplikacji w...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[9] => Array
(
[id] => 9
[site_id] => 1
[status_id] => 5
[name] => zespół delecji
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 9-zespol_delecji
[url] => /9-zespol_delecji
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[137] => Array
(
[id] => 137
[site_id] => 1
[status_id] => 5
[name] => Genetyczne uwarunkowania kraniostenoz
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/137/posterw_erze.png
[video] => resources/data/material/137/kutkowska_genetycz_uwarunkow_kraniostenoz.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n.med. Anna Kutkowska-Kaźmierczak
)
[authors_data] => Array
(
[0] => Array
(
[id] => 64
[site_id] => 1
[status_id] => 5
[name] => dr n.med. Anna Kutkowska-Kaźmierczak
[firstname] => Anna
[lastname] => Kutkowska-Kaźmierczak
[title] => dr n.med.
[affiliation] => Zakład Genetyki Klinicznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 64-anna_kutkowska_kazmierczak
[url] => eksperci/64-anna_kutkowska_kazmierczak
)
)
[authors_ids] => Array
(
[0] => 64
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 137-genetyczne_uwarunkowania_kraniostenoz
[url] => wideo/137-genetyczne_uwarunkowania_kraniostenoz
[short_name] => Genetyczne uwarunkowania kraniostenoz
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[138] => Array
(
[id] => 138
[site_id] => 1
[status_id] => 5
[name] => Niepełnosprawność intelektualna – podłoże genetyczne
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/138/posterw_erze.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n.med. Anna Kutkowska-Kaźmierczak
)
[authors_data] => Array
(
[0] => Array
(
[id] => 64
[site_id] => 1
[status_id] => 5
[name] => dr n.med. Anna Kutkowska-Kaźmierczak
[firstname] => Anna
[lastname] => Kutkowska-Kaźmierczak
[title] => dr n.med.
[affiliation] => Zakład Genetyki Klinicznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 64-anna_kutkowska_kazmierczak
[url] => eksperci/64-anna_kutkowska_kazmierczak
)
)
[authors_ids] => Array
(
[0] => 64
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 138-niepelnosprawnosc_intelektualna__podloze_genetyczne
[url] => wideo/138-niepelnosprawnosc_intelektualna__podloze_genetyczne
[short_name] => Niepełnosprawność intelektualna – podłoże genetycz...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[139] => Array
(
[id] => 139
[site_id] => 1
[status_id] => 5
[name] => Niedosłuch w erze genomowej - możliwości diagnostyczne
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/139/posterw_erze.png
[video] => resources/data/material/139/niepokoj_niedosluch.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Niepokój
)
[authors_data] => Array
(
[0] => Array
(
[id] => 68
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Niepokój
[firstname] => Katarzyna
[lastname] => Niepokój
[title] => dr n. med.
[affiliation] => Zakład Genetyki Medycznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 68-katarzyna_niepokoj
[url] => eksperci/68-katarzyna_niepokoj
)
)
[authors_ids] => Array
(
[0] => 68
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 139-niedosluch_w_erze_genomowej___mozliwosci_diagnostyczne
[url] => wideo/139-niedosluch_w_erze_genomowej___mozliwosci_diagnostyczne
[short_name] => Niedosłuch w erze genomowej - możliwości diagnosty...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[140] => Array
(
[id] => 140
[site_id] => 1
[status_id] => 5
[name] => Zastosowanie sekwencjonowania w diagnostyce molekularnej
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/140/posterw_erze.png
[video] => resources/data/material/140/wertheim_zastosowanie_sekwencjonowania_w_diagnostyce_molekularnej.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 140-zastosowanie_sekwencjonowania_w_diagnostyce_molekularnej
[url] => wideo/140-zastosowanie_sekwencjonowania_w_diagnostyce_molekularnej
[short_name] => Zastosowanie sekwencjonowania w diagnostyce moleku...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[141] => Array
(
[id] => 141
[site_id] => 1
[status_id] => 5
[name] => Interpretacja wyników badań molekularnych na przykładzie genetycznie uwarunkowanych chorób skóry
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/141/posterw_erze.png
[video] => resources/data/material/141/interpretacja_wynikow_badan_molekularnych_na_przykladzie_genetycznie_uwarunkowanych_chorob_skory_wertheimtyssarowska_12_min_uciety_poczatek_zdania.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 141-interpretacja_wynikow_badan_molekularnych_na_przykladzie_genetycznie_uwarunkowanych_chorob_skory
[url] => wideo/141-interpretacja_wynikow_badan_molekularnych_na_przykladzie_genetycznie_uwarunkowanych_chorob_skory
[short_name] => Interpretacja wyników badań molekularnych na przyk...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[142] => Array
(
[id] => 142
[site_id] => 1
[status_id] => 5
[name] => Diagnostyka mukowiscydozy i chorób CFTR zależnych 30 lat po odkryciu genu CFTR
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/142/posterw_erze.png
[video] => resources/data/material/142/wertheim_diagnostyka_mukowiscydzy.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 142-diagnostyka_mukowiscydozy_i_chorob_cftr_zaleznych_30_lat_po_odkryciu_genu_cftr
[url] => wideo/142-diagnostyka_mukowiscydozy_i_chorob_cftr_zaleznych_30_lat_po_odkryciu_genu_cftr
[short_name] => Diagnostyka mukowiscydozy i chorób CFTR zależnych ...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[143] => Array
(
[id] => 143
[site_id] => 1
[status_id] => 5
[name] => Badania molekularne w diagnostyce galaktozemii
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/143/posterw_erze.png
[video] => resources/data/material/143/wertheim_bad_molek_w_diagnost_galaktozemii.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 143-badania_molekularne_w_diagnostyce_galaktozemii
[url] => wideo/143-badania_molekularne_w_diagnostyce_galaktozemii
[short_name] => Badania molekularne w diagnostyce galaktozemii
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
)
)
[sort] => 1
[status_code] => active
[authors] => Array
(
[0] => dr n. med. Magdalena Bartnik-Głaska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 66
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Magdalena Bartnik-Głaska
[firstname] => Magdalena
[lastname] => Bartnik-Głaska
[title] => dr n. med.
[affiliation] => Zakład Genetyki Medycznej, Instytut Matki i Dziecka, Warszawa
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 66-magdalena_bartnik_glaska
[url] => eksperci/66-magdalena_bartnik_glaska
)
)
[authors_ids] => Array
(
[0] => 66
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 134-postepowanie_diagnostyczne_w_niepelnosprawnosci_intelektualnej
[url] => wideo/134-postepowanie_diagnostyczne_w_niepelnosprawnosci_intelektualnej
[short_name] => Postępowanie diagnostyczne w niepełnosprawności in...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
[logotypy] => Array
(
)
[pliki] => Array
(
[103] => Array
(
[id] => 103
[site_id] => 1
[status_id] => 5
[entity_key] => material
[entity_id] => 134
[name] => Postępowanie diagnostyczne w niepełnosprawności intelektualnej
[file] => resources/data/pliki/material/134/postepowanie_diagnostyczne_w_niepelnosprawnosci_intelektualnej.pdf
[sort] => 100
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
[135] => Array
(
[id] => 135
[name] => Zespoły mikrodelecyjne i mikroduplikacyjne
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/135/posterw_erze.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
[linked] => Array
(
[128] => Array
(
[id] => 128
[site_id] => 1
[status_id] => 5
[name] => RASopatie – diagnostyka molekularna wrodzonych zaburzeń rozwojowych
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/128/posterw_erze.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med., prof IMiD Monika Gos
)
[authors_data] => Array
(
[0] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => dr n. med., prof IMiD Monika Gos
[firstname] => Monika
[lastname] => Gos
[title] => dr n. med., prof IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-monika_gos
[url] => eksperci/13-monika_gos
)
)
[authors_ids] => Array
(
[0] => 13
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 128-rasopatie__diagnostyka_molekularna_wrodzonych_zaburzen_rozwojowych
[url] => wideo/128-rasopatie__diagnostyka_molekularna_wrodzonych_zaburzen_rozwojowych
[short_name] => RASopatie – diagnostyka molekularna wrodzonych zab...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[129] => Array
(
[id] => 129
[site_id] => 1
[status_id] => 5
[name] => Zastosowanie metod cytogenetycznych w diagnostyce zaburzeń wieku rozwojowego
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/129/posterw_erze.png
[video] => resources/data/material/129/wisniowiecka_zastosowanie_cytogenetyki.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Barbara Wiśniowiecka-Kowalnik
)
[authors_data] => Array
(
[0] => Array
(
[id] => 7
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Barbara Wiśniowiecka-Kowalnik
[firstname] => Barbara
[lastname] => Wiśniowiecka-Kowalnik
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 7-barbara_wisniowiecka_kowalnik
[url] => eksperci/7-barbara_wisniowiecka_kowalnik
)
)
[authors_ids] => Array
(
[0] => 7
)
[topics] => Array
(
[0] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 129-zastosowanie_metod_cytogenetycznych_w_diagnostyce_zaburzen_wieku_rozwojowego
[url] => wideo/129-zastosowanie_metod_cytogenetycznych_w_diagnostyce_zaburzen_wieku_rozwojowego
[short_name] => Zastosowanie metod cytogenetycznych w diagnostyce ...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[131] => Array
(
[id] => 131
[site_id] => 1
[status_id] => 5
[name] => Typy dziedziczenia chorób genetycznych i poradnictwo genetyczne
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/131/posterw_erze.png
[video] => resources/data/material/131/kutkowska_typy_dziedziczenia.mp4
[content] =>
[ext] => Array
(
[linked] => Array
(
[0] => Array
(
[id] =>
)
)
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n.med. Anna Kutkowska-Kaźmierczak
)
[authors_data] => Array
(
[0] => Array
(
[id] => 64
[site_id] => 1
[status_id] => 5
[name] => dr n.med. Anna Kutkowska-Kaźmierczak
[firstname] => Anna
[lastname] => Kutkowska-Kaźmierczak
[title] => dr n.med.
[affiliation] => Zakład Genetyki Klinicznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 64-anna_kutkowska_kazmierczak
[url] => eksperci/64-anna_kutkowska_kazmierczak
)
)
[authors_ids] => Array
(
[0] => 64
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 131-typy_dziedziczenia_chorob_genetycznych_i_poradnictwo_genetyczne
[url] => wideo/131-typy_dziedziczenia_chorob_genetycznych_i_poradnictwo_genetyczne
[short_name] => Typy dziedziczenia chorób genetycznych i poradnict...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[132] => Array
(
[id] => 132
[site_id] => 1
[status_id] => 5
[name] => Diagnostyka wrodzonych wad metabolizmu
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/132/posterw_erze.png
[video] => resources/data/material/132/rygiel_diagnostyka_wrodzonych_wad_metabolizmu.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab. n. med., prof. IMID Agnieszka Rygiel
)
[authors_data] => Array
(
[0] => Array
(
[id] => 65
[site_id] => 1
[status_id] => 5
[name] => dr hab. n. med., prof. IMID Agnieszka Rygiel
[firstname] => Agnieszka
[lastname] => Rygiel
[title] => dr hab. n. med., prof. IMID
[affiliation] => Zakład Genetyki Medycznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 65-agnieszka_rygiel
[url] => eksperci/65-agnieszka_rygiel
)
)
[authors_ids] => Array
(
[0] => 65
)
[topics] => Array
(
[0] => 2
[1] => 4
[2] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 132-diagnostyka_wrodzonych_wad_metabolizmu
[url] => wideo/132-diagnostyka_wrodzonych_wad_metabolizmu
[short_name] => Diagnostyka wrodzonych wad metabolizmu
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[2] => Array
(
[id] => 2
[site_id] => 1
[status_id] => 5
[name] => metabolizm
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 2-metabolizm
[url] => /2-metabolizm
)
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[133] => Array
(
[id] => 133
[site_id] => 1
[status_id] => 5
[name] => Diagnostyka molekularna genetycznie uwarunkowanego zapalenia trzustki
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/133/posterw_erze.png
[video] => resources/data/material/133/rygiel_diagn_molek_genet_uwarunk_zapalenia_trzustki.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab. n. med., prof. IMID Agnieszka Rygiel
)
[authors_data] => Array
(
[0] => Array
(
[id] => 65
[site_id] => 1
[status_id] => 5
[name] => dr hab. n. med., prof. IMID Agnieszka Rygiel
[firstname] => Agnieszka
[lastname] => Rygiel
[title] => dr hab. n. med., prof. IMID
[affiliation] => Zakład Genetyki Medycznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 65-agnieszka_rygiel
[url] => eksperci/65-agnieszka_rygiel
)
)
[authors_ids] => Array
(
[0] => 65
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 133-diagnostyka_molekularna_genetycznie_uwarunkowanego_zapalenia_trzustki
[url] => wideo/133-diagnostyka_molekularna_genetycznie_uwarunkowanego_zapalenia_trzustki
[short_name] => Diagnostyka molekularna genetycznie uwarunkowanego...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[134] => Array
(
[id] => 134
[site_id] => 1
[status_id] => 5
[name] => Postępowanie diagnostyczne w niepełnosprawności intelektualnej
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/134/posterw_erze.png
[video] => resources/data/material/134/postepowanie_diagnostyczne_w_niepelnosprawnosci_intelektualnej_brak_nazwy_kursu.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Magdalena Bartnik-Głaska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 66
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Magdalena Bartnik-Głaska
[firstname] => Magdalena
[lastname] => Bartnik-Głaska
[title] => dr n. med.
[affiliation] => Zakład Genetyki Medycznej, Instytut Matki i Dziecka, Warszawa
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 66-magdalena_bartnik_glaska
[url] => eksperci/66-magdalena_bartnik_glaska
)
)
[authors_ids] => Array
(
[0] => 66
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 134-postepowanie_diagnostyczne_w_niepelnosprawnosci_intelektualnej
[url] => wideo/134-postepowanie_diagnostyczne_w_niepelnosprawnosci_intelektualnej
[short_name] => Postępowanie diagnostyczne w niepełnosprawności in...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[136] => Array
(
[id] => 136
[site_id] => 1
[status_id] => 5
[name] => „Już” znane zespoły mikrodelecji/mikroduplikacji w diagnostyce zaburzeń wieku rozwojowego
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/136/posterw_erze.png
[video] => resources/data/material/136/kedzior_juz_znane_zespoly_mikrodelecji.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr Marta Kędzior
)
[authors_data] => Array
(
[0] => Array
(
[id] => 67
[site_id] => 1
[status_id] => 5
[name] => dr Marta Kędzior
[firstname] => Marta
[lastname] => Kędzior
[title] => dr
[affiliation] => Zakład Genetyki Medycznej, IMiD
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 67-marta_kedzior
[url] => eksperci/67-marta_kedzior
)
)
[authors_ids] => Array
(
[0] => 67
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 9
[3] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 136-juz_znane_zespoly_mikrodelecjimikroduplikacji_w_diagnostyce_zaburzen_wieku_rozwojowego
[url] => wideo/136-juz_znane_zespoly_mikrodelecjimikroduplikacji_w_diagnostyce_zaburzen_wieku_rozwojowego
[short_name] => „Już” znane zespoły mikrodelecji/mikroduplikacji w...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[9] => Array
(
[id] => 9
[site_id] => 1
[status_id] => 5
[name] => zespół delecji
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 9-zespol_delecji
[url] => /9-zespol_delecji
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[137] => Array
(
[id] => 137
[site_id] => 1
[status_id] => 5
[name] => Genetyczne uwarunkowania kraniostenoz
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/137/posterw_erze.png
[video] => resources/data/material/137/kutkowska_genetycz_uwarunkow_kraniostenoz.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n.med. Anna Kutkowska-Kaźmierczak
)
[authors_data] => Array
(
[0] => Array
(
[id] => 64
[site_id] => 1
[status_id] => 5
[name] => dr n.med. Anna Kutkowska-Kaźmierczak
[firstname] => Anna
[lastname] => Kutkowska-Kaźmierczak
[title] => dr n.med.
[affiliation] => Zakład Genetyki Klinicznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 64-anna_kutkowska_kazmierczak
[url] => eksperci/64-anna_kutkowska_kazmierczak
)
)
[authors_ids] => Array
(
[0] => 64
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 137-genetyczne_uwarunkowania_kraniostenoz
[url] => wideo/137-genetyczne_uwarunkowania_kraniostenoz
[short_name] => Genetyczne uwarunkowania kraniostenoz
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[138] => Array
(
[id] => 138
[site_id] => 1
[status_id] => 5
[name] => Niepełnosprawność intelektualna – podłoże genetyczne
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/138/posterw_erze.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n.med. Anna Kutkowska-Kaźmierczak
)
[authors_data] => Array
(
[0] => Array
(
[id] => 64
[site_id] => 1
[status_id] => 5
[name] => dr n.med. Anna Kutkowska-Kaźmierczak
[firstname] => Anna
[lastname] => Kutkowska-Kaźmierczak
[title] => dr n.med.
[affiliation] => Zakład Genetyki Klinicznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 64-anna_kutkowska_kazmierczak
[url] => eksperci/64-anna_kutkowska_kazmierczak
)
)
[authors_ids] => Array
(
[0] => 64
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 138-niepelnosprawnosc_intelektualna__podloze_genetyczne
[url] => wideo/138-niepelnosprawnosc_intelektualna__podloze_genetyczne
[short_name] => Niepełnosprawność intelektualna – podłoże genetycz...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[139] => Array
(
[id] => 139
[site_id] => 1
[status_id] => 5
[name] => Niedosłuch w erze genomowej - możliwości diagnostyczne
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/139/posterw_erze.png
[video] => resources/data/material/139/niepokoj_niedosluch.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Niepokój
)
[authors_data] => Array
(
[0] => Array
(
[id] => 68
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Niepokój
[firstname] => Katarzyna
[lastname] => Niepokój
[title] => dr n. med.
[affiliation] => Zakład Genetyki Medycznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 68-katarzyna_niepokoj
[url] => eksperci/68-katarzyna_niepokoj
)
)
[authors_ids] => Array
(
[0] => 68
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 139-niedosluch_w_erze_genomowej___mozliwosci_diagnostyczne
[url] => wideo/139-niedosluch_w_erze_genomowej___mozliwosci_diagnostyczne
[short_name] => Niedosłuch w erze genomowej - możliwości diagnosty...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[140] => Array
(
[id] => 140
[site_id] => 1
[status_id] => 5
[name] => Zastosowanie sekwencjonowania w diagnostyce molekularnej
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/140/posterw_erze.png
[video] => resources/data/material/140/wertheim_zastosowanie_sekwencjonowania_w_diagnostyce_molekularnej.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 140-zastosowanie_sekwencjonowania_w_diagnostyce_molekularnej
[url] => wideo/140-zastosowanie_sekwencjonowania_w_diagnostyce_molekularnej
[short_name] => Zastosowanie sekwencjonowania w diagnostyce moleku...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[141] => Array
(
[id] => 141
[site_id] => 1
[status_id] => 5
[name] => Interpretacja wyników badań molekularnych na przykładzie genetycznie uwarunkowanych chorób skóry
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/141/posterw_erze.png
[video] => resources/data/material/141/interpretacja_wynikow_badan_molekularnych_na_przykladzie_genetycznie_uwarunkowanych_chorob_skory_wertheimtyssarowska_12_min_uciety_poczatek_zdania.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 141-interpretacja_wynikow_badan_molekularnych_na_przykladzie_genetycznie_uwarunkowanych_chorob_skory
[url] => wideo/141-interpretacja_wynikow_badan_molekularnych_na_przykladzie_genetycznie_uwarunkowanych_chorob_skory
[short_name] => Interpretacja wyników badań molekularnych na przyk...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[142] => Array
(
[id] => 142
[site_id] => 1
[status_id] => 5
[name] => Diagnostyka mukowiscydozy i chorób CFTR zależnych 30 lat po odkryciu genu CFTR
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/142/posterw_erze.png
[video] => resources/data/material/142/wertheim_diagnostyka_mukowiscydzy.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 142-diagnostyka_mukowiscydozy_i_chorob_cftr_zaleznych_30_lat_po_odkryciu_genu_cftr
[url] => wideo/142-diagnostyka_mukowiscydozy_i_chorob_cftr_zaleznych_30_lat_po_odkryciu_genu_cftr
[short_name] => Diagnostyka mukowiscydozy i chorób CFTR zależnych ...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[143] => Array
(
[id] => 143
[site_id] => 1
[status_id] => 5
[name] => Badania molekularne w diagnostyce galaktozemii
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/143/posterw_erze.png
[video] => resources/data/material/143/wertheim_bad_molek_w_diagnost_galaktozemii.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 143-badania_molekularne_w_diagnostyce_galaktozemii
[url] => wideo/143-badania_molekularne_w_diagnostyce_galaktozemii
[short_name] => Badania molekularne w diagnostyce galaktozemii
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
)
)
[sort] => 1
[status_code] => active
[authors] => Array
(
[0] => dr n.med. Anna Kutkowska-Kaźmierczak
)
[authors_data] => Array
(
[0] => Array
(
[id] => 64
[site_id] => 1
[status_id] => 5
[name] => dr n.med. Anna Kutkowska-Kaźmierczak
[firstname] => Anna
[lastname] => Kutkowska-Kaźmierczak
[title] => dr n.med.
[affiliation] => Zakład Genetyki Klinicznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 64-anna_kutkowska_kazmierczak
[url] => eksperci/64-anna_kutkowska_kazmierczak
)
)
[authors_ids] => Array
(
[0] => 64
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 9
[3] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 135-zespoly_mikrodelecyjne_i_mikroduplikacyjne
[url] => wideo/135-zespoly_mikrodelecyjne_i_mikroduplikacyjne
[short_name] => Zespoły mikrodelecyjne i mikroduplikacyjne
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[9] => Array
(
[id] => 9
[site_id] => 1
[status_id] => 5
[name] => zespół delecji
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 9-zespol_delecji
[url] => /9-zespol_delecji
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
[logotypy] => Array
(
)
[pliki] => Array
(
[104] => Array
(
[id] => 104
[site_id] => 1
[status_id] => 5
[entity_key] => material
[entity_id] => 135
[name] => Zespoły mikrodelecjne i mikroduplikacjne
[file] => resources/data/pliki/material/135/zespoly_mikrodelecjne_i_mikroduplikacjne.pdf
[sort] => 101
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
[136] => Array
(
[id] => 136
[name] => „Już” znane zespoły mikrodelecji/mikroduplikacji w diagnostyce zaburzeń wieku rozwojowego
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/136/posterw_erze.png
[video] => resources/data/material/136/kedzior_juz_znane_zespoly_mikrodelecji.mp4
[content] =>
[ext] => Array
(
[files_header] =>
[linked] => Array
(
[128] => Array
(
[id] => 128
[site_id] => 1
[status_id] => 5
[name] => RASopatie – diagnostyka molekularna wrodzonych zaburzeń rozwojowych
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/128/posterw_erze.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med., prof IMiD Monika Gos
)
[authors_data] => Array
(
[0] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => dr n. med., prof IMiD Monika Gos
[firstname] => Monika
[lastname] => Gos
[title] => dr n. med., prof IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-monika_gos
[url] => eksperci/13-monika_gos
)
)
[authors_ids] => Array
(
[0] => 13
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 128-rasopatie__diagnostyka_molekularna_wrodzonych_zaburzen_rozwojowych
[url] => wideo/128-rasopatie__diagnostyka_molekularna_wrodzonych_zaburzen_rozwojowych
[short_name] => RASopatie – diagnostyka molekularna wrodzonych zab...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[129] => Array
(
[id] => 129
[site_id] => 1
[status_id] => 5
[name] => Zastosowanie metod cytogenetycznych w diagnostyce zaburzeń wieku rozwojowego
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/129/posterw_erze.png
[video] => resources/data/material/129/wisniowiecka_zastosowanie_cytogenetyki.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Barbara Wiśniowiecka-Kowalnik
)
[authors_data] => Array
(
[0] => Array
(
[id] => 7
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Barbara Wiśniowiecka-Kowalnik
[firstname] => Barbara
[lastname] => Wiśniowiecka-Kowalnik
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 7-barbara_wisniowiecka_kowalnik
[url] => eksperci/7-barbara_wisniowiecka_kowalnik
)
)
[authors_ids] => Array
(
[0] => 7
)
[topics] => Array
(
[0] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 129-zastosowanie_metod_cytogenetycznych_w_diagnostyce_zaburzen_wieku_rozwojowego
[url] => wideo/129-zastosowanie_metod_cytogenetycznych_w_diagnostyce_zaburzen_wieku_rozwojowego
[short_name] => Zastosowanie metod cytogenetycznych w diagnostyce ...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[131] => Array
(
[id] => 131
[site_id] => 1
[status_id] => 5
[name] => Typy dziedziczenia chorób genetycznych i poradnictwo genetyczne
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/131/posterw_erze.png
[video] => resources/data/material/131/kutkowska_typy_dziedziczenia.mp4
[content] =>
[ext] => Array
(
[linked] => Array
(
[0] => Array
(
[id] =>
)
)
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n.med. Anna Kutkowska-Kaźmierczak
)
[authors_data] => Array
(
[0] => Array
(
[id] => 64
[site_id] => 1
[status_id] => 5
[name] => dr n.med. Anna Kutkowska-Kaźmierczak
[firstname] => Anna
[lastname] => Kutkowska-Kaźmierczak
[title] => dr n.med.
[affiliation] => Zakład Genetyki Klinicznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 64-anna_kutkowska_kazmierczak
[url] => eksperci/64-anna_kutkowska_kazmierczak
)
)
[authors_ids] => Array
(
[0] => 64
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 131-typy_dziedziczenia_chorob_genetycznych_i_poradnictwo_genetyczne
[url] => wideo/131-typy_dziedziczenia_chorob_genetycznych_i_poradnictwo_genetyczne
[short_name] => Typy dziedziczenia chorób genetycznych i poradnict...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[132] => Array
(
[id] => 132
[site_id] => 1
[status_id] => 5
[name] => Diagnostyka wrodzonych wad metabolizmu
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/132/posterw_erze.png
[video] => resources/data/material/132/rygiel_diagnostyka_wrodzonych_wad_metabolizmu.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab. n. med., prof. IMID Agnieszka Rygiel
)
[authors_data] => Array
(
[0] => Array
(
[id] => 65
[site_id] => 1
[status_id] => 5
[name] => dr hab. n. med., prof. IMID Agnieszka Rygiel
[firstname] => Agnieszka
[lastname] => Rygiel
[title] => dr hab. n. med., prof. IMID
[affiliation] => Zakład Genetyki Medycznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 65-agnieszka_rygiel
[url] => eksperci/65-agnieszka_rygiel
)
)
[authors_ids] => Array
(
[0] => 65
)
[topics] => Array
(
[0] => 2
[1] => 4
[2] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 132-diagnostyka_wrodzonych_wad_metabolizmu
[url] => wideo/132-diagnostyka_wrodzonych_wad_metabolizmu
[short_name] => Diagnostyka wrodzonych wad metabolizmu
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[2] => Array
(
[id] => 2
[site_id] => 1
[status_id] => 5
[name] => metabolizm
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 2-metabolizm
[url] => /2-metabolizm
)
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[133] => Array
(
[id] => 133
[site_id] => 1
[status_id] => 5
[name] => Diagnostyka molekularna genetycznie uwarunkowanego zapalenia trzustki
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/133/posterw_erze.png
[video] => resources/data/material/133/rygiel_diagn_molek_genet_uwarunk_zapalenia_trzustki.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab. n. med., prof. IMID Agnieszka Rygiel
)
[authors_data] => Array
(
[0] => Array
(
[id] => 65
[site_id] => 1
[status_id] => 5
[name] => dr hab. n. med., prof. IMID Agnieszka Rygiel
[firstname] => Agnieszka
[lastname] => Rygiel
[title] => dr hab. n. med., prof. IMID
[affiliation] => Zakład Genetyki Medycznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 65-agnieszka_rygiel
[url] => eksperci/65-agnieszka_rygiel
)
)
[authors_ids] => Array
(
[0] => 65
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 133-diagnostyka_molekularna_genetycznie_uwarunkowanego_zapalenia_trzustki
[url] => wideo/133-diagnostyka_molekularna_genetycznie_uwarunkowanego_zapalenia_trzustki
[short_name] => Diagnostyka molekularna genetycznie uwarunkowanego...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[134] => Array
(
[id] => 134
[site_id] => 1
[status_id] => 5
[name] => Postępowanie diagnostyczne w niepełnosprawności intelektualnej
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/134/posterw_erze.png
[video] => resources/data/material/134/postepowanie_diagnostyczne_w_niepelnosprawnosci_intelektualnej_brak_nazwy_kursu.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Magdalena Bartnik-Głaska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 66
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Magdalena Bartnik-Głaska
[firstname] => Magdalena
[lastname] => Bartnik-Głaska
[title] => dr n. med.
[affiliation] => Zakład Genetyki Medycznej, Instytut Matki i Dziecka, Warszawa
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 66-magdalena_bartnik_glaska
[url] => eksperci/66-magdalena_bartnik_glaska
)
)
[authors_ids] => Array
(
[0] => 66
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 134-postepowanie_diagnostyczne_w_niepelnosprawnosci_intelektualnej
[url] => wideo/134-postepowanie_diagnostyczne_w_niepelnosprawnosci_intelektualnej
[short_name] => Postępowanie diagnostyczne w niepełnosprawności in...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[135] => Array
(
[id] => 135
[site_id] => 1
[status_id] => 5
[name] => Zespoły mikrodelecyjne i mikroduplikacyjne
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/135/posterw_erze.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n.med. Anna Kutkowska-Kaźmierczak
)
[authors_data] => Array
(
[0] => Array
(
[id] => 64
[site_id] => 1
[status_id] => 5
[name] => dr n.med. Anna Kutkowska-Kaźmierczak
[firstname] => Anna
[lastname] => Kutkowska-Kaźmierczak
[title] => dr n.med.
[affiliation] => Zakład Genetyki Klinicznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 64-anna_kutkowska_kazmierczak
[url] => eksperci/64-anna_kutkowska_kazmierczak
)
)
[authors_ids] => Array
(
[0] => 64
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 9
[3] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 135-zespoly_mikrodelecyjne_i_mikroduplikacyjne
[url] => wideo/135-zespoly_mikrodelecyjne_i_mikroduplikacyjne
[short_name] => Zespoły mikrodelecyjne i mikroduplikacyjne
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[9] => Array
(
[id] => 9
[site_id] => 1
[status_id] => 5
[name] => zespół delecji
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 9-zespol_delecji
[url] => /9-zespol_delecji
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[137] => Array
(
[id] => 137
[site_id] => 1
[status_id] => 5
[name] => Genetyczne uwarunkowania kraniostenoz
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/137/posterw_erze.png
[video] => resources/data/material/137/kutkowska_genetycz_uwarunkow_kraniostenoz.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n.med. Anna Kutkowska-Kaźmierczak
)
[authors_data] => Array
(
[0] => Array
(
[id] => 64
[site_id] => 1
[status_id] => 5
[name] => dr n.med. Anna Kutkowska-Kaźmierczak
[firstname] => Anna
[lastname] => Kutkowska-Kaźmierczak
[title] => dr n.med.
[affiliation] => Zakład Genetyki Klinicznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 64-anna_kutkowska_kazmierczak
[url] => eksperci/64-anna_kutkowska_kazmierczak
)
)
[authors_ids] => Array
(
[0] => 64
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 137-genetyczne_uwarunkowania_kraniostenoz
[url] => wideo/137-genetyczne_uwarunkowania_kraniostenoz
[short_name] => Genetyczne uwarunkowania kraniostenoz
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[138] => Array
(
[id] => 138
[site_id] => 1
[status_id] => 5
[name] => Niepełnosprawność intelektualna – podłoże genetyczne
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/138/posterw_erze.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n.med. Anna Kutkowska-Kaźmierczak
)
[authors_data] => Array
(
[0] => Array
(
[id] => 64
[site_id] => 1
[status_id] => 5
[name] => dr n.med. Anna Kutkowska-Kaźmierczak
[firstname] => Anna
[lastname] => Kutkowska-Kaźmierczak
[title] => dr n.med.
[affiliation] => Zakład Genetyki Klinicznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 64-anna_kutkowska_kazmierczak
[url] => eksperci/64-anna_kutkowska_kazmierczak
)
)
[authors_ids] => Array
(
[0] => 64
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 138-niepelnosprawnosc_intelektualna__podloze_genetyczne
[url] => wideo/138-niepelnosprawnosc_intelektualna__podloze_genetyczne
[short_name] => Niepełnosprawność intelektualna – podłoże genetycz...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[139] => Array
(
[id] => 139
[site_id] => 1
[status_id] => 5
[name] => Niedosłuch w erze genomowej - możliwości diagnostyczne
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/139/posterw_erze.png
[video] => resources/data/material/139/niepokoj_niedosluch.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Niepokój
)
[authors_data] => Array
(
[0] => Array
(
[id] => 68
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Niepokój
[firstname] => Katarzyna
[lastname] => Niepokój
[title] => dr n. med.
[affiliation] => Zakład Genetyki Medycznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 68-katarzyna_niepokoj
[url] => eksperci/68-katarzyna_niepokoj
)
)
[authors_ids] => Array
(
[0] => 68
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 139-niedosluch_w_erze_genomowej___mozliwosci_diagnostyczne
[url] => wideo/139-niedosluch_w_erze_genomowej___mozliwosci_diagnostyczne
[short_name] => Niedosłuch w erze genomowej - możliwości diagnosty...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[140] => Array
(
[id] => 140
[site_id] => 1
[status_id] => 5
[name] => Zastosowanie sekwencjonowania w diagnostyce molekularnej
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/140/posterw_erze.png
[video] => resources/data/material/140/wertheim_zastosowanie_sekwencjonowania_w_diagnostyce_molekularnej.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 140-zastosowanie_sekwencjonowania_w_diagnostyce_molekularnej
[url] => wideo/140-zastosowanie_sekwencjonowania_w_diagnostyce_molekularnej
[short_name] => Zastosowanie sekwencjonowania w diagnostyce moleku...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[141] => Array
(
[id] => 141
[site_id] => 1
[status_id] => 5
[name] => Interpretacja wyników badań molekularnych na przykładzie genetycznie uwarunkowanych chorób skóry
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/141/posterw_erze.png
[video] => resources/data/material/141/interpretacja_wynikow_badan_molekularnych_na_przykladzie_genetycznie_uwarunkowanych_chorob_skory_wertheimtyssarowska_12_min_uciety_poczatek_zdania.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 141-interpretacja_wynikow_badan_molekularnych_na_przykladzie_genetycznie_uwarunkowanych_chorob_skory
[url] => wideo/141-interpretacja_wynikow_badan_molekularnych_na_przykladzie_genetycznie_uwarunkowanych_chorob_skory
[short_name] => Interpretacja wyników badań molekularnych na przyk...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[142] => Array
(
[id] => 142
[site_id] => 1
[status_id] => 5
[name] => Diagnostyka mukowiscydozy i chorób CFTR zależnych 30 lat po odkryciu genu CFTR
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/142/posterw_erze.png
[video] => resources/data/material/142/wertheim_diagnostyka_mukowiscydzy.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 142-diagnostyka_mukowiscydozy_i_chorob_cftr_zaleznych_30_lat_po_odkryciu_genu_cftr
[url] => wideo/142-diagnostyka_mukowiscydozy_i_chorob_cftr_zaleznych_30_lat_po_odkryciu_genu_cftr
[short_name] => Diagnostyka mukowiscydozy i chorób CFTR zależnych ...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[143] => Array
(
[id] => 143
[site_id] => 1
[status_id] => 5
[name] => Badania molekularne w diagnostyce galaktozemii
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/143/posterw_erze.png
[video] => resources/data/material/143/wertheim_bad_molek_w_diagnost_galaktozemii.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 143-badania_molekularne_w_diagnostyce_galaktozemii
[url] => wideo/143-badania_molekularne_w_diagnostyce_galaktozemii
[short_name] => Badania molekularne w diagnostyce galaktozemii
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
)
)
[sort] => 1
[status_code] => active
[authors] => Array
(
[0] => dr Marta Kędzior
)
[authors_data] => Array
(
[0] => Array
(
[id] => 67
[site_id] => 1
[status_id] => 5
[name] => dr Marta Kędzior
[firstname] => Marta
[lastname] => Kędzior
[title] => dr
[affiliation] => Zakład Genetyki Medycznej, IMiD
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 67-marta_kedzior
[url] => eksperci/67-marta_kedzior
)
)
[authors_ids] => Array
(
[0] => 67
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 9
[3] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 136-juz_znane_zespoly_mikrodelecjimikroduplikacji_w_diagnostyce_zaburzen_wieku_rozwojowego
[url] => wideo/136-juz_znane_zespoly_mikrodelecjimikroduplikacji_w_diagnostyce_zaburzen_wieku_rozwojowego
[short_name] => „Już” znane zespoły mikrodelecji/mikroduplikacji w...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[9] => Array
(
[id] => 9
[site_id] => 1
[status_id] => 5
[name] => zespół delecji
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 9-zespol_delecji
[url] => /9-zespol_delecji
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
[logotypy] => Array
(
)
[pliki] => Array
(
[105] => Array
(
[id] => 105
[site_id] => 1
[status_id] => 5
[entity_key] => material
[entity_id] => 136
[name] => „Już” znane zespoły mikrodelecji/mikroduplikacji w diagnostyce zaburzeń wieku rozwojowego
[file] => resources/data/pliki/material/136/znane_zespoly_mikrodelecji_mikroduplikacji_w_diagnostyce_zaburzen_wieku_rozwojowego.pdf
[sort] => 102
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
[137] => Array
(
[id] => 137
[name] => Genetyczne uwarunkowania kraniostenoz
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/137/posterw_erze.png
[video] => resources/data/material/137/kutkowska_genetycz_uwarunkow_kraniostenoz.mp4
[content] =>
[ext] => Array
(
[files_header] =>
[linked] => Array
(
[128] => Array
(
[id] => 128
[site_id] => 1
[status_id] => 5
[name] => RASopatie – diagnostyka molekularna wrodzonych zaburzeń rozwojowych
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/128/posterw_erze.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med., prof IMiD Monika Gos
)
[authors_data] => Array
(
[0] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => dr n. med., prof IMiD Monika Gos
[firstname] => Monika
[lastname] => Gos
[title] => dr n. med., prof IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-monika_gos
[url] => eksperci/13-monika_gos
)
)
[authors_ids] => Array
(
[0] => 13
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 128-rasopatie__diagnostyka_molekularna_wrodzonych_zaburzen_rozwojowych
[url] => wideo/128-rasopatie__diagnostyka_molekularna_wrodzonych_zaburzen_rozwojowych
[short_name] => RASopatie – diagnostyka molekularna wrodzonych zab...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[129] => Array
(
[id] => 129
[site_id] => 1
[status_id] => 5
[name] => Zastosowanie metod cytogenetycznych w diagnostyce zaburzeń wieku rozwojowego
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/129/posterw_erze.png
[video] => resources/data/material/129/wisniowiecka_zastosowanie_cytogenetyki.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Barbara Wiśniowiecka-Kowalnik
)
[authors_data] => Array
(
[0] => Array
(
[id] => 7
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Barbara Wiśniowiecka-Kowalnik
[firstname] => Barbara
[lastname] => Wiśniowiecka-Kowalnik
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 7-barbara_wisniowiecka_kowalnik
[url] => eksperci/7-barbara_wisniowiecka_kowalnik
)
)
[authors_ids] => Array
(
[0] => 7
)
[topics] => Array
(
[0] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 129-zastosowanie_metod_cytogenetycznych_w_diagnostyce_zaburzen_wieku_rozwojowego
[url] => wideo/129-zastosowanie_metod_cytogenetycznych_w_diagnostyce_zaburzen_wieku_rozwojowego
[short_name] => Zastosowanie metod cytogenetycznych w diagnostyce ...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[131] => Array
(
[id] => 131
[site_id] => 1
[status_id] => 5
[name] => Typy dziedziczenia chorób genetycznych i poradnictwo genetyczne
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/131/posterw_erze.png
[video] => resources/data/material/131/kutkowska_typy_dziedziczenia.mp4
[content] =>
[ext] => Array
(
[linked] => Array
(
[0] => Array
(
[id] =>
)
)
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n.med. Anna Kutkowska-Kaźmierczak
)
[authors_data] => Array
(
[0] => Array
(
[id] => 64
[site_id] => 1
[status_id] => 5
[name] => dr n.med. Anna Kutkowska-Kaźmierczak
[firstname] => Anna
[lastname] => Kutkowska-Kaźmierczak
[title] => dr n.med.
[affiliation] => Zakład Genetyki Klinicznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 64-anna_kutkowska_kazmierczak
[url] => eksperci/64-anna_kutkowska_kazmierczak
)
)
[authors_ids] => Array
(
[0] => 64
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 131-typy_dziedziczenia_chorob_genetycznych_i_poradnictwo_genetyczne
[url] => wideo/131-typy_dziedziczenia_chorob_genetycznych_i_poradnictwo_genetyczne
[short_name] => Typy dziedziczenia chorób genetycznych i poradnict...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[132] => Array
(
[id] => 132
[site_id] => 1
[status_id] => 5
[name] => Diagnostyka wrodzonych wad metabolizmu
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/132/posterw_erze.png
[video] => resources/data/material/132/rygiel_diagnostyka_wrodzonych_wad_metabolizmu.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab. n. med., prof. IMID Agnieszka Rygiel
)
[authors_data] => Array
(
[0] => Array
(
[id] => 65
[site_id] => 1
[status_id] => 5
[name] => dr hab. n. med., prof. IMID Agnieszka Rygiel
[firstname] => Agnieszka
[lastname] => Rygiel
[title] => dr hab. n. med., prof. IMID
[affiliation] => Zakład Genetyki Medycznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 65-agnieszka_rygiel
[url] => eksperci/65-agnieszka_rygiel
)
)
[authors_ids] => Array
(
[0] => 65
)
[topics] => Array
(
[0] => 2
[1] => 4
[2] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 132-diagnostyka_wrodzonych_wad_metabolizmu
[url] => wideo/132-diagnostyka_wrodzonych_wad_metabolizmu
[short_name] => Diagnostyka wrodzonych wad metabolizmu
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[2] => Array
(
[id] => 2
[site_id] => 1
[status_id] => 5
[name] => metabolizm
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 2-metabolizm
[url] => /2-metabolizm
)
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[133] => Array
(
[id] => 133
[site_id] => 1
[status_id] => 5
[name] => Diagnostyka molekularna genetycznie uwarunkowanego zapalenia trzustki
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/133/posterw_erze.png
[video] => resources/data/material/133/rygiel_diagn_molek_genet_uwarunk_zapalenia_trzustki.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab. n. med., prof. IMID Agnieszka Rygiel
)
[authors_data] => Array
(
[0] => Array
(
[id] => 65
[site_id] => 1
[status_id] => 5
[name] => dr hab. n. med., prof. IMID Agnieszka Rygiel
[firstname] => Agnieszka
[lastname] => Rygiel
[title] => dr hab. n. med., prof. IMID
[affiliation] => Zakład Genetyki Medycznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 65-agnieszka_rygiel
[url] => eksperci/65-agnieszka_rygiel
)
)
[authors_ids] => Array
(
[0] => 65
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 133-diagnostyka_molekularna_genetycznie_uwarunkowanego_zapalenia_trzustki
[url] => wideo/133-diagnostyka_molekularna_genetycznie_uwarunkowanego_zapalenia_trzustki
[short_name] => Diagnostyka molekularna genetycznie uwarunkowanego...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[134] => Array
(
[id] => 134
[site_id] => 1
[status_id] => 5
[name] => Postępowanie diagnostyczne w niepełnosprawności intelektualnej
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/134/posterw_erze.png
[video] => resources/data/material/134/postepowanie_diagnostyczne_w_niepelnosprawnosci_intelektualnej_brak_nazwy_kursu.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Magdalena Bartnik-Głaska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 66
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Magdalena Bartnik-Głaska
[firstname] => Magdalena
[lastname] => Bartnik-Głaska
[title] => dr n. med.
[affiliation] => Zakład Genetyki Medycznej, Instytut Matki i Dziecka, Warszawa
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 66-magdalena_bartnik_glaska
[url] => eksperci/66-magdalena_bartnik_glaska
)
)
[authors_ids] => Array
(
[0] => 66
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 134-postepowanie_diagnostyczne_w_niepelnosprawnosci_intelektualnej
[url] => wideo/134-postepowanie_diagnostyczne_w_niepelnosprawnosci_intelektualnej
[short_name] => Postępowanie diagnostyczne w niepełnosprawności in...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[135] => Array
(
[id] => 135
[site_id] => 1
[status_id] => 5
[name] => Zespoły mikrodelecyjne i mikroduplikacyjne
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/135/posterw_erze.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n.med. Anna Kutkowska-Kaźmierczak
)
[authors_data] => Array
(
[0] => Array
(
[id] => 64
[site_id] => 1
[status_id] => 5
[name] => dr n.med. Anna Kutkowska-Kaźmierczak
[firstname] => Anna
[lastname] => Kutkowska-Kaźmierczak
[title] => dr n.med.
[affiliation] => Zakład Genetyki Klinicznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 64-anna_kutkowska_kazmierczak
[url] => eksperci/64-anna_kutkowska_kazmierczak
)
)
[authors_ids] => Array
(
[0] => 64
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 9
[3] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 135-zespoly_mikrodelecyjne_i_mikroduplikacyjne
[url] => wideo/135-zespoly_mikrodelecyjne_i_mikroduplikacyjne
[short_name] => Zespoły mikrodelecyjne i mikroduplikacyjne
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[9] => Array
(
[id] => 9
[site_id] => 1
[status_id] => 5
[name] => zespół delecji
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 9-zespol_delecji
[url] => /9-zespol_delecji
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[136] => Array
(
[id] => 136
[site_id] => 1
[status_id] => 5
[name] => „Już” znane zespoły mikrodelecji/mikroduplikacji w diagnostyce zaburzeń wieku rozwojowego
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/136/posterw_erze.png
[video] => resources/data/material/136/kedzior_juz_znane_zespoly_mikrodelecji.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr Marta Kędzior
)
[authors_data] => Array
(
[0] => Array
(
[id] => 67
[site_id] => 1
[status_id] => 5
[name] => dr Marta Kędzior
[firstname] => Marta
[lastname] => Kędzior
[title] => dr
[affiliation] => Zakład Genetyki Medycznej, IMiD
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 67-marta_kedzior
[url] => eksperci/67-marta_kedzior
)
)
[authors_ids] => Array
(
[0] => 67
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 9
[3] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 136-juz_znane_zespoly_mikrodelecjimikroduplikacji_w_diagnostyce_zaburzen_wieku_rozwojowego
[url] => wideo/136-juz_znane_zespoly_mikrodelecjimikroduplikacji_w_diagnostyce_zaburzen_wieku_rozwojowego
[short_name] => „Już” znane zespoły mikrodelecji/mikroduplikacji w...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[9] => Array
(
[id] => 9
[site_id] => 1
[status_id] => 5
[name] => zespół delecji
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 9-zespol_delecji
[url] => /9-zespol_delecji
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[138] => Array
(
[id] => 138
[site_id] => 1
[status_id] => 5
[name] => Niepełnosprawność intelektualna – podłoże genetyczne
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/138/posterw_erze.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n.med. Anna Kutkowska-Kaźmierczak
)
[authors_data] => Array
(
[0] => Array
(
[id] => 64
[site_id] => 1
[status_id] => 5
[name] => dr n.med. Anna Kutkowska-Kaźmierczak
[firstname] => Anna
[lastname] => Kutkowska-Kaźmierczak
[title] => dr n.med.
[affiliation] => Zakład Genetyki Klinicznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 64-anna_kutkowska_kazmierczak
[url] => eksperci/64-anna_kutkowska_kazmierczak
)
)
[authors_ids] => Array
(
[0] => 64
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 138-niepelnosprawnosc_intelektualna__podloze_genetyczne
[url] => wideo/138-niepelnosprawnosc_intelektualna__podloze_genetyczne
[short_name] => Niepełnosprawność intelektualna – podłoże genetycz...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[139] => Array
(
[id] => 139
[site_id] => 1
[status_id] => 5
[name] => Niedosłuch w erze genomowej - możliwości diagnostyczne
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/139/posterw_erze.png
[video] => resources/data/material/139/niepokoj_niedosluch.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Niepokój
)
[authors_data] => Array
(
[0] => Array
(
[id] => 68
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Niepokój
[firstname] => Katarzyna
[lastname] => Niepokój
[title] => dr n. med.
[affiliation] => Zakład Genetyki Medycznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 68-katarzyna_niepokoj
[url] => eksperci/68-katarzyna_niepokoj
)
)
[authors_ids] => Array
(
[0] => 68
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 139-niedosluch_w_erze_genomowej___mozliwosci_diagnostyczne
[url] => wideo/139-niedosluch_w_erze_genomowej___mozliwosci_diagnostyczne
[short_name] => Niedosłuch w erze genomowej - możliwości diagnosty...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[140] => Array
(
[id] => 140
[site_id] => 1
[status_id] => 5
[name] => Zastosowanie sekwencjonowania w diagnostyce molekularnej
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/140/posterw_erze.png
[video] => resources/data/material/140/wertheim_zastosowanie_sekwencjonowania_w_diagnostyce_molekularnej.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 140-zastosowanie_sekwencjonowania_w_diagnostyce_molekularnej
[url] => wideo/140-zastosowanie_sekwencjonowania_w_diagnostyce_molekularnej
[short_name] => Zastosowanie sekwencjonowania w diagnostyce moleku...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[141] => Array
(
[id] => 141
[site_id] => 1
[status_id] => 5
[name] => Interpretacja wyników badań molekularnych na przykładzie genetycznie uwarunkowanych chorób skóry
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/141/posterw_erze.png
[video] => resources/data/material/141/interpretacja_wynikow_badan_molekularnych_na_przykladzie_genetycznie_uwarunkowanych_chorob_skory_wertheimtyssarowska_12_min_uciety_poczatek_zdania.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 141-interpretacja_wynikow_badan_molekularnych_na_przykladzie_genetycznie_uwarunkowanych_chorob_skory
[url] => wideo/141-interpretacja_wynikow_badan_molekularnych_na_przykladzie_genetycznie_uwarunkowanych_chorob_skory
[short_name] => Interpretacja wyników badań molekularnych na przyk...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[142] => Array
(
[id] => 142
[site_id] => 1
[status_id] => 5
[name] => Diagnostyka mukowiscydozy i chorób CFTR zależnych 30 lat po odkryciu genu CFTR
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/142/posterw_erze.png
[video] => resources/data/material/142/wertheim_diagnostyka_mukowiscydzy.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 142-diagnostyka_mukowiscydozy_i_chorob_cftr_zaleznych_30_lat_po_odkryciu_genu_cftr
[url] => wideo/142-diagnostyka_mukowiscydozy_i_chorob_cftr_zaleznych_30_lat_po_odkryciu_genu_cftr
[short_name] => Diagnostyka mukowiscydozy i chorób CFTR zależnych ...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[143] => Array
(
[id] => 143
[site_id] => 1
[status_id] => 5
[name] => Badania molekularne w diagnostyce galaktozemii
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/143/posterw_erze.png
[video] => resources/data/material/143/wertheim_bad_molek_w_diagnost_galaktozemii.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 143-badania_molekularne_w_diagnostyce_galaktozemii
[url] => wideo/143-badania_molekularne_w_diagnostyce_galaktozemii
[short_name] => Badania molekularne w diagnostyce galaktozemii
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
)
)
[sort] => 1
[status_code] => active
[authors] => Array
(
[0] => dr n.med. Anna Kutkowska-Kaźmierczak
)
[authors_data] => Array
(
[0] => Array
(
[id] => 64
[site_id] => 1
[status_id] => 5
[name] => dr n.med. Anna Kutkowska-Kaźmierczak
[firstname] => Anna
[lastname] => Kutkowska-Kaźmierczak
[title] => dr n.med.
[affiliation] => Zakład Genetyki Klinicznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 64-anna_kutkowska_kazmierczak
[url] => eksperci/64-anna_kutkowska_kazmierczak
)
)
[authors_ids] => Array
(
[0] => 64
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 137-genetyczne_uwarunkowania_kraniostenoz
[url] => wideo/137-genetyczne_uwarunkowania_kraniostenoz
[short_name] => Genetyczne uwarunkowania kraniostenoz
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
[logotypy] => Array
(
)
[pliki] => Array
(
[106] => Array
(
[id] => 106
[site_id] => 1
[status_id] => 5
[entity_key] => material
[entity_id] => 137
[name] => Genetyczne uwarunkowania kraniostenoz
[file] => resources/data/pliki/material/137/genetyczne_uwarunowania_kraniostenoz.pdf
[sort] => 103
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
[138] => Array
(
[id] => 138
[name] => Niepełnosprawność intelektualna – podłoże genetyczne
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/138/posterw_erze.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
[linked] => Array
(
[128] => Array
(
[id] => 128
[site_id] => 1
[status_id] => 5
[name] => RASopatie – diagnostyka molekularna wrodzonych zaburzeń rozwojowych
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/128/posterw_erze.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med., prof IMiD Monika Gos
)
[authors_data] => Array
(
[0] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => dr n. med., prof IMiD Monika Gos
[firstname] => Monika
[lastname] => Gos
[title] => dr n. med., prof IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-monika_gos
[url] => eksperci/13-monika_gos
)
)
[authors_ids] => Array
(
[0] => 13
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 128-rasopatie__diagnostyka_molekularna_wrodzonych_zaburzen_rozwojowych
[url] => wideo/128-rasopatie__diagnostyka_molekularna_wrodzonych_zaburzen_rozwojowych
[short_name] => RASopatie – diagnostyka molekularna wrodzonych zab...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[129] => Array
(
[id] => 129
[site_id] => 1
[status_id] => 5
[name] => Zastosowanie metod cytogenetycznych w diagnostyce zaburzeń wieku rozwojowego
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/129/posterw_erze.png
[video] => resources/data/material/129/wisniowiecka_zastosowanie_cytogenetyki.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Barbara Wiśniowiecka-Kowalnik
)
[authors_data] => Array
(
[0] => Array
(
[id] => 7
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Barbara Wiśniowiecka-Kowalnik
[firstname] => Barbara
[lastname] => Wiśniowiecka-Kowalnik
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 7-barbara_wisniowiecka_kowalnik
[url] => eksperci/7-barbara_wisniowiecka_kowalnik
)
)
[authors_ids] => Array
(
[0] => 7
)
[topics] => Array
(
[0] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 129-zastosowanie_metod_cytogenetycznych_w_diagnostyce_zaburzen_wieku_rozwojowego
[url] => wideo/129-zastosowanie_metod_cytogenetycznych_w_diagnostyce_zaburzen_wieku_rozwojowego
[short_name] => Zastosowanie metod cytogenetycznych w diagnostyce ...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[131] => Array
(
[id] => 131
[site_id] => 1
[status_id] => 5
[name] => Typy dziedziczenia chorób genetycznych i poradnictwo genetyczne
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/131/posterw_erze.png
[video] => resources/data/material/131/kutkowska_typy_dziedziczenia.mp4
[content] =>
[ext] => Array
(
[linked] => Array
(
[0] => Array
(
[id] =>
)
)
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n.med. Anna Kutkowska-Kaźmierczak
)
[authors_data] => Array
(
[0] => Array
(
[id] => 64
[site_id] => 1
[status_id] => 5
[name] => dr n.med. Anna Kutkowska-Kaźmierczak
[firstname] => Anna
[lastname] => Kutkowska-Kaźmierczak
[title] => dr n.med.
[affiliation] => Zakład Genetyki Klinicznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 64-anna_kutkowska_kazmierczak
[url] => eksperci/64-anna_kutkowska_kazmierczak
)
)
[authors_ids] => Array
(
[0] => 64
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 131-typy_dziedziczenia_chorob_genetycznych_i_poradnictwo_genetyczne
[url] => wideo/131-typy_dziedziczenia_chorob_genetycznych_i_poradnictwo_genetyczne
[short_name] => Typy dziedziczenia chorób genetycznych i poradnict...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[132] => Array
(
[id] => 132
[site_id] => 1
[status_id] => 5
[name] => Diagnostyka wrodzonych wad metabolizmu
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/132/posterw_erze.png
[video] => resources/data/material/132/rygiel_diagnostyka_wrodzonych_wad_metabolizmu.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab. n. med., prof. IMID Agnieszka Rygiel
)
[authors_data] => Array
(
[0] => Array
(
[id] => 65
[site_id] => 1
[status_id] => 5
[name] => dr hab. n. med., prof. IMID Agnieszka Rygiel
[firstname] => Agnieszka
[lastname] => Rygiel
[title] => dr hab. n. med., prof. IMID
[affiliation] => Zakład Genetyki Medycznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 65-agnieszka_rygiel
[url] => eksperci/65-agnieszka_rygiel
)
)
[authors_ids] => Array
(
[0] => 65
)
[topics] => Array
(
[0] => 2
[1] => 4
[2] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 132-diagnostyka_wrodzonych_wad_metabolizmu
[url] => wideo/132-diagnostyka_wrodzonych_wad_metabolizmu
[short_name] => Diagnostyka wrodzonych wad metabolizmu
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[2] => Array
(
[id] => 2
[site_id] => 1
[status_id] => 5
[name] => metabolizm
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 2-metabolizm
[url] => /2-metabolizm
)
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[133] => Array
(
[id] => 133
[site_id] => 1
[status_id] => 5
[name] => Diagnostyka molekularna genetycznie uwarunkowanego zapalenia trzustki
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/133/posterw_erze.png
[video] => resources/data/material/133/rygiel_diagn_molek_genet_uwarunk_zapalenia_trzustki.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab. n. med., prof. IMID Agnieszka Rygiel
)
[authors_data] => Array
(
[0] => Array
(
[id] => 65
[site_id] => 1
[status_id] => 5
[name] => dr hab. n. med., prof. IMID Agnieszka Rygiel
[firstname] => Agnieszka
[lastname] => Rygiel
[title] => dr hab. n. med., prof. IMID
[affiliation] => Zakład Genetyki Medycznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 65-agnieszka_rygiel
[url] => eksperci/65-agnieszka_rygiel
)
)
[authors_ids] => Array
(
[0] => 65
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 133-diagnostyka_molekularna_genetycznie_uwarunkowanego_zapalenia_trzustki
[url] => wideo/133-diagnostyka_molekularna_genetycznie_uwarunkowanego_zapalenia_trzustki
[short_name] => Diagnostyka molekularna genetycznie uwarunkowanego...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[134] => Array
(
[id] => 134
[site_id] => 1
[status_id] => 5
[name] => Postępowanie diagnostyczne w niepełnosprawności intelektualnej
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/134/posterw_erze.png
[video] => resources/data/material/134/postepowanie_diagnostyczne_w_niepelnosprawnosci_intelektualnej_brak_nazwy_kursu.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Magdalena Bartnik-Głaska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 66
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Magdalena Bartnik-Głaska
[firstname] => Magdalena
[lastname] => Bartnik-Głaska
[title] => dr n. med.
[affiliation] => Zakład Genetyki Medycznej, Instytut Matki i Dziecka, Warszawa
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 66-magdalena_bartnik_glaska
[url] => eksperci/66-magdalena_bartnik_glaska
)
)
[authors_ids] => Array
(
[0] => 66
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 134-postepowanie_diagnostyczne_w_niepelnosprawnosci_intelektualnej
[url] => wideo/134-postepowanie_diagnostyczne_w_niepelnosprawnosci_intelektualnej
[short_name] => Postępowanie diagnostyczne w niepełnosprawności in...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[135] => Array
(
[id] => 135
[site_id] => 1
[status_id] => 5
[name] => Zespoły mikrodelecyjne i mikroduplikacyjne
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/135/posterw_erze.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n.med. Anna Kutkowska-Kaźmierczak
)
[authors_data] => Array
(
[0] => Array
(
[id] => 64
[site_id] => 1
[status_id] => 5
[name] => dr n.med. Anna Kutkowska-Kaźmierczak
[firstname] => Anna
[lastname] => Kutkowska-Kaźmierczak
[title] => dr n.med.
[affiliation] => Zakład Genetyki Klinicznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 64-anna_kutkowska_kazmierczak
[url] => eksperci/64-anna_kutkowska_kazmierczak
)
)
[authors_ids] => Array
(
[0] => 64
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 9
[3] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 135-zespoly_mikrodelecyjne_i_mikroduplikacyjne
[url] => wideo/135-zespoly_mikrodelecyjne_i_mikroduplikacyjne
[short_name] => Zespoły mikrodelecyjne i mikroduplikacyjne
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[9] => Array
(
[id] => 9
[site_id] => 1
[status_id] => 5
[name] => zespół delecji
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 9-zespol_delecji
[url] => /9-zespol_delecji
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[136] => Array
(
[id] => 136
[site_id] => 1
[status_id] => 5
[name] => „Już” znane zespoły mikrodelecji/mikroduplikacji w diagnostyce zaburzeń wieku rozwojowego
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/136/posterw_erze.png
[video] => resources/data/material/136/kedzior_juz_znane_zespoly_mikrodelecji.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr Marta Kędzior
)
[authors_data] => Array
(
[0] => Array
(
[id] => 67
[site_id] => 1
[status_id] => 5
[name] => dr Marta Kędzior
[firstname] => Marta
[lastname] => Kędzior
[title] => dr
[affiliation] => Zakład Genetyki Medycznej, IMiD
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 67-marta_kedzior
[url] => eksperci/67-marta_kedzior
)
)
[authors_ids] => Array
(
[0] => 67
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 9
[3] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 136-juz_znane_zespoly_mikrodelecjimikroduplikacji_w_diagnostyce_zaburzen_wieku_rozwojowego
[url] => wideo/136-juz_znane_zespoly_mikrodelecjimikroduplikacji_w_diagnostyce_zaburzen_wieku_rozwojowego
[short_name] => „Już” znane zespoły mikrodelecji/mikroduplikacji w...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[9] => Array
(
[id] => 9
[site_id] => 1
[status_id] => 5
[name] => zespół delecji
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 9-zespol_delecji
[url] => /9-zespol_delecji
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[137] => Array
(
[id] => 137
[site_id] => 1
[status_id] => 5
[name] => Genetyczne uwarunkowania kraniostenoz
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/137/posterw_erze.png
[video] => resources/data/material/137/kutkowska_genetycz_uwarunkow_kraniostenoz.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n.med. Anna Kutkowska-Kaźmierczak
)
[authors_data] => Array
(
[0] => Array
(
[id] => 64
[site_id] => 1
[status_id] => 5
[name] => dr n.med. Anna Kutkowska-Kaźmierczak
[firstname] => Anna
[lastname] => Kutkowska-Kaźmierczak
[title] => dr n.med.
[affiliation] => Zakład Genetyki Klinicznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 64-anna_kutkowska_kazmierczak
[url] => eksperci/64-anna_kutkowska_kazmierczak
)
)
[authors_ids] => Array
(
[0] => 64
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 137-genetyczne_uwarunkowania_kraniostenoz
[url] => wideo/137-genetyczne_uwarunkowania_kraniostenoz
[short_name] => Genetyczne uwarunkowania kraniostenoz
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[139] => Array
(
[id] => 139
[site_id] => 1
[status_id] => 5
[name] => Niedosłuch w erze genomowej - możliwości diagnostyczne
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/139/posterw_erze.png
[video] => resources/data/material/139/niepokoj_niedosluch.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Niepokój
)
[authors_data] => Array
(
[0] => Array
(
[id] => 68
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Niepokój
[firstname] => Katarzyna
[lastname] => Niepokój
[title] => dr n. med.
[affiliation] => Zakład Genetyki Medycznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 68-katarzyna_niepokoj
[url] => eksperci/68-katarzyna_niepokoj
)
)
[authors_ids] => Array
(
[0] => 68
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 139-niedosluch_w_erze_genomowej___mozliwosci_diagnostyczne
[url] => wideo/139-niedosluch_w_erze_genomowej___mozliwosci_diagnostyczne
[short_name] => Niedosłuch w erze genomowej - możliwości diagnosty...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[140] => Array
(
[id] => 140
[site_id] => 1
[status_id] => 5
[name] => Zastosowanie sekwencjonowania w diagnostyce molekularnej
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/140/posterw_erze.png
[video] => resources/data/material/140/wertheim_zastosowanie_sekwencjonowania_w_diagnostyce_molekularnej.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 140-zastosowanie_sekwencjonowania_w_diagnostyce_molekularnej
[url] => wideo/140-zastosowanie_sekwencjonowania_w_diagnostyce_molekularnej
[short_name] => Zastosowanie sekwencjonowania w diagnostyce moleku...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[141] => Array
(
[id] => 141
[site_id] => 1
[status_id] => 5
[name] => Interpretacja wyników badań molekularnych na przykładzie genetycznie uwarunkowanych chorób skóry
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/141/posterw_erze.png
[video] => resources/data/material/141/interpretacja_wynikow_badan_molekularnych_na_przykladzie_genetycznie_uwarunkowanych_chorob_skory_wertheimtyssarowska_12_min_uciety_poczatek_zdania.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 141-interpretacja_wynikow_badan_molekularnych_na_przykladzie_genetycznie_uwarunkowanych_chorob_skory
[url] => wideo/141-interpretacja_wynikow_badan_molekularnych_na_przykladzie_genetycznie_uwarunkowanych_chorob_skory
[short_name] => Interpretacja wyników badań molekularnych na przyk...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[142] => Array
(
[id] => 142
[site_id] => 1
[status_id] => 5
[name] => Diagnostyka mukowiscydozy i chorób CFTR zależnych 30 lat po odkryciu genu CFTR
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/142/posterw_erze.png
[video] => resources/data/material/142/wertheim_diagnostyka_mukowiscydzy.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 142-diagnostyka_mukowiscydozy_i_chorob_cftr_zaleznych_30_lat_po_odkryciu_genu_cftr
[url] => wideo/142-diagnostyka_mukowiscydozy_i_chorob_cftr_zaleznych_30_lat_po_odkryciu_genu_cftr
[short_name] => Diagnostyka mukowiscydozy i chorób CFTR zależnych ...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[143] => Array
(
[id] => 143
[site_id] => 1
[status_id] => 5
[name] => Badania molekularne w diagnostyce galaktozemii
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/143/posterw_erze.png
[video] => resources/data/material/143/wertheim_bad_molek_w_diagnost_galaktozemii.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 143-badania_molekularne_w_diagnostyce_galaktozemii
[url] => wideo/143-badania_molekularne_w_diagnostyce_galaktozemii
[short_name] => Badania molekularne w diagnostyce galaktozemii
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
)
)
[sort] => 1
[status_code] => active
[authors] => Array
(
[0] => dr n.med. Anna Kutkowska-Kaźmierczak
)
[authors_data] => Array
(
[0] => Array
(
[id] => 64
[site_id] => 1
[status_id] => 5
[name] => dr n.med. Anna Kutkowska-Kaźmierczak
[firstname] => Anna
[lastname] => Kutkowska-Kaźmierczak
[title] => dr n.med.
[affiliation] => Zakład Genetyki Klinicznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 64-anna_kutkowska_kazmierczak
[url] => eksperci/64-anna_kutkowska_kazmierczak
)
)
[authors_ids] => Array
(
[0] => 64
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 138-niepelnosprawnosc_intelektualna__podloze_genetyczne
[url] => wideo/138-niepelnosprawnosc_intelektualna__podloze_genetyczne
[short_name] => Niepełnosprawność intelektualna – podłoże genetycz...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
[logotypy] => Array
(
)
[pliki] => Array
(
[107] => Array
(
[id] => 107
[site_id] => 1
[status_id] => 5
[entity_key] => material
[entity_id] => 138
[name] => Niepełnosprawność intelektualna – podłoże genetyczne
[file] => resources/data/pliki/material/138/niepelnosprawnosc_intelektualna_podloze_genetyczne.pdf
[sort] => 104
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
[139] => Array
(
[id] => 139
[name] => Niedosłuch w erze genomowej - możliwości diagnostyczne
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/139/posterw_erze.png
[video] => resources/data/material/139/niepokoj_niedosluch.mp4
[content] =>
[ext] => Array
(
[files_header] =>
[linked] => Array
(
[128] => Array
(
[id] => 128
[site_id] => 1
[status_id] => 5
[name] => RASopatie – diagnostyka molekularna wrodzonych zaburzeń rozwojowych
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/128/posterw_erze.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med., prof IMiD Monika Gos
)
[authors_data] => Array
(
[0] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => dr n. med., prof IMiD Monika Gos
[firstname] => Monika
[lastname] => Gos
[title] => dr n. med., prof IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-monika_gos
[url] => eksperci/13-monika_gos
)
)
[authors_ids] => Array
(
[0] => 13
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 128-rasopatie__diagnostyka_molekularna_wrodzonych_zaburzen_rozwojowych
[url] => wideo/128-rasopatie__diagnostyka_molekularna_wrodzonych_zaburzen_rozwojowych
[short_name] => RASopatie – diagnostyka molekularna wrodzonych zab...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[129] => Array
(
[id] => 129
[site_id] => 1
[status_id] => 5
[name] => Zastosowanie metod cytogenetycznych w diagnostyce zaburzeń wieku rozwojowego
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/129/posterw_erze.png
[video] => resources/data/material/129/wisniowiecka_zastosowanie_cytogenetyki.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Barbara Wiśniowiecka-Kowalnik
)
[authors_data] => Array
(
[0] => Array
(
[id] => 7
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Barbara Wiśniowiecka-Kowalnik
[firstname] => Barbara
[lastname] => Wiśniowiecka-Kowalnik
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 7-barbara_wisniowiecka_kowalnik
[url] => eksperci/7-barbara_wisniowiecka_kowalnik
)
)
[authors_ids] => Array
(
[0] => 7
)
[topics] => Array
(
[0] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 129-zastosowanie_metod_cytogenetycznych_w_diagnostyce_zaburzen_wieku_rozwojowego
[url] => wideo/129-zastosowanie_metod_cytogenetycznych_w_diagnostyce_zaburzen_wieku_rozwojowego
[short_name] => Zastosowanie metod cytogenetycznych w diagnostyce ...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[131] => Array
(
[id] => 131
[site_id] => 1
[status_id] => 5
[name] => Typy dziedziczenia chorób genetycznych i poradnictwo genetyczne
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/131/posterw_erze.png
[video] => resources/data/material/131/kutkowska_typy_dziedziczenia.mp4
[content] =>
[ext] => Array
(
[linked] => Array
(
[0] => Array
(
[id] =>
)
)
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n.med. Anna Kutkowska-Kaźmierczak
)
[authors_data] => Array
(
[0] => Array
(
[id] => 64
[site_id] => 1
[status_id] => 5
[name] => dr n.med. Anna Kutkowska-Kaźmierczak
[firstname] => Anna
[lastname] => Kutkowska-Kaźmierczak
[title] => dr n.med.
[affiliation] => Zakład Genetyki Klinicznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 64-anna_kutkowska_kazmierczak
[url] => eksperci/64-anna_kutkowska_kazmierczak
)
)
[authors_ids] => Array
(
[0] => 64
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 131-typy_dziedziczenia_chorob_genetycznych_i_poradnictwo_genetyczne
[url] => wideo/131-typy_dziedziczenia_chorob_genetycznych_i_poradnictwo_genetyczne
[short_name] => Typy dziedziczenia chorób genetycznych i poradnict...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[132] => Array
(
[id] => 132
[site_id] => 1
[status_id] => 5
[name] => Diagnostyka wrodzonych wad metabolizmu
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/132/posterw_erze.png
[video] => resources/data/material/132/rygiel_diagnostyka_wrodzonych_wad_metabolizmu.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab. n. med., prof. IMID Agnieszka Rygiel
)
[authors_data] => Array
(
[0] => Array
(
[id] => 65
[site_id] => 1
[status_id] => 5
[name] => dr hab. n. med., prof. IMID Agnieszka Rygiel
[firstname] => Agnieszka
[lastname] => Rygiel
[title] => dr hab. n. med., prof. IMID
[affiliation] => Zakład Genetyki Medycznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 65-agnieszka_rygiel
[url] => eksperci/65-agnieszka_rygiel
)
)
[authors_ids] => Array
(
[0] => 65
)
[topics] => Array
(
[0] => 2
[1] => 4
[2] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 132-diagnostyka_wrodzonych_wad_metabolizmu
[url] => wideo/132-diagnostyka_wrodzonych_wad_metabolizmu
[short_name] => Diagnostyka wrodzonych wad metabolizmu
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[2] => Array
(
[id] => 2
[site_id] => 1
[status_id] => 5
[name] => metabolizm
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 2-metabolizm
[url] => /2-metabolizm
)
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[133] => Array
(
[id] => 133
[site_id] => 1
[status_id] => 5
[name] => Diagnostyka molekularna genetycznie uwarunkowanego zapalenia trzustki
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/133/posterw_erze.png
[video] => resources/data/material/133/rygiel_diagn_molek_genet_uwarunk_zapalenia_trzustki.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab. n. med., prof. IMID Agnieszka Rygiel
)
[authors_data] => Array
(
[0] => Array
(
[id] => 65
[site_id] => 1
[status_id] => 5
[name] => dr hab. n. med., prof. IMID Agnieszka Rygiel
[firstname] => Agnieszka
[lastname] => Rygiel
[title] => dr hab. n. med., prof. IMID
[affiliation] => Zakład Genetyki Medycznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 65-agnieszka_rygiel
[url] => eksperci/65-agnieszka_rygiel
)
)
[authors_ids] => Array
(
[0] => 65
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 133-diagnostyka_molekularna_genetycznie_uwarunkowanego_zapalenia_trzustki
[url] => wideo/133-diagnostyka_molekularna_genetycznie_uwarunkowanego_zapalenia_trzustki
[short_name] => Diagnostyka molekularna genetycznie uwarunkowanego...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[134] => Array
(
[id] => 134
[site_id] => 1
[status_id] => 5
[name] => Postępowanie diagnostyczne w niepełnosprawności intelektualnej
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/134/posterw_erze.png
[video] => resources/data/material/134/postepowanie_diagnostyczne_w_niepelnosprawnosci_intelektualnej_brak_nazwy_kursu.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Magdalena Bartnik-Głaska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 66
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Magdalena Bartnik-Głaska
[firstname] => Magdalena
[lastname] => Bartnik-Głaska
[title] => dr n. med.
[affiliation] => Zakład Genetyki Medycznej, Instytut Matki i Dziecka, Warszawa
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 66-magdalena_bartnik_glaska
[url] => eksperci/66-magdalena_bartnik_glaska
)
)
[authors_ids] => Array
(
[0] => 66
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 134-postepowanie_diagnostyczne_w_niepelnosprawnosci_intelektualnej
[url] => wideo/134-postepowanie_diagnostyczne_w_niepelnosprawnosci_intelektualnej
[short_name] => Postępowanie diagnostyczne w niepełnosprawności in...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[135] => Array
(
[id] => 135
[site_id] => 1
[status_id] => 5
[name] => Zespoły mikrodelecyjne i mikroduplikacyjne
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/135/posterw_erze.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n.med. Anna Kutkowska-Kaźmierczak
)
[authors_data] => Array
(
[0] => Array
(
[id] => 64
[site_id] => 1
[status_id] => 5
[name] => dr n.med. Anna Kutkowska-Kaźmierczak
[firstname] => Anna
[lastname] => Kutkowska-Kaźmierczak
[title] => dr n.med.
[affiliation] => Zakład Genetyki Klinicznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 64-anna_kutkowska_kazmierczak
[url] => eksperci/64-anna_kutkowska_kazmierczak
)
)
[authors_ids] => Array
(
[0] => 64
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 9
[3] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 135-zespoly_mikrodelecyjne_i_mikroduplikacyjne
[url] => wideo/135-zespoly_mikrodelecyjne_i_mikroduplikacyjne
[short_name] => Zespoły mikrodelecyjne i mikroduplikacyjne
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[9] => Array
(
[id] => 9
[site_id] => 1
[status_id] => 5
[name] => zespół delecji
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 9-zespol_delecji
[url] => /9-zespol_delecji
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[136] => Array
(
[id] => 136
[site_id] => 1
[status_id] => 5
[name] => „Już” znane zespoły mikrodelecji/mikroduplikacji w diagnostyce zaburzeń wieku rozwojowego
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/136/posterw_erze.png
[video] => resources/data/material/136/kedzior_juz_znane_zespoly_mikrodelecji.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr Marta Kędzior
)
[authors_data] => Array
(
[0] => Array
(
[id] => 67
[site_id] => 1
[status_id] => 5
[name] => dr Marta Kędzior
[firstname] => Marta
[lastname] => Kędzior
[title] => dr
[affiliation] => Zakład Genetyki Medycznej, IMiD
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 67-marta_kedzior
[url] => eksperci/67-marta_kedzior
)
)
[authors_ids] => Array
(
[0] => 67
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 9
[3] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 136-juz_znane_zespoly_mikrodelecjimikroduplikacji_w_diagnostyce_zaburzen_wieku_rozwojowego
[url] => wideo/136-juz_znane_zespoly_mikrodelecjimikroduplikacji_w_diagnostyce_zaburzen_wieku_rozwojowego
[short_name] => „Już” znane zespoły mikrodelecji/mikroduplikacji w...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[9] => Array
(
[id] => 9
[site_id] => 1
[status_id] => 5
[name] => zespół delecji
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 9-zespol_delecji
[url] => /9-zespol_delecji
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[137] => Array
(
[id] => 137
[site_id] => 1
[status_id] => 5
[name] => Genetyczne uwarunkowania kraniostenoz
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/137/posterw_erze.png
[video] => resources/data/material/137/kutkowska_genetycz_uwarunkow_kraniostenoz.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n.med. Anna Kutkowska-Kaźmierczak
)
[authors_data] => Array
(
[0] => Array
(
[id] => 64
[site_id] => 1
[status_id] => 5
[name] => dr n.med. Anna Kutkowska-Kaźmierczak
[firstname] => Anna
[lastname] => Kutkowska-Kaźmierczak
[title] => dr n.med.
[affiliation] => Zakład Genetyki Klinicznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 64-anna_kutkowska_kazmierczak
[url] => eksperci/64-anna_kutkowska_kazmierczak
)
)
[authors_ids] => Array
(
[0] => 64
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 137-genetyczne_uwarunkowania_kraniostenoz
[url] => wideo/137-genetyczne_uwarunkowania_kraniostenoz
[short_name] => Genetyczne uwarunkowania kraniostenoz
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[138] => Array
(
[id] => 138
[site_id] => 1
[status_id] => 5
[name] => Niepełnosprawność intelektualna – podłoże genetyczne
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/138/posterw_erze.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n.med. Anna Kutkowska-Kaźmierczak
)
[authors_data] => Array
(
[0] => Array
(
[id] => 64
[site_id] => 1
[status_id] => 5
[name] => dr n.med. Anna Kutkowska-Kaźmierczak
[firstname] => Anna
[lastname] => Kutkowska-Kaźmierczak
[title] => dr n.med.
[affiliation] => Zakład Genetyki Klinicznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 64-anna_kutkowska_kazmierczak
[url] => eksperci/64-anna_kutkowska_kazmierczak
)
)
[authors_ids] => Array
(
[0] => 64
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 138-niepelnosprawnosc_intelektualna__podloze_genetyczne
[url] => wideo/138-niepelnosprawnosc_intelektualna__podloze_genetyczne
[short_name] => Niepełnosprawność intelektualna – podłoże genetycz...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[140] => Array
(
[id] => 140
[site_id] => 1
[status_id] => 5
[name] => Zastosowanie sekwencjonowania w diagnostyce molekularnej
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/140/posterw_erze.png
[video] => resources/data/material/140/wertheim_zastosowanie_sekwencjonowania_w_diagnostyce_molekularnej.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 140-zastosowanie_sekwencjonowania_w_diagnostyce_molekularnej
[url] => wideo/140-zastosowanie_sekwencjonowania_w_diagnostyce_molekularnej
[short_name] => Zastosowanie sekwencjonowania w diagnostyce moleku...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[141] => Array
(
[id] => 141
[site_id] => 1
[status_id] => 5
[name] => Interpretacja wyników badań molekularnych na przykładzie genetycznie uwarunkowanych chorób skóry
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/141/posterw_erze.png
[video] => resources/data/material/141/interpretacja_wynikow_badan_molekularnych_na_przykladzie_genetycznie_uwarunkowanych_chorob_skory_wertheimtyssarowska_12_min_uciety_poczatek_zdania.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 141-interpretacja_wynikow_badan_molekularnych_na_przykladzie_genetycznie_uwarunkowanych_chorob_skory
[url] => wideo/141-interpretacja_wynikow_badan_molekularnych_na_przykladzie_genetycznie_uwarunkowanych_chorob_skory
[short_name] => Interpretacja wyników badań molekularnych na przyk...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[142] => Array
(
[id] => 142
[site_id] => 1
[status_id] => 5
[name] => Diagnostyka mukowiscydozy i chorób CFTR zależnych 30 lat po odkryciu genu CFTR
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/142/posterw_erze.png
[video] => resources/data/material/142/wertheim_diagnostyka_mukowiscydzy.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 142-diagnostyka_mukowiscydozy_i_chorob_cftr_zaleznych_30_lat_po_odkryciu_genu_cftr
[url] => wideo/142-diagnostyka_mukowiscydozy_i_chorob_cftr_zaleznych_30_lat_po_odkryciu_genu_cftr
[short_name] => Diagnostyka mukowiscydozy i chorób CFTR zależnych ...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[143] => Array
(
[id] => 143
[site_id] => 1
[status_id] => 5
[name] => Badania molekularne w diagnostyce galaktozemii
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/143/posterw_erze.png
[video] => resources/data/material/143/wertheim_bad_molek_w_diagnost_galaktozemii.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 143-badania_molekularne_w_diagnostyce_galaktozemii
[url] => wideo/143-badania_molekularne_w_diagnostyce_galaktozemii
[short_name] => Badania molekularne w diagnostyce galaktozemii
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
)
)
[sort] => 1
[status_code] => active
[authors] => Array
(
[0] => dr n. med. Katarzyna Niepokój
)
[authors_data] => Array
(
[0] => Array
(
[id] => 68
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Niepokój
[firstname] => Katarzyna
[lastname] => Niepokój
[title] => dr n. med.
[affiliation] => Zakład Genetyki Medycznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 68-katarzyna_niepokoj
[url] => eksperci/68-katarzyna_niepokoj
)
)
[authors_ids] => Array
(
[0] => 68
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 139-niedosluch_w_erze_genomowej___mozliwosci_diagnostyczne
[url] => wideo/139-niedosluch_w_erze_genomowej___mozliwosci_diagnostyczne
[short_name] => Niedosłuch w erze genomowej - możliwości diagnosty...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
[logotypy] => Array
(
)
[pliki] => Array
(
[108] => Array
(
[id] => 108
[site_id] => 1
[status_id] => 5
[entity_key] => material
[entity_id] => 139
[name] => Niedosłuch w erze genomowej - możliwości diagnostyczne
[file] => resources/data/pliki/material/139/niedusluch_w_erze_genomowej_mozliwosci_diagnostyczne.pdf
[sort] => 105
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
[140] => Array
(
[id] => 140
[name] => Zastosowanie sekwencjonowania w diagnostyce molekularnej
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/140/posterw_erze.png
[video] => resources/data/material/140/wertheim_zastosowanie_sekwencjonowania_w_diagnostyce_molekularnej.mp4
[content] =>
[ext] => Array
(
[files_header] =>
[linked] => Array
(
[128] => Array
(
[id] => 128
[site_id] => 1
[status_id] => 5
[name] => RASopatie – diagnostyka molekularna wrodzonych zaburzeń rozwojowych
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/128/posterw_erze.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med., prof IMiD Monika Gos
)
[authors_data] => Array
(
[0] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => dr n. med., prof IMiD Monika Gos
[firstname] => Monika
[lastname] => Gos
[title] => dr n. med., prof IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-monika_gos
[url] => eksperci/13-monika_gos
)
)
[authors_ids] => Array
(
[0] => 13
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 128-rasopatie__diagnostyka_molekularna_wrodzonych_zaburzen_rozwojowych
[url] => wideo/128-rasopatie__diagnostyka_molekularna_wrodzonych_zaburzen_rozwojowych
[short_name] => RASopatie – diagnostyka molekularna wrodzonych zab...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[129] => Array
(
[id] => 129
[site_id] => 1
[status_id] => 5
[name] => Zastosowanie metod cytogenetycznych w diagnostyce zaburzeń wieku rozwojowego
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/129/posterw_erze.png
[video] => resources/data/material/129/wisniowiecka_zastosowanie_cytogenetyki.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Barbara Wiśniowiecka-Kowalnik
)
[authors_data] => Array
(
[0] => Array
(
[id] => 7
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Barbara Wiśniowiecka-Kowalnik
[firstname] => Barbara
[lastname] => Wiśniowiecka-Kowalnik
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 7-barbara_wisniowiecka_kowalnik
[url] => eksperci/7-barbara_wisniowiecka_kowalnik
)
)
[authors_ids] => Array
(
[0] => 7
)
[topics] => Array
(
[0] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 129-zastosowanie_metod_cytogenetycznych_w_diagnostyce_zaburzen_wieku_rozwojowego
[url] => wideo/129-zastosowanie_metod_cytogenetycznych_w_diagnostyce_zaburzen_wieku_rozwojowego
[short_name] => Zastosowanie metod cytogenetycznych w diagnostyce ...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[131] => Array
(
[id] => 131
[site_id] => 1
[status_id] => 5
[name] => Typy dziedziczenia chorób genetycznych i poradnictwo genetyczne
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/131/posterw_erze.png
[video] => resources/data/material/131/kutkowska_typy_dziedziczenia.mp4
[content] =>
[ext] => Array
(
[linked] => Array
(
[0] => Array
(
[id] =>
)
)
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n.med. Anna Kutkowska-Kaźmierczak
)
[authors_data] => Array
(
[0] => Array
(
[id] => 64
[site_id] => 1
[status_id] => 5
[name] => dr n.med. Anna Kutkowska-Kaźmierczak
[firstname] => Anna
[lastname] => Kutkowska-Kaźmierczak
[title] => dr n.med.
[affiliation] => Zakład Genetyki Klinicznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 64-anna_kutkowska_kazmierczak
[url] => eksperci/64-anna_kutkowska_kazmierczak
)
)
[authors_ids] => Array
(
[0] => 64
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 131-typy_dziedziczenia_chorob_genetycznych_i_poradnictwo_genetyczne
[url] => wideo/131-typy_dziedziczenia_chorob_genetycznych_i_poradnictwo_genetyczne
[short_name] => Typy dziedziczenia chorób genetycznych i poradnict...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[132] => Array
(
[id] => 132
[site_id] => 1
[status_id] => 5
[name] => Diagnostyka wrodzonych wad metabolizmu
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/132/posterw_erze.png
[video] => resources/data/material/132/rygiel_diagnostyka_wrodzonych_wad_metabolizmu.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab. n. med., prof. IMID Agnieszka Rygiel
)
[authors_data] => Array
(
[0] => Array
(
[id] => 65
[site_id] => 1
[status_id] => 5
[name] => dr hab. n. med., prof. IMID Agnieszka Rygiel
[firstname] => Agnieszka
[lastname] => Rygiel
[title] => dr hab. n. med., prof. IMID
[affiliation] => Zakład Genetyki Medycznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 65-agnieszka_rygiel
[url] => eksperci/65-agnieszka_rygiel
)
)
[authors_ids] => Array
(
[0] => 65
)
[topics] => Array
(
[0] => 2
[1] => 4
[2] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 132-diagnostyka_wrodzonych_wad_metabolizmu
[url] => wideo/132-diagnostyka_wrodzonych_wad_metabolizmu
[short_name] => Diagnostyka wrodzonych wad metabolizmu
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[2] => Array
(
[id] => 2
[site_id] => 1
[status_id] => 5
[name] => metabolizm
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 2-metabolizm
[url] => /2-metabolizm
)
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[133] => Array
(
[id] => 133
[site_id] => 1
[status_id] => 5
[name] => Diagnostyka molekularna genetycznie uwarunkowanego zapalenia trzustki
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/133/posterw_erze.png
[video] => resources/data/material/133/rygiel_diagn_molek_genet_uwarunk_zapalenia_trzustki.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab. n. med., prof. IMID Agnieszka Rygiel
)
[authors_data] => Array
(
[0] => Array
(
[id] => 65
[site_id] => 1
[status_id] => 5
[name] => dr hab. n. med., prof. IMID Agnieszka Rygiel
[firstname] => Agnieszka
[lastname] => Rygiel
[title] => dr hab. n. med., prof. IMID
[affiliation] => Zakład Genetyki Medycznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 65-agnieszka_rygiel
[url] => eksperci/65-agnieszka_rygiel
)
)
[authors_ids] => Array
(
[0] => 65
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 133-diagnostyka_molekularna_genetycznie_uwarunkowanego_zapalenia_trzustki
[url] => wideo/133-diagnostyka_molekularna_genetycznie_uwarunkowanego_zapalenia_trzustki
[short_name] => Diagnostyka molekularna genetycznie uwarunkowanego...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[134] => Array
(
[id] => 134
[site_id] => 1
[status_id] => 5
[name] => Postępowanie diagnostyczne w niepełnosprawności intelektualnej
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/134/posterw_erze.png
[video] => resources/data/material/134/postepowanie_diagnostyczne_w_niepelnosprawnosci_intelektualnej_brak_nazwy_kursu.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Magdalena Bartnik-Głaska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 66
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Magdalena Bartnik-Głaska
[firstname] => Magdalena
[lastname] => Bartnik-Głaska
[title] => dr n. med.
[affiliation] => Zakład Genetyki Medycznej, Instytut Matki i Dziecka, Warszawa
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 66-magdalena_bartnik_glaska
[url] => eksperci/66-magdalena_bartnik_glaska
)
)
[authors_ids] => Array
(
[0] => 66
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 134-postepowanie_diagnostyczne_w_niepelnosprawnosci_intelektualnej
[url] => wideo/134-postepowanie_diagnostyczne_w_niepelnosprawnosci_intelektualnej
[short_name] => Postępowanie diagnostyczne w niepełnosprawności in...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[135] => Array
(
[id] => 135
[site_id] => 1
[status_id] => 5
[name] => Zespoły mikrodelecyjne i mikroduplikacyjne
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/135/posterw_erze.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n.med. Anna Kutkowska-Kaźmierczak
)
[authors_data] => Array
(
[0] => Array
(
[id] => 64
[site_id] => 1
[status_id] => 5
[name] => dr n.med. Anna Kutkowska-Kaźmierczak
[firstname] => Anna
[lastname] => Kutkowska-Kaźmierczak
[title] => dr n.med.
[affiliation] => Zakład Genetyki Klinicznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 64-anna_kutkowska_kazmierczak
[url] => eksperci/64-anna_kutkowska_kazmierczak
)
)
[authors_ids] => Array
(
[0] => 64
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 9
[3] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 135-zespoly_mikrodelecyjne_i_mikroduplikacyjne
[url] => wideo/135-zespoly_mikrodelecyjne_i_mikroduplikacyjne
[short_name] => Zespoły mikrodelecyjne i mikroduplikacyjne
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[9] => Array
(
[id] => 9
[site_id] => 1
[status_id] => 5
[name] => zespół delecji
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 9-zespol_delecji
[url] => /9-zespol_delecji
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[136] => Array
(
[id] => 136
[site_id] => 1
[status_id] => 5
[name] => „Już” znane zespoły mikrodelecji/mikroduplikacji w diagnostyce zaburzeń wieku rozwojowego
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/136/posterw_erze.png
[video] => resources/data/material/136/kedzior_juz_znane_zespoly_mikrodelecji.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr Marta Kędzior
)
[authors_data] => Array
(
[0] => Array
(
[id] => 67
[site_id] => 1
[status_id] => 5
[name] => dr Marta Kędzior
[firstname] => Marta
[lastname] => Kędzior
[title] => dr
[affiliation] => Zakład Genetyki Medycznej, IMiD
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 67-marta_kedzior
[url] => eksperci/67-marta_kedzior
)
)
[authors_ids] => Array
(
[0] => 67
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 9
[3] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 136-juz_znane_zespoly_mikrodelecjimikroduplikacji_w_diagnostyce_zaburzen_wieku_rozwojowego
[url] => wideo/136-juz_znane_zespoly_mikrodelecjimikroduplikacji_w_diagnostyce_zaburzen_wieku_rozwojowego
[short_name] => „Już” znane zespoły mikrodelecji/mikroduplikacji w...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[9] => Array
(
[id] => 9
[site_id] => 1
[status_id] => 5
[name] => zespół delecji
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 9-zespol_delecji
[url] => /9-zespol_delecji
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[137] => Array
(
[id] => 137
[site_id] => 1
[status_id] => 5
[name] => Genetyczne uwarunkowania kraniostenoz
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/137/posterw_erze.png
[video] => resources/data/material/137/kutkowska_genetycz_uwarunkow_kraniostenoz.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n.med. Anna Kutkowska-Kaźmierczak
)
[authors_data] => Array
(
[0] => Array
(
[id] => 64
[site_id] => 1
[status_id] => 5
[name] => dr n.med. Anna Kutkowska-Kaźmierczak
[firstname] => Anna
[lastname] => Kutkowska-Kaźmierczak
[title] => dr n.med.
[affiliation] => Zakład Genetyki Klinicznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 64-anna_kutkowska_kazmierczak
[url] => eksperci/64-anna_kutkowska_kazmierczak
)
)
[authors_ids] => Array
(
[0] => 64
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 137-genetyczne_uwarunkowania_kraniostenoz
[url] => wideo/137-genetyczne_uwarunkowania_kraniostenoz
[short_name] => Genetyczne uwarunkowania kraniostenoz
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[138] => Array
(
[id] => 138
[site_id] => 1
[status_id] => 5
[name] => Niepełnosprawność intelektualna – podłoże genetyczne
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/138/posterw_erze.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n.med. Anna Kutkowska-Kaźmierczak
)
[authors_data] => Array
(
[0] => Array
(
[id] => 64
[site_id] => 1
[status_id] => 5
[name] => dr n.med. Anna Kutkowska-Kaźmierczak
[firstname] => Anna
[lastname] => Kutkowska-Kaźmierczak
[title] => dr n.med.
[affiliation] => Zakład Genetyki Klinicznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 64-anna_kutkowska_kazmierczak
[url] => eksperci/64-anna_kutkowska_kazmierczak
)
)
[authors_ids] => Array
(
[0] => 64
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 138-niepelnosprawnosc_intelektualna__podloze_genetyczne
[url] => wideo/138-niepelnosprawnosc_intelektualna__podloze_genetyczne
[short_name] => Niepełnosprawność intelektualna – podłoże genetycz...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[139] => Array
(
[id] => 139
[site_id] => 1
[status_id] => 5
[name] => Niedosłuch w erze genomowej - możliwości diagnostyczne
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/139/posterw_erze.png
[video] => resources/data/material/139/niepokoj_niedosluch.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Niepokój
)
[authors_data] => Array
(
[0] => Array
(
[id] => 68
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Niepokój
[firstname] => Katarzyna
[lastname] => Niepokój
[title] => dr n. med.
[affiliation] => Zakład Genetyki Medycznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 68-katarzyna_niepokoj
[url] => eksperci/68-katarzyna_niepokoj
)
)
[authors_ids] => Array
(
[0] => 68
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 139-niedosluch_w_erze_genomowej___mozliwosci_diagnostyczne
[url] => wideo/139-niedosluch_w_erze_genomowej___mozliwosci_diagnostyczne
[short_name] => Niedosłuch w erze genomowej - możliwości diagnosty...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[141] => Array
(
[id] => 141
[site_id] => 1
[status_id] => 5
[name] => Interpretacja wyników badań molekularnych na przykładzie genetycznie uwarunkowanych chorób skóry
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/141/posterw_erze.png
[video] => resources/data/material/141/interpretacja_wynikow_badan_molekularnych_na_przykladzie_genetycznie_uwarunkowanych_chorob_skory_wertheimtyssarowska_12_min_uciety_poczatek_zdania.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 141-interpretacja_wynikow_badan_molekularnych_na_przykladzie_genetycznie_uwarunkowanych_chorob_skory
[url] => wideo/141-interpretacja_wynikow_badan_molekularnych_na_przykladzie_genetycznie_uwarunkowanych_chorob_skory
[short_name] => Interpretacja wyników badań molekularnych na przyk...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[142] => Array
(
[id] => 142
[site_id] => 1
[status_id] => 5
[name] => Diagnostyka mukowiscydozy i chorób CFTR zależnych 30 lat po odkryciu genu CFTR
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/142/posterw_erze.png
[video] => resources/data/material/142/wertheim_diagnostyka_mukowiscydzy.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 142-diagnostyka_mukowiscydozy_i_chorob_cftr_zaleznych_30_lat_po_odkryciu_genu_cftr
[url] => wideo/142-diagnostyka_mukowiscydozy_i_chorob_cftr_zaleznych_30_lat_po_odkryciu_genu_cftr
[short_name] => Diagnostyka mukowiscydozy i chorób CFTR zależnych ...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[143] => Array
(
[id] => 143
[site_id] => 1
[status_id] => 5
[name] => Badania molekularne w diagnostyce galaktozemii
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/143/posterw_erze.png
[video] => resources/data/material/143/wertheim_bad_molek_w_diagnost_galaktozemii.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 143-badania_molekularne_w_diagnostyce_galaktozemii
[url] => wideo/143-badania_molekularne_w_diagnostyce_galaktozemii
[short_name] => Badania molekularne w diagnostyce galaktozemii
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
)
)
[sort] => 1
[status_code] => active
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 140-zastosowanie_sekwencjonowania_w_diagnostyce_molekularnej
[url] => wideo/140-zastosowanie_sekwencjonowania_w_diagnostyce_molekularnej
[short_name] => Zastosowanie sekwencjonowania w diagnostyce moleku...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
[logotypy] => Array
(
)
[pliki] => Array
(
[109] => Array
(
[id] => 109
[site_id] => 1
[status_id] => 5
[entity_key] => material
[entity_id] => 140
[name] => Zastosowanie sekwencjonowania w diagnostyce molekularnej
[file] => resources/data/pliki/material/140/zastosowanie_sekwencjonowania_w_diagnostyce_molekularnej.pdf
[sort] => 106
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
[141] => Array
(
[id] => 141
[name] => Interpretacja wyników badań molekularnych na przykładzie genetycznie uwarunkowanych chorób skóry
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/141/posterw_erze.png
[video] => resources/data/material/141/interpretacja_wynikow_badan_molekularnych_na_przykladzie_genetycznie_uwarunkowanych_chorob_skory_wertheimtyssarowska_12_min_uciety_poczatek_zdania.mp4
[content] =>
[ext] => Array
(
[files_header] =>
[linked] => Array
(
[128] => Array
(
[id] => 128
[site_id] => 1
[status_id] => 5
[name] => RASopatie – diagnostyka molekularna wrodzonych zaburzeń rozwojowych
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/128/posterw_erze.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med., prof IMiD Monika Gos
)
[authors_data] => Array
(
[0] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => dr n. med., prof IMiD Monika Gos
[firstname] => Monika
[lastname] => Gos
[title] => dr n. med., prof IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-monika_gos
[url] => eksperci/13-monika_gos
)
)
[authors_ids] => Array
(
[0] => 13
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 128-rasopatie__diagnostyka_molekularna_wrodzonych_zaburzen_rozwojowych
[url] => wideo/128-rasopatie__diagnostyka_molekularna_wrodzonych_zaburzen_rozwojowych
[short_name] => RASopatie – diagnostyka molekularna wrodzonych zab...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[129] => Array
(
[id] => 129
[site_id] => 1
[status_id] => 5
[name] => Zastosowanie metod cytogenetycznych w diagnostyce zaburzeń wieku rozwojowego
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/129/posterw_erze.png
[video] => resources/data/material/129/wisniowiecka_zastosowanie_cytogenetyki.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Barbara Wiśniowiecka-Kowalnik
)
[authors_data] => Array
(
[0] => Array
(
[id] => 7
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Barbara Wiśniowiecka-Kowalnik
[firstname] => Barbara
[lastname] => Wiśniowiecka-Kowalnik
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 7-barbara_wisniowiecka_kowalnik
[url] => eksperci/7-barbara_wisniowiecka_kowalnik
)
)
[authors_ids] => Array
(
[0] => 7
)
[topics] => Array
(
[0] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 129-zastosowanie_metod_cytogenetycznych_w_diagnostyce_zaburzen_wieku_rozwojowego
[url] => wideo/129-zastosowanie_metod_cytogenetycznych_w_diagnostyce_zaburzen_wieku_rozwojowego
[short_name] => Zastosowanie metod cytogenetycznych w diagnostyce ...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[131] => Array
(
[id] => 131
[site_id] => 1
[status_id] => 5
[name] => Typy dziedziczenia chorób genetycznych i poradnictwo genetyczne
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/131/posterw_erze.png
[video] => resources/data/material/131/kutkowska_typy_dziedziczenia.mp4
[content] =>
[ext] => Array
(
[linked] => Array
(
[0] => Array
(
[id] =>
)
)
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n.med. Anna Kutkowska-Kaźmierczak
)
[authors_data] => Array
(
[0] => Array
(
[id] => 64
[site_id] => 1
[status_id] => 5
[name] => dr n.med. Anna Kutkowska-Kaźmierczak
[firstname] => Anna
[lastname] => Kutkowska-Kaźmierczak
[title] => dr n.med.
[affiliation] => Zakład Genetyki Klinicznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 64-anna_kutkowska_kazmierczak
[url] => eksperci/64-anna_kutkowska_kazmierczak
)
)
[authors_ids] => Array
(
[0] => 64
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 131-typy_dziedziczenia_chorob_genetycznych_i_poradnictwo_genetyczne
[url] => wideo/131-typy_dziedziczenia_chorob_genetycznych_i_poradnictwo_genetyczne
[short_name] => Typy dziedziczenia chorób genetycznych i poradnict...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[132] => Array
(
[id] => 132
[site_id] => 1
[status_id] => 5
[name] => Diagnostyka wrodzonych wad metabolizmu
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/132/posterw_erze.png
[video] => resources/data/material/132/rygiel_diagnostyka_wrodzonych_wad_metabolizmu.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab. n. med., prof. IMID Agnieszka Rygiel
)
[authors_data] => Array
(
[0] => Array
(
[id] => 65
[site_id] => 1
[status_id] => 5
[name] => dr hab. n. med., prof. IMID Agnieszka Rygiel
[firstname] => Agnieszka
[lastname] => Rygiel
[title] => dr hab. n. med., prof. IMID
[affiliation] => Zakład Genetyki Medycznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 65-agnieszka_rygiel
[url] => eksperci/65-agnieszka_rygiel
)
)
[authors_ids] => Array
(
[0] => 65
)
[topics] => Array
(
[0] => 2
[1] => 4
[2] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 132-diagnostyka_wrodzonych_wad_metabolizmu
[url] => wideo/132-diagnostyka_wrodzonych_wad_metabolizmu
[short_name] => Diagnostyka wrodzonych wad metabolizmu
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[2] => Array
(
[id] => 2
[site_id] => 1
[status_id] => 5
[name] => metabolizm
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 2-metabolizm
[url] => /2-metabolizm
)
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[133] => Array
(
[id] => 133
[site_id] => 1
[status_id] => 5
[name] => Diagnostyka molekularna genetycznie uwarunkowanego zapalenia trzustki
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/133/posterw_erze.png
[video] => resources/data/material/133/rygiel_diagn_molek_genet_uwarunk_zapalenia_trzustki.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab. n. med., prof. IMID Agnieszka Rygiel
)
[authors_data] => Array
(
[0] => Array
(
[id] => 65
[site_id] => 1
[status_id] => 5
[name] => dr hab. n. med., prof. IMID Agnieszka Rygiel
[firstname] => Agnieszka
[lastname] => Rygiel
[title] => dr hab. n. med., prof. IMID
[affiliation] => Zakład Genetyki Medycznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 65-agnieszka_rygiel
[url] => eksperci/65-agnieszka_rygiel
)
)
[authors_ids] => Array
(
[0] => 65
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 133-diagnostyka_molekularna_genetycznie_uwarunkowanego_zapalenia_trzustki
[url] => wideo/133-diagnostyka_molekularna_genetycznie_uwarunkowanego_zapalenia_trzustki
[short_name] => Diagnostyka molekularna genetycznie uwarunkowanego...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[134] => Array
(
[id] => 134
[site_id] => 1
[status_id] => 5
[name] => Postępowanie diagnostyczne w niepełnosprawności intelektualnej
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/134/posterw_erze.png
[video] => resources/data/material/134/postepowanie_diagnostyczne_w_niepelnosprawnosci_intelektualnej_brak_nazwy_kursu.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Magdalena Bartnik-Głaska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 66
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Magdalena Bartnik-Głaska
[firstname] => Magdalena
[lastname] => Bartnik-Głaska
[title] => dr n. med.
[affiliation] => Zakład Genetyki Medycznej, Instytut Matki i Dziecka, Warszawa
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 66-magdalena_bartnik_glaska
[url] => eksperci/66-magdalena_bartnik_glaska
)
)
[authors_ids] => Array
(
[0] => 66
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 134-postepowanie_diagnostyczne_w_niepelnosprawnosci_intelektualnej
[url] => wideo/134-postepowanie_diagnostyczne_w_niepelnosprawnosci_intelektualnej
[short_name] => Postępowanie diagnostyczne w niepełnosprawności in...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[135] => Array
(
[id] => 135
[site_id] => 1
[status_id] => 5
[name] => Zespoły mikrodelecyjne i mikroduplikacyjne
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/135/posterw_erze.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n.med. Anna Kutkowska-Kaźmierczak
)
[authors_data] => Array
(
[0] => Array
(
[id] => 64
[site_id] => 1
[status_id] => 5
[name] => dr n.med. Anna Kutkowska-Kaźmierczak
[firstname] => Anna
[lastname] => Kutkowska-Kaźmierczak
[title] => dr n.med.
[affiliation] => Zakład Genetyki Klinicznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 64-anna_kutkowska_kazmierczak
[url] => eksperci/64-anna_kutkowska_kazmierczak
)
)
[authors_ids] => Array
(
[0] => 64
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 9
[3] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 135-zespoly_mikrodelecyjne_i_mikroduplikacyjne
[url] => wideo/135-zespoly_mikrodelecyjne_i_mikroduplikacyjne
[short_name] => Zespoły mikrodelecyjne i mikroduplikacyjne
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[9] => Array
(
[id] => 9
[site_id] => 1
[status_id] => 5
[name] => zespół delecji
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 9-zespol_delecji
[url] => /9-zespol_delecji
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[136] => Array
(
[id] => 136
[site_id] => 1
[status_id] => 5
[name] => „Już” znane zespoły mikrodelecji/mikroduplikacji w diagnostyce zaburzeń wieku rozwojowego
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/136/posterw_erze.png
[video] => resources/data/material/136/kedzior_juz_znane_zespoly_mikrodelecji.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr Marta Kędzior
)
[authors_data] => Array
(
[0] => Array
(
[id] => 67
[site_id] => 1
[status_id] => 5
[name] => dr Marta Kędzior
[firstname] => Marta
[lastname] => Kędzior
[title] => dr
[affiliation] => Zakład Genetyki Medycznej, IMiD
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 67-marta_kedzior
[url] => eksperci/67-marta_kedzior
)
)
[authors_ids] => Array
(
[0] => 67
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 9
[3] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 136-juz_znane_zespoly_mikrodelecjimikroduplikacji_w_diagnostyce_zaburzen_wieku_rozwojowego
[url] => wideo/136-juz_znane_zespoly_mikrodelecjimikroduplikacji_w_diagnostyce_zaburzen_wieku_rozwojowego
[short_name] => „Już” znane zespoły mikrodelecji/mikroduplikacji w...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[9] => Array
(
[id] => 9
[site_id] => 1
[status_id] => 5
[name] => zespół delecji
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 9-zespol_delecji
[url] => /9-zespol_delecji
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[137] => Array
(
[id] => 137
[site_id] => 1
[status_id] => 5
[name] => Genetyczne uwarunkowania kraniostenoz
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/137/posterw_erze.png
[video] => resources/data/material/137/kutkowska_genetycz_uwarunkow_kraniostenoz.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n.med. Anna Kutkowska-Kaźmierczak
)
[authors_data] => Array
(
[0] => Array
(
[id] => 64
[site_id] => 1
[status_id] => 5
[name] => dr n.med. Anna Kutkowska-Kaźmierczak
[firstname] => Anna
[lastname] => Kutkowska-Kaźmierczak
[title] => dr n.med.
[affiliation] => Zakład Genetyki Klinicznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 64-anna_kutkowska_kazmierczak
[url] => eksperci/64-anna_kutkowska_kazmierczak
)
)
[authors_ids] => Array
(
[0] => 64
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 137-genetyczne_uwarunkowania_kraniostenoz
[url] => wideo/137-genetyczne_uwarunkowania_kraniostenoz
[short_name] => Genetyczne uwarunkowania kraniostenoz
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[138] => Array
(
[id] => 138
[site_id] => 1
[status_id] => 5
[name] => Niepełnosprawność intelektualna – podłoże genetyczne
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/138/posterw_erze.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n.med. Anna Kutkowska-Kaźmierczak
)
[authors_data] => Array
(
[0] => Array
(
[id] => 64
[site_id] => 1
[status_id] => 5
[name] => dr n.med. Anna Kutkowska-Kaźmierczak
[firstname] => Anna
[lastname] => Kutkowska-Kaźmierczak
[title] => dr n.med.
[affiliation] => Zakład Genetyki Klinicznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 64-anna_kutkowska_kazmierczak
[url] => eksperci/64-anna_kutkowska_kazmierczak
)
)
[authors_ids] => Array
(
[0] => 64
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 138-niepelnosprawnosc_intelektualna__podloze_genetyczne
[url] => wideo/138-niepelnosprawnosc_intelektualna__podloze_genetyczne
[short_name] => Niepełnosprawność intelektualna – podłoże genetycz...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[139] => Array
(
[id] => 139
[site_id] => 1
[status_id] => 5
[name] => Niedosłuch w erze genomowej - możliwości diagnostyczne
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/139/posterw_erze.png
[video] => resources/data/material/139/niepokoj_niedosluch.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Niepokój
)
[authors_data] => Array
(
[0] => Array
(
[id] => 68
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Niepokój
[firstname] => Katarzyna
[lastname] => Niepokój
[title] => dr n. med.
[affiliation] => Zakład Genetyki Medycznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 68-katarzyna_niepokoj
[url] => eksperci/68-katarzyna_niepokoj
)
)
[authors_ids] => Array
(
[0] => 68
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 139-niedosluch_w_erze_genomowej___mozliwosci_diagnostyczne
[url] => wideo/139-niedosluch_w_erze_genomowej___mozliwosci_diagnostyczne
[short_name] => Niedosłuch w erze genomowej - możliwości diagnosty...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[140] => Array
(
[id] => 140
[site_id] => 1
[status_id] => 5
[name] => Zastosowanie sekwencjonowania w diagnostyce molekularnej
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/140/posterw_erze.png
[video] => resources/data/material/140/wertheim_zastosowanie_sekwencjonowania_w_diagnostyce_molekularnej.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 140-zastosowanie_sekwencjonowania_w_diagnostyce_molekularnej
[url] => wideo/140-zastosowanie_sekwencjonowania_w_diagnostyce_molekularnej
[short_name] => Zastosowanie sekwencjonowania w diagnostyce moleku...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[142] => Array
(
[id] => 142
[site_id] => 1
[status_id] => 5
[name] => Diagnostyka mukowiscydozy i chorób CFTR zależnych 30 lat po odkryciu genu CFTR
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/142/posterw_erze.png
[video] => resources/data/material/142/wertheim_diagnostyka_mukowiscydzy.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 142-diagnostyka_mukowiscydozy_i_chorob_cftr_zaleznych_30_lat_po_odkryciu_genu_cftr
[url] => wideo/142-diagnostyka_mukowiscydozy_i_chorob_cftr_zaleznych_30_lat_po_odkryciu_genu_cftr
[short_name] => Diagnostyka mukowiscydozy i chorób CFTR zależnych ...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[143] => Array
(
[id] => 143
[site_id] => 1
[status_id] => 5
[name] => Badania molekularne w diagnostyce galaktozemii
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/143/posterw_erze.png
[video] => resources/data/material/143/wertheim_bad_molek_w_diagnost_galaktozemii.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 143-badania_molekularne_w_diagnostyce_galaktozemii
[url] => wideo/143-badania_molekularne_w_diagnostyce_galaktozemii
[short_name] => Badania molekularne w diagnostyce galaktozemii
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
)
)
[sort] => 1
[status_code] => active
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 141-interpretacja_wynikow_badan_molekularnych_na_przykladzie_genetycznie_uwarunkowanych_chorob_skory
[url] => wideo/141-interpretacja_wynikow_badan_molekularnych_na_przykladzie_genetycznie_uwarunkowanych_chorob_skory
[short_name] => Interpretacja wyników badań molekularnych na przyk...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
[logotypy] => Array
(
)
[pliki] => Array
(
[110] => Array
(
[id] => 110
[site_id] => 1
[status_id] => 5
[entity_key] => material
[entity_id] => 141
[name] => Interpretacja wyników badań molekularnych na przykładzie genetycznie uwarunkowanych chorób skóry
[file] => resources/data/pliki/material/141/interpretacja_wynikow_badan_molekularnych_na_przykladzie_genetycznie_uwarunkowanych.pdf
[sort] => 107
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
[142] => Array
(
[id] => 142
[name] => Diagnostyka mukowiscydozy i chorób CFTR zależnych 30 lat po odkryciu genu CFTR
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/142/posterw_erze.png
[video] => resources/data/material/142/wertheim_diagnostyka_mukowiscydzy.mp4
[content] =>
[ext] => Array
(
[files_header] =>
[linked] => Array
(
[128] => Array
(
[id] => 128
[site_id] => 1
[status_id] => 5
[name] => RASopatie – diagnostyka molekularna wrodzonych zaburzeń rozwojowych
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/128/posterw_erze.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med., prof IMiD Monika Gos
)
[authors_data] => Array
(
[0] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => dr n. med., prof IMiD Monika Gos
[firstname] => Monika
[lastname] => Gos
[title] => dr n. med., prof IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-monika_gos
[url] => eksperci/13-monika_gos
)
)
[authors_ids] => Array
(
[0] => 13
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 128-rasopatie__diagnostyka_molekularna_wrodzonych_zaburzen_rozwojowych
[url] => wideo/128-rasopatie__diagnostyka_molekularna_wrodzonych_zaburzen_rozwojowych
[short_name] => RASopatie – diagnostyka molekularna wrodzonych zab...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[129] => Array
(
[id] => 129
[site_id] => 1
[status_id] => 5
[name] => Zastosowanie metod cytogenetycznych w diagnostyce zaburzeń wieku rozwojowego
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/129/posterw_erze.png
[video] => resources/data/material/129/wisniowiecka_zastosowanie_cytogenetyki.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Barbara Wiśniowiecka-Kowalnik
)
[authors_data] => Array
(
[0] => Array
(
[id] => 7
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Barbara Wiśniowiecka-Kowalnik
[firstname] => Barbara
[lastname] => Wiśniowiecka-Kowalnik
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 7-barbara_wisniowiecka_kowalnik
[url] => eksperci/7-barbara_wisniowiecka_kowalnik
)
)
[authors_ids] => Array
(
[0] => 7
)
[topics] => Array
(
[0] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 129-zastosowanie_metod_cytogenetycznych_w_diagnostyce_zaburzen_wieku_rozwojowego
[url] => wideo/129-zastosowanie_metod_cytogenetycznych_w_diagnostyce_zaburzen_wieku_rozwojowego
[short_name] => Zastosowanie metod cytogenetycznych w diagnostyce ...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[131] => Array
(
[id] => 131
[site_id] => 1
[status_id] => 5
[name] => Typy dziedziczenia chorób genetycznych i poradnictwo genetyczne
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/131/posterw_erze.png
[video] => resources/data/material/131/kutkowska_typy_dziedziczenia.mp4
[content] =>
[ext] => Array
(
[linked] => Array
(
[0] => Array
(
[id] =>
)
)
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n.med. Anna Kutkowska-Kaźmierczak
)
[authors_data] => Array
(
[0] => Array
(
[id] => 64
[site_id] => 1
[status_id] => 5
[name] => dr n.med. Anna Kutkowska-Kaźmierczak
[firstname] => Anna
[lastname] => Kutkowska-Kaźmierczak
[title] => dr n.med.
[affiliation] => Zakład Genetyki Klinicznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 64-anna_kutkowska_kazmierczak
[url] => eksperci/64-anna_kutkowska_kazmierczak
)
)
[authors_ids] => Array
(
[0] => 64
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 131-typy_dziedziczenia_chorob_genetycznych_i_poradnictwo_genetyczne
[url] => wideo/131-typy_dziedziczenia_chorob_genetycznych_i_poradnictwo_genetyczne
[short_name] => Typy dziedziczenia chorób genetycznych i poradnict...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[132] => Array
(
[id] => 132
[site_id] => 1
[status_id] => 5
[name] => Diagnostyka wrodzonych wad metabolizmu
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/132/posterw_erze.png
[video] => resources/data/material/132/rygiel_diagnostyka_wrodzonych_wad_metabolizmu.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab. n. med., prof. IMID Agnieszka Rygiel
)
[authors_data] => Array
(
[0] => Array
(
[id] => 65
[site_id] => 1
[status_id] => 5
[name] => dr hab. n. med., prof. IMID Agnieszka Rygiel
[firstname] => Agnieszka
[lastname] => Rygiel
[title] => dr hab. n. med., prof. IMID
[affiliation] => Zakład Genetyki Medycznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 65-agnieszka_rygiel
[url] => eksperci/65-agnieszka_rygiel
)
)
[authors_ids] => Array
(
[0] => 65
)
[topics] => Array
(
[0] => 2
[1] => 4
[2] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 132-diagnostyka_wrodzonych_wad_metabolizmu
[url] => wideo/132-diagnostyka_wrodzonych_wad_metabolizmu
[short_name] => Diagnostyka wrodzonych wad metabolizmu
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[2] => Array
(
[id] => 2
[site_id] => 1
[status_id] => 5
[name] => metabolizm
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 2-metabolizm
[url] => /2-metabolizm
)
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[133] => Array
(
[id] => 133
[site_id] => 1
[status_id] => 5
[name] => Diagnostyka molekularna genetycznie uwarunkowanego zapalenia trzustki
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/133/posterw_erze.png
[video] => resources/data/material/133/rygiel_diagn_molek_genet_uwarunk_zapalenia_trzustki.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab. n. med., prof. IMID Agnieszka Rygiel
)
[authors_data] => Array
(
[0] => Array
(
[id] => 65
[site_id] => 1
[status_id] => 5
[name] => dr hab. n. med., prof. IMID Agnieszka Rygiel
[firstname] => Agnieszka
[lastname] => Rygiel
[title] => dr hab. n. med., prof. IMID
[affiliation] => Zakład Genetyki Medycznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 65-agnieszka_rygiel
[url] => eksperci/65-agnieszka_rygiel
)
)
[authors_ids] => Array
(
[0] => 65
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 133-diagnostyka_molekularna_genetycznie_uwarunkowanego_zapalenia_trzustki
[url] => wideo/133-diagnostyka_molekularna_genetycznie_uwarunkowanego_zapalenia_trzustki
[short_name] => Diagnostyka molekularna genetycznie uwarunkowanego...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[134] => Array
(
[id] => 134
[site_id] => 1
[status_id] => 5
[name] => Postępowanie diagnostyczne w niepełnosprawności intelektualnej
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/134/posterw_erze.png
[video] => resources/data/material/134/postepowanie_diagnostyczne_w_niepelnosprawnosci_intelektualnej_brak_nazwy_kursu.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Magdalena Bartnik-Głaska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 66
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Magdalena Bartnik-Głaska
[firstname] => Magdalena
[lastname] => Bartnik-Głaska
[title] => dr n. med.
[affiliation] => Zakład Genetyki Medycznej, Instytut Matki i Dziecka, Warszawa
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 66-magdalena_bartnik_glaska
[url] => eksperci/66-magdalena_bartnik_glaska
)
)
[authors_ids] => Array
(
[0] => 66
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 134-postepowanie_diagnostyczne_w_niepelnosprawnosci_intelektualnej
[url] => wideo/134-postepowanie_diagnostyczne_w_niepelnosprawnosci_intelektualnej
[short_name] => Postępowanie diagnostyczne w niepełnosprawności in...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[135] => Array
(
[id] => 135
[site_id] => 1
[status_id] => 5
[name] => Zespoły mikrodelecyjne i mikroduplikacyjne
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/135/posterw_erze.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n.med. Anna Kutkowska-Kaźmierczak
)
[authors_data] => Array
(
[0] => Array
(
[id] => 64
[site_id] => 1
[status_id] => 5
[name] => dr n.med. Anna Kutkowska-Kaźmierczak
[firstname] => Anna
[lastname] => Kutkowska-Kaźmierczak
[title] => dr n.med.
[affiliation] => Zakład Genetyki Klinicznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 64-anna_kutkowska_kazmierczak
[url] => eksperci/64-anna_kutkowska_kazmierczak
)
)
[authors_ids] => Array
(
[0] => 64
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 9
[3] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 135-zespoly_mikrodelecyjne_i_mikroduplikacyjne
[url] => wideo/135-zespoly_mikrodelecyjne_i_mikroduplikacyjne
[short_name] => Zespoły mikrodelecyjne i mikroduplikacyjne
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[9] => Array
(
[id] => 9
[site_id] => 1
[status_id] => 5
[name] => zespół delecji
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 9-zespol_delecji
[url] => /9-zespol_delecji
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[136] => Array
(
[id] => 136
[site_id] => 1
[status_id] => 5
[name] => „Już” znane zespoły mikrodelecji/mikroduplikacji w diagnostyce zaburzeń wieku rozwojowego
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/136/posterw_erze.png
[video] => resources/data/material/136/kedzior_juz_znane_zespoly_mikrodelecji.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr Marta Kędzior
)
[authors_data] => Array
(
[0] => Array
(
[id] => 67
[site_id] => 1
[status_id] => 5
[name] => dr Marta Kędzior
[firstname] => Marta
[lastname] => Kędzior
[title] => dr
[affiliation] => Zakład Genetyki Medycznej, IMiD
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 67-marta_kedzior
[url] => eksperci/67-marta_kedzior
)
)
[authors_ids] => Array
(
[0] => 67
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 9
[3] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 136-juz_znane_zespoly_mikrodelecjimikroduplikacji_w_diagnostyce_zaburzen_wieku_rozwojowego
[url] => wideo/136-juz_znane_zespoly_mikrodelecjimikroduplikacji_w_diagnostyce_zaburzen_wieku_rozwojowego
[short_name] => „Już” znane zespoły mikrodelecji/mikroduplikacji w...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[9] => Array
(
[id] => 9
[site_id] => 1
[status_id] => 5
[name] => zespół delecji
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 9-zespol_delecji
[url] => /9-zespol_delecji
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[137] => Array
(
[id] => 137
[site_id] => 1
[status_id] => 5
[name] => Genetyczne uwarunkowania kraniostenoz
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/137/posterw_erze.png
[video] => resources/data/material/137/kutkowska_genetycz_uwarunkow_kraniostenoz.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n.med. Anna Kutkowska-Kaźmierczak
)
[authors_data] => Array
(
[0] => Array
(
[id] => 64
[site_id] => 1
[status_id] => 5
[name] => dr n.med. Anna Kutkowska-Kaźmierczak
[firstname] => Anna
[lastname] => Kutkowska-Kaźmierczak
[title] => dr n.med.
[affiliation] => Zakład Genetyki Klinicznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 64-anna_kutkowska_kazmierczak
[url] => eksperci/64-anna_kutkowska_kazmierczak
)
)
[authors_ids] => Array
(
[0] => 64
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 137-genetyczne_uwarunkowania_kraniostenoz
[url] => wideo/137-genetyczne_uwarunkowania_kraniostenoz
[short_name] => Genetyczne uwarunkowania kraniostenoz
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[138] => Array
(
[id] => 138
[site_id] => 1
[status_id] => 5
[name] => Niepełnosprawność intelektualna – podłoże genetyczne
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/138/posterw_erze.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n.med. Anna Kutkowska-Kaźmierczak
)
[authors_data] => Array
(
[0] => Array
(
[id] => 64
[site_id] => 1
[status_id] => 5
[name] => dr n.med. Anna Kutkowska-Kaźmierczak
[firstname] => Anna
[lastname] => Kutkowska-Kaźmierczak
[title] => dr n.med.
[affiliation] => Zakład Genetyki Klinicznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 64-anna_kutkowska_kazmierczak
[url] => eksperci/64-anna_kutkowska_kazmierczak
)
)
[authors_ids] => Array
(
[0] => 64
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 138-niepelnosprawnosc_intelektualna__podloze_genetyczne
[url] => wideo/138-niepelnosprawnosc_intelektualna__podloze_genetyczne
[short_name] => Niepełnosprawność intelektualna – podłoże genetycz...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[139] => Array
(
[id] => 139
[site_id] => 1
[status_id] => 5
[name] => Niedosłuch w erze genomowej - możliwości diagnostyczne
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/139/posterw_erze.png
[video] => resources/data/material/139/niepokoj_niedosluch.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Niepokój
)
[authors_data] => Array
(
[0] => Array
(
[id] => 68
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Niepokój
[firstname] => Katarzyna
[lastname] => Niepokój
[title] => dr n. med.
[affiliation] => Zakład Genetyki Medycznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 68-katarzyna_niepokoj
[url] => eksperci/68-katarzyna_niepokoj
)
)
[authors_ids] => Array
(
[0] => 68
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 139-niedosluch_w_erze_genomowej___mozliwosci_diagnostyczne
[url] => wideo/139-niedosluch_w_erze_genomowej___mozliwosci_diagnostyczne
[short_name] => Niedosłuch w erze genomowej - możliwości diagnosty...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[140] => Array
(
[id] => 140
[site_id] => 1
[status_id] => 5
[name] => Zastosowanie sekwencjonowania w diagnostyce molekularnej
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/140/posterw_erze.png
[video] => resources/data/material/140/wertheim_zastosowanie_sekwencjonowania_w_diagnostyce_molekularnej.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 140-zastosowanie_sekwencjonowania_w_diagnostyce_molekularnej
[url] => wideo/140-zastosowanie_sekwencjonowania_w_diagnostyce_molekularnej
[short_name] => Zastosowanie sekwencjonowania w diagnostyce moleku...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[141] => Array
(
[id] => 141
[site_id] => 1
[status_id] => 5
[name] => Interpretacja wyników badań molekularnych na przykładzie genetycznie uwarunkowanych chorób skóry
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/141/posterw_erze.png
[video] => resources/data/material/141/interpretacja_wynikow_badan_molekularnych_na_przykladzie_genetycznie_uwarunkowanych_chorob_skory_wertheimtyssarowska_12_min_uciety_poczatek_zdania.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 141-interpretacja_wynikow_badan_molekularnych_na_przykladzie_genetycznie_uwarunkowanych_chorob_skory
[url] => wideo/141-interpretacja_wynikow_badan_molekularnych_na_przykladzie_genetycznie_uwarunkowanych_chorob_skory
[short_name] => Interpretacja wyników badań molekularnych na przyk...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[143] => Array
(
[id] => 143
[site_id] => 1
[status_id] => 5
[name] => Badania molekularne w diagnostyce galaktozemii
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/143/posterw_erze.png
[video] => resources/data/material/143/wertheim_bad_molek_w_diagnost_galaktozemii.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 143-badania_molekularne_w_diagnostyce_galaktozemii
[url] => wideo/143-badania_molekularne_w_diagnostyce_galaktozemii
[short_name] => Badania molekularne w diagnostyce galaktozemii
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
)
)
[sort] => 1
[status_code] => active
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 142-diagnostyka_mukowiscydozy_i_chorob_cftr_zaleznych_30_lat_po_odkryciu_genu_cftr
[url] => wideo/142-diagnostyka_mukowiscydozy_i_chorob_cftr_zaleznych_30_lat_po_odkryciu_genu_cftr
[short_name] => Diagnostyka mukowiscydozy i chorób CFTR zależnych ...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
[logotypy] => Array
(
)
[pliki] => Array
(
[111] => Array
(
[id] => 111
[site_id] => 1
[status_id] => 5
[entity_key] => material
[entity_id] => 142
[name] => Diagnostyka mukowiscydozy i chorób CFTR zależnych 30 lat po odkryciu genu CFTR
[file] => resources/data/pliki/material/142/diagnostyka_mukowiscydozy_i_chorob_cftr_zaleznych_30_lat_po_odkryciu_genu_cftr.pdf
[sort] => 108
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
[143] => Array
(
[id] => 143
[name] => Badania molekularne w diagnostyce galaktozemii
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/143/posterw_erze.png
[video] => resources/data/material/143/wertheim_bad_molek_w_diagnost_galaktozemii.mp4
[content] =>
[ext] => Array
(
[files_header] =>
[linked] => Array
(
[128] => Array
(
[id] => 128
[site_id] => 1
[status_id] => 5
[name] => RASopatie – diagnostyka molekularna wrodzonych zaburzeń rozwojowych
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/128/posterw_erze.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med., prof IMiD Monika Gos
)
[authors_data] => Array
(
[0] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => dr n. med., prof IMiD Monika Gos
[firstname] => Monika
[lastname] => Gos
[title] => dr n. med., prof IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-monika_gos
[url] => eksperci/13-monika_gos
)
)
[authors_ids] => Array
(
[0] => 13
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 128-rasopatie__diagnostyka_molekularna_wrodzonych_zaburzen_rozwojowych
[url] => wideo/128-rasopatie__diagnostyka_molekularna_wrodzonych_zaburzen_rozwojowych
[short_name] => RASopatie – diagnostyka molekularna wrodzonych zab...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[129] => Array
(
[id] => 129
[site_id] => 1
[status_id] => 5
[name] => Zastosowanie metod cytogenetycznych w diagnostyce zaburzeń wieku rozwojowego
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/129/posterw_erze.png
[video] => resources/data/material/129/wisniowiecka_zastosowanie_cytogenetyki.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Barbara Wiśniowiecka-Kowalnik
)
[authors_data] => Array
(
[0] => Array
(
[id] => 7
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Barbara Wiśniowiecka-Kowalnik
[firstname] => Barbara
[lastname] => Wiśniowiecka-Kowalnik
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 7-barbara_wisniowiecka_kowalnik
[url] => eksperci/7-barbara_wisniowiecka_kowalnik
)
)
[authors_ids] => Array
(
[0] => 7
)
[topics] => Array
(
[0] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 129-zastosowanie_metod_cytogenetycznych_w_diagnostyce_zaburzen_wieku_rozwojowego
[url] => wideo/129-zastosowanie_metod_cytogenetycznych_w_diagnostyce_zaburzen_wieku_rozwojowego
[short_name] => Zastosowanie metod cytogenetycznych w diagnostyce ...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[131] => Array
(
[id] => 131
[site_id] => 1
[status_id] => 5
[name] => Typy dziedziczenia chorób genetycznych i poradnictwo genetyczne
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/131/posterw_erze.png
[video] => resources/data/material/131/kutkowska_typy_dziedziczenia.mp4
[content] =>
[ext] => Array
(
[linked] => Array
(
[0] => Array
(
[id] =>
)
)
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n.med. Anna Kutkowska-Kaźmierczak
)
[authors_data] => Array
(
[0] => Array
(
[id] => 64
[site_id] => 1
[status_id] => 5
[name] => dr n.med. Anna Kutkowska-Kaźmierczak
[firstname] => Anna
[lastname] => Kutkowska-Kaźmierczak
[title] => dr n.med.
[affiliation] => Zakład Genetyki Klinicznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 64-anna_kutkowska_kazmierczak
[url] => eksperci/64-anna_kutkowska_kazmierczak
)
)
[authors_ids] => Array
(
[0] => 64
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 131-typy_dziedziczenia_chorob_genetycznych_i_poradnictwo_genetyczne
[url] => wideo/131-typy_dziedziczenia_chorob_genetycznych_i_poradnictwo_genetyczne
[short_name] => Typy dziedziczenia chorób genetycznych i poradnict...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[132] => Array
(
[id] => 132
[site_id] => 1
[status_id] => 5
[name] => Diagnostyka wrodzonych wad metabolizmu
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/132/posterw_erze.png
[video] => resources/data/material/132/rygiel_diagnostyka_wrodzonych_wad_metabolizmu.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab. n. med., prof. IMID Agnieszka Rygiel
)
[authors_data] => Array
(
[0] => Array
(
[id] => 65
[site_id] => 1
[status_id] => 5
[name] => dr hab. n. med., prof. IMID Agnieszka Rygiel
[firstname] => Agnieszka
[lastname] => Rygiel
[title] => dr hab. n. med., prof. IMID
[affiliation] => Zakład Genetyki Medycznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 65-agnieszka_rygiel
[url] => eksperci/65-agnieszka_rygiel
)
)
[authors_ids] => Array
(
[0] => 65
)
[topics] => Array
(
[0] => 2
[1] => 4
[2] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 132-diagnostyka_wrodzonych_wad_metabolizmu
[url] => wideo/132-diagnostyka_wrodzonych_wad_metabolizmu
[short_name] => Diagnostyka wrodzonych wad metabolizmu
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[2] => Array
(
[id] => 2
[site_id] => 1
[status_id] => 5
[name] => metabolizm
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 2-metabolizm
[url] => /2-metabolizm
)
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[133] => Array
(
[id] => 133
[site_id] => 1
[status_id] => 5
[name] => Diagnostyka molekularna genetycznie uwarunkowanego zapalenia trzustki
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/133/posterw_erze.png
[video] => resources/data/material/133/rygiel_diagn_molek_genet_uwarunk_zapalenia_trzustki.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab. n. med., prof. IMID Agnieszka Rygiel
)
[authors_data] => Array
(
[0] => Array
(
[id] => 65
[site_id] => 1
[status_id] => 5
[name] => dr hab. n. med., prof. IMID Agnieszka Rygiel
[firstname] => Agnieszka
[lastname] => Rygiel
[title] => dr hab. n. med., prof. IMID
[affiliation] => Zakład Genetyki Medycznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 65-agnieszka_rygiel
[url] => eksperci/65-agnieszka_rygiel
)
)
[authors_ids] => Array
(
[0] => 65
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 133-diagnostyka_molekularna_genetycznie_uwarunkowanego_zapalenia_trzustki
[url] => wideo/133-diagnostyka_molekularna_genetycznie_uwarunkowanego_zapalenia_trzustki
[short_name] => Diagnostyka molekularna genetycznie uwarunkowanego...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[134] => Array
(
[id] => 134
[site_id] => 1
[status_id] => 5
[name] => Postępowanie diagnostyczne w niepełnosprawności intelektualnej
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/134/posterw_erze.png
[video] => resources/data/material/134/postepowanie_diagnostyczne_w_niepelnosprawnosci_intelektualnej_brak_nazwy_kursu.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Magdalena Bartnik-Głaska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 66
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Magdalena Bartnik-Głaska
[firstname] => Magdalena
[lastname] => Bartnik-Głaska
[title] => dr n. med.
[affiliation] => Zakład Genetyki Medycznej, Instytut Matki i Dziecka, Warszawa
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 66-magdalena_bartnik_glaska
[url] => eksperci/66-magdalena_bartnik_glaska
)
)
[authors_ids] => Array
(
[0] => 66
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 134-postepowanie_diagnostyczne_w_niepelnosprawnosci_intelektualnej
[url] => wideo/134-postepowanie_diagnostyczne_w_niepelnosprawnosci_intelektualnej
[short_name] => Postępowanie diagnostyczne w niepełnosprawności in...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[135] => Array
(
[id] => 135
[site_id] => 1
[status_id] => 5
[name] => Zespoły mikrodelecyjne i mikroduplikacyjne
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/135/posterw_erze.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n.med. Anna Kutkowska-Kaźmierczak
)
[authors_data] => Array
(
[0] => Array
(
[id] => 64
[site_id] => 1
[status_id] => 5
[name] => dr n.med. Anna Kutkowska-Kaźmierczak
[firstname] => Anna
[lastname] => Kutkowska-Kaźmierczak
[title] => dr n.med.
[affiliation] => Zakład Genetyki Klinicznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 64-anna_kutkowska_kazmierczak
[url] => eksperci/64-anna_kutkowska_kazmierczak
)
)
[authors_ids] => Array
(
[0] => 64
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 9
[3] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 135-zespoly_mikrodelecyjne_i_mikroduplikacyjne
[url] => wideo/135-zespoly_mikrodelecyjne_i_mikroduplikacyjne
[short_name] => Zespoły mikrodelecyjne i mikroduplikacyjne
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[9] => Array
(
[id] => 9
[site_id] => 1
[status_id] => 5
[name] => zespół delecji
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 9-zespol_delecji
[url] => /9-zespol_delecji
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[136] => Array
(
[id] => 136
[site_id] => 1
[status_id] => 5
[name] => „Już” znane zespoły mikrodelecji/mikroduplikacji w diagnostyce zaburzeń wieku rozwojowego
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/136/posterw_erze.png
[video] => resources/data/material/136/kedzior_juz_znane_zespoly_mikrodelecji.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr Marta Kędzior
)
[authors_data] => Array
(
[0] => Array
(
[id] => 67
[site_id] => 1
[status_id] => 5
[name] => dr Marta Kędzior
[firstname] => Marta
[lastname] => Kędzior
[title] => dr
[affiliation] => Zakład Genetyki Medycznej, IMiD
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 67-marta_kedzior
[url] => eksperci/67-marta_kedzior
)
)
[authors_ids] => Array
(
[0] => 67
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 9
[3] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 136-juz_znane_zespoly_mikrodelecjimikroduplikacji_w_diagnostyce_zaburzen_wieku_rozwojowego
[url] => wideo/136-juz_znane_zespoly_mikrodelecjimikroduplikacji_w_diagnostyce_zaburzen_wieku_rozwojowego
[short_name] => „Już” znane zespoły mikrodelecji/mikroduplikacji w...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[9] => Array
(
[id] => 9
[site_id] => 1
[status_id] => 5
[name] => zespół delecji
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 9-zespol_delecji
[url] => /9-zespol_delecji
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[137] => Array
(
[id] => 137
[site_id] => 1
[status_id] => 5
[name] => Genetyczne uwarunkowania kraniostenoz
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/137/posterw_erze.png
[video] => resources/data/material/137/kutkowska_genetycz_uwarunkow_kraniostenoz.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n.med. Anna Kutkowska-Kaźmierczak
)
[authors_data] => Array
(
[0] => Array
(
[id] => 64
[site_id] => 1
[status_id] => 5
[name] => dr n.med. Anna Kutkowska-Kaźmierczak
[firstname] => Anna
[lastname] => Kutkowska-Kaźmierczak
[title] => dr n.med.
[affiliation] => Zakład Genetyki Klinicznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 64-anna_kutkowska_kazmierczak
[url] => eksperci/64-anna_kutkowska_kazmierczak
)
)
[authors_ids] => Array
(
[0] => 64
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 137-genetyczne_uwarunkowania_kraniostenoz
[url] => wideo/137-genetyczne_uwarunkowania_kraniostenoz
[short_name] => Genetyczne uwarunkowania kraniostenoz
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[138] => Array
(
[id] => 138
[site_id] => 1
[status_id] => 5
[name] => Niepełnosprawność intelektualna – podłoże genetyczne
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/138/posterw_erze.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n.med. Anna Kutkowska-Kaźmierczak
)
[authors_data] => Array
(
[0] => Array
(
[id] => 64
[site_id] => 1
[status_id] => 5
[name] => dr n.med. Anna Kutkowska-Kaźmierczak
[firstname] => Anna
[lastname] => Kutkowska-Kaźmierczak
[title] => dr n.med.
[affiliation] => Zakład Genetyki Klinicznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 64-anna_kutkowska_kazmierczak
[url] => eksperci/64-anna_kutkowska_kazmierczak
)
)
[authors_ids] => Array
(
[0] => 64
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 138-niepelnosprawnosc_intelektualna__podloze_genetyczne
[url] => wideo/138-niepelnosprawnosc_intelektualna__podloze_genetyczne
[short_name] => Niepełnosprawność intelektualna – podłoże genetycz...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[139] => Array
(
[id] => 139
[site_id] => 1
[status_id] => 5
[name] => Niedosłuch w erze genomowej - możliwości diagnostyczne
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/139/posterw_erze.png
[video] => resources/data/material/139/niepokoj_niedosluch.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Niepokój
)
[authors_data] => Array
(
[0] => Array
(
[id] => 68
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Niepokój
[firstname] => Katarzyna
[lastname] => Niepokój
[title] => dr n. med.
[affiliation] => Zakład Genetyki Medycznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 68-katarzyna_niepokoj
[url] => eksperci/68-katarzyna_niepokoj
)
)
[authors_ids] => Array
(
[0] => 68
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 139-niedosluch_w_erze_genomowej___mozliwosci_diagnostyczne
[url] => wideo/139-niedosluch_w_erze_genomowej___mozliwosci_diagnostyczne
[short_name] => Niedosłuch w erze genomowej - możliwości diagnosty...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[140] => Array
(
[id] => 140
[site_id] => 1
[status_id] => 5
[name] => Zastosowanie sekwencjonowania w diagnostyce molekularnej
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/140/posterw_erze.png
[video] => resources/data/material/140/wertheim_zastosowanie_sekwencjonowania_w_diagnostyce_molekularnej.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 140-zastosowanie_sekwencjonowania_w_diagnostyce_molekularnej
[url] => wideo/140-zastosowanie_sekwencjonowania_w_diagnostyce_molekularnej
[short_name] => Zastosowanie sekwencjonowania w diagnostyce moleku...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[141] => Array
(
[id] => 141
[site_id] => 1
[status_id] => 5
[name] => Interpretacja wyników badań molekularnych na przykładzie genetycznie uwarunkowanych chorób skóry
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/141/posterw_erze.png
[video] => resources/data/material/141/interpretacja_wynikow_badan_molekularnych_na_przykladzie_genetycznie_uwarunkowanych_chorob_skory_wertheimtyssarowska_12_min_uciety_poczatek_zdania.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 141-interpretacja_wynikow_badan_molekularnych_na_przykladzie_genetycznie_uwarunkowanych_chorob_skory
[url] => wideo/141-interpretacja_wynikow_badan_molekularnych_na_przykladzie_genetycznie_uwarunkowanych_chorob_skory
[short_name] => Interpretacja wyników badań molekularnych na przyk...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[142] => Array
(
[id] => 142
[site_id] => 1
[status_id] => 5
[name] => Diagnostyka mukowiscydozy i chorób CFTR zależnych 30 lat po odkryciu genu CFTR
[type_id] => 1
[group_id] => 18
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/142/posterw_erze.png
[video] => resources/data/material/142/wertheim_diagnostyka_mukowiscydzy.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 142-diagnostyka_mukowiscydozy_i_chorob_cftr_zaleznych_30_lat_po_odkryciu_genu_cftr
[url] => wideo/142-diagnostyka_mukowiscydozy_i_chorob_cftr_zaleznych_30_lat_po_odkryciu_genu_cftr
[short_name] => Diagnostyka mukowiscydozy i chorób CFTR zależnych ...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
)
)
[sort] => 1
[status_code] => active
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 143-badania_molekularne_w_diagnostyce_galaktozemii
[url] => wideo/143-badania_molekularne_w_diagnostyce_galaktozemii
[short_name] => Badania molekularne w diagnostyce galaktozemii
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 18
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Choroby genetyczne wieku rozwojowego – możliwości diagnostyczne w erze badań genomowych.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
[fields] => Array
(
[0] => Array
(
[text] => {user.ext.pani}
[image] =>
[type] => C
[pos] => 90,0
[font] => 20
)
[1] => Array
(
[text] => {user.ext.firstname} {user.ext.lastname}
[image] =>
[type] => C
[pos] => 105,0
[font] => 25
)
[2] => Array
(
[text] => {user.ext.ukonczyla} kurs on-line:
[image] =>
[type] => C
[pos] => 120,0
[font] => 15
)
[3] => Array
(
[text] => {group.name}
[image] =>
[type] => TC
[pos] => 130,45,120,10
[font] => 25
)
[4] => Array
(
[text] => Warszawa, {now}
[image] =>
[type] => C
[pos] => 190,0
[font] => 10
)
[5] => Array
(
[text] => Przyznane punkty edukacyjne: 2
[image] =>
[type] => C
[pos] => 200,0
[font] => 10
)
)
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
[url] => kursy/18-choroby_genetyczne_wieku_rozwojowego__mozliwosci_diagnostyczne_w_erze_badan_genomowych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
[logotypy] => Array
(
)
[pliki] => Array
(
[112] => Array
(
[id] => 112
[site_id] => 1
[status_id] => 5
[entity_key] => material
[entity_id] => 143
[name] => Badania molekularne w diagnostyce galaktozemii
[file] => resources/data/pliki/material/143/badania_molekularne_w_diagnostyce_galaktozemii.pdf
[sort] => 109
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
)
[quiz_questions] => Array
(
[384] => Array
(
[id] => 384
[site_id] => 1
[status_id] => 5
[group_id] => 18
[type_id] => 1
[name] => Metody cytogenetyczne umożliwiające analizę całego genomu to:
[ext] =>
[sort] => 0
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[type_name] => pojedyncza odpowiedź
[type_code] => single
[answers] => Array
(
[1411] => Array
(
[id] => 1411
[site_id] => 1
[status_id] => 5
[question_id] => 384
[name] => Tylko 2
[correct] => 0
[ext] =>
[sort] => 1404
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[1412] => Array
(
[id] => 1412
[site_id] => 1
[status_id] => 5
[question_id] => 384
[name] => 1, 2, 3
[correct] => 0
[ext] =>
[sort] => 1405
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[1413] => Array
(
[id] => 1413
[site_id] => 1
[status_id] => 5
[question_id] => 384
[name] => 2, 3, 5
[correct] => 0
[ext] =>
[sort] => 1406
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[1414] => Array
(
[id] => 1414
[site_id] => 1
[status_id] => 5
[question_id] => 384
[name] => Wszystkie odpowiedzi są prawdziwe
[correct] => 1
[ext] =>
[sort] => 1407
[correct_yesno] => Tak
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
[385] => Array
(
[id] => 385
[site_id] => 1
[status_id] => 5
[group_id] => 18
[type_id] => 1
[name] => Wskaż nieprawidłową odpowiedź: Weryfikacja obecności mikrodelecji regionu AZF chromosomu Y umożliwia m.in.
[ext] =>
[sort] => 0
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[type_name] => pojedyncza odpowiedź
[type_code] => single
[answers] => Array
(
[1415] => Array
(
[id] => 1415
[site_id] => 1
[status_id] => 5
[question_id] => 385
[name] => a) Ustalenie przyczyny niepłodności
[correct] => 0
[ext] =>
[sort] => 1408
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[1416] => Array
(
[id] => 1416
[site_id] => 1
[status_id] => 5
[question_id] => 385
[name] => b) Zaplanowanie dalszego postępowania z parą
[correct] => 0
[ext] =>
[sort] => 1409
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[1417] => Array
(
[id] => 1417
[site_id] => 1
[status_id] => 5
[question_id] => 385
[name] => c) Ocenę szansy sukcesu w TESE, ART
[correct] => 0
[ext] =>
[sort] => 1410
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[1418] => Array
(
[id] => 1418
[site_id] => 1
[status_id] => 5
[question_id] => 385
[name] => d) Ocenę ryzyka przekazania niepłodności potomstwu płci żeńskiej
[correct] => 1
[ext] =>
[sort] => 1411
[correct_yesno] => Tak
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
[386] => Array
(
[id] => 386
[site_id] => 1
[status_id] => 5
[group_id] => 18
[type_id] => 1
[name] => Wskaż zdanie prawdziwe:
[ext] =>
[sort] => 0
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[type_name] => pojedyncza odpowiedź
[type_code] => single
[answers] => Array
(
[1419] => Array
(
[id] => 1419
[site_id] => 1
[status_id] => 5
[question_id] => 386
[name] => a) CBAVD jest wynikiem mutacji tylko w genie CFTR
[correct] => 0
[ext] =>
[sort] => 1412
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[1420] => Array
(
[id] => 1420
[site_id] => 1
[status_id] => 5
[question_id] => 386
[name] => b) Premutacje genu FMR1 są przyczyną przedwczesnego wygasania funkcji jajników
[correct] => 1
[ext] =>
[sort] => 1413
[correct_yesno] => Tak
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[1421] => Array
(
[id] => 1421
[site_id] => 1
[status_id] => 5
[question_id] => 386
[name] => c) Jednym ze wskazań do badania genu CFTR jest występowanie CBAVD z towarzyszącą agenezją nerki
[correct] => 0
[ext] =>
[sort] => 1414
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[1422] => Array
(
[id] => 1422
[site_id] => 1
[status_id] => 5
[question_id] => 386
[name] => d) Prawidłowy wynik kariotypu, analizy regionu AZF chromosomu Y i genu CFTR oznacza, że przyczyną oligozoospermii u Pacjenta nie jest czynnik genetyczny.
[correct] => 0
[ext] =>
[sort] => 1415
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
[387] => Array
(
[id] => 387
[site_id] => 1
[status_id] => 5
[group_id] => 18
[type_id] => 1
[name] => Zaznacz odpowiedź prawidłową dotyczącą techniki MLPA wykorzystywanej w szybkiej diagnostyce aneuploidii u płodu:
[ext] =>
[sort] => 0
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[type_name] => pojedyncza odpowiedź
[type_code] => single
[answers] => Array
(
[1423] => Array
(
[id] => 1423
[site_id] => 1
[status_id] => 5
[question_id] => 387
[name] => a) wykrywa aberracje zrównoważone, nie wykrywa kontaminacji krwią matczyną
[correct] => 0
[ext] =>
[sort] => 1416
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[1424] => Array
(
[id] => 1424
[site_id] => 1
[status_id] => 5
[question_id] => 387
[name] => b) nie wykrywa kontaminacji krwią matczyną, nie wykrywa mozaikowości, nie wykrywa triploidii
[correct] => 1
[ext] =>
[sort] => 1417
[correct_yesno] => Tak
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[1425] => Array
(
[id] => 1425
[site_id] => 1
[status_id] => 5
[question_id] => 387
[name] => c) wykrywa aberracje zrównoważone, wykrywa triploidię
[correct] => 0
[ext] =>
[sort] => 1418
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[1426] => Array
(
[id] => 1426
[site_id] => 1
[status_id] => 5
[question_id] => 387
[name] => d) wykrywa triploidię, nie wykrywa aberracji zrównoważonych
[correct] => 0
[ext] =>
[sort] => 1419
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
[388] => Array
(
[id] => 388
[site_id] => 1
[status_id] => 5
[group_id] => 18
[type_id] => 1
[name] => Które zdania NIE dotyczą zespołu Klinefeltera:
[ext] =>
[sort] => 0
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[type_name] => pojedyncza odpowiedź
[type_code] => single
[answers] => Array
(
[1427] => Array
(
[id] => 1427
[site_id] => 1
[status_id] => 5
[question_id] => 388
[name] => a) jest najczęstszą genetyczną przyczyną niepłodności męskiej
[correct] => 0
[ext] =>
[sort] => 1420
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[1428] => Array
(
[id] => 1428
[site_id] => 1
[status_id] => 5
[question_id] => 388
[name] => b) związany jest z azoospermią lub znaczną oligozoospermią
[correct] => 0
[ext] =>
[sort] => 1421
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[1429] => Array
(
[id] => 1429
[site_id] => 1
[status_id] => 5
[question_id] => 388
[name] => c) zazwyczaj stwierdza się kariotyp mozaikowy
[correct] => 1
[ext] =>
[sort] => 1422
[correct_yesno] => Tak
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[1430] => Array
(
[id] => 1430
[site_id] => 1
[status_id] => 5
[question_id] => 388
[name] => d) występuje z częstością 1 na 500 mężczyzn
[correct] => 0
[ext] =>
[sort] => 1423
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
[133] => Array
(
[id] => 133
[site_id] => 1
[status_id] => 5
[group_id] => 18
[type_id] => 1
[name] => W dziedziczeniu autosomalnym recesywnym: 1. Rodzice najczęściej są nosicielami mutacji w genie związanym z chorobą dziecka. 2. Rodzice nosiciele ponoszą ryzyko wynoszące 25% wystąpienia choroby u kolejnego potomstwa. 3. Nosiciel mutacji w jednym allelu genu jest osobą zdrową. 4. Osoba z chorobą o uwarunkowaniu autosomalnym recesywnym ma szanse na zdrowe potomstwo, jeśli u partnera zostanie wykluczone nosicielstwo mutacji w genie związanym z chorobą. 5. Pokrewieństwo zwiększa ryzyko wystąpienia choroby o tym uwarunkowaniu genetycznym. Odpowiedź prawidłowa to:
[ext] =>
[sort] => 0
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[type_name] => pojedyncza odpowiedź
[type_code] => single
[answers] => Array
(
[443] => Array
(
[id] => 443
[site_id] => 1
[status_id] => 5
[question_id] => 133
[name] => a. tylko 2
[correct] => 0
[ext] =>
[sort] => 436
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[444] => Array
(
[id] => 444
[site_id] => 1
[status_id] => 5
[question_id] => 133
[name] => b. 1, 2, 3
[correct] => 0
[ext] =>
[sort] => 437
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[445] => Array
(
[id] => 445
[site_id] => 1
[status_id] => 5
[question_id] => 133
[name] => c. 2, 3, 5
[correct] => 0
[ext] =>
[sort] => 438
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[446] => Array
(
[id] => 446
[site_id] => 1
[status_id] => 5
[question_id] => 133
[name] => Wszystkie odpowiedzi są prawdziwe
[correct] => 1
[ext] =>
[sort] => 439
[correct_yesno] => Tak
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
[389] => Array
(
[id] => 389
[site_id] => 1
[status_id] => 5
[group_id] => 18
[type_id] => 1
[name] => Zaznacz BŁĘDNE zdanie dotyczące chromosomów markerowych stwierdzanych u osób z niepłodnością
[ext] =>
[sort] => 0
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[type_name] => pojedyncza odpowiedź
[type_code] => single
[answers] => Array
(
[1431] => Array
(
[id] => 1431
[site_id] => 1
[status_id] => 5
[question_id] => 389
[name] => a) Najczęściej stwierdza się markery pochodzące z chromosomów akrocentrycznych
[correct] => 0
[ext] =>
[sort] => 1424
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[1432] => Array
(
[id] => 1432
[site_id] => 1
[status_id] => 5
[question_id] => 389
[name] => b) Chromosomy markerowe wpływają na niepowodzenia rozrodu nosicieli, ponieważ zawierają geny związane z niepłodnością
[correct] => 1
[ext] =>
[sort] => 1425
[correct_yesno] => Tak
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[1433] => Array
(
[id] => 1433
[site_id] => 1
[status_id] => 5
[question_id] => 389
[name] => c) U osób niepłodnych najczęściej stwierdza się markery pochodzące z chromosomu 15.
[correct] => 0
[ext] =>
[sort] => 1426
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[1434] => Array
(
[id] => 1434
[site_id] => 1
[status_id] => 5
[question_id] => 389
[name] => d) Obecność chromosomu markerowego zaburza proces gametogenezy
[correct] => 0
[ext] =>
[sort] => 1427
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
[134] => Array
(
[id] => 134
[site_id] => 1
[status_id] => 5
[group_id] => 18
[type_id] => 1
[name] => Zaznacz odpowiedź prawdziwą: 1. Na podstawie analizy rodowodu nie można podejrzewać sposobu dziedziczenia choroby. 2. W chorobach o dziedziczeniu sprzężonym z chromosomem X recesywnym u matek nosicielek choroby może nie być żadnych objawów klinicznych, a chorują wyłącznie synowie. 3. W chorobach o uwarunkowaniu autosomalnym dominującym osoba chora ponosi ryzyko wynoszące 100% wystąpienia choroby u potomstwa. 4. W chorobach o dziedziczeniu sprzężonym z chromosomem X dominującym chorują wyłącznie kobiety, ponieważ najczęściej są one letalne dla płci męskiej. Odpowiedź prawidłowa to:
[ext] =>
[sort] => 0
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[type_name] => pojedyncza odpowiedź
[type_code] => single
[answers] => Array
(
[447] => Array
(
[id] => 447
[site_id] => 1
[status_id] => 5
[question_id] => 134
[name] => a. 1, 3
[correct] => 0
[ext] =>
[sort] => 440
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[448] => Array
(
[id] => 448
[site_id] => 1
[status_id] => 5
[question_id] => 134
[name] => b. 1, 2, 3
[correct] => 0
[ext] =>
[sort] => 441
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[449] => Array
(
[id] => 449
[site_id] => 1
[status_id] => 5
[question_id] => 134
[name] => c. 2, 4
[correct] => 1
[ext] =>
[sort] => 442
[correct_yesno] => Tak
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[450] => Array
(
[id] => 450
[site_id] => 1
[status_id] => 5
[question_id] => 134
[name] => d. 2, 3, 4
[correct] => 0
[ext] =>
[sort] => 443
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
[390] => Array
(
[id] => 390
[site_id] => 1
[status_id] => 5
[group_id] => 18
[type_id] => 1
[name] => Aby ustalić typ trisomii (prosta czy translokacyjna) należy wykonać badanie:
[ext] =>
[sort] => 0
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[type_name] => pojedyncza odpowiedź
[type_code] => single
[answers] => Array
(
[1435] => Array
(
[id] => 1435
[site_id] => 1
[status_id] => 5
[question_id] => 390
[name] => a) QF-PCR
[correct] => 0
[ext] =>
[sort] => 1428
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[1436] => Array
(
[id] => 1436
[site_id] => 1
[status_id] => 5
[question_id] => 390
[name] => b) Rapid FISH
[correct] => 0
[ext] =>
[sort] => 1429
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[1437] => Array
(
[id] => 1437
[site_id] => 1
[status_id] => 5
[question_id] => 390
[name] => c) MLPA
[correct] => 0
[ext] =>
[sort] => 1430
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[1438] => Array
(
[id] => 1438
[site_id] => 1
[status_id] => 5
[question_id] => 390
[name] => d) Kariotyp
[correct] => 1
[ext] =>
[sort] => 1431
[correct_yesno] => Tak
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
[135] => Array
(
[id] => 135
[site_id] => 1
[status_id] => 5
[group_id] => 18
[type_id] => 1
[name] => Zespół Crouzona: 1. Należy do zespołów kraniostenoz. 2. Występuje w tym zespole przedwczesne zarastanie szwów czaszkowych. 3. Charakteryzuje się brakiem występowania wad kończyn i wad innych narządów poza nieprawidłowościami budowy czaszki. 4. Brak kraniostenozy nie wyklucza rozpoznania tego zespołu. Odpowiedź prawidłowa to:
[ext] =>
[sort] => 0
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[type_name] => pojedyncza odpowiedź
[type_code] => single
[answers] => Array
(
[451] => Array
(
[id] => 451
[site_id] => 1
[status_id] => 5
[question_id] => 135
[name] => a. Tylko 1
[correct] => 0
[ext] =>
[sort] => 444
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[452] => Array
(
[id] => 452
[site_id] => 1
[status_id] => 5
[question_id] => 135
[name] => b. 1 i 2
[correct] => 0
[ext] =>
[sort] => 445
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[453] => Array
(
[id] => 453
[site_id] => 1
[status_id] => 5
[question_id] => 135
[name] => c. 2 i 3
[correct] => 0
[ext] =>
[sort] => 446
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[454] => Array
(
[id] => 454
[site_id] => 1
[status_id] => 5
[question_id] => 135
[name] => d. Wszystkie odpowiedzi są prawidłowe
[correct] => 1
[ext] =>
[sort] => 447
[correct_yesno] => Tak
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
[391] => Array
(
[id] => 391
[site_id] => 1
[status_id] => 5
[group_id] => 18
[type_id] => 1
[name] => Zaznacz BŁĘDNE zdanie:
[ext] =>
[sort] => 0
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[type_name] => pojedyncza odpowiedź
[type_code] => single
[answers] => Array
(
[1439] => Array
(
[id] => 1439
[site_id] => 1
[status_id] => 5
[question_id] => 391
[name] => a) Wszystkie kobiety ciężarne powinny mieć zaproponowane przesiewowe badania prenatalne
[correct] => 0
[ext] =>
[sort] => 1432
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[1440] => Array
(
[id] => 1440
[site_id] => 1
[status_id] => 5
[question_id] => 391
[name] => b) Badania inwazyjne powinny być wykonane po uprzednich badaniach przesiewowych
[correct] => 0
[ext] =>
[sort] => 1433
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[1441] => Array
(
[id] => 1441
[site_id] => 1
[status_id] => 5
[question_id] => 391
[name] => c) Badania przesiewowe nie określają ryzyka wystąpienia aberracji chromosomowych
[correct] => 1
[ext] =>
[sort] => 1434
[correct_yesno] => Tak
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[1442] => Array
(
[id] => 1442
[site_id] => 1
[status_id] => 5
[question_id] => 391
[name] => d) Kobietom, które decydują się na pominięcie etapu skriningowego, należy umożliwić wykonanie badania inwazyjnego po uprzednim poinformowaniu o możliwych powikłaniach
[correct] => 0
[ext] =>
[sort] => 1435
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
[136] => Array
(
[id] => 136
[site_id] => 1
[status_id] => 5
[group_id] => 18
[type_id] => 1
[name] => Metody cytogenetyczne umożliwiające analizę całego genomu to:
[ext] =>
[sort] => 0
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[type_name] => pojedyncza odpowiedź
[type_code] => single
[answers] => Array
(
[455] => Array
(
[id] => 455
[site_id] => 1
[status_id] => 5
[question_id] => 136
[name] => a. FISH i aCGH
[correct] => 0
[ext] =>
[sort] => 448
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[456] => Array
(
[id] => 456
[site_id] => 1
[status_id] => 5
[question_id] => 136
[name] => b. MLPA i kariotyp
[correct] => 0
[ext] =>
[sort] => 449
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[457] => Array
(
[id] => 457
[site_id] => 1
[status_id] => 5
[question_id] => 136
[name] => c. kariotyp i aCGH
[correct] => 1
[ext] =>
[sort] => 450
[correct_yesno] => Tak
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[458] => Array
(
[id] => 458
[site_id] => 1
[status_id] => 5
[question_id] => 136
[name] => d. MLPA i FISH
[correct] => 0
[ext] =>
[sort] => 451
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
[392] => Array
(
[id] => 392
[site_id] => 1
[status_id] => 5
[group_id] => 18
[type_id] => 1
[name] => Które czynniki genetyczne należą do najczęstszych przyczyn niepowodzeń ciąży?
[ext] =>
[sort] => 0
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[type_name] => pojedyncza odpowiedź
[type_code] => single
[answers] => Array
(
[1443] => Array
(
[id] => 1443
[site_id] => 1
[status_id] => 5
[question_id] => 392
[name] => a) choroby jednogenowe zarodka/płodu
[correct] => 0
[ext] =>
[sort] => 1436
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[1444] => Array
(
[id] => 1444
[site_id] => 1
[status_id] => 5
[question_id] => 392
[name] => b) disomia jednorodzicielska
[correct] => 0
[ext] =>
[sort] => 1437
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[1445] => Array
(
[id] => 1445
[site_id] => 1
[status_id] => 5
[question_id] => 392
[name] => c) aberracje chromosomowe
[correct] => 1
[ext] =>
[sort] => 1438
[correct_yesno] => Tak
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[1446] => Array
(
[id] => 1446
[site_id] => 1
[status_id] => 5
[question_id] => 392
[name] => d) polimorfizmy i mutacje w genach, związane z różnymi procesami zachodzącymi w komórkach, takimi jak na przykład: immunosupresja, apoptoza, angiogeneza, czy przekazywanie sygnałów w komórce.
[correct] => 0
[ext] =>
[sort] => 1439
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
[137] => Array
(
[id] => 137
[site_id] => 1
[status_id] => 5
[group_id] => 18
[type_id] => 1
[name] => Które z metod pozwalają na identyfikację translokacji zrównoważonych?
[ext] =>
[sort] => 0
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[type_name] => pojedyncza odpowiedź
[type_code] => single
[answers] => Array
(
[459] => Array
(
[id] => 459
[site_id] => 1
[status_id] => 5
[question_id] => 137
[name] => a. kariotyp i FISH
[correct] => 1
[ext] =>
[sort] => 452
[correct_yesno] => Tak
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[460] => Array
(
[id] => 460
[site_id] => 1
[status_id] => 5
[question_id] => 137
[name] => b. kariotyp i aCGH
[correct] => 0
[ext] =>
[sort] => 453
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[461] => Array
(
[id] => 461
[site_id] => 1
[status_id] => 5
[question_id] => 137
[name] => c. aCGH i MLPA
[correct] => 0
[ext] =>
[sort] => 454
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[462] => Array
(
[id] => 462
[site_id] => 1
[status_id] => 5
[question_id] => 137
[name] => d. FISH i MLPA
[correct] => 0
[ext] =>
[sort] => 455
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
[393] => Array
(
[id] => 393
[site_id] => 1
[status_id] => 5
[group_id] => 18
[type_id] => 1
[name] => Zaznacz PRAWIDŁOWE zdanie:
[ext] =>
[sort] => 0
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[type_name] => pojedyncza odpowiedź
[type_code] => single
[answers] => Array
(
[1447] => Array
(
[id] => 1447
[site_id] => 1
[status_id] => 5
[question_id] => 393
[name] => a) Wrodzone nietrzymanie barwnika spowodowane jest mutacją w genie MECP2 w locus Xq28, kodującym aktywator jądrowego czynnika transkrypcyjnego kappa B. U płci męskiej wada jest zazwyczaj letalna. Istotą choroby jest niezdolność komórek podstawnych skóry do gromadzenia melaniny, która gromadzi się w skórze właściwej oraz w makrofagach indukując stan zapalny.
[correct] => 0
[ext] =>
[sort] => 1440
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[1448] => Array
(
[id] => 1448
[site_id] => 1
[status_id] => 5
[question_id] => 393
[name] => b) Zespół Retta spowodowany jest mutacją lub aberracją w genie IKBKG, locus Xq28. Jest to szereg zaburzeń neurorozwojowych, które w większości wypadków prowadzą do znacznej i głębokiej niepełnosprawności ruchowej oraz znacząco ograniczają możliwość komunikacji z otoczeniem.
[correct] => 0
[ext] =>
[sort] => 1441
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[1449] => Array
(
[id] => 1449
[site_id] => 1
[status_id] => 5
[question_id] => 393
[name] => c) Zespół Aicardiego to zespół wrodzonych wad genetycznych charakteryzujący się częściowym lub całkowitym brakiem ciała modzelowatego, obecnością zmian w siatkówce i napadów drgawkowych.
[correct] => 1
[ext] =>
[sort] => 1442
[correct_yesno] => Tak
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[1450] => Array
(
[id] => 1450
[site_id] => 1
[status_id] => 5
[question_id] => 393
[name] => d) Letalne dysplazje kostne u płodu, takie jak dysplazja tanatoforyczna oraz wrodzona łamliwości kości typu III odpowiedzialne są za przyczynę utraty ciąży.
[correct] => 0
[ext] =>
[sort] => 1443
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
[138] => Array
(
[id] => 138
[site_id] => 1
[status_id] => 5
[group_id] => 18
[type_id] => 1
[name] => Termin sekwencjonowanie następnej generacji oznacza :
[ext] =>
[sort] => 0
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[type_name] => pojedyncza odpowiedź
[type_code] => single
[answers] => Array
(
[463] => Array
(
[id] => 463
[site_id] => 1
[status_id] => 5
[question_id] => 138
[name] => a. Analizę całego genomu
[correct] => 0
[ext] =>
[sort] => 456
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[464] => Array
(
[id] => 464
[site_id] => 1
[status_id] => 5
[question_id] => 138
[name] => b. Analizę całego eksomu
[correct] => 0
[ext] =>
[sort] => 457
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[465] => Array
(
[id] => 465
[site_id] => 1
[status_id] => 5
[question_id] => 138
[name] => c. Sposób badania, ale nie jego zakres
[correct] => 1
[ext] =>
[sort] => 458
[correct_yesno] => Tak
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[466] => Array
(
[id] => 466
[site_id] => 1
[status_id] => 5
[question_id] => 138
[name] => d. Analizę panelu genów
[correct] => 0
[ext] =>
[sort] => 459
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
[394] => Array
(
[id] => 394
[site_id] => 1
[status_id] => 5
[group_id] => 18
[type_id] => 1
[name] => Oznaczenie płci płodu jest konieczne w przypadku diagnostyki prenatalnej:
[ext] =>
[sort] => 0
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[type_name] => pojedyncza odpowiedź
[type_code] => single
[answers] => Array
(
[1451] => Array
(
[id] => 1451
[site_id] => 1
[status_id] => 5
[question_id] => 394
[name] => a) Mukowiscydozy
[correct] => 0
[ext] =>
[sort] => 1444
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[1452] => Array
(
[id] => 1452
[site_id] => 1
[status_id] => 5
[question_id] => 394
[name] => b) Zespołu duplikacji MECP2
[correct] => 1
[ext] =>
[sort] => 1445
[correct_yesno] => Tak
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[1453] => Array
(
[id] => 1453
[site_id] => 1
[status_id] => 5
[question_id] => 394
[name] => c) Rdzeniowego zaniku mięśni
[correct] => 0
[ext] =>
[sort] => 1446
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[1454] => Array
(
[id] => 1454
[site_id] => 1
[status_id] => 5
[question_id] => 394
[name] => d) Zespołu Angelmana
[correct] => 0
[ext] =>
[sort] => 1447
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
[139] => Array
(
[id] => 139
[site_id] => 1
[status_id] => 5
[group_id] => 18
[type_id] => 2
[name] => Zaznacz zdanie fałszywe:
[ext] =>
[sort] => 0
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[type_name] => wielokrotna odpowiedź
[type_code] => multi
[answers] => Array
(
[467] => Array
(
[id] => 467
[site_id] => 1
[status_id] => 5
[question_id] => 139
[name] => a. Pokrycie badanych regionów genu odnosi się do liczby odczytów tych fragmentów
[correct] => 0
[ext] =>
[sort] => 460
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[468] => Array
(
[id] => 468
[site_id] => 1
[status_id] => 5
[question_id] => 139
[name] => b. Każde laboratorium definiuje we własnym zakresie liczbę i rodzaj genów analizowanych w ramach danego panelu na podstawie baz danych i dostępnej literatury
[correct] => 0
[ext] =>
[sort] => 461
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[469] => Array
(
[id] => 469
[site_id] => 1
[status_id] => 5
[question_id] => 139
[name] => c. Ocena patogenności wariantów jest jednym z podstawowych wyzwań diagnostyki molekularnej
[correct] => 0
[ext] =>
[sort] => 462
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[470] => Array
(
[id] => 470
[site_id] => 1
[status_id] => 5
[question_id] => 139
[name] => d. Sekwencjonowanie Sangera nie umożliwia identyfikacji nowych mutacji, nie opisanych wcześniej w piśmiennictwie
[correct] => 1
[ext] =>
[sort] => 463
[correct_yesno] => Tak
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
[395] => Array
(
[id] => 395
[site_id] => 1
[status_id] => 5
[group_id] => 18
[type_id] => 1
[name] => Do Poradni Genetycznej zgłosiła się 25-letnia kobieta z potwierdzonym molekularnie przedwczesnym wygasaniem czynności jajników związanym z FraX (premutacja w genie FMR1) w celu ewentualnej diagnostyki prenatalnej. Do przeprowadzenia badania wykorzystana zostanie technika:
[ext] =>
[sort] => 0
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[type_name] => pojedyncza odpowiedź
[type_code] => single
[answers] => Array
(
[1455] => Array
(
[id] => 1455
[site_id] => 1
[status_id] => 5
[question_id] => 395
[name] => a) PCR z analizą GeneScan i/lub Triplet-Primed PCR (TP-PCR)
[correct] => 1
[ext] =>
[sort] => 1448
[correct_yesno] => Tak
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[1456] => Array
(
[id] => 1456
[site_id] => 1
[status_id] => 5
[question_id] => 395
[name] => b) Sekwencjonowanie następnej generacji celowane
[correct] => 0
[ext] =>
[sort] => 1449
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[1457] => Array
(
[id] => 1457
[site_id] => 1
[status_id] => 5
[question_id] => 395
[name] => c) Sekwencjonowanie techniką Sangera genu FMR1
[correct] => 0
[ext] =>
[sort] => 1450
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[1458] => Array
(
[id] => 1458
[site_id] => 1
[status_id] => 5
[question_id] => 395
[name] => d) Pacjentce nie powinno się wykonywać diagnostyki prenatalnej
[correct] => 0
[ext] =>
[sort] => 1451
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
[140] => Array
(
[id] => 140
[site_id] => 1
[status_id] => 5
[group_id] => 18
[type_id] => 1
[name] => Stwierdzenie, że u danego pacjenta najprawdopodobniej wystąpiła mutacja de novo możliwe jest poprzez:
[ext] =>
[sort] => 0
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[type_name] => pojedyncza odpowiedź
[type_code] => single
[answers] => Array
(
[471] => Array
(
[id] => 471
[site_id] => 1
[status_id] => 5
[question_id] => 140
[name] => a. Zastosowanie sekwencjonowania NGS jako metody diagnostycznej
[correct] => 0
[ext] =>
[sort] => 464
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[472] => Array
(
[id] => 472
[site_id] => 1
[status_id] => 5
[question_id] => 140
[name] => b. Analizę rodowodu i fakt, iż choroba nie występowała wcześniej u żadnego z krewnych Pacjenta bez konieczności wykonania analiz u rodziców pacjenta
[correct] => 0
[ext] =>
[sort] => 465
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[473] => Array
(
[id] => 473
[site_id] => 1
[status_id] => 5
[question_id] => 140
[name] => c. Wykonanie badania rodziców pacjenta i wykluczenie u obojga z nich obecności danej mutacji
[correct] => 1
[ext] =>
[sort] => 466
[correct_yesno] => Tak
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
[396] => Array
(
[id] => 396
[site_id] => 1
[status_id] => 5
[group_id] => 18
[type_id] => 1
[name] => Ryzyko otrzymania wyniku fałszywie pozytywnego dla trisomii w badaniu przesiewowym z wykorzystaniem wolnego płodowego DNA rośnie w przypadku:
[ext] =>
[sort] => 0
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[type_name] => pojedyncza odpowiedź
[type_code] => single
[answers] => Array
(
[1459] => Array
(
[id] => 1459
[site_id] => 1
[status_id] => 5
[question_id] => 396
[name] => a) „vanishing twin”
[correct] => 0
[ext] =>
[sort] => 1452
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[1460] => Array
(
[id] => 1460
[site_id] => 1
[status_id] => 5
[question_id] => 396
[name] => b) Nieprawidłowości chromosomowych u matki
[correct] => 0
[ext] =>
[sort] => 1453
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[1461] => Array
(
[id] => 1461
[site_id] => 1
[status_id] => 5
[question_id] => 396
[name] => c) Mozaikowości
[correct] => 0
[ext] =>
[sort] => 1454
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[1462] => Array
(
[id] => 1462
[site_id] => 1
[status_id] => 5
[question_id] => 396
[name] => d) Wszystkie powyżej
[correct] => 1
[ext] =>
[sort] => 1455
[correct_yesno] => Tak
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
[141] => Array
(
[id] => 141
[site_id] => 1
[status_id] => 5
[group_id] => 18
[type_id] => 1
[name] => Określenie Kraniostenoza oznacza:
[ext] =>
[sort] => 0
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[type_name] => pojedyncza odpowiedź
[type_code] => single
[answers] => Array
(
[474] => Array
(
[id] => 474
[site_id] => 1
[status_id] => 5
[question_id] => 141
[name] => a. Ścieśnienie czaszki na skutek przedwczesnego zarastania szwów czaszkowych
[correct] => 1
[ext] =>
[sort] => 467
[correct_yesno] => Tak
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[475] => Array
(
[id] => 475
[site_id] => 1
[status_id] => 5
[question_id] => 141
[name] => b. Zarośnięcie pojedynczego szwu
[correct] => 0
[ext] =>
[sort] => 468
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[476] => Array
(
[id] => 476
[site_id] => 1
[status_id] => 5
[question_id] => 141
[name] => c. Zwężenie w strukturach wewnątrz czaszki
[correct] => 0
[ext] =>
[sort] => 469
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[477] => Array
(
[id] => 477
[site_id] => 1
[status_id] => 5
[question_id] => 141
[name] => d. Zwężenie dotyczące oczodołów
[correct] => 0
[ext] =>
[sort] => 470
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
[397] => Array
(
[id] => 397
[site_id] => 1
[status_id] => 5
[group_id] => 18
[type_id] => 1
[name] => Ryzyko otrzymania wyniku fałszywie negatywnego dla trisomii w badaniu przesiewowym z wykorzystaniem wolnego płodowego DNA rośnie w przypadku:
[ext] =>
[sort] => 0
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[type_name] => pojedyncza odpowiedź
[type_code] => single
[answers] => Array
(
[1463] => Array
(
[id] => 1463
[site_id] => 1
[status_id] => 5
[question_id] => 397
[name] => a) Aberracja obecna jedynie w komórkach płodu, brak w trofoblaście (TFM ang. true fetal mosaicism)
[correct] => 0
[ext] =>
[sort] => 1456
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[1464] => Array
(
[id] => 1464
[site_id] => 1
[status_id] => 5
[question_id] => 397
[name] => b) Zbyt niski % frakcji płodowego DNA (>4%)
[correct] => 0
[ext] =>
[sort] => 1457
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[1465] => Array
(
[id] => 1465
[site_id] => 1
[status_id] => 5
[question_id] => 397
[name] => c) Złe przechowywanie próbek z krwią pacjentek
[correct] => 0
[ext] =>
[sort] => 1458
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[1466] => Array
(
[id] => 1466
[site_id] => 1
[status_id] => 5
[question_id] => 397
[name] => d) Wszystkie powyżej
[correct] => 1
[ext] =>
[sort] => 1459
[correct_yesno] => Tak
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
[142] => Array
(
[id] => 142
[site_id] => 1
[status_id] => 5
[group_id] => 18
[type_id] => 1
[name] => Do genów, których patogenne mutacje uznawane są za przyczynę rozwoju przewlekłego zapalenia trzustki i dziedziczą się autosomalnie dominująco zaliczamy:
[ext] =>
[sort] => 0
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[type_name] => pojedyncza odpowiedź
[type_code] => single
[answers] => Array
(
[478] => Array
(
[id] => 478
[site_id] => 1
[status_id] => 5
[question_id] => 142
[name] => a. gen PRSS1
[correct] => 0
[ext] =>
[sort] => 471
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[479] => Array
(
[id] => 479
[site_id] => 1
[status_id] => 5
[question_id] => 142
[name] => b. gen CFTR, SPINK1, CTRC
[correct] => 0
[ext] =>
[sort] => 472
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[480] => Array
(
[id] => 480
[site_id] => 1
[status_id] => 5
[question_id] => 142
[name] => c. gen CPA1
[correct] => 0
[ext] =>
[sort] => 473
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[481] => Array
(
[id] => 481
[site_id] => 1
[status_id] => 5
[question_id] => 142
[name] => d. odpowiedzi A i C są prawidłowe
[correct] => 1
[ext] =>
[sort] => 474
[correct_yesno] => Tak
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
[398] => Array
(
[id] => 398
[site_id] => 1
[status_id] => 5
[group_id] => 18
[type_id] => 1
[name] => Podczas badania całoeksomowego badamy:
[ext] =>
[sort] => 0
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[type_name] => pojedyncza odpowiedź
[type_code] => single
[answers] => Array
(
[1467] => Array
(
[id] => 1467
[site_id] => 1
[status_id] => 5
[question_id] => 398
[name] => a) Wszystkie części kodujące genomu
[correct] => 1
[ext] =>
[sort] => 1460
[correct_yesno] => Tak
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[1468] => Array
(
[id] => 1468
[site_id] => 1
[status_id] => 5
[question_id] => 398
[name] => b) Kilka lub kilkanaście wybranych genów
[correct] => 0
[ext] =>
[sort] => 1461
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[1469] => Array
(
[id] => 1469
[site_id] => 1
[status_id] => 5
[question_id] => 398
[name] => c) Części niekodujące genomu
[correct] => 0
[ext] =>
[sort] => 1462
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[1470] => Array
(
[id] => 1470
[site_id] => 1
[status_id] => 5
[question_id] => 398
[name] => d) Wszystkie powyżej
[correct] => 0
[ext] =>
[sort] => 1463
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
[143] => Array
(
[id] => 143
[site_id] => 1
[status_id] => 5
[group_id] => 18
[type_id] => 1
[name] => Według polskich i europejskich rekomendacji badania genetyczne u pacjentów z przewlekłym zapaleniem trzustki należy wykonać w przypadku:
[ext] =>
[sort] => 0
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[type_name] => pojedyncza odpowiedź
[type_code] => single
[answers] => Array
(
[482] => Array
(
[id] => 482
[site_id] => 1
[status_id] => 5
[question_id] => 143
[name] => a. alkoholowego PZT
[correct] => 0
[ext] =>
[sort] => 475
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[483] => Array
(
[id] => 483
[site_id] => 1
[status_id] => 5
[question_id] => 143
[name] => b. u pacjentów z pozytywnym wywiadem rodzinnym
[correct] => 0
[ext] =>
[sort] => 476
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[484] => Array
(
[id] => 484
[site_id] => 1
[status_id] => 5
[question_id] => 143
[name] => c. u pacjentów z o wczesnym początku zachorowania lub/i niejasnej etiologii
[correct] => 0
[ext] =>
[sort] => 477
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[485] => Array
(
[id] => 485
[site_id] => 1
[status_id] => 5
[question_id] => 143
[name] => d. odpowiedz B i C są prawidłowe
[correct] => 1
[ext] =>
[sort] => 478
[correct_yesno] => Tak
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
[144] => Array
(
[id] => 144
[site_id] => 1
[status_id] => 5
[group_id] => 18
[type_id] => 1
[name] => Wrodzone Wady Metabolizmu mogą dziedziczyć się :
[ext] =>
[sort] => 0
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[type_name] => pojedyncza odpowiedź
[type_code] => single
[answers] => Array
(
[486] => Array
(
[id] => 486
[site_id] => 1
[status_id] => 5
[question_id] => 144
[name] => a. jedynie autosomalnie recesywnie
[correct] => 0
[ext] =>
[sort] => 479
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[487] => Array
(
[id] => 487
[site_id] => 1
[status_id] => 5
[question_id] => 144
[name] => b. autosomalnie dominująco i rzadziej autosomalnie recesywnie
[correct] => 0
[ext] =>
[sort] => 480
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[488] => Array
(
[id] => 488
[site_id] => 1
[status_id] => 5
[question_id] => 144
[name] => c. w sposób sprzężony z chromosomem X
[correct] => 0
[ext] =>
[sort] => 481
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[489] => Array
(
[id] => 489
[site_id] => 1
[status_id] => 5
[question_id] => 144
[name] => d. zazwyczaj dziedziczone w sposób autosomalny recesywny, rzadziej autosomalnie dominująco bądź w sposób sprzężony z chromosomem X, ale odstępstwa od praw Mendla są też możliwe
[correct] => 1
[ext] =>
[sort] => 482
[correct_yesno] => Tak
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
[145] => Array
(
[id] => 145
[site_id] => 1
[status_id] => 5
[group_id] => 18
[type_id] => 1
[name] => Wskaż zdanie prawdziwe:
[ext] =>
[sort] => 0
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[type_name] => pojedyncza odpowiedź
[type_code] => single
[answers] => Array
(
[490] => Array
(
[id] => 490
[site_id] => 1
[status_id] => 5
[question_id] => 145
[name] => a. Fenyloketonuria odpowiada za podwyższone stężenie fenyloalaniny we krwi
[correct] => 0
[ext] =>
[sort] => 483
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[491] => Array
(
[id] => 491
[site_id] => 1
[status_id] => 5
[question_id] => 145
[name] => b. Fenyloketonuria jest najczęstszą wrodzoną wadą w metabolizmie aminokwasów.
[correct] => 0
[ext] =>
[sort] => 484
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[492] => Array
(
[id] => 492
[site_id] => 1
[status_id] => 5
[question_id] => 145
[name] => c. Jedynym obecnie skutecznym sposobem leczenia postaci klasycznej fenyloketonurii jest dieta z ograniczoną ilością fenyloalaniny
[correct] => 0
[ext] =>
[sort] => 485
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[493] => Array
(
[id] => 493
[site_id] => 1
[status_id] => 5
[question_id] => 145
[name] => d. Wszystkie powyższe zdania są prawdziwe
[correct] => 1
[ext] =>
[sort] => 486
[correct_yesno] => Tak
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
[146] => Array
(
[id] => 146
[site_id] => 1
[status_id] => 5
[group_id] => 18
[type_id] => 1
[name] => RASoptie to grupa chorób charakteryzujących się:
[ext] =>
[sort] => 0
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[type_name] => pojedyncza odpowiedź
[type_code] => single
[answers] => Array
(
[494] => Array
(
[id] => 494
[site_id] => 1
[status_id] => 5
[question_id] => 146
[name] => a. homogennością kliniczną
[correct] => 0
[ext] =>
[sort] => 487
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[495] => Array
(
[id] => 495
[site_id] => 1
[status_id] => 5
[question_id] => 146
[name] => b. heterogennością genetyczną
[correct] => 1
[ext] =>
[sort] => 488
[correct_yesno] => Tak
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[496] => Array
(
[id] => 496
[site_id] => 1
[status_id] => 5
[question_id] => 146
[name] => c. występowaniem wad izolowanych
[correct] => 0
[ext] =>
[sort] => 489
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[497] => Array
(
[id] => 497
[site_id] => 1
[status_id] => 5
[question_id] => 146
[name] => d. homogennością genetyczną
[correct] => 0
[ext] =>
[sort] => 490
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
[147] => Array
(
[id] => 147
[site_id] => 1
[status_id] => 5
[group_id] => 18
[type_id] => 1
[name] => Do grupy RASopatii nie zaliczamy:
[ext] =>
[sort] => 0
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[type_name] => pojedyncza odpowiedź
[type_code] => single
[answers] => Array
(
[498] => Array
(
[id] => 498
[site_id] => 1
[status_id] => 5
[question_id] => 147
[name] => a. zespołu Noonan
[correct] => 0
[ext] =>
[sort] => 491
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[499] => Array
(
[id] => 499
[site_id] => 1
[status_id] => 5
[question_id] => 147
[name] => b. zespołu Blooma
[correct] => 1
[ext] =>
[sort] => 492
[correct_yesno] => Tak
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[500] => Array
(
[id] => 500
[site_id] => 1
[status_id] => 5
[question_id] => 147
[name] => c. zespołu Costello
[correct] => 0
[ext] =>
[sort] => 493
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[501] => Array
(
[id] => 501
[site_id] => 1
[status_id] => 5
[question_id] => 147
[name] => d. zespołu Legiusa
[correct] => 0
[ext] =>
[sort] => 494
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
[148] => Array
(
[id] => 148
[site_id] => 1
[status_id] => 5
[group_id] => 18
[type_id] => 1
[name] => Wskaż zdanie prawdziwe:
[ext] =>
[sort] => 0
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[type_name] => pojedyncza odpowiedź
[type_code] => single
[answers] => Array
(
[502] => Array
(
[id] => 502
[site_id] => 1
[status_id] => 5
[question_id] => 148
[name] => a. Niektóre choroby np. pęcherzowe oddzielenie się naskórka typu dystroficznego mogą być dziedziczone w sposób recesywny albo dominujący nawet jeśli mutacje zawsze występują w tym samym genie
[correct] => 1
[ext] =>
[sort] => 495
[correct_yesno] => Tak
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[503] => Array
(
[id] => 503
[site_id] => 1
[status_id] => 5
[question_id] => 148
[name] => b. Identyfikacja mutacji w jednym allelu genu związanego fenotypowo z daną jednostką chorobową o dziedziczeniu autosomalnym recesywnym uprawnia do stwierdzenia, że na pewno w drugim allelu tego genu znajduje się mutacja i że choroba jest wynikiem mutacji tego właśnie genu.
[correct] => 0
[ext] =>
[sort] => 496
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[504] => Array
(
[id] => 504
[site_id] => 1
[status_id] => 5
[question_id] => 148
[name] => c. Niewykrycie mutacji z wykorzystaniem sekwencjonowania eksomowego oznacza, że na pewno mutacja nie występuje w analizowanych genach.
[correct] => 0
[ext] =>
[sort] => 497
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[505] => Array
(
[id] => 505
[site_id] => 1
[status_id] => 5
[question_id] => 148
[name] => d. Wybór sekwencjonowania eksomowego jest zawsze optymalnym rozwiązaniem diagnostycznym
[correct] => 0
[ext] =>
[sort] => 498
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
)
[quiz_active] => 0
[materials_count] => 15
)
[19] => Array
(
[id] => 19
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[sort] => 1
[status_code] => active
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
[materials] => Array
(
[144] => Array
(
[id] => 144
[name] => Badania molekularne. Od kliniki do interpretacji wyniku.
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/144/postergen_i_geno.png
[video] => resources/data/material/144/5_badania_molekularne_–_od_kliniki_do_interpretacji_wyniku_dr_hab._dorota_hoffmanzacharska.mp4
[content] =>
[ext] => Array
(
[files_header] =>
[linked] => Array
(
[145] => Array
(
[id] => 145
[site_id] => 1
[status_id] => 5
[name] => Choroba Huntingtona
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/145/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 145-choroba_huntingtona
[url] => wideo/145-choroba_huntingtona
[short_name] => Choroba Huntingtona
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[146] => Array
(
[id] => 146
[site_id] => 1
[status_id] => 5
[name] => Wspólne drogi zaburzeń neurorozwojowych
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/146/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 146-wspolne_drogi_zaburzen_neurorozwojowych
[url] => wideo/146-wspolne_drogi_zaburzen_neurorozwojowych
[short_name] => Wspólne drogi zaburzeń neurorozwojowych
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[147] => Array
(
[id] => 147
[site_id] => 1
[status_id] => 5
[name] => Genetyka chorób neurologicznych o późnym początku
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/147/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Maciej Geremek
)
[authors_data] => Array
(
[0] => Array
(
[id] => 69
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Maciej Geremek
[firstname] => Maciej
[lastname] => Geremek
[title] => dr n. med.
[affiliation] => Zakład genetyki Medycznej IMiD
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 69-maciej_geremek
[url] => eksperci/69-maciej_geremek
)
)
[authors_ids] => Array
(
[0] => 69
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 147-genetyka_chorob_neurologicznych_o_poznym_poczatku
[url] => wideo/147-genetyka_chorob_neurologicznych_o_poznym_poczatku
[short_name] => Genetyka chorób neurologicznych o późnym początku
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[148] => Array
(
[id] => 148
[site_id] => 1
[status_id] => 5
[name] => Neurogenetyka molekularna
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/148/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 148-neurogenetyka_molekularna
[url] => wideo/148-neurogenetyka_molekularna
[short_name] => Neurogenetyka molekularna
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[149] => Array
(
[id] => 149
[site_id] => 1
[status_id] => 5
[name] => Poradnictwo genetyczne w odniesieniu do chorób neurologicznych
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/149/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Ewa Obersztyn
)
[authors_data] => Array
(
[0] => Array
(
[id] => 14
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Ewa Obersztyn
[firstname] => Ewa
[lastname] => Obersztyn
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 14-ewa_obersztyn
[url] => eksperci/14-ewa_obersztyn
)
)
[authors_ids] => Array
(
[0] => 14
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 149-poradnictwo_genetyczne_w_odniesieniu_do_chorob_neurologicznych
[url] => wideo/149-poradnictwo_genetyczne_w_odniesieniu_do_chorob_neurologicznych
[short_name] => Poradnictwo genetyczne w odniesieniu do chorób neu...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[150] => Array
(
[id] => 150
[site_id] => 1
[status_id] => 5
[name] => Niepełnosprawność intelektualna –badania cytogenetyczne.
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/150/postergen_i_geno.png
[video] => resources/data/material/150/5_niepelnosprawnosc_intelektualna_–_badania_molekularne_dr_sylwia_rzonca.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => mgr Kamila Ziemkiewicz
)
[authors_data] => Array
(
[0] => Array
(
[id] => 11
[site_id] => 1
[status_id] => 5
[name] => mgr Kamila Ziemkiewicz
[firstname] => Kamila
[lastname] => Ziemkiewicz
[title] => mgr
[affiliation] =>
[avatar] => resources/data/eksperci/11/kziemkiewicz.png
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 11-kamila_ziemkiewicz
[url] => eksperci/11-kamila_ziemkiewicz
)
)
[authors_ids] => Array
(
[0] => 11
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 12
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 150-niepelnosprawnosc_intelektualna_badania_cytogenetyczne
[url] => wideo/150-niepelnosprawnosc_intelektualna_badania_cytogenetyczne
[short_name] => Niepełnosprawność intelektualna –badania cytogenet...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[12] => Array
(
[id] => 12
[site_id] => 1
[status_id] => 5
[name] => cytogenetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 12-cytogenetyka
[url] => /12-cytogenetyka
)
)
[artykuly] => Array
(
)
)
[151] => Array
(
[id] => 151
[site_id] => 1
[status_id] => 5
[name] => Techniki cytogenetyczne w diagnostyce chorób układu nerwowego.
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/151/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => mgr Kamila Ziemkiewicz
)
[authors_data] => Array
(
[0] => Array
(
[id] => 11
[site_id] => 1
[status_id] => 5
[name] => mgr Kamila Ziemkiewicz
[firstname] => Kamila
[lastname] => Ziemkiewicz
[title] => mgr
[affiliation] =>
[avatar] => resources/data/eksperci/11/kziemkiewicz.png
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 11-kamila_ziemkiewicz
[url] => eksperci/11-kamila_ziemkiewicz
)
)
[authors_ids] => Array
(
[0] => 11
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 12
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 151-techniki_cytogenetyczne_w_diagnostyce_chorob_ukladu_nerwowego
[url] => wideo/151-techniki_cytogenetyczne_w_diagnostyce_chorob_ukladu_nerwowego
[short_name] => Techniki cytogenetyczne w diagnostyce chorób układ...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[12] => Array
(
[id] => 12
[site_id] => 1
[status_id] => 5
[name] => cytogenetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 12-cytogenetyka
[url] => /12-cytogenetyka
)
)
[artykuly] => Array
(
)
)
[152] => Array
(
[id] => 152
[site_id] => 1
[status_id] => 5
[name] => Choroby nerwów obwodowych
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/152/postergen_i_geno.png
[video] => resources/data/material/152/5_choroby_nerwowobwodowych_potulska.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab. n. med. Anna Potulska-Chromik
)
[authors_data] => Array
(
[0] => Array
(
[id] => 70
[site_id] => 1
[status_id] => 5
[name] => dr hab. n. med. Anna Potulska-Chromik
[firstname] => Anna
[lastname] => Potulska-Chromik
[title] => dr hab. n. med.
[affiliation] => Klinika Neurologii WUM
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 70-anna_potulska_chromik
[url] => eksperci/70-anna_potulska_chromik
)
)
[authors_ids] => Array
(
[0] => 70
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 152-choroby_nerwow_obwodowych
[url] => wideo/152-choroby_nerwow_obwodowych
[short_name] => Choroby nerwów obwodowych
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[153] => Array
(
[id] => 153
[site_id] => 1
[status_id] => 5
[name] => Choroby nerwowo-mięśniowe
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/153/postergen_i_geno.png
[video] => resources/data/material/153/5_choroby_nerwowomiesniowe_dr_hab._monika_gos.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med., prof IMiD Monika Gos
)
[authors_data] => Array
(
[0] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => dr n. med., prof IMiD Monika Gos
[firstname] => Monika
[lastname] => Gos
[title] => dr n. med., prof IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-monika_gos
[url] => eksperci/13-monika_gos
)
)
[authors_ids] => Array
(
[0] => 13
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 153-choroby_nerwowo_miesniowe
[url] => wideo/153-choroby_nerwowo_miesniowe
[short_name] => Choroby nerwowo-mięśniowe
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[154] => Array
(
[id] => 154
[site_id] => 1
[status_id] => 5
[name] => Rdzeniowy zanik mięśni - od mutacji do terapii
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/154/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med., prof IMiD Monika Gos
)
[authors_data] => Array
(
[0] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => dr n. med., prof IMiD Monika Gos
[firstname] => Monika
[lastname] => Gos
[title] => dr n. med., prof IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-monika_gos
[url] => eksperci/13-monika_gos
)
)
[authors_ids] => Array
(
[0] => 13
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
[3] => 14
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 154-rdzeniowy_zanik_miesni___od_mutacji_do_terapii
[url] => wideo/154-rdzeniowy_zanik_miesni___od_mutacji_do_terapii
[short_name] => Rdzeniowy zanik mięśni - od mutacji do terapii
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
[14] => Array
(
[id] => 14
[site_id] => 1
[status_id] => 5
[name] => choroby rzadkie
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 14-choroby_rzadkie
[url] => /14-choroby_rzadkie
)
)
[artykuly] => Array
(
)
)
[155] => Array
(
[id] => 155
[site_id] => 1
[status_id] => 5
[name] => Niepełnosprawność intelektualna – badania molekularne
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/155/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Sylwia Rzońca
)
[authors_data] => Array
(
[0] => Array
(
[id] => 10
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Sylwia Rzońca
[firstname] => Sylwia
[lastname] => Rzońca
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 10-sylwia_rzonca
[url] => eksperci/10-sylwia_rzonca
)
)
[authors_ids] => Array
(
[0] => 10
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 155-niepelnosprawnosc_intelektualna__badania_molekularne
[url] => wideo/155-niepelnosprawnosc_intelektualna__badania_molekularne
[short_name] => Niepełnosprawność intelektualna – badania molekula...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[156] => Array
(
[id] => 156
[site_id] => 1
[status_id] => 5
[name] => Choroby neurologiczne o późnym wieku zachorowania - wyzwania diagnostyki i poradnictwa
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/156/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 156-choroby_neurologiczne_o_poznym_wieku_zachorowania___wyzwania_diagnostyki_i_poradnictwa
[url] => wideo/156-choroby_neurologiczne_o_poznym_wieku_zachorowania___wyzwania_diagnostyki_i_poradnictwa
[short_name] => Choroby neurologiczne o późnym wieku zachorowania ...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[158] => Array
(
[id] => 158
[site_id] => 1
[status_id] => 5
[name] => Badania cytogenetyczne – od kliniki do interpretacji wyniku
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/158/postergen_i_geno.png
[video] => resources/data/material/158/5_badania_cytogenetyczne_–_od_kliniki_do_interpretacji_wyniku.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med.,prof IMiD Beata Nowakowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 9
[site_id] => 1
[status_id] => 5
[name] => dr n. med.,prof IMiD Beata Nowakowska
[firstname] => Beata
[lastname] => Nowakowska
[title] => dr n. med.,prof IMiD
[affiliation] => Zakład Genetyki Medycznej, Zespół Pracowni Cytogenetyki, IMID
[avatar] => resources/data/eksperci/9/dr_nowakowska_v2.jpg
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 9-beata_nowakowska
[url] => eksperci/9-beata_nowakowska
)
)
[authors_ids] => Array
(
[0] => 9
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 12
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 158-badania_cytogenetyczne__od_kliniki_do_interpretacji_wyniku
[url] => wideo/158-badania_cytogenetyczne__od_kliniki_do_interpretacji_wyniku
[short_name] => Badania cytogenetyczne – od kliniki do interpretac...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[12] => Array
(
[id] => 12
[site_id] => 1
[status_id] => 5
[name] => cytogenetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 12-cytogenetyka
[url] => /12-cytogenetyka
)
)
[artykuly] => Array
(
)
)
)
)
[sort] => 1
[status_code] => active
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
[3] => 14
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 144-badania_molekularne_od_kliniki_do_interpretacji_wyniku
[url] => wideo/144-badania_molekularne_od_kliniki_do_interpretacji_wyniku
[short_name] => Badania molekularne. Od kliniki do interpretacji w...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
[14] => Array
(
[id] => 14
[site_id] => 1
[status_id] => 5
[name] => choroby rzadkie
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 14-choroby_rzadkie
[url] => /14-choroby_rzadkie
)
)
[artykuly] => Array
(
)
[logotypy] => Array
(
)
[pliki] => Array
(
[113] => Array
(
[id] => 113
[site_id] => 1
[status_id] => 5
[entity_key] => material
[entity_id] => 144
[name] => Badania molekularne. Od kliniki do interpretacji wyniku.
[file] => resources/data/pliki/material/144/25.06_w6_dhz_materialy_.pdf
[sort] => 110
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
[145] => Array
(
[id] => 145
[name] => Choroba Huntingtona
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/145/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
[linked] => Array
(
[144] => Array
(
[id] => 144
[site_id] => 1
[status_id] => 5
[name] => Badania molekularne. Od kliniki do interpretacji wyniku.
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/144/postergen_i_geno.png
[video] => resources/data/material/144/5_badania_molekularne_–_od_kliniki_do_interpretacji_wyniku_dr_hab._dorota_hoffmanzacharska.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
[3] => 14
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 144-badania_molekularne_od_kliniki_do_interpretacji_wyniku
[url] => wideo/144-badania_molekularne_od_kliniki_do_interpretacji_wyniku
[short_name] => Badania molekularne. Od kliniki do interpretacji w...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
[14] => Array
(
[id] => 14
[site_id] => 1
[status_id] => 5
[name] => choroby rzadkie
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 14-choroby_rzadkie
[url] => /14-choroby_rzadkie
)
)
[artykuly] => Array
(
)
)
[146] => Array
(
[id] => 146
[site_id] => 1
[status_id] => 5
[name] => Wspólne drogi zaburzeń neurorozwojowych
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/146/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 146-wspolne_drogi_zaburzen_neurorozwojowych
[url] => wideo/146-wspolne_drogi_zaburzen_neurorozwojowych
[short_name] => Wspólne drogi zaburzeń neurorozwojowych
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[147] => Array
(
[id] => 147
[site_id] => 1
[status_id] => 5
[name] => Genetyka chorób neurologicznych o późnym początku
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/147/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Maciej Geremek
)
[authors_data] => Array
(
[0] => Array
(
[id] => 69
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Maciej Geremek
[firstname] => Maciej
[lastname] => Geremek
[title] => dr n. med.
[affiliation] => Zakład genetyki Medycznej IMiD
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 69-maciej_geremek
[url] => eksperci/69-maciej_geremek
)
)
[authors_ids] => Array
(
[0] => 69
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 147-genetyka_chorob_neurologicznych_o_poznym_poczatku
[url] => wideo/147-genetyka_chorob_neurologicznych_o_poznym_poczatku
[short_name] => Genetyka chorób neurologicznych o późnym początku
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[148] => Array
(
[id] => 148
[site_id] => 1
[status_id] => 5
[name] => Neurogenetyka molekularna
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/148/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 148-neurogenetyka_molekularna
[url] => wideo/148-neurogenetyka_molekularna
[short_name] => Neurogenetyka molekularna
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[149] => Array
(
[id] => 149
[site_id] => 1
[status_id] => 5
[name] => Poradnictwo genetyczne w odniesieniu do chorób neurologicznych
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/149/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Ewa Obersztyn
)
[authors_data] => Array
(
[0] => Array
(
[id] => 14
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Ewa Obersztyn
[firstname] => Ewa
[lastname] => Obersztyn
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 14-ewa_obersztyn
[url] => eksperci/14-ewa_obersztyn
)
)
[authors_ids] => Array
(
[0] => 14
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 149-poradnictwo_genetyczne_w_odniesieniu_do_chorob_neurologicznych
[url] => wideo/149-poradnictwo_genetyczne_w_odniesieniu_do_chorob_neurologicznych
[short_name] => Poradnictwo genetyczne w odniesieniu do chorób neu...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[150] => Array
(
[id] => 150
[site_id] => 1
[status_id] => 5
[name] => Niepełnosprawność intelektualna –badania cytogenetyczne.
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/150/postergen_i_geno.png
[video] => resources/data/material/150/5_niepelnosprawnosc_intelektualna_–_badania_molekularne_dr_sylwia_rzonca.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => mgr Kamila Ziemkiewicz
)
[authors_data] => Array
(
[0] => Array
(
[id] => 11
[site_id] => 1
[status_id] => 5
[name] => mgr Kamila Ziemkiewicz
[firstname] => Kamila
[lastname] => Ziemkiewicz
[title] => mgr
[affiliation] =>
[avatar] => resources/data/eksperci/11/kziemkiewicz.png
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 11-kamila_ziemkiewicz
[url] => eksperci/11-kamila_ziemkiewicz
)
)
[authors_ids] => Array
(
[0] => 11
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 12
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 150-niepelnosprawnosc_intelektualna_badania_cytogenetyczne
[url] => wideo/150-niepelnosprawnosc_intelektualna_badania_cytogenetyczne
[short_name] => Niepełnosprawność intelektualna –badania cytogenet...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[12] => Array
(
[id] => 12
[site_id] => 1
[status_id] => 5
[name] => cytogenetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 12-cytogenetyka
[url] => /12-cytogenetyka
)
)
[artykuly] => Array
(
)
)
[151] => Array
(
[id] => 151
[site_id] => 1
[status_id] => 5
[name] => Techniki cytogenetyczne w diagnostyce chorób układu nerwowego.
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/151/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => mgr Kamila Ziemkiewicz
)
[authors_data] => Array
(
[0] => Array
(
[id] => 11
[site_id] => 1
[status_id] => 5
[name] => mgr Kamila Ziemkiewicz
[firstname] => Kamila
[lastname] => Ziemkiewicz
[title] => mgr
[affiliation] =>
[avatar] => resources/data/eksperci/11/kziemkiewicz.png
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 11-kamila_ziemkiewicz
[url] => eksperci/11-kamila_ziemkiewicz
)
)
[authors_ids] => Array
(
[0] => 11
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 12
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 151-techniki_cytogenetyczne_w_diagnostyce_chorob_ukladu_nerwowego
[url] => wideo/151-techniki_cytogenetyczne_w_diagnostyce_chorob_ukladu_nerwowego
[short_name] => Techniki cytogenetyczne w diagnostyce chorób układ...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[12] => Array
(
[id] => 12
[site_id] => 1
[status_id] => 5
[name] => cytogenetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 12-cytogenetyka
[url] => /12-cytogenetyka
)
)
[artykuly] => Array
(
)
)
[152] => Array
(
[id] => 152
[site_id] => 1
[status_id] => 5
[name] => Choroby nerwów obwodowych
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/152/postergen_i_geno.png
[video] => resources/data/material/152/5_choroby_nerwowobwodowych_potulska.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab. n. med. Anna Potulska-Chromik
)
[authors_data] => Array
(
[0] => Array
(
[id] => 70
[site_id] => 1
[status_id] => 5
[name] => dr hab. n. med. Anna Potulska-Chromik
[firstname] => Anna
[lastname] => Potulska-Chromik
[title] => dr hab. n. med.
[affiliation] => Klinika Neurologii WUM
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 70-anna_potulska_chromik
[url] => eksperci/70-anna_potulska_chromik
)
)
[authors_ids] => Array
(
[0] => 70
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 152-choroby_nerwow_obwodowych
[url] => wideo/152-choroby_nerwow_obwodowych
[short_name] => Choroby nerwów obwodowych
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[153] => Array
(
[id] => 153
[site_id] => 1
[status_id] => 5
[name] => Choroby nerwowo-mięśniowe
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/153/postergen_i_geno.png
[video] => resources/data/material/153/5_choroby_nerwowomiesniowe_dr_hab._monika_gos.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med., prof IMiD Monika Gos
)
[authors_data] => Array
(
[0] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => dr n. med., prof IMiD Monika Gos
[firstname] => Monika
[lastname] => Gos
[title] => dr n. med., prof IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-monika_gos
[url] => eksperci/13-monika_gos
)
)
[authors_ids] => Array
(
[0] => 13
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 153-choroby_nerwowo_miesniowe
[url] => wideo/153-choroby_nerwowo_miesniowe
[short_name] => Choroby nerwowo-mięśniowe
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[154] => Array
(
[id] => 154
[site_id] => 1
[status_id] => 5
[name] => Rdzeniowy zanik mięśni - od mutacji do terapii
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/154/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med., prof IMiD Monika Gos
)
[authors_data] => Array
(
[0] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => dr n. med., prof IMiD Monika Gos
[firstname] => Monika
[lastname] => Gos
[title] => dr n. med., prof IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-monika_gos
[url] => eksperci/13-monika_gos
)
)
[authors_ids] => Array
(
[0] => 13
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
[3] => 14
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 154-rdzeniowy_zanik_miesni___od_mutacji_do_terapii
[url] => wideo/154-rdzeniowy_zanik_miesni___od_mutacji_do_terapii
[short_name] => Rdzeniowy zanik mięśni - od mutacji do terapii
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
[14] => Array
(
[id] => 14
[site_id] => 1
[status_id] => 5
[name] => choroby rzadkie
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 14-choroby_rzadkie
[url] => /14-choroby_rzadkie
)
)
[artykuly] => Array
(
)
)
[155] => Array
(
[id] => 155
[site_id] => 1
[status_id] => 5
[name] => Niepełnosprawność intelektualna – badania molekularne
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/155/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Sylwia Rzońca
)
[authors_data] => Array
(
[0] => Array
(
[id] => 10
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Sylwia Rzońca
[firstname] => Sylwia
[lastname] => Rzońca
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 10-sylwia_rzonca
[url] => eksperci/10-sylwia_rzonca
)
)
[authors_ids] => Array
(
[0] => 10
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 155-niepelnosprawnosc_intelektualna__badania_molekularne
[url] => wideo/155-niepelnosprawnosc_intelektualna__badania_molekularne
[short_name] => Niepełnosprawność intelektualna – badania molekula...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[156] => Array
(
[id] => 156
[site_id] => 1
[status_id] => 5
[name] => Choroby neurologiczne o późnym wieku zachorowania - wyzwania diagnostyki i poradnictwa
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/156/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 156-choroby_neurologiczne_o_poznym_wieku_zachorowania___wyzwania_diagnostyki_i_poradnictwa
[url] => wideo/156-choroby_neurologiczne_o_poznym_wieku_zachorowania___wyzwania_diagnostyki_i_poradnictwa
[short_name] => Choroby neurologiczne o późnym wieku zachorowania ...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[158] => Array
(
[id] => 158
[site_id] => 1
[status_id] => 5
[name] => Badania cytogenetyczne – od kliniki do interpretacji wyniku
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/158/postergen_i_geno.png
[video] => resources/data/material/158/5_badania_cytogenetyczne_–_od_kliniki_do_interpretacji_wyniku.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med.,prof IMiD Beata Nowakowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 9
[site_id] => 1
[status_id] => 5
[name] => dr n. med.,prof IMiD Beata Nowakowska
[firstname] => Beata
[lastname] => Nowakowska
[title] => dr n. med.,prof IMiD
[affiliation] => Zakład Genetyki Medycznej, Zespół Pracowni Cytogenetyki, IMID
[avatar] => resources/data/eksperci/9/dr_nowakowska_v2.jpg
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 9-beata_nowakowska
[url] => eksperci/9-beata_nowakowska
)
)
[authors_ids] => Array
(
[0] => 9
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 12
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 158-badania_cytogenetyczne__od_kliniki_do_interpretacji_wyniku
[url] => wideo/158-badania_cytogenetyczne__od_kliniki_do_interpretacji_wyniku
[short_name] => Badania cytogenetyczne – od kliniki do interpretac...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[12] => Array
(
[id] => 12
[site_id] => 1
[status_id] => 5
[name] => cytogenetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 12-cytogenetyka
[url] => /12-cytogenetyka
)
)
[artykuly] => Array
(
)
)
)
)
[sort] => 1
[status_code] => active
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 145-choroba_huntingtona
[url] => wideo/145-choroba_huntingtona
[short_name] => Choroba Huntingtona
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
[logotypy] => Array
(
)
[pliki] => Array
(
[114] => Array
(
[id] => 114
[site_id] => 1
[status_id] => 5
[entity_key] => material
[entity_id] => 145
[name] => Choroba Huntingtona
[file] => resources/data/pliki/material/145/25.06_w5_dhz_materialy_.pdf
[sort] => 111
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
[146] => Array
(
[id] => 146
[name] => Wspólne drogi zaburzeń neurorozwojowych
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/146/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
[linked] => Array
(
[144] => Array
(
[id] => 144
[site_id] => 1
[status_id] => 5
[name] => Badania molekularne. Od kliniki do interpretacji wyniku.
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/144/postergen_i_geno.png
[video] => resources/data/material/144/5_badania_molekularne_–_od_kliniki_do_interpretacji_wyniku_dr_hab._dorota_hoffmanzacharska.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
[3] => 14
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 144-badania_molekularne_od_kliniki_do_interpretacji_wyniku
[url] => wideo/144-badania_molekularne_od_kliniki_do_interpretacji_wyniku
[short_name] => Badania molekularne. Od kliniki do interpretacji w...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
[14] => Array
(
[id] => 14
[site_id] => 1
[status_id] => 5
[name] => choroby rzadkie
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 14-choroby_rzadkie
[url] => /14-choroby_rzadkie
)
)
[artykuly] => Array
(
)
)
[145] => Array
(
[id] => 145
[site_id] => 1
[status_id] => 5
[name] => Choroba Huntingtona
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/145/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 145-choroba_huntingtona
[url] => wideo/145-choroba_huntingtona
[short_name] => Choroba Huntingtona
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[147] => Array
(
[id] => 147
[site_id] => 1
[status_id] => 5
[name] => Genetyka chorób neurologicznych o późnym początku
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/147/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Maciej Geremek
)
[authors_data] => Array
(
[0] => Array
(
[id] => 69
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Maciej Geremek
[firstname] => Maciej
[lastname] => Geremek
[title] => dr n. med.
[affiliation] => Zakład genetyki Medycznej IMiD
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 69-maciej_geremek
[url] => eksperci/69-maciej_geremek
)
)
[authors_ids] => Array
(
[0] => 69
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 147-genetyka_chorob_neurologicznych_o_poznym_poczatku
[url] => wideo/147-genetyka_chorob_neurologicznych_o_poznym_poczatku
[short_name] => Genetyka chorób neurologicznych o późnym początku
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[148] => Array
(
[id] => 148
[site_id] => 1
[status_id] => 5
[name] => Neurogenetyka molekularna
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/148/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 148-neurogenetyka_molekularna
[url] => wideo/148-neurogenetyka_molekularna
[short_name] => Neurogenetyka molekularna
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[149] => Array
(
[id] => 149
[site_id] => 1
[status_id] => 5
[name] => Poradnictwo genetyczne w odniesieniu do chorób neurologicznych
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/149/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Ewa Obersztyn
)
[authors_data] => Array
(
[0] => Array
(
[id] => 14
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Ewa Obersztyn
[firstname] => Ewa
[lastname] => Obersztyn
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 14-ewa_obersztyn
[url] => eksperci/14-ewa_obersztyn
)
)
[authors_ids] => Array
(
[0] => 14
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 149-poradnictwo_genetyczne_w_odniesieniu_do_chorob_neurologicznych
[url] => wideo/149-poradnictwo_genetyczne_w_odniesieniu_do_chorob_neurologicznych
[short_name] => Poradnictwo genetyczne w odniesieniu do chorób neu...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[150] => Array
(
[id] => 150
[site_id] => 1
[status_id] => 5
[name] => Niepełnosprawność intelektualna –badania cytogenetyczne.
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/150/postergen_i_geno.png
[video] => resources/data/material/150/5_niepelnosprawnosc_intelektualna_–_badania_molekularne_dr_sylwia_rzonca.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => mgr Kamila Ziemkiewicz
)
[authors_data] => Array
(
[0] => Array
(
[id] => 11
[site_id] => 1
[status_id] => 5
[name] => mgr Kamila Ziemkiewicz
[firstname] => Kamila
[lastname] => Ziemkiewicz
[title] => mgr
[affiliation] =>
[avatar] => resources/data/eksperci/11/kziemkiewicz.png
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 11-kamila_ziemkiewicz
[url] => eksperci/11-kamila_ziemkiewicz
)
)
[authors_ids] => Array
(
[0] => 11
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 12
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 150-niepelnosprawnosc_intelektualna_badania_cytogenetyczne
[url] => wideo/150-niepelnosprawnosc_intelektualna_badania_cytogenetyczne
[short_name] => Niepełnosprawność intelektualna –badania cytogenet...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[12] => Array
(
[id] => 12
[site_id] => 1
[status_id] => 5
[name] => cytogenetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 12-cytogenetyka
[url] => /12-cytogenetyka
)
)
[artykuly] => Array
(
)
)
[151] => Array
(
[id] => 151
[site_id] => 1
[status_id] => 5
[name] => Techniki cytogenetyczne w diagnostyce chorób układu nerwowego.
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/151/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => mgr Kamila Ziemkiewicz
)
[authors_data] => Array
(
[0] => Array
(
[id] => 11
[site_id] => 1
[status_id] => 5
[name] => mgr Kamila Ziemkiewicz
[firstname] => Kamila
[lastname] => Ziemkiewicz
[title] => mgr
[affiliation] =>
[avatar] => resources/data/eksperci/11/kziemkiewicz.png
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 11-kamila_ziemkiewicz
[url] => eksperci/11-kamila_ziemkiewicz
)
)
[authors_ids] => Array
(
[0] => 11
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 12
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 151-techniki_cytogenetyczne_w_diagnostyce_chorob_ukladu_nerwowego
[url] => wideo/151-techniki_cytogenetyczne_w_diagnostyce_chorob_ukladu_nerwowego
[short_name] => Techniki cytogenetyczne w diagnostyce chorób układ...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[12] => Array
(
[id] => 12
[site_id] => 1
[status_id] => 5
[name] => cytogenetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 12-cytogenetyka
[url] => /12-cytogenetyka
)
)
[artykuly] => Array
(
)
)
[152] => Array
(
[id] => 152
[site_id] => 1
[status_id] => 5
[name] => Choroby nerwów obwodowych
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/152/postergen_i_geno.png
[video] => resources/data/material/152/5_choroby_nerwowobwodowych_potulska.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab. n. med. Anna Potulska-Chromik
)
[authors_data] => Array
(
[0] => Array
(
[id] => 70
[site_id] => 1
[status_id] => 5
[name] => dr hab. n. med. Anna Potulska-Chromik
[firstname] => Anna
[lastname] => Potulska-Chromik
[title] => dr hab. n. med.
[affiliation] => Klinika Neurologii WUM
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 70-anna_potulska_chromik
[url] => eksperci/70-anna_potulska_chromik
)
)
[authors_ids] => Array
(
[0] => 70
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 152-choroby_nerwow_obwodowych
[url] => wideo/152-choroby_nerwow_obwodowych
[short_name] => Choroby nerwów obwodowych
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[153] => Array
(
[id] => 153
[site_id] => 1
[status_id] => 5
[name] => Choroby nerwowo-mięśniowe
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/153/postergen_i_geno.png
[video] => resources/data/material/153/5_choroby_nerwowomiesniowe_dr_hab._monika_gos.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med., prof IMiD Monika Gos
)
[authors_data] => Array
(
[0] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => dr n. med., prof IMiD Monika Gos
[firstname] => Monika
[lastname] => Gos
[title] => dr n. med., prof IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-monika_gos
[url] => eksperci/13-monika_gos
)
)
[authors_ids] => Array
(
[0] => 13
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 153-choroby_nerwowo_miesniowe
[url] => wideo/153-choroby_nerwowo_miesniowe
[short_name] => Choroby nerwowo-mięśniowe
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[154] => Array
(
[id] => 154
[site_id] => 1
[status_id] => 5
[name] => Rdzeniowy zanik mięśni - od mutacji do terapii
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/154/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med., prof IMiD Monika Gos
)
[authors_data] => Array
(
[0] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => dr n. med., prof IMiD Monika Gos
[firstname] => Monika
[lastname] => Gos
[title] => dr n. med., prof IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-monika_gos
[url] => eksperci/13-monika_gos
)
)
[authors_ids] => Array
(
[0] => 13
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
[3] => 14
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 154-rdzeniowy_zanik_miesni___od_mutacji_do_terapii
[url] => wideo/154-rdzeniowy_zanik_miesni___od_mutacji_do_terapii
[short_name] => Rdzeniowy zanik mięśni - od mutacji do terapii
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
[14] => Array
(
[id] => 14
[site_id] => 1
[status_id] => 5
[name] => choroby rzadkie
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 14-choroby_rzadkie
[url] => /14-choroby_rzadkie
)
)
[artykuly] => Array
(
)
)
[155] => Array
(
[id] => 155
[site_id] => 1
[status_id] => 5
[name] => Niepełnosprawność intelektualna – badania molekularne
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/155/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Sylwia Rzońca
)
[authors_data] => Array
(
[0] => Array
(
[id] => 10
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Sylwia Rzońca
[firstname] => Sylwia
[lastname] => Rzońca
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 10-sylwia_rzonca
[url] => eksperci/10-sylwia_rzonca
)
)
[authors_ids] => Array
(
[0] => 10
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 155-niepelnosprawnosc_intelektualna__badania_molekularne
[url] => wideo/155-niepelnosprawnosc_intelektualna__badania_molekularne
[short_name] => Niepełnosprawność intelektualna – badania molekula...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[156] => Array
(
[id] => 156
[site_id] => 1
[status_id] => 5
[name] => Choroby neurologiczne o późnym wieku zachorowania - wyzwania diagnostyki i poradnictwa
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/156/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 156-choroby_neurologiczne_o_poznym_wieku_zachorowania___wyzwania_diagnostyki_i_poradnictwa
[url] => wideo/156-choroby_neurologiczne_o_poznym_wieku_zachorowania___wyzwania_diagnostyki_i_poradnictwa
[short_name] => Choroby neurologiczne o późnym wieku zachorowania ...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[158] => Array
(
[id] => 158
[site_id] => 1
[status_id] => 5
[name] => Badania cytogenetyczne – od kliniki do interpretacji wyniku
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/158/postergen_i_geno.png
[video] => resources/data/material/158/5_badania_cytogenetyczne_–_od_kliniki_do_interpretacji_wyniku.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med.,prof IMiD Beata Nowakowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 9
[site_id] => 1
[status_id] => 5
[name] => dr n. med.,prof IMiD Beata Nowakowska
[firstname] => Beata
[lastname] => Nowakowska
[title] => dr n. med.,prof IMiD
[affiliation] => Zakład Genetyki Medycznej, Zespół Pracowni Cytogenetyki, IMID
[avatar] => resources/data/eksperci/9/dr_nowakowska_v2.jpg
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 9-beata_nowakowska
[url] => eksperci/9-beata_nowakowska
)
)
[authors_ids] => Array
(
[0] => 9
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 12
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 158-badania_cytogenetyczne__od_kliniki_do_interpretacji_wyniku
[url] => wideo/158-badania_cytogenetyczne__od_kliniki_do_interpretacji_wyniku
[short_name] => Badania cytogenetyczne – od kliniki do interpretac...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[12] => Array
(
[id] => 12
[site_id] => 1
[status_id] => 5
[name] => cytogenetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 12-cytogenetyka
[url] => /12-cytogenetyka
)
)
[artykuly] => Array
(
)
)
)
)
[sort] => 1
[status_code] => active
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 146-wspolne_drogi_zaburzen_neurorozwojowych
[url] => wideo/146-wspolne_drogi_zaburzen_neurorozwojowych
[short_name] => Wspólne drogi zaburzeń neurorozwojowych
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
[logotypy] => Array
(
)
[pliki] => Array
(
[115] => Array
(
[id] => 115
[site_id] => 1
[status_id] => 5
[entity_key] => material
[entity_id] => 146
[name] => Wspólne drogi zaburzeń neurorozwojowych
[file] => resources/data/pliki/material/146/24.06_w6_dhz_.pdf
[sort] => 112
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
[147] => Array
(
[id] => 147
[name] => Genetyka chorób neurologicznych o późnym początku
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/147/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
[linked] => Array
(
[144] => Array
(
[id] => 144
[site_id] => 1
[status_id] => 5
[name] => Badania molekularne. Od kliniki do interpretacji wyniku.
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/144/postergen_i_geno.png
[video] => resources/data/material/144/5_badania_molekularne_–_od_kliniki_do_interpretacji_wyniku_dr_hab._dorota_hoffmanzacharska.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
[3] => 14
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 144-badania_molekularne_od_kliniki_do_interpretacji_wyniku
[url] => wideo/144-badania_molekularne_od_kliniki_do_interpretacji_wyniku
[short_name] => Badania molekularne. Od kliniki do interpretacji w...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
[14] => Array
(
[id] => 14
[site_id] => 1
[status_id] => 5
[name] => choroby rzadkie
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 14-choroby_rzadkie
[url] => /14-choroby_rzadkie
)
)
[artykuly] => Array
(
)
)
[145] => Array
(
[id] => 145
[site_id] => 1
[status_id] => 5
[name] => Choroba Huntingtona
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/145/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 145-choroba_huntingtona
[url] => wideo/145-choroba_huntingtona
[short_name] => Choroba Huntingtona
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[146] => Array
(
[id] => 146
[site_id] => 1
[status_id] => 5
[name] => Wspólne drogi zaburzeń neurorozwojowych
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/146/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 146-wspolne_drogi_zaburzen_neurorozwojowych
[url] => wideo/146-wspolne_drogi_zaburzen_neurorozwojowych
[short_name] => Wspólne drogi zaburzeń neurorozwojowych
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[148] => Array
(
[id] => 148
[site_id] => 1
[status_id] => 5
[name] => Neurogenetyka molekularna
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/148/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 148-neurogenetyka_molekularna
[url] => wideo/148-neurogenetyka_molekularna
[short_name] => Neurogenetyka molekularna
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[149] => Array
(
[id] => 149
[site_id] => 1
[status_id] => 5
[name] => Poradnictwo genetyczne w odniesieniu do chorób neurologicznych
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/149/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Ewa Obersztyn
)
[authors_data] => Array
(
[0] => Array
(
[id] => 14
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Ewa Obersztyn
[firstname] => Ewa
[lastname] => Obersztyn
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 14-ewa_obersztyn
[url] => eksperci/14-ewa_obersztyn
)
)
[authors_ids] => Array
(
[0] => 14
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 149-poradnictwo_genetyczne_w_odniesieniu_do_chorob_neurologicznych
[url] => wideo/149-poradnictwo_genetyczne_w_odniesieniu_do_chorob_neurologicznych
[short_name] => Poradnictwo genetyczne w odniesieniu do chorób neu...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[150] => Array
(
[id] => 150
[site_id] => 1
[status_id] => 5
[name] => Niepełnosprawność intelektualna –badania cytogenetyczne.
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/150/postergen_i_geno.png
[video] => resources/data/material/150/5_niepelnosprawnosc_intelektualna_–_badania_molekularne_dr_sylwia_rzonca.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => mgr Kamila Ziemkiewicz
)
[authors_data] => Array
(
[0] => Array
(
[id] => 11
[site_id] => 1
[status_id] => 5
[name] => mgr Kamila Ziemkiewicz
[firstname] => Kamila
[lastname] => Ziemkiewicz
[title] => mgr
[affiliation] =>
[avatar] => resources/data/eksperci/11/kziemkiewicz.png
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 11-kamila_ziemkiewicz
[url] => eksperci/11-kamila_ziemkiewicz
)
)
[authors_ids] => Array
(
[0] => 11
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 12
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 150-niepelnosprawnosc_intelektualna_badania_cytogenetyczne
[url] => wideo/150-niepelnosprawnosc_intelektualna_badania_cytogenetyczne
[short_name] => Niepełnosprawność intelektualna –badania cytogenet...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[12] => Array
(
[id] => 12
[site_id] => 1
[status_id] => 5
[name] => cytogenetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 12-cytogenetyka
[url] => /12-cytogenetyka
)
)
[artykuly] => Array
(
)
)
[151] => Array
(
[id] => 151
[site_id] => 1
[status_id] => 5
[name] => Techniki cytogenetyczne w diagnostyce chorób układu nerwowego.
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/151/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => mgr Kamila Ziemkiewicz
)
[authors_data] => Array
(
[0] => Array
(
[id] => 11
[site_id] => 1
[status_id] => 5
[name] => mgr Kamila Ziemkiewicz
[firstname] => Kamila
[lastname] => Ziemkiewicz
[title] => mgr
[affiliation] =>
[avatar] => resources/data/eksperci/11/kziemkiewicz.png
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 11-kamila_ziemkiewicz
[url] => eksperci/11-kamila_ziemkiewicz
)
)
[authors_ids] => Array
(
[0] => 11
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 12
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 151-techniki_cytogenetyczne_w_diagnostyce_chorob_ukladu_nerwowego
[url] => wideo/151-techniki_cytogenetyczne_w_diagnostyce_chorob_ukladu_nerwowego
[short_name] => Techniki cytogenetyczne w diagnostyce chorób układ...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[12] => Array
(
[id] => 12
[site_id] => 1
[status_id] => 5
[name] => cytogenetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 12-cytogenetyka
[url] => /12-cytogenetyka
)
)
[artykuly] => Array
(
)
)
[152] => Array
(
[id] => 152
[site_id] => 1
[status_id] => 5
[name] => Choroby nerwów obwodowych
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/152/postergen_i_geno.png
[video] => resources/data/material/152/5_choroby_nerwowobwodowych_potulska.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab. n. med. Anna Potulska-Chromik
)
[authors_data] => Array
(
[0] => Array
(
[id] => 70
[site_id] => 1
[status_id] => 5
[name] => dr hab. n. med. Anna Potulska-Chromik
[firstname] => Anna
[lastname] => Potulska-Chromik
[title] => dr hab. n. med.
[affiliation] => Klinika Neurologii WUM
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 70-anna_potulska_chromik
[url] => eksperci/70-anna_potulska_chromik
)
)
[authors_ids] => Array
(
[0] => 70
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 152-choroby_nerwow_obwodowych
[url] => wideo/152-choroby_nerwow_obwodowych
[short_name] => Choroby nerwów obwodowych
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[153] => Array
(
[id] => 153
[site_id] => 1
[status_id] => 5
[name] => Choroby nerwowo-mięśniowe
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/153/postergen_i_geno.png
[video] => resources/data/material/153/5_choroby_nerwowomiesniowe_dr_hab._monika_gos.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med., prof IMiD Monika Gos
)
[authors_data] => Array
(
[0] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => dr n. med., prof IMiD Monika Gos
[firstname] => Monika
[lastname] => Gos
[title] => dr n. med., prof IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-monika_gos
[url] => eksperci/13-monika_gos
)
)
[authors_ids] => Array
(
[0] => 13
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 153-choroby_nerwowo_miesniowe
[url] => wideo/153-choroby_nerwowo_miesniowe
[short_name] => Choroby nerwowo-mięśniowe
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[154] => Array
(
[id] => 154
[site_id] => 1
[status_id] => 5
[name] => Rdzeniowy zanik mięśni - od mutacji do terapii
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/154/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med., prof IMiD Monika Gos
)
[authors_data] => Array
(
[0] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => dr n. med., prof IMiD Monika Gos
[firstname] => Monika
[lastname] => Gos
[title] => dr n. med., prof IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-monika_gos
[url] => eksperci/13-monika_gos
)
)
[authors_ids] => Array
(
[0] => 13
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
[3] => 14
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 154-rdzeniowy_zanik_miesni___od_mutacji_do_terapii
[url] => wideo/154-rdzeniowy_zanik_miesni___od_mutacji_do_terapii
[short_name] => Rdzeniowy zanik mięśni - od mutacji do terapii
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
[14] => Array
(
[id] => 14
[site_id] => 1
[status_id] => 5
[name] => choroby rzadkie
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 14-choroby_rzadkie
[url] => /14-choroby_rzadkie
)
)
[artykuly] => Array
(
)
)
[155] => Array
(
[id] => 155
[site_id] => 1
[status_id] => 5
[name] => Niepełnosprawność intelektualna – badania molekularne
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/155/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Sylwia Rzońca
)
[authors_data] => Array
(
[0] => Array
(
[id] => 10
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Sylwia Rzońca
[firstname] => Sylwia
[lastname] => Rzońca
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 10-sylwia_rzonca
[url] => eksperci/10-sylwia_rzonca
)
)
[authors_ids] => Array
(
[0] => 10
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 155-niepelnosprawnosc_intelektualna__badania_molekularne
[url] => wideo/155-niepelnosprawnosc_intelektualna__badania_molekularne
[short_name] => Niepełnosprawność intelektualna – badania molekula...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[156] => Array
(
[id] => 156
[site_id] => 1
[status_id] => 5
[name] => Choroby neurologiczne o późnym wieku zachorowania - wyzwania diagnostyki i poradnictwa
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/156/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 156-choroby_neurologiczne_o_poznym_wieku_zachorowania___wyzwania_diagnostyki_i_poradnictwa
[url] => wideo/156-choroby_neurologiczne_o_poznym_wieku_zachorowania___wyzwania_diagnostyki_i_poradnictwa
[short_name] => Choroby neurologiczne o późnym wieku zachorowania ...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[158] => Array
(
[id] => 158
[site_id] => 1
[status_id] => 5
[name] => Badania cytogenetyczne – od kliniki do interpretacji wyniku
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/158/postergen_i_geno.png
[video] => resources/data/material/158/5_badania_cytogenetyczne_–_od_kliniki_do_interpretacji_wyniku.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med.,prof IMiD Beata Nowakowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 9
[site_id] => 1
[status_id] => 5
[name] => dr n. med.,prof IMiD Beata Nowakowska
[firstname] => Beata
[lastname] => Nowakowska
[title] => dr n. med.,prof IMiD
[affiliation] => Zakład Genetyki Medycznej, Zespół Pracowni Cytogenetyki, IMID
[avatar] => resources/data/eksperci/9/dr_nowakowska_v2.jpg
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 9-beata_nowakowska
[url] => eksperci/9-beata_nowakowska
)
)
[authors_ids] => Array
(
[0] => 9
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 12
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 158-badania_cytogenetyczne__od_kliniki_do_interpretacji_wyniku
[url] => wideo/158-badania_cytogenetyczne__od_kliniki_do_interpretacji_wyniku
[short_name] => Badania cytogenetyczne – od kliniki do interpretac...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[12] => Array
(
[id] => 12
[site_id] => 1
[status_id] => 5
[name] => cytogenetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 12-cytogenetyka
[url] => /12-cytogenetyka
)
)
[artykuly] => Array
(
)
)
)
)
[sort] => 1
[status_code] => active
[authors] => Array
(
[0] => dr n. med. Maciej Geremek
)
[authors_data] => Array
(
[0] => Array
(
[id] => 69
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Maciej Geremek
[firstname] => Maciej
[lastname] => Geremek
[title] => dr n. med.
[affiliation] => Zakład genetyki Medycznej IMiD
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 69-maciej_geremek
[url] => eksperci/69-maciej_geremek
)
)
[authors_ids] => Array
(
[0] => 69
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 147-genetyka_chorob_neurologicznych_o_poznym_poczatku
[url] => wideo/147-genetyka_chorob_neurologicznych_o_poznym_poczatku
[short_name] => Genetyka chorób neurologicznych o późnym początku
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
[logotypy] => Array
(
)
[pliki] => Array
(
[116] => Array
(
[id] => 116
[site_id] => 1
[status_id] => 5
[entity_key] => material
[entity_id] => 147
[name] => Genetyka chorób neurologicznych o późnym początku
[file] => resources/data/pliki/material/147/25.06.w4short.pdf
[sort] => 113
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
[148] => Array
(
[id] => 148
[name] => Neurogenetyka molekularna
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/148/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
[linked] => Array
(
[144] => Array
(
[id] => 144
[site_id] => 1
[status_id] => 5
[name] => Badania molekularne. Od kliniki do interpretacji wyniku.
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/144/postergen_i_geno.png
[video] => resources/data/material/144/5_badania_molekularne_–_od_kliniki_do_interpretacji_wyniku_dr_hab._dorota_hoffmanzacharska.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
[3] => 14
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 144-badania_molekularne_od_kliniki_do_interpretacji_wyniku
[url] => wideo/144-badania_molekularne_od_kliniki_do_interpretacji_wyniku
[short_name] => Badania molekularne. Od kliniki do interpretacji w...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
[14] => Array
(
[id] => 14
[site_id] => 1
[status_id] => 5
[name] => choroby rzadkie
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 14-choroby_rzadkie
[url] => /14-choroby_rzadkie
)
)
[artykuly] => Array
(
)
)
[145] => Array
(
[id] => 145
[site_id] => 1
[status_id] => 5
[name] => Choroba Huntingtona
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/145/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 145-choroba_huntingtona
[url] => wideo/145-choroba_huntingtona
[short_name] => Choroba Huntingtona
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[146] => Array
(
[id] => 146
[site_id] => 1
[status_id] => 5
[name] => Wspólne drogi zaburzeń neurorozwojowych
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/146/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 146-wspolne_drogi_zaburzen_neurorozwojowych
[url] => wideo/146-wspolne_drogi_zaburzen_neurorozwojowych
[short_name] => Wspólne drogi zaburzeń neurorozwojowych
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[147] => Array
(
[id] => 147
[site_id] => 1
[status_id] => 5
[name] => Genetyka chorób neurologicznych o późnym początku
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/147/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Maciej Geremek
)
[authors_data] => Array
(
[0] => Array
(
[id] => 69
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Maciej Geremek
[firstname] => Maciej
[lastname] => Geremek
[title] => dr n. med.
[affiliation] => Zakład genetyki Medycznej IMiD
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 69-maciej_geremek
[url] => eksperci/69-maciej_geremek
)
)
[authors_ids] => Array
(
[0] => 69
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 147-genetyka_chorob_neurologicznych_o_poznym_poczatku
[url] => wideo/147-genetyka_chorob_neurologicznych_o_poznym_poczatku
[short_name] => Genetyka chorób neurologicznych o późnym początku
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[149] => Array
(
[id] => 149
[site_id] => 1
[status_id] => 5
[name] => Poradnictwo genetyczne w odniesieniu do chorób neurologicznych
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/149/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Ewa Obersztyn
)
[authors_data] => Array
(
[0] => Array
(
[id] => 14
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Ewa Obersztyn
[firstname] => Ewa
[lastname] => Obersztyn
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 14-ewa_obersztyn
[url] => eksperci/14-ewa_obersztyn
)
)
[authors_ids] => Array
(
[0] => 14
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 149-poradnictwo_genetyczne_w_odniesieniu_do_chorob_neurologicznych
[url] => wideo/149-poradnictwo_genetyczne_w_odniesieniu_do_chorob_neurologicznych
[short_name] => Poradnictwo genetyczne w odniesieniu do chorób neu...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[150] => Array
(
[id] => 150
[site_id] => 1
[status_id] => 5
[name] => Niepełnosprawność intelektualna –badania cytogenetyczne.
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/150/postergen_i_geno.png
[video] => resources/data/material/150/5_niepelnosprawnosc_intelektualna_–_badania_molekularne_dr_sylwia_rzonca.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => mgr Kamila Ziemkiewicz
)
[authors_data] => Array
(
[0] => Array
(
[id] => 11
[site_id] => 1
[status_id] => 5
[name] => mgr Kamila Ziemkiewicz
[firstname] => Kamila
[lastname] => Ziemkiewicz
[title] => mgr
[affiliation] =>
[avatar] => resources/data/eksperci/11/kziemkiewicz.png
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 11-kamila_ziemkiewicz
[url] => eksperci/11-kamila_ziemkiewicz
)
)
[authors_ids] => Array
(
[0] => 11
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 12
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 150-niepelnosprawnosc_intelektualna_badania_cytogenetyczne
[url] => wideo/150-niepelnosprawnosc_intelektualna_badania_cytogenetyczne
[short_name] => Niepełnosprawność intelektualna –badania cytogenet...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[12] => Array
(
[id] => 12
[site_id] => 1
[status_id] => 5
[name] => cytogenetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 12-cytogenetyka
[url] => /12-cytogenetyka
)
)
[artykuly] => Array
(
)
)
[151] => Array
(
[id] => 151
[site_id] => 1
[status_id] => 5
[name] => Techniki cytogenetyczne w diagnostyce chorób układu nerwowego.
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/151/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => mgr Kamila Ziemkiewicz
)
[authors_data] => Array
(
[0] => Array
(
[id] => 11
[site_id] => 1
[status_id] => 5
[name] => mgr Kamila Ziemkiewicz
[firstname] => Kamila
[lastname] => Ziemkiewicz
[title] => mgr
[affiliation] =>
[avatar] => resources/data/eksperci/11/kziemkiewicz.png
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 11-kamila_ziemkiewicz
[url] => eksperci/11-kamila_ziemkiewicz
)
)
[authors_ids] => Array
(
[0] => 11
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 12
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 151-techniki_cytogenetyczne_w_diagnostyce_chorob_ukladu_nerwowego
[url] => wideo/151-techniki_cytogenetyczne_w_diagnostyce_chorob_ukladu_nerwowego
[short_name] => Techniki cytogenetyczne w diagnostyce chorób układ...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[12] => Array
(
[id] => 12
[site_id] => 1
[status_id] => 5
[name] => cytogenetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 12-cytogenetyka
[url] => /12-cytogenetyka
)
)
[artykuly] => Array
(
)
)
[152] => Array
(
[id] => 152
[site_id] => 1
[status_id] => 5
[name] => Choroby nerwów obwodowych
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/152/postergen_i_geno.png
[video] => resources/data/material/152/5_choroby_nerwowobwodowych_potulska.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab. n. med. Anna Potulska-Chromik
)
[authors_data] => Array
(
[0] => Array
(
[id] => 70
[site_id] => 1
[status_id] => 5
[name] => dr hab. n. med. Anna Potulska-Chromik
[firstname] => Anna
[lastname] => Potulska-Chromik
[title] => dr hab. n. med.
[affiliation] => Klinika Neurologii WUM
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 70-anna_potulska_chromik
[url] => eksperci/70-anna_potulska_chromik
)
)
[authors_ids] => Array
(
[0] => 70
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 152-choroby_nerwow_obwodowych
[url] => wideo/152-choroby_nerwow_obwodowych
[short_name] => Choroby nerwów obwodowych
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[153] => Array
(
[id] => 153
[site_id] => 1
[status_id] => 5
[name] => Choroby nerwowo-mięśniowe
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/153/postergen_i_geno.png
[video] => resources/data/material/153/5_choroby_nerwowomiesniowe_dr_hab._monika_gos.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med., prof IMiD Monika Gos
)
[authors_data] => Array
(
[0] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => dr n. med., prof IMiD Monika Gos
[firstname] => Monika
[lastname] => Gos
[title] => dr n. med., prof IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-monika_gos
[url] => eksperci/13-monika_gos
)
)
[authors_ids] => Array
(
[0] => 13
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 153-choroby_nerwowo_miesniowe
[url] => wideo/153-choroby_nerwowo_miesniowe
[short_name] => Choroby nerwowo-mięśniowe
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[154] => Array
(
[id] => 154
[site_id] => 1
[status_id] => 5
[name] => Rdzeniowy zanik mięśni - od mutacji do terapii
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/154/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med., prof IMiD Monika Gos
)
[authors_data] => Array
(
[0] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => dr n. med., prof IMiD Monika Gos
[firstname] => Monika
[lastname] => Gos
[title] => dr n. med., prof IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-monika_gos
[url] => eksperci/13-monika_gos
)
)
[authors_ids] => Array
(
[0] => 13
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
[3] => 14
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 154-rdzeniowy_zanik_miesni___od_mutacji_do_terapii
[url] => wideo/154-rdzeniowy_zanik_miesni___od_mutacji_do_terapii
[short_name] => Rdzeniowy zanik mięśni - od mutacji do terapii
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
[14] => Array
(
[id] => 14
[site_id] => 1
[status_id] => 5
[name] => choroby rzadkie
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 14-choroby_rzadkie
[url] => /14-choroby_rzadkie
)
)
[artykuly] => Array
(
)
)
[155] => Array
(
[id] => 155
[site_id] => 1
[status_id] => 5
[name] => Niepełnosprawność intelektualna – badania molekularne
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/155/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Sylwia Rzońca
)
[authors_data] => Array
(
[0] => Array
(
[id] => 10
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Sylwia Rzońca
[firstname] => Sylwia
[lastname] => Rzońca
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 10-sylwia_rzonca
[url] => eksperci/10-sylwia_rzonca
)
)
[authors_ids] => Array
(
[0] => 10
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 155-niepelnosprawnosc_intelektualna__badania_molekularne
[url] => wideo/155-niepelnosprawnosc_intelektualna__badania_molekularne
[short_name] => Niepełnosprawność intelektualna – badania molekula...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[156] => Array
(
[id] => 156
[site_id] => 1
[status_id] => 5
[name] => Choroby neurologiczne o późnym wieku zachorowania - wyzwania diagnostyki i poradnictwa
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/156/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 156-choroby_neurologiczne_o_poznym_wieku_zachorowania___wyzwania_diagnostyki_i_poradnictwa
[url] => wideo/156-choroby_neurologiczne_o_poznym_wieku_zachorowania___wyzwania_diagnostyki_i_poradnictwa
[short_name] => Choroby neurologiczne o późnym wieku zachorowania ...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[158] => Array
(
[id] => 158
[site_id] => 1
[status_id] => 5
[name] => Badania cytogenetyczne – od kliniki do interpretacji wyniku
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/158/postergen_i_geno.png
[video] => resources/data/material/158/5_badania_cytogenetyczne_–_od_kliniki_do_interpretacji_wyniku.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med.,prof IMiD Beata Nowakowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 9
[site_id] => 1
[status_id] => 5
[name] => dr n. med.,prof IMiD Beata Nowakowska
[firstname] => Beata
[lastname] => Nowakowska
[title] => dr n. med.,prof IMiD
[affiliation] => Zakład Genetyki Medycznej, Zespół Pracowni Cytogenetyki, IMID
[avatar] => resources/data/eksperci/9/dr_nowakowska_v2.jpg
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 9-beata_nowakowska
[url] => eksperci/9-beata_nowakowska
)
)
[authors_ids] => Array
(
[0] => 9
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 12
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 158-badania_cytogenetyczne__od_kliniki_do_interpretacji_wyniku
[url] => wideo/158-badania_cytogenetyczne__od_kliniki_do_interpretacji_wyniku
[short_name] => Badania cytogenetyczne – od kliniki do interpretac...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[12] => Array
(
[id] => 12
[site_id] => 1
[status_id] => 5
[name] => cytogenetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 12-cytogenetyka
[url] => /12-cytogenetyka
)
)
[artykuly] => Array
(
)
)
)
)
[sort] => 1
[status_code] => active
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 148-neurogenetyka_molekularna
[url] => wideo/148-neurogenetyka_molekularna
[short_name] => Neurogenetyka molekularna
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
[logotypy] => Array
(
)
[pliki] => Array
(
[117] => Array
(
[id] => 117
[site_id] => 1
[status_id] => 5
[entity_key] => material
[entity_id] => 148
[name] => Neurogenetyka molekularna
[file] => resources/data/pliki/material/148/24.06_w3_dhz_materialy.pdf
[sort] => 114
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
[149] => Array
(
[id] => 149
[name] => Poradnictwo genetyczne w odniesieniu do chorób neurologicznych
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/149/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
[linked] => Array
(
[144] => Array
(
[id] => 144
[site_id] => 1
[status_id] => 5
[name] => Badania molekularne. Od kliniki do interpretacji wyniku.
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/144/postergen_i_geno.png
[video] => resources/data/material/144/5_badania_molekularne_–_od_kliniki_do_interpretacji_wyniku_dr_hab._dorota_hoffmanzacharska.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
[3] => 14
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 144-badania_molekularne_od_kliniki_do_interpretacji_wyniku
[url] => wideo/144-badania_molekularne_od_kliniki_do_interpretacji_wyniku
[short_name] => Badania molekularne. Od kliniki do interpretacji w...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
[14] => Array
(
[id] => 14
[site_id] => 1
[status_id] => 5
[name] => choroby rzadkie
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 14-choroby_rzadkie
[url] => /14-choroby_rzadkie
)
)
[artykuly] => Array
(
)
)
[145] => Array
(
[id] => 145
[site_id] => 1
[status_id] => 5
[name] => Choroba Huntingtona
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/145/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 145-choroba_huntingtona
[url] => wideo/145-choroba_huntingtona
[short_name] => Choroba Huntingtona
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[146] => Array
(
[id] => 146
[site_id] => 1
[status_id] => 5
[name] => Wspólne drogi zaburzeń neurorozwojowych
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/146/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 146-wspolne_drogi_zaburzen_neurorozwojowych
[url] => wideo/146-wspolne_drogi_zaburzen_neurorozwojowych
[short_name] => Wspólne drogi zaburzeń neurorozwojowych
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[147] => Array
(
[id] => 147
[site_id] => 1
[status_id] => 5
[name] => Genetyka chorób neurologicznych o późnym początku
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/147/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Maciej Geremek
)
[authors_data] => Array
(
[0] => Array
(
[id] => 69
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Maciej Geremek
[firstname] => Maciej
[lastname] => Geremek
[title] => dr n. med.
[affiliation] => Zakład genetyki Medycznej IMiD
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 69-maciej_geremek
[url] => eksperci/69-maciej_geremek
)
)
[authors_ids] => Array
(
[0] => 69
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 147-genetyka_chorob_neurologicznych_o_poznym_poczatku
[url] => wideo/147-genetyka_chorob_neurologicznych_o_poznym_poczatku
[short_name] => Genetyka chorób neurologicznych o późnym początku
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[148] => Array
(
[id] => 148
[site_id] => 1
[status_id] => 5
[name] => Neurogenetyka molekularna
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/148/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 148-neurogenetyka_molekularna
[url] => wideo/148-neurogenetyka_molekularna
[short_name] => Neurogenetyka molekularna
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[150] => Array
(
[id] => 150
[site_id] => 1
[status_id] => 5
[name] => Niepełnosprawność intelektualna –badania cytogenetyczne.
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/150/postergen_i_geno.png
[video] => resources/data/material/150/5_niepelnosprawnosc_intelektualna_–_badania_molekularne_dr_sylwia_rzonca.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => mgr Kamila Ziemkiewicz
)
[authors_data] => Array
(
[0] => Array
(
[id] => 11
[site_id] => 1
[status_id] => 5
[name] => mgr Kamila Ziemkiewicz
[firstname] => Kamila
[lastname] => Ziemkiewicz
[title] => mgr
[affiliation] =>
[avatar] => resources/data/eksperci/11/kziemkiewicz.png
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 11-kamila_ziemkiewicz
[url] => eksperci/11-kamila_ziemkiewicz
)
)
[authors_ids] => Array
(
[0] => 11
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 12
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 150-niepelnosprawnosc_intelektualna_badania_cytogenetyczne
[url] => wideo/150-niepelnosprawnosc_intelektualna_badania_cytogenetyczne
[short_name] => Niepełnosprawność intelektualna –badania cytogenet...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[12] => Array
(
[id] => 12
[site_id] => 1
[status_id] => 5
[name] => cytogenetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 12-cytogenetyka
[url] => /12-cytogenetyka
)
)
[artykuly] => Array
(
)
)
[151] => Array
(
[id] => 151
[site_id] => 1
[status_id] => 5
[name] => Techniki cytogenetyczne w diagnostyce chorób układu nerwowego.
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/151/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => mgr Kamila Ziemkiewicz
)
[authors_data] => Array
(
[0] => Array
(
[id] => 11
[site_id] => 1
[status_id] => 5
[name] => mgr Kamila Ziemkiewicz
[firstname] => Kamila
[lastname] => Ziemkiewicz
[title] => mgr
[affiliation] =>
[avatar] => resources/data/eksperci/11/kziemkiewicz.png
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 11-kamila_ziemkiewicz
[url] => eksperci/11-kamila_ziemkiewicz
)
)
[authors_ids] => Array
(
[0] => 11
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 12
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 151-techniki_cytogenetyczne_w_diagnostyce_chorob_ukladu_nerwowego
[url] => wideo/151-techniki_cytogenetyczne_w_diagnostyce_chorob_ukladu_nerwowego
[short_name] => Techniki cytogenetyczne w diagnostyce chorób układ...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[12] => Array
(
[id] => 12
[site_id] => 1
[status_id] => 5
[name] => cytogenetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 12-cytogenetyka
[url] => /12-cytogenetyka
)
)
[artykuly] => Array
(
)
)
[152] => Array
(
[id] => 152
[site_id] => 1
[status_id] => 5
[name] => Choroby nerwów obwodowych
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/152/postergen_i_geno.png
[video] => resources/data/material/152/5_choroby_nerwowobwodowych_potulska.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab. n. med. Anna Potulska-Chromik
)
[authors_data] => Array
(
[0] => Array
(
[id] => 70
[site_id] => 1
[status_id] => 5
[name] => dr hab. n. med. Anna Potulska-Chromik
[firstname] => Anna
[lastname] => Potulska-Chromik
[title] => dr hab. n. med.
[affiliation] => Klinika Neurologii WUM
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 70-anna_potulska_chromik
[url] => eksperci/70-anna_potulska_chromik
)
)
[authors_ids] => Array
(
[0] => 70
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 152-choroby_nerwow_obwodowych
[url] => wideo/152-choroby_nerwow_obwodowych
[short_name] => Choroby nerwów obwodowych
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[153] => Array
(
[id] => 153
[site_id] => 1
[status_id] => 5
[name] => Choroby nerwowo-mięśniowe
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/153/postergen_i_geno.png
[video] => resources/data/material/153/5_choroby_nerwowomiesniowe_dr_hab._monika_gos.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med., prof IMiD Monika Gos
)
[authors_data] => Array
(
[0] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => dr n. med., prof IMiD Monika Gos
[firstname] => Monika
[lastname] => Gos
[title] => dr n. med., prof IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-monika_gos
[url] => eksperci/13-monika_gos
)
)
[authors_ids] => Array
(
[0] => 13
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 153-choroby_nerwowo_miesniowe
[url] => wideo/153-choroby_nerwowo_miesniowe
[short_name] => Choroby nerwowo-mięśniowe
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[154] => Array
(
[id] => 154
[site_id] => 1
[status_id] => 5
[name] => Rdzeniowy zanik mięśni - od mutacji do terapii
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/154/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med., prof IMiD Monika Gos
)
[authors_data] => Array
(
[0] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => dr n. med., prof IMiD Monika Gos
[firstname] => Monika
[lastname] => Gos
[title] => dr n. med., prof IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-monika_gos
[url] => eksperci/13-monika_gos
)
)
[authors_ids] => Array
(
[0] => 13
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
[3] => 14
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 154-rdzeniowy_zanik_miesni___od_mutacji_do_terapii
[url] => wideo/154-rdzeniowy_zanik_miesni___od_mutacji_do_terapii
[short_name] => Rdzeniowy zanik mięśni - od mutacji do terapii
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
[14] => Array
(
[id] => 14
[site_id] => 1
[status_id] => 5
[name] => choroby rzadkie
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 14-choroby_rzadkie
[url] => /14-choroby_rzadkie
)
)
[artykuly] => Array
(
)
)
[155] => Array
(
[id] => 155
[site_id] => 1
[status_id] => 5
[name] => Niepełnosprawność intelektualna – badania molekularne
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/155/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Sylwia Rzońca
)
[authors_data] => Array
(
[0] => Array
(
[id] => 10
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Sylwia Rzońca
[firstname] => Sylwia
[lastname] => Rzońca
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 10-sylwia_rzonca
[url] => eksperci/10-sylwia_rzonca
)
)
[authors_ids] => Array
(
[0] => 10
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 155-niepelnosprawnosc_intelektualna__badania_molekularne
[url] => wideo/155-niepelnosprawnosc_intelektualna__badania_molekularne
[short_name] => Niepełnosprawność intelektualna – badania molekula...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[156] => Array
(
[id] => 156
[site_id] => 1
[status_id] => 5
[name] => Choroby neurologiczne o późnym wieku zachorowania - wyzwania diagnostyki i poradnictwa
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/156/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 156-choroby_neurologiczne_o_poznym_wieku_zachorowania___wyzwania_diagnostyki_i_poradnictwa
[url] => wideo/156-choroby_neurologiczne_o_poznym_wieku_zachorowania___wyzwania_diagnostyki_i_poradnictwa
[short_name] => Choroby neurologiczne o późnym wieku zachorowania ...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[158] => Array
(
[id] => 158
[site_id] => 1
[status_id] => 5
[name] => Badania cytogenetyczne – od kliniki do interpretacji wyniku
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/158/postergen_i_geno.png
[video] => resources/data/material/158/5_badania_cytogenetyczne_–_od_kliniki_do_interpretacji_wyniku.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med.,prof IMiD Beata Nowakowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 9
[site_id] => 1
[status_id] => 5
[name] => dr n. med.,prof IMiD Beata Nowakowska
[firstname] => Beata
[lastname] => Nowakowska
[title] => dr n. med.,prof IMiD
[affiliation] => Zakład Genetyki Medycznej, Zespół Pracowni Cytogenetyki, IMID
[avatar] => resources/data/eksperci/9/dr_nowakowska_v2.jpg
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 9-beata_nowakowska
[url] => eksperci/9-beata_nowakowska
)
)
[authors_ids] => Array
(
[0] => 9
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 12
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 158-badania_cytogenetyczne__od_kliniki_do_interpretacji_wyniku
[url] => wideo/158-badania_cytogenetyczne__od_kliniki_do_interpretacji_wyniku
[short_name] => Badania cytogenetyczne – od kliniki do interpretac...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[12] => Array
(
[id] => 12
[site_id] => 1
[status_id] => 5
[name] => cytogenetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 12-cytogenetyka
[url] => /12-cytogenetyka
)
)
[artykuly] => Array
(
)
)
)
)
[sort] => 1
[status_code] => active
[authors] => Array
(
[0] => dr n. med. Ewa Obersztyn
)
[authors_data] => Array
(
[0] => Array
(
[id] => 14
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Ewa Obersztyn
[firstname] => Ewa
[lastname] => Obersztyn
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 14-ewa_obersztyn
[url] => eksperci/14-ewa_obersztyn
)
)
[authors_ids] => Array
(
[0] => 14
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 149-poradnictwo_genetyczne_w_odniesieniu_do_chorob_neurologicznych
[url] => wideo/149-poradnictwo_genetyczne_w_odniesieniu_do_chorob_neurologicznych
[short_name] => Poradnictwo genetyczne w odniesieniu do chorób neu...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
[logotypy] => Array
(
)
[pliki] => Array
(
[118] => Array
(
[id] => 118
[site_id] => 1
[status_id] => 5
[entity_key] => material
[entity_id] => 149
[name] => Poradnictwo genetyczne w odniesieniu do chorób neurologicznych
[file] => resources/data/pliki/material/149/24.06_w1_eo_materialy.pdf
[sort] => 115
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
[150] => Array
(
[id] => 150
[name] => Niepełnosprawność intelektualna –badania cytogenetyczne.
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/150/postergen_i_geno.png
[video] => resources/data/material/150/5_niepelnosprawnosc_intelektualna_–_badania_molekularne_dr_sylwia_rzonca.mp4
[content] =>
[ext] => Array
(
[files_header] =>
[linked] => Array
(
[144] => Array
(
[id] => 144
[site_id] => 1
[status_id] => 5
[name] => Badania molekularne. Od kliniki do interpretacji wyniku.
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/144/postergen_i_geno.png
[video] => resources/data/material/144/5_badania_molekularne_–_od_kliniki_do_interpretacji_wyniku_dr_hab._dorota_hoffmanzacharska.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
[3] => 14
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 144-badania_molekularne_od_kliniki_do_interpretacji_wyniku
[url] => wideo/144-badania_molekularne_od_kliniki_do_interpretacji_wyniku
[short_name] => Badania molekularne. Od kliniki do interpretacji w...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
[14] => Array
(
[id] => 14
[site_id] => 1
[status_id] => 5
[name] => choroby rzadkie
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 14-choroby_rzadkie
[url] => /14-choroby_rzadkie
)
)
[artykuly] => Array
(
)
)
[145] => Array
(
[id] => 145
[site_id] => 1
[status_id] => 5
[name] => Choroba Huntingtona
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/145/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 145-choroba_huntingtona
[url] => wideo/145-choroba_huntingtona
[short_name] => Choroba Huntingtona
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[146] => Array
(
[id] => 146
[site_id] => 1
[status_id] => 5
[name] => Wspólne drogi zaburzeń neurorozwojowych
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/146/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 146-wspolne_drogi_zaburzen_neurorozwojowych
[url] => wideo/146-wspolne_drogi_zaburzen_neurorozwojowych
[short_name] => Wspólne drogi zaburzeń neurorozwojowych
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[147] => Array
(
[id] => 147
[site_id] => 1
[status_id] => 5
[name] => Genetyka chorób neurologicznych o późnym początku
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/147/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Maciej Geremek
)
[authors_data] => Array
(
[0] => Array
(
[id] => 69
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Maciej Geremek
[firstname] => Maciej
[lastname] => Geremek
[title] => dr n. med.
[affiliation] => Zakład genetyki Medycznej IMiD
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 69-maciej_geremek
[url] => eksperci/69-maciej_geremek
)
)
[authors_ids] => Array
(
[0] => 69
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 147-genetyka_chorob_neurologicznych_o_poznym_poczatku
[url] => wideo/147-genetyka_chorob_neurologicznych_o_poznym_poczatku
[short_name] => Genetyka chorób neurologicznych o późnym początku
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[148] => Array
(
[id] => 148
[site_id] => 1
[status_id] => 5
[name] => Neurogenetyka molekularna
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/148/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 148-neurogenetyka_molekularna
[url] => wideo/148-neurogenetyka_molekularna
[short_name] => Neurogenetyka molekularna
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[149] => Array
(
[id] => 149
[site_id] => 1
[status_id] => 5
[name] => Poradnictwo genetyczne w odniesieniu do chorób neurologicznych
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/149/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Ewa Obersztyn
)
[authors_data] => Array
(
[0] => Array
(
[id] => 14
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Ewa Obersztyn
[firstname] => Ewa
[lastname] => Obersztyn
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 14-ewa_obersztyn
[url] => eksperci/14-ewa_obersztyn
)
)
[authors_ids] => Array
(
[0] => 14
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 149-poradnictwo_genetyczne_w_odniesieniu_do_chorob_neurologicznych
[url] => wideo/149-poradnictwo_genetyczne_w_odniesieniu_do_chorob_neurologicznych
[short_name] => Poradnictwo genetyczne w odniesieniu do chorób neu...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[151] => Array
(
[id] => 151
[site_id] => 1
[status_id] => 5
[name] => Techniki cytogenetyczne w diagnostyce chorób układu nerwowego.
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/151/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => mgr Kamila Ziemkiewicz
)
[authors_data] => Array
(
[0] => Array
(
[id] => 11
[site_id] => 1
[status_id] => 5
[name] => mgr Kamila Ziemkiewicz
[firstname] => Kamila
[lastname] => Ziemkiewicz
[title] => mgr
[affiliation] =>
[avatar] => resources/data/eksperci/11/kziemkiewicz.png
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 11-kamila_ziemkiewicz
[url] => eksperci/11-kamila_ziemkiewicz
)
)
[authors_ids] => Array
(
[0] => 11
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 12
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 151-techniki_cytogenetyczne_w_diagnostyce_chorob_ukladu_nerwowego
[url] => wideo/151-techniki_cytogenetyczne_w_diagnostyce_chorob_ukladu_nerwowego
[short_name] => Techniki cytogenetyczne w diagnostyce chorób układ...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[12] => Array
(
[id] => 12
[site_id] => 1
[status_id] => 5
[name] => cytogenetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 12-cytogenetyka
[url] => /12-cytogenetyka
)
)
[artykuly] => Array
(
)
)
[152] => Array
(
[id] => 152
[site_id] => 1
[status_id] => 5
[name] => Choroby nerwów obwodowych
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/152/postergen_i_geno.png
[video] => resources/data/material/152/5_choroby_nerwowobwodowych_potulska.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab. n. med. Anna Potulska-Chromik
)
[authors_data] => Array
(
[0] => Array
(
[id] => 70
[site_id] => 1
[status_id] => 5
[name] => dr hab. n. med. Anna Potulska-Chromik
[firstname] => Anna
[lastname] => Potulska-Chromik
[title] => dr hab. n. med.
[affiliation] => Klinika Neurologii WUM
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 70-anna_potulska_chromik
[url] => eksperci/70-anna_potulska_chromik
)
)
[authors_ids] => Array
(
[0] => 70
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 152-choroby_nerwow_obwodowych
[url] => wideo/152-choroby_nerwow_obwodowych
[short_name] => Choroby nerwów obwodowych
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[153] => Array
(
[id] => 153
[site_id] => 1
[status_id] => 5
[name] => Choroby nerwowo-mięśniowe
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/153/postergen_i_geno.png
[video] => resources/data/material/153/5_choroby_nerwowomiesniowe_dr_hab._monika_gos.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med., prof IMiD Monika Gos
)
[authors_data] => Array
(
[0] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => dr n. med., prof IMiD Monika Gos
[firstname] => Monika
[lastname] => Gos
[title] => dr n. med., prof IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-monika_gos
[url] => eksperci/13-monika_gos
)
)
[authors_ids] => Array
(
[0] => 13
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 153-choroby_nerwowo_miesniowe
[url] => wideo/153-choroby_nerwowo_miesniowe
[short_name] => Choroby nerwowo-mięśniowe
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[154] => Array
(
[id] => 154
[site_id] => 1
[status_id] => 5
[name] => Rdzeniowy zanik mięśni - od mutacji do terapii
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/154/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med., prof IMiD Monika Gos
)
[authors_data] => Array
(
[0] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => dr n. med., prof IMiD Monika Gos
[firstname] => Monika
[lastname] => Gos
[title] => dr n. med., prof IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-monika_gos
[url] => eksperci/13-monika_gos
)
)
[authors_ids] => Array
(
[0] => 13
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
[3] => 14
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 154-rdzeniowy_zanik_miesni___od_mutacji_do_terapii
[url] => wideo/154-rdzeniowy_zanik_miesni___od_mutacji_do_terapii
[short_name] => Rdzeniowy zanik mięśni - od mutacji do terapii
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
[14] => Array
(
[id] => 14
[site_id] => 1
[status_id] => 5
[name] => choroby rzadkie
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 14-choroby_rzadkie
[url] => /14-choroby_rzadkie
)
)
[artykuly] => Array
(
)
)
[155] => Array
(
[id] => 155
[site_id] => 1
[status_id] => 5
[name] => Niepełnosprawność intelektualna – badania molekularne
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/155/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Sylwia Rzońca
)
[authors_data] => Array
(
[0] => Array
(
[id] => 10
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Sylwia Rzońca
[firstname] => Sylwia
[lastname] => Rzońca
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 10-sylwia_rzonca
[url] => eksperci/10-sylwia_rzonca
)
)
[authors_ids] => Array
(
[0] => 10
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 155-niepelnosprawnosc_intelektualna__badania_molekularne
[url] => wideo/155-niepelnosprawnosc_intelektualna__badania_molekularne
[short_name] => Niepełnosprawność intelektualna – badania molekula...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[156] => Array
(
[id] => 156
[site_id] => 1
[status_id] => 5
[name] => Choroby neurologiczne o późnym wieku zachorowania - wyzwania diagnostyki i poradnictwa
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/156/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 156-choroby_neurologiczne_o_poznym_wieku_zachorowania___wyzwania_diagnostyki_i_poradnictwa
[url] => wideo/156-choroby_neurologiczne_o_poznym_wieku_zachorowania___wyzwania_diagnostyki_i_poradnictwa
[short_name] => Choroby neurologiczne o późnym wieku zachorowania ...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[158] => Array
(
[id] => 158
[site_id] => 1
[status_id] => 5
[name] => Badania cytogenetyczne – od kliniki do interpretacji wyniku
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/158/postergen_i_geno.png
[video] => resources/data/material/158/5_badania_cytogenetyczne_–_od_kliniki_do_interpretacji_wyniku.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med.,prof IMiD Beata Nowakowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 9
[site_id] => 1
[status_id] => 5
[name] => dr n. med.,prof IMiD Beata Nowakowska
[firstname] => Beata
[lastname] => Nowakowska
[title] => dr n. med.,prof IMiD
[affiliation] => Zakład Genetyki Medycznej, Zespół Pracowni Cytogenetyki, IMID
[avatar] => resources/data/eksperci/9/dr_nowakowska_v2.jpg
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 9-beata_nowakowska
[url] => eksperci/9-beata_nowakowska
)
)
[authors_ids] => Array
(
[0] => 9
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 12
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 158-badania_cytogenetyczne__od_kliniki_do_interpretacji_wyniku
[url] => wideo/158-badania_cytogenetyczne__od_kliniki_do_interpretacji_wyniku
[short_name] => Badania cytogenetyczne – od kliniki do interpretac...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[12] => Array
(
[id] => 12
[site_id] => 1
[status_id] => 5
[name] => cytogenetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 12-cytogenetyka
[url] => /12-cytogenetyka
)
)
[artykuly] => Array
(
)
)
)
)
[sort] => 1
[status_code] => active
[authors] => Array
(
[0] => mgr Kamila Ziemkiewicz
)
[authors_data] => Array
(
[0] => Array
(
[id] => 11
[site_id] => 1
[status_id] => 5
[name] => mgr Kamila Ziemkiewicz
[firstname] => Kamila
[lastname] => Ziemkiewicz
[title] => mgr
[affiliation] =>
[avatar] => resources/data/eksperci/11/kziemkiewicz.png
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 11-kamila_ziemkiewicz
[url] => eksperci/11-kamila_ziemkiewicz
)
)
[authors_ids] => Array
(
[0] => 11
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 12
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 150-niepelnosprawnosc_intelektualna_badania_cytogenetyczne
[url] => wideo/150-niepelnosprawnosc_intelektualna_badania_cytogenetyczne
[short_name] => Niepełnosprawność intelektualna –badania cytogenet...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[12] => Array
(
[id] => 12
[site_id] => 1
[status_id] => 5
[name] => cytogenetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 12-cytogenetyka
[url] => /12-cytogenetyka
)
)
[artykuly] => Array
(
)
[logotypy] => Array
(
)
[pliki] => Array
(
[119] => Array
(
[id] => 119
[site_id] => 1
[status_id] => 5
[entity_key] => material
[entity_id] => 150
[name] => Niepełnosprawność intelektualna –badania cytogenetyczne.
[file] => resources/data/pliki/material/150/24.06_w4_kz_materialy.pdf
[sort] => 116
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
[151] => Array
(
[id] => 151
[name] => Techniki cytogenetyczne w diagnostyce chorób układu nerwowego.
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/151/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
[linked] => Array
(
[144] => Array
(
[id] => 144
[site_id] => 1
[status_id] => 5
[name] => Badania molekularne. Od kliniki do interpretacji wyniku.
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/144/postergen_i_geno.png
[video] => resources/data/material/144/5_badania_molekularne_–_od_kliniki_do_interpretacji_wyniku_dr_hab._dorota_hoffmanzacharska.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
[3] => 14
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 144-badania_molekularne_od_kliniki_do_interpretacji_wyniku
[url] => wideo/144-badania_molekularne_od_kliniki_do_interpretacji_wyniku
[short_name] => Badania molekularne. Od kliniki do interpretacji w...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
[14] => Array
(
[id] => 14
[site_id] => 1
[status_id] => 5
[name] => choroby rzadkie
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 14-choroby_rzadkie
[url] => /14-choroby_rzadkie
)
)
[artykuly] => Array
(
)
)
[145] => Array
(
[id] => 145
[site_id] => 1
[status_id] => 5
[name] => Choroba Huntingtona
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/145/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 145-choroba_huntingtona
[url] => wideo/145-choroba_huntingtona
[short_name] => Choroba Huntingtona
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[146] => Array
(
[id] => 146
[site_id] => 1
[status_id] => 5
[name] => Wspólne drogi zaburzeń neurorozwojowych
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/146/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 146-wspolne_drogi_zaburzen_neurorozwojowych
[url] => wideo/146-wspolne_drogi_zaburzen_neurorozwojowych
[short_name] => Wspólne drogi zaburzeń neurorozwojowych
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[147] => Array
(
[id] => 147
[site_id] => 1
[status_id] => 5
[name] => Genetyka chorób neurologicznych o późnym początku
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/147/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Maciej Geremek
)
[authors_data] => Array
(
[0] => Array
(
[id] => 69
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Maciej Geremek
[firstname] => Maciej
[lastname] => Geremek
[title] => dr n. med.
[affiliation] => Zakład genetyki Medycznej IMiD
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 69-maciej_geremek
[url] => eksperci/69-maciej_geremek
)
)
[authors_ids] => Array
(
[0] => 69
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 147-genetyka_chorob_neurologicznych_o_poznym_poczatku
[url] => wideo/147-genetyka_chorob_neurologicznych_o_poznym_poczatku
[short_name] => Genetyka chorób neurologicznych o późnym początku
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[148] => Array
(
[id] => 148
[site_id] => 1
[status_id] => 5
[name] => Neurogenetyka molekularna
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/148/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 148-neurogenetyka_molekularna
[url] => wideo/148-neurogenetyka_molekularna
[short_name] => Neurogenetyka molekularna
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[149] => Array
(
[id] => 149
[site_id] => 1
[status_id] => 5
[name] => Poradnictwo genetyczne w odniesieniu do chorób neurologicznych
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/149/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Ewa Obersztyn
)
[authors_data] => Array
(
[0] => Array
(
[id] => 14
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Ewa Obersztyn
[firstname] => Ewa
[lastname] => Obersztyn
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 14-ewa_obersztyn
[url] => eksperci/14-ewa_obersztyn
)
)
[authors_ids] => Array
(
[0] => 14
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 149-poradnictwo_genetyczne_w_odniesieniu_do_chorob_neurologicznych
[url] => wideo/149-poradnictwo_genetyczne_w_odniesieniu_do_chorob_neurologicznych
[short_name] => Poradnictwo genetyczne w odniesieniu do chorób neu...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[150] => Array
(
[id] => 150
[site_id] => 1
[status_id] => 5
[name] => Niepełnosprawność intelektualna –badania cytogenetyczne.
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/150/postergen_i_geno.png
[video] => resources/data/material/150/5_niepelnosprawnosc_intelektualna_–_badania_molekularne_dr_sylwia_rzonca.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => mgr Kamila Ziemkiewicz
)
[authors_data] => Array
(
[0] => Array
(
[id] => 11
[site_id] => 1
[status_id] => 5
[name] => mgr Kamila Ziemkiewicz
[firstname] => Kamila
[lastname] => Ziemkiewicz
[title] => mgr
[affiliation] =>
[avatar] => resources/data/eksperci/11/kziemkiewicz.png
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 11-kamila_ziemkiewicz
[url] => eksperci/11-kamila_ziemkiewicz
)
)
[authors_ids] => Array
(
[0] => 11
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 12
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 150-niepelnosprawnosc_intelektualna_badania_cytogenetyczne
[url] => wideo/150-niepelnosprawnosc_intelektualna_badania_cytogenetyczne
[short_name] => Niepełnosprawność intelektualna –badania cytogenet...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[12] => Array
(
[id] => 12
[site_id] => 1
[status_id] => 5
[name] => cytogenetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 12-cytogenetyka
[url] => /12-cytogenetyka
)
)
[artykuly] => Array
(
)
)
[152] => Array
(
[id] => 152
[site_id] => 1
[status_id] => 5
[name] => Choroby nerwów obwodowych
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/152/postergen_i_geno.png
[video] => resources/data/material/152/5_choroby_nerwowobwodowych_potulska.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab. n. med. Anna Potulska-Chromik
)
[authors_data] => Array
(
[0] => Array
(
[id] => 70
[site_id] => 1
[status_id] => 5
[name] => dr hab. n. med. Anna Potulska-Chromik
[firstname] => Anna
[lastname] => Potulska-Chromik
[title] => dr hab. n. med.
[affiliation] => Klinika Neurologii WUM
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 70-anna_potulska_chromik
[url] => eksperci/70-anna_potulska_chromik
)
)
[authors_ids] => Array
(
[0] => 70
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 152-choroby_nerwow_obwodowych
[url] => wideo/152-choroby_nerwow_obwodowych
[short_name] => Choroby nerwów obwodowych
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[153] => Array
(
[id] => 153
[site_id] => 1
[status_id] => 5
[name] => Choroby nerwowo-mięśniowe
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/153/postergen_i_geno.png
[video] => resources/data/material/153/5_choroby_nerwowomiesniowe_dr_hab._monika_gos.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med., prof IMiD Monika Gos
)
[authors_data] => Array
(
[0] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => dr n. med., prof IMiD Monika Gos
[firstname] => Monika
[lastname] => Gos
[title] => dr n. med., prof IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-monika_gos
[url] => eksperci/13-monika_gos
)
)
[authors_ids] => Array
(
[0] => 13
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 153-choroby_nerwowo_miesniowe
[url] => wideo/153-choroby_nerwowo_miesniowe
[short_name] => Choroby nerwowo-mięśniowe
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[154] => Array
(
[id] => 154
[site_id] => 1
[status_id] => 5
[name] => Rdzeniowy zanik mięśni - od mutacji do terapii
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/154/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med., prof IMiD Monika Gos
)
[authors_data] => Array
(
[0] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => dr n. med., prof IMiD Monika Gos
[firstname] => Monika
[lastname] => Gos
[title] => dr n. med., prof IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-monika_gos
[url] => eksperci/13-monika_gos
)
)
[authors_ids] => Array
(
[0] => 13
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
[3] => 14
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 154-rdzeniowy_zanik_miesni___od_mutacji_do_terapii
[url] => wideo/154-rdzeniowy_zanik_miesni___od_mutacji_do_terapii
[short_name] => Rdzeniowy zanik mięśni - od mutacji do terapii
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
[14] => Array
(
[id] => 14
[site_id] => 1
[status_id] => 5
[name] => choroby rzadkie
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 14-choroby_rzadkie
[url] => /14-choroby_rzadkie
)
)
[artykuly] => Array
(
)
)
[155] => Array
(
[id] => 155
[site_id] => 1
[status_id] => 5
[name] => Niepełnosprawność intelektualna – badania molekularne
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/155/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Sylwia Rzońca
)
[authors_data] => Array
(
[0] => Array
(
[id] => 10
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Sylwia Rzońca
[firstname] => Sylwia
[lastname] => Rzońca
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 10-sylwia_rzonca
[url] => eksperci/10-sylwia_rzonca
)
)
[authors_ids] => Array
(
[0] => 10
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 155-niepelnosprawnosc_intelektualna__badania_molekularne
[url] => wideo/155-niepelnosprawnosc_intelektualna__badania_molekularne
[short_name] => Niepełnosprawność intelektualna – badania molekula...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[156] => Array
(
[id] => 156
[site_id] => 1
[status_id] => 5
[name] => Choroby neurologiczne o późnym wieku zachorowania - wyzwania diagnostyki i poradnictwa
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/156/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 156-choroby_neurologiczne_o_poznym_wieku_zachorowania___wyzwania_diagnostyki_i_poradnictwa
[url] => wideo/156-choroby_neurologiczne_o_poznym_wieku_zachorowania___wyzwania_diagnostyki_i_poradnictwa
[short_name] => Choroby neurologiczne o późnym wieku zachorowania ...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[158] => Array
(
[id] => 158
[site_id] => 1
[status_id] => 5
[name] => Badania cytogenetyczne – od kliniki do interpretacji wyniku
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/158/postergen_i_geno.png
[video] => resources/data/material/158/5_badania_cytogenetyczne_–_od_kliniki_do_interpretacji_wyniku.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med.,prof IMiD Beata Nowakowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 9
[site_id] => 1
[status_id] => 5
[name] => dr n. med.,prof IMiD Beata Nowakowska
[firstname] => Beata
[lastname] => Nowakowska
[title] => dr n. med.,prof IMiD
[affiliation] => Zakład Genetyki Medycznej, Zespół Pracowni Cytogenetyki, IMID
[avatar] => resources/data/eksperci/9/dr_nowakowska_v2.jpg
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 9-beata_nowakowska
[url] => eksperci/9-beata_nowakowska
)
)
[authors_ids] => Array
(
[0] => 9
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 12
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 158-badania_cytogenetyczne__od_kliniki_do_interpretacji_wyniku
[url] => wideo/158-badania_cytogenetyczne__od_kliniki_do_interpretacji_wyniku
[short_name] => Badania cytogenetyczne – od kliniki do interpretac...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[12] => Array
(
[id] => 12
[site_id] => 1
[status_id] => 5
[name] => cytogenetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 12-cytogenetyka
[url] => /12-cytogenetyka
)
)
[artykuly] => Array
(
)
)
)
)
[sort] => 1
[status_code] => active
[authors] => Array
(
[0] => mgr Kamila Ziemkiewicz
)
[authors_data] => Array
(
[0] => Array
(
[id] => 11
[site_id] => 1
[status_id] => 5
[name] => mgr Kamila Ziemkiewicz
[firstname] => Kamila
[lastname] => Ziemkiewicz
[title] => mgr
[affiliation] =>
[avatar] => resources/data/eksperci/11/kziemkiewicz.png
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 11-kamila_ziemkiewicz
[url] => eksperci/11-kamila_ziemkiewicz
)
)
[authors_ids] => Array
(
[0] => 11
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 12
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 151-techniki_cytogenetyczne_w_diagnostyce_chorob_ukladu_nerwowego
[url] => wideo/151-techniki_cytogenetyczne_w_diagnostyce_chorob_ukladu_nerwowego
[short_name] => Techniki cytogenetyczne w diagnostyce chorób układ...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[12] => Array
(
[id] => 12
[site_id] => 1
[status_id] => 5
[name] => cytogenetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 12-cytogenetyka
[url] => /12-cytogenetyka
)
)
[artykuly] => Array
(
)
[logotypy] => Array
(
)
[pliki] => Array
(
[120] => Array
(
[id] => 120
[site_id] => 1
[status_id] => 5
[entity_key] => material
[entity_id] => 151
[name] => Techniki cytogenetyczne w diagnostyce chorób układu nerwowego.
[file] => resources/data/pliki/material/151/24.06_w2_kz_materialy.pdf
[sort] => 117
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
[152] => Array
(
[id] => 152
[name] => Choroby nerwów obwodowych
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/152/postergen_i_geno.png
[video] => resources/data/material/152/5_choroby_nerwowobwodowych_potulska.mp4
[content] =>
[ext] => Array
(
[files_header] =>
[linked] => Array
(
[144] => Array
(
[id] => 144
[site_id] => 1
[status_id] => 5
[name] => Badania molekularne. Od kliniki do interpretacji wyniku.
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/144/postergen_i_geno.png
[video] => resources/data/material/144/5_badania_molekularne_–_od_kliniki_do_interpretacji_wyniku_dr_hab._dorota_hoffmanzacharska.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
[3] => 14
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 144-badania_molekularne_od_kliniki_do_interpretacji_wyniku
[url] => wideo/144-badania_molekularne_od_kliniki_do_interpretacji_wyniku
[short_name] => Badania molekularne. Od kliniki do interpretacji w...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
[14] => Array
(
[id] => 14
[site_id] => 1
[status_id] => 5
[name] => choroby rzadkie
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 14-choroby_rzadkie
[url] => /14-choroby_rzadkie
)
)
[artykuly] => Array
(
)
)
[145] => Array
(
[id] => 145
[site_id] => 1
[status_id] => 5
[name] => Choroba Huntingtona
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/145/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 145-choroba_huntingtona
[url] => wideo/145-choroba_huntingtona
[short_name] => Choroba Huntingtona
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[146] => Array
(
[id] => 146
[site_id] => 1
[status_id] => 5
[name] => Wspólne drogi zaburzeń neurorozwojowych
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/146/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 146-wspolne_drogi_zaburzen_neurorozwojowych
[url] => wideo/146-wspolne_drogi_zaburzen_neurorozwojowych
[short_name] => Wspólne drogi zaburzeń neurorozwojowych
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[147] => Array
(
[id] => 147
[site_id] => 1
[status_id] => 5
[name] => Genetyka chorób neurologicznych o późnym początku
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/147/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Maciej Geremek
)
[authors_data] => Array
(
[0] => Array
(
[id] => 69
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Maciej Geremek
[firstname] => Maciej
[lastname] => Geremek
[title] => dr n. med.
[affiliation] => Zakład genetyki Medycznej IMiD
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 69-maciej_geremek
[url] => eksperci/69-maciej_geremek
)
)
[authors_ids] => Array
(
[0] => 69
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 147-genetyka_chorob_neurologicznych_o_poznym_poczatku
[url] => wideo/147-genetyka_chorob_neurologicznych_o_poznym_poczatku
[short_name] => Genetyka chorób neurologicznych o późnym początku
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[148] => Array
(
[id] => 148
[site_id] => 1
[status_id] => 5
[name] => Neurogenetyka molekularna
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/148/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 148-neurogenetyka_molekularna
[url] => wideo/148-neurogenetyka_molekularna
[short_name] => Neurogenetyka molekularna
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[149] => Array
(
[id] => 149
[site_id] => 1
[status_id] => 5
[name] => Poradnictwo genetyczne w odniesieniu do chorób neurologicznych
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/149/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Ewa Obersztyn
)
[authors_data] => Array
(
[0] => Array
(
[id] => 14
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Ewa Obersztyn
[firstname] => Ewa
[lastname] => Obersztyn
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 14-ewa_obersztyn
[url] => eksperci/14-ewa_obersztyn
)
)
[authors_ids] => Array
(
[0] => 14
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 149-poradnictwo_genetyczne_w_odniesieniu_do_chorob_neurologicznych
[url] => wideo/149-poradnictwo_genetyczne_w_odniesieniu_do_chorob_neurologicznych
[short_name] => Poradnictwo genetyczne w odniesieniu do chorób neu...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[150] => Array
(
[id] => 150
[site_id] => 1
[status_id] => 5
[name] => Niepełnosprawność intelektualna –badania cytogenetyczne.
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/150/postergen_i_geno.png
[video] => resources/data/material/150/5_niepelnosprawnosc_intelektualna_–_badania_molekularne_dr_sylwia_rzonca.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => mgr Kamila Ziemkiewicz
)
[authors_data] => Array
(
[0] => Array
(
[id] => 11
[site_id] => 1
[status_id] => 5
[name] => mgr Kamila Ziemkiewicz
[firstname] => Kamila
[lastname] => Ziemkiewicz
[title] => mgr
[affiliation] =>
[avatar] => resources/data/eksperci/11/kziemkiewicz.png
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 11-kamila_ziemkiewicz
[url] => eksperci/11-kamila_ziemkiewicz
)
)
[authors_ids] => Array
(
[0] => 11
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 12
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 150-niepelnosprawnosc_intelektualna_badania_cytogenetyczne
[url] => wideo/150-niepelnosprawnosc_intelektualna_badania_cytogenetyczne
[short_name] => Niepełnosprawność intelektualna –badania cytogenet...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[12] => Array
(
[id] => 12
[site_id] => 1
[status_id] => 5
[name] => cytogenetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 12-cytogenetyka
[url] => /12-cytogenetyka
)
)
[artykuly] => Array
(
)
)
[151] => Array
(
[id] => 151
[site_id] => 1
[status_id] => 5
[name] => Techniki cytogenetyczne w diagnostyce chorób układu nerwowego.
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/151/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => mgr Kamila Ziemkiewicz
)
[authors_data] => Array
(
[0] => Array
(
[id] => 11
[site_id] => 1
[status_id] => 5
[name] => mgr Kamila Ziemkiewicz
[firstname] => Kamila
[lastname] => Ziemkiewicz
[title] => mgr
[affiliation] =>
[avatar] => resources/data/eksperci/11/kziemkiewicz.png
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 11-kamila_ziemkiewicz
[url] => eksperci/11-kamila_ziemkiewicz
)
)
[authors_ids] => Array
(
[0] => 11
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 12
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 151-techniki_cytogenetyczne_w_diagnostyce_chorob_ukladu_nerwowego
[url] => wideo/151-techniki_cytogenetyczne_w_diagnostyce_chorob_ukladu_nerwowego
[short_name] => Techniki cytogenetyczne w diagnostyce chorób układ...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[12] => Array
(
[id] => 12
[site_id] => 1
[status_id] => 5
[name] => cytogenetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 12-cytogenetyka
[url] => /12-cytogenetyka
)
)
[artykuly] => Array
(
)
)
[153] => Array
(
[id] => 153
[site_id] => 1
[status_id] => 5
[name] => Choroby nerwowo-mięśniowe
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/153/postergen_i_geno.png
[video] => resources/data/material/153/5_choroby_nerwowomiesniowe_dr_hab._monika_gos.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med., prof IMiD Monika Gos
)
[authors_data] => Array
(
[0] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => dr n. med., prof IMiD Monika Gos
[firstname] => Monika
[lastname] => Gos
[title] => dr n. med., prof IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-monika_gos
[url] => eksperci/13-monika_gos
)
)
[authors_ids] => Array
(
[0] => 13
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 153-choroby_nerwowo_miesniowe
[url] => wideo/153-choroby_nerwowo_miesniowe
[short_name] => Choroby nerwowo-mięśniowe
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[154] => Array
(
[id] => 154
[site_id] => 1
[status_id] => 5
[name] => Rdzeniowy zanik mięśni - od mutacji do terapii
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/154/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med., prof IMiD Monika Gos
)
[authors_data] => Array
(
[0] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => dr n. med., prof IMiD Monika Gos
[firstname] => Monika
[lastname] => Gos
[title] => dr n. med., prof IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-monika_gos
[url] => eksperci/13-monika_gos
)
)
[authors_ids] => Array
(
[0] => 13
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
[3] => 14
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 154-rdzeniowy_zanik_miesni___od_mutacji_do_terapii
[url] => wideo/154-rdzeniowy_zanik_miesni___od_mutacji_do_terapii
[short_name] => Rdzeniowy zanik mięśni - od mutacji do terapii
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
[14] => Array
(
[id] => 14
[site_id] => 1
[status_id] => 5
[name] => choroby rzadkie
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 14-choroby_rzadkie
[url] => /14-choroby_rzadkie
)
)
[artykuly] => Array
(
)
)
[155] => Array
(
[id] => 155
[site_id] => 1
[status_id] => 5
[name] => Niepełnosprawność intelektualna – badania molekularne
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/155/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Sylwia Rzońca
)
[authors_data] => Array
(
[0] => Array
(
[id] => 10
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Sylwia Rzońca
[firstname] => Sylwia
[lastname] => Rzońca
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 10-sylwia_rzonca
[url] => eksperci/10-sylwia_rzonca
)
)
[authors_ids] => Array
(
[0] => 10
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 155-niepelnosprawnosc_intelektualna__badania_molekularne
[url] => wideo/155-niepelnosprawnosc_intelektualna__badania_molekularne
[short_name] => Niepełnosprawność intelektualna – badania molekula...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[156] => Array
(
[id] => 156
[site_id] => 1
[status_id] => 5
[name] => Choroby neurologiczne o późnym wieku zachorowania - wyzwania diagnostyki i poradnictwa
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/156/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 156-choroby_neurologiczne_o_poznym_wieku_zachorowania___wyzwania_diagnostyki_i_poradnictwa
[url] => wideo/156-choroby_neurologiczne_o_poznym_wieku_zachorowania___wyzwania_diagnostyki_i_poradnictwa
[short_name] => Choroby neurologiczne o późnym wieku zachorowania ...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[158] => Array
(
[id] => 158
[site_id] => 1
[status_id] => 5
[name] => Badania cytogenetyczne – od kliniki do interpretacji wyniku
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/158/postergen_i_geno.png
[video] => resources/data/material/158/5_badania_cytogenetyczne_–_od_kliniki_do_interpretacji_wyniku.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med.,prof IMiD Beata Nowakowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 9
[site_id] => 1
[status_id] => 5
[name] => dr n. med.,prof IMiD Beata Nowakowska
[firstname] => Beata
[lastname] => Nowakowska
[title] => dr n. med.,prof IMiD
[affiliation] => Zakład Genetyki Medycznej, Zespół Pracowni Cytogenetyki, IMID
[avatar] => resources/data/eksperci/9/dr_nowakowska_v2.jpg
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 9-beata_nowakowska
[url] => eksperci/9-beata_nowakowska
)
)
[authors_ids] => Array
(
[0] => 9
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 12
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 158-badania_cytogenetyczne__od_kliniki_do_interpretacji_wyniku
[url] => wideo/158-badania_cytogenetyczne__od_kliniki_do_interpretacji_wyniku
[short_name] => Badania cytogenetyczne – od kliniki do interpretac...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[12] => Array
(
[id] => 12
[site_id] => 1
[status_id] => 5
[name] => cytogenetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 12-cytogenetyka
[url] => /12-cytogenetyka
)
)
[artykuly] => Array
(
)
)
)
)
[sort] => 1
[status_code] => active
[authors] => Array
(
[0] => dr hab. n. med. Anna Potulska-Chromik
)
[authors_data] => Array
(
[0] => Array
(
[id] => 70
[site_id] => 1
[status_id] => 5
[name] => dr hab. n. med. Anna Potulska-Chromik
[firstname] => Anna
[lastname] => Potulska-Chromik
[title] => dr hab. n. med.
[affiliation] => Klinika Neurologii WUM
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 70-anna_potulska_chromik
[url] => eksperci/70-anna_potulska_chromik
)
)
[authors_ids] => Array
(
[0] => 70
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 152-choroby_nerwow_obwodowych
[url] => wideo/152-choroby_nerwow_obwodowych
[short_name] => Choroby nerwów obwodowych
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
[logotypy] => Array
(
)
[pliki] => Array
(
[121] => Array
(
[id] => 121
[site_id] => 1
[status_id] => 5
[entity_key] => material
[entity_id] => 152
[name] => Choroby nerwów obwodowych
[file] => resources/data/pliki/material/152/25.06w3_apch.pdf
[sort] => 118
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
[153] => Array
(
[id] => 153
[name] => Choroby nerwowo-mięśniowe
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/153/postergen_i_geno.png
[video] => resources/data/material/153/5_choroby_nerwowomiesniowe_dr_hab._monika_gos.mp4
[content] =>
[ext] => Array
(
[files_header] =>
[linked] => Array
(
[144] => Array
(
[id] => 144
[site_id] => 1
[status_id] => 5
[name] => Badania molekularne. Od kliniki do interpretacji wyniku.
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/144/postergen_i_geno.png
[video] => resources/data/material/144/5_badania_molekularne_–_od_kliniki_do_interpretacji_wyniku_dr_hab._dorota_hoffmanzacharska.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
[3] => 14
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 144-badania_molekularne_od_kliniki_do_interpretacji_wyniku
[url] => wideo/144-badania_molekularne_od_kliniki_do_interpretacji_wyniku
[short_name] => Badania molekularne. Od kliniki do interpretacji w...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
[14] => Array
(
[id] => 14
[site_id] => 1
[status_id] => 5
[name] => choroby rzadkie
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 14-choroby_rzadkie
[url] => /14-choroby_rzadkie
)
)
[artykuly] => Array
(
)
)
[145] => Array
(
[id] => 145
[site_id] => 1
[status_id] => 5
[name] => Choroba Huntingtona
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/145/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 145-choroba_huntingtona
[url] => wideo/145-choroba_huntingtona
[short_name] => Choroba Huntingtona
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[146] => Array
(
[id] => 146
[site_id] => 1
[status_id] => 5
[name] => Wspólne drogi zaburzeń neurorozwojowych
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/146/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 146-wspolne_drogi_zaburzen_neurorozwojowych
[url] => wideo/146-wspolne_drogi_zaburzen_neurorozwojowych
[short_name] => Wspólne drogi zaburzeń neurorozwojowych
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[147] => Array
(
[id] => 147
[site_id] => 1
[status_id] => 5
[name] => Genetyka chorób neurologicznych o późnym początku
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/147/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Maciej Geremek
)
[authors_data] => Array
(
[0] => Array
(
[id] => 69
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Maciej Geremek
[firstname] => Maciej
[lastname] => Geremek
[title] => dr n. med.
[affiliation] => Zakład genetyki Medycznej IMiD
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 69-maciej_geremek
[url] => eksperci/69-maciej_geremek
)
)
[authors_ids] => Array
(
[0] => 69
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 147-genetyka_chorob_neurologicznych_o_poznym_poczatku
[url] => wideo/147-genetyka_chorob_neurologicznych_o_poznym_poczatku
[short_name] => Genetyka chorób neurologicznych o późnym początku
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[148] => Array
(
[id] => 148
[site_id] => 1
[status_id] => 5
[name] => Neurogenetyka molekularna
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/148/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 148-neurogenetyka_molekularna
[url] => wideo/148-neurogenetyka_molekularna
[short_name] => Neurogenetyka molekularna
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[149] => Array
(
[id] => 149
[site_id] => 1
[status_id] => 5
[name] => Poradnictwo genetyczne w odniesieniu do chorób neurologicznych
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/149/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Ewa Obersztyn
)
[authors_data] => Array
(
[0] => Array
(
[id] => 14
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Ewa Obersztyn
[firstname] => Ewa
[lastname] => Obersztyn
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 14-ewa_obersztyn
[url] => eksperci/14-ewa_obersztyn
)
)
[authors_ids] => Array
(
[0] => 14
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 149-poradnictwo_genetyczne_w_odniesieniu_do_chorob_neurologicznych
[url] => wideo/149-poradnictwo_genetyczne_w_odniesieniu_do_chorob_neurologicznych
[short_name] => Poradnictwo genetyczne w odniesieniu do chorób neu...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[150] => Array
(
[id] => 150
[site_id] => 1
[status_id] => 5
[name] => Niepełnosprawność intelektualna –badania cytogenetyczne.
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/150/postergen_i_geno.png
[video] => resources/data/material/150/5_niepelnosprawnosc_intelektualna_–_badania_molekularne_dr_sylwia_rzonca.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => mgr Kamila Ziemkiewicz
)
[authors_data] => Array
(
[0] => Array
(
[id] => 11
[site_id] => 1
[status_id] => 5
[name] => mgr Kamila Ziemkiewicz
[firstname] => Kamila
[lastname] => Ziemkiewicz
[title] => mgr
[affiliation] =>
[avatar] => resources/data/eksperci/11/kziemkiewicz.png
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 11-kamila_ziemkiewicz
[url] => eksperci/11-kamila_ziemkiewicz
)
)
[authors_ids] => Array
(
[0] => 11
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 12
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 150-niepelnosprawnosc_intelektualna_badania_cytogenetyczne
[url] => wideo/150-niepelnosprawnosc_intelektualna_badania_cytogenetyczne
[short_name] => Niepełnosprawność intelektualna –badania cytogenet...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[12] => Array
(
[id] => 12
[site_id] => 1
[status_id] => 5
[name] => cytogenetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 12-cytogenetyka
[url] => /12-cytogenetyka
)
)
[artykuly] => Array
(
)
)
[151] => Array
(
[id] => 151
[site_id] => 1
[status_id] => 5
[name] => Techniki cytogenetyczne w diagnostyce chorób układu nerwowego.
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/151/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => mgr Kamila Ziemkiewicz
)
[authors_data] => Array
(
[0] => Array
(
[id] => 11
[site_id] => 1
[status_id] => 5
[name] => mgr Kamila Ziemkiewicz
[firstname] => Kamila
[lastname] => Ziemkiewicz
[title] => mgr
[affiliation] =>
[avatar] => resources/data/eksperci/11/kziemkiewicz.png
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 11-kamila_ziemkiewicz
[url] => eksperci/11-kamila_ziemkiewicz
)
)
[authors_ids] => Array
(
[0] => 11
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 12
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 151-techniki_cytogenetyczne_w_diagnostyce_chorob_ukladu_nerwowego
[url] => wideo/151-techniki_cytogenetyczne_w_diagnostyce_chorob_ukladu_nerwowego
[short_name] => Techniki cytogenetyczne w diagnostyce chorób układ...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[12] => Array
(
[id] => 12
[site_id] => 1
[status_id] => 5
[name] => cytogenetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 12-cytogenetyka
[url] => /12-cytogenetyka
)
)
[artykuly] => Array
(
)
)
[152] => Array
(
[id] => 152
[site_id] => 1
[status_id] => 5
[name] => Choroby nerwów obwodowych
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/152/postergen_i_geno.png
[video] => resources/data/material/152/5_choroby_nerwowobwodowych_potulska.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab. n. med. Anna Potulska-Chromik
)
[authors_data] => Array
(
[0] => Array
(
[id] => 70
[site_id] => 1
[status_id] => 5
[name] => dr hab. n. med. Anna Potulska-Chromik
[firstname] => Anna
[lastname] => Potulska-Chromik
[title] => dr hab. n. med.
[affiliation] => Klinika Neurologii WUM
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 70-anna_potulska_chromik
[url] => eksperci/70-anna_potulska_chromik
)
)
[authors_ids] => Array
(
[0] => 70
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 152-choroby_nerwow_obwodowych
[url] => wideo/152-choroby_nerwow_obwodowych
[short_name] => Choroby nerwów obwodowych
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[154] => Array
(
[id] => 154
[site_id] => 1
[status_id] => 5
[name] => Rdzeniowy zanik mięśni - od mutacji do terapii
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/154/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med., prof IMiD Monika Gos
)
[authors_data] => Array
(
[0] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => dr n. med., prof IMiD Monika Gos
[firstname] => Monika
[lastname] => Gos
[title] => dr n. med., prof IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-monika_gos
[url] => eksperci/13-monika_gos
)
)
[authors_ids] => Array
(
[0] => 13
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
[3] => 14
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 154-rdzeniowy_zanik_miesni___od_mutacji_do_terapii
[url] => wideo/154-rdzeniowy_zanik_miesni___od_mutacji_do_terapii
[short_name] => Rdzeniowy zanik mięśni - od mutacji do terapii
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
[14] => Array
(
[id] => 14
[site_id] => 1
[status_id] => 5
[name] => choroby rzadkie
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 14-choroby_rzadkie
[url] => /14-choroby_rzadkie
)
)
[artykuly] => Array
(
)
)
[155] => Array
(
[id] => 155
[site_id] => 1
[status_id] => 5
[name] => Niepełnosprawność intelektualna – badania molekularne
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/155/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Sylwia Rzońca
)
[authors_data] => Array
(
[0] => Array
(
[id] => 10
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Sylwia Rzońca
[firstname] => Sylwia
[lastname] => Rzońca
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 10-sylwia_rzonca
[url] => eksperci/10-sylwia_rzonca
)
)
[authors_ids] => Array
(
[0] => 10
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 155-niepelnosprawnosc_intelektualna__badania_molekularne
[url] => wideo/155-niepelnosprawnosc_intelektualna__badania_molekularne
[short_name] => Niepełnosprawność intelektualna – badania molekula...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[156] => Array
(
[id] => 156
[site_id] => 1
[status_id] => 5
[name] => Choroby neurologiczne o późnym wieku zachorowania - wyzwania diagnostyki i poradnictwa
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/156/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 156-choroby_neurologiczne_o_poznym_wieku_zachorowania___wyzwania_diagnostyki_i_poradnictwa
[url] => wideo/156-choroby_neurologiczne_o_poznym_wieku_zachorowania___wyzwania_diagnostyki_i_poradnictwa
[short_name] => Choroby neurologiczne o późnym wieku zachorowania ...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[158] => Array
(
[id] => 158
[site_id] => 1
[status_id] => 5
[name] => Badania cytogenetyczne – od kliniki do interpretacji wyniku
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/158/postergen_i_geno.png
[video] => resources/data/material/158/5_badania_cytogenetyczne_–_od_kliniki_do_interpretacji_wyniku.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med.,prof IMiD Beata Nowakowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 9
[site_id] => 1
[status_id] => 5
[name] => dr n. med.,prof IMiD Beata Nowakowska
[firstname] => Beata
[lastname] => Nowakowska
[title] => dr n. med.,prof IMiD
[affiliation] => Zakład Genetyki Medycznej, Zespół Pracowni Cytogenetyki, IMID
[avatar] => resources/data/eksperci/9/dr_nowakowska_v2.jpg
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 9-beata_nowakowska
[url] => eksperci/9-beata_nowakowska
)
)
[authors_ids] => Array
(
[0] => 9
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 12
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 158-badania_cytogenetyczne__od_kliniki_do_interpretacji_wyniku
[url] => wideo/158-badania_cytogenetyczne__od_kliniki_do_interpretacji_wyniku
[short_name] => Badania cytogenetyczne – od kliniki do interpretac...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[12] => Array
(
[id] => 12
[site_id] => 1
[status_id] => 5
[name] => cytogenetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 12-cytogenetyka
[url] => /12-cytogenetyka
)
)
[artykuly] => Array
(
)
)
)
)
[sort] => 1
[status_code] => active
[authors] => Array
(
[0] => dr n. med., prof IMiD Monika Gos
)
[authors_data] => Array
(
[0] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => dr n. med., prof IMiD Monika Gos
[firstname] => Monika
[lastname] => Gos
[title] => dr n. med., prof IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-monika_gos
[url] => eksperci/13-monika_gos
)
)
[authors_ids] => Array
(
[0] => 13
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 153-choroby_nerwowo_miesniowe
[url] => wideo/153-choroby_nerwowo_miesniowe
[short_name] => Choroby nerwowo-mięśniowe
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
[logotypy] => Array
(
)
[pliki] => Array
(
[122] => Array
(
[id] => 122
[site_id] => 1
[status_id] => 5
[entity_key] => material
[entity_id] => 153
[name] => Choroby nerwowo-mięśniowe
[file] => resources/data/pliki/material/153/25.06_w1_mg_materialy.pdf
[sort] => 119
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
[154] => Array
(
[id] => 154
[name] => Rdzeniowy zanik mięśni - od mutacji do terapii
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/154/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
[linked] => Array
(
[144] => Array
(
[id] => 144
[site_id] => 1
[status_id] => 5
[name] => Badania molekularne. Od kliniki do interpretacji wyniku.
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/144/postergen_i_geno.png
[video] => resources/data/material/144/5_badania_molekularne_–_od_kliniki_do_interpretacji_wyniku_dr_hab._dorota_hoffmanzacharska.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
[3] => 14
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 144-badania_molekularne_od_kliniki_do_interpretacji_wyniku
[url] => wideo/144-badania_molekularne_od_kliniki_do_interpretacji_wyniku
[short_name] => Badania molekularne. Od kliniki do interpretacji w...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
[14] => Array
(
[id] => 14
[site_id] => 1
[status_id] => 5
[name] => choroby rzadkie
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 14-choroby_rzadkie
[url] => /14-choroby_rzadkie
)
)
[artykuly] => Array
(
)
)
[145] => Array
(
[id] => 145
[site_id] => 1
[status_id] => 5
[name] => Choroba Huntingtona
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/145/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 145-choroba_huntingtona
[url] => wideo/145-choroba_huntingtona
[short_name] => Choroba Huntingtona
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[146] => Array
(
[id] => 146
[site_id] => 1
[status_id] => 5
[name] => Wspólne drogi zaburzeń neurorozwojowych
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/146/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 146-wspolne_drogi_zaburzen_neurorozwojowych
[url] => wideo/146-wspolne_drogi_zaburzen_neurorozwojowych
[short_name] => Wspólne drogi zaburzeń neurorozwojowych
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[147] => Array
(
[id] => 147
[site_id] => 1
[status_id] => 5
[name] => Genetyka chorób neurologicznych o późnym początku
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/147/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Maciej Geremek
)
[authors_data] => Array
(
[0] => Array
(
[id] => 69
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Maciej Geremek
[firstname] => Maciej
[lastname] => Geremek
[title] => dr n. med.
[affiliation] => Zakład genetyki Medycznej IMiD
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 69-maciej_geremek
[url] => eksperci/69-maciej_geremek
)
)
[authors_ids] => Array
(
[0] => 69
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 147-genetyka_chorob_neurologicznych_o_poznym_poczatku
[url] => wideo/147-genetyka_chorob_neurologicznych_o_poznym_poczatku
[short_name] => Genetyka chorób neurologicznych o późnym początku
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[148] => Array
(
[id] => 148
[site_id] => 1
[status_id] => 5
[name] => Neurogenetyka molekularna
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/148/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 148-neurogenetyka_molekularna
[url] => wideo/148-neurogenetyka_molekularna
[short_name] => Neurogenetyka molekularna
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[149] => Array
(
[id] => 149
[site_id] => 1
[status_id] => 5
[name] => Poradnictwo genetyczne w odniesieniu do chorób neurologicznych
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/149/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Ewa Obersztyn
)
[authors_data] => Array
(
[0] => Array
(
[id] => 14
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Ewa Obersztyn
[firstname] => Ewa
[lastname] => Obersztyn
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 14-ewa_obersztyn
[url] => eksperci/14-ewa_obersztyn
)
)
[authors_ids] => Array
(
[0] => 14
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 149-poradnictwo_genetyczne_w_odniesieniu_do_chorob_neurologicznych
[url] => wideo/149-poradnictwo_genetyczne_w_odniesieniu_do_chorob_neurologicznych
[short_name] => Poradnictwo genetyczne w odniesieniu do chorób neu...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[150] => Array
(
[id] => 150
[site_id] => 1
[status_id] => 5
[name] => Niepełnosprawność intelektualna –badania cytogenetyczne.
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/150/postergen_i_geno.png
[video] => resources/data/material/150/5_niepelnosprawnosc_intelektualna_–_badania_molekularne_dr_sylwia_rzonca.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => mgr Kamila Ziemkiewicz
)
[authors_data] => Array
(
[0] => Array
(
[id] => 11
[site_id] => 1
[status_id] => 5
[name] => mgr Kamila Ziemkiewicz
[firstname] => Kamila
[lastname] => Ziemkiewicz
[title] => mgr
[affiliation] =>
[avatar] => resources/data/eksperci/11/kziemkiewicz.png
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 11-kamila_ziemkiewicz
[url] => eksperci/11-kamila_ziemkiewicz
)
)
[authors_ids] => Array
(
[0] => 11
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 12
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 150-niepelnosprawnosc_intelektualna_badania_cytogenetyczne
[url] => wideo/150-niepelnosprawnosc_intelektualna_badania_cytogenetyczne
[short_name] => Niepełnosprawność intelektualna –badania cytogenet...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[12] => Array
(
[id] => 12
[site_id] => 1
[status_id] => 5
[name] => cytogenetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 12-cytogenetyka
[url] => /12-cytogenetyka
)
)
[artykuly] => Array
(
)
)
[151] => Array
(
[id] => 151
[site_id] => 1
[status_id] => 5
[name] => Techniki cytogenetyczne w diagnostyce chorób układu nerwowego.
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/151/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => mgr Kamila Ziemkiewicz
)
[authors_data] => Array
(
[0] => Array
(
[id] => 11
[site_id] => 1
[status_id] => 5
[name] => mgr Kamila Ziemkiewicz
[firstname] => Kamila
[lastname] => Ziemkiewicz
[title] => mgr
[affiliation] =>
[avatar] => resources/data/eksperci/11/kziemkiewicz.png
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 11-kamila_ziemkiewicz
[url] => eksperci/11-kamila_ziemkiewicz
)
)
[authors_ids] => Array
(
[0] => 11
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 12
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 151-techniki_cytogenetyczne_w_diagnostyce_chorob_ukladu_nerwowego
[url] => wideo/151-techniki_cytogenetyczne_w_diagnostyce_chorob_ukladu_nerwowego
[short_name] => Techniki cytogenetyczne w diagnostyce chorób układ...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[12] => Array
(
[id] => 12
[site_id] => 1
[status_id] => 5
[name] => cytogenetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 12-cytogenetyka
[url] => /12-cytogenetyka
)
)
[artykuly] => Array
(
)
)
[152] => Array
(
[id] => 152
[site_id] => 1
[status_id] => 5
[name] => Choroby nerwów obwodowych
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/152/postergen_i_geno.png
[video] => resources/data/material/152/5_choroby_nerwowobwodowych_potulska.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab. n. med. Anna Potulska-Chromik
)
[authors_data] => Array
(
[0] => Array
(
[id] => 70
[site_id] => 1
[status_id] => 5
[name] => dr hab. n. med. Anna Potulska-Chromik
[firstname] => Anna
[lastname] => Potulska-Chromik
[title] => dr hab. n. med.
[affiliation] => Klinika Neurologii WUM
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 70-anna_potulska_chromik
[url] => eksperci/70-anna_potulska_chromik
)
)
[authors_ids] => Array
(
[0] => 70
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 152-choroby_nerwow_obwodowych
[url] => wideo/152-choroby_nerwow_obwodowych
[short_name] => Choroby nerwów obwodowych
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[153] => Array
(
[id] => 153
[site_id] => 1
[status_id] => 5
[name] => Choroby nerwowo-mięśniowe
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/153/postergen_i_geno.png
[video] => resources/data/material/153/5_choroby_nerwowomiesniowe_dr_hab._monika_gos.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med., prof IMiD Monika Gos
)
[authors_data] => Array
(
[0] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => dr n. med., prof IMiD Monika Gos
[firstname] => Monika
[lastname] => Gos
[title] => dr n. med., prof IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-monika_gos
[url] => eksperci/13-monika_gos
)
)
[authors_ids] => Array
(
[0] => 13
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 153-choroby_nerwowo_miesniowe
[url] => wideo/153-choroby_nerwowo_miesniowe
[short_name] => Choroby nerwowo-mięśniowe
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[155] => Array
(
[id] => 155
[site_id] => 1
[status_id] => 5
[name] => Niepełnosprawność intelektualna – badania molekularne
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/155/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Sylwia Rzońca
)
[authors_data] => Array
(
[0] => Array
(
[id] => 10
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Sylwia Rzońca
[firstname] => Sylwia
[lastname] => Rzońca
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 10-sylwia_rzonca
[url] => eksperci/10-sylwia_rzonca
)
)
[authors_ids] => Array
(
[0] => 10
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 155-niepelnosprawnosc_intelektualna__badania_molekularne
[url] => wideo/155-niepelnosprawnosc_intelektualna__badania_molekularne
[short_name] => Niepełnosprawność intelektualna – badania molekula...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[156] => Array
(
[id] => 156
[site_id] => 1
[status_id] => 5
[name] => Choroby neurologiczne o późnym wieku zachorowania - wyzwania diagnostyki i poradnictwa
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/156/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 156-choroby_neurologiczne_o_poznym_wieku_zachorowania___wyzwania_diagnostyki_i_poradnictwa
[url] => wideo/156-choroby_neurologiczne_o_poznym_wieku_zachorowania___wyzwania_diagnostyki_i_poradnictwa
[short_name] => Choroby neurologiczne o późnym wieku zachorowania ...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[158] => Array
(
[id] => 158
[site_id] => 1
[status_id] => 5
[name] => Badania cytogenetyczne – od kliniki do interpretacji wyniku
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/158/postergen_i_geno.png
[video] => resources/data/material/158/5_badania_cytogenetyczne_–_od_kliniki_do_interpretacji_wyniku.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med.,prof IMiD Beata Nowakowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 9
[site_id] => 1
[status_id] => 5
[name] => dr n. med.,prof IMiD Beata Nowakowska
[firstname] => Beata
[lastname] => Nowakowska
[title] => dr n. med.,prof IMiD
[affiliation] => Zakład Genetyki Medycznej, Zespół Pracowni Cytogenetyki, IMID
[avatar] => resources/data/eksperci/9/dr_nowakowska_v2.jpg
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 9-beata_nowakowska
[url] => eksperci/9-beata_nowakowska
)
)
[authors_ids] => Array
(
[0] => 9
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 12
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 158-badania_cytogenetyczne__od_kliniki_do_interpretacji_wyniku
[url] => wideo/158-badania_cytogenetyczne__od_kliniki_do_interpretacji_wyniku
[short_name] => Badania cytogenetyczne – od kliniki do interpretac...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[12] => Array
(
[id] => 12
[site_id] => 1
[status_id] => 5
[name] => cytogenetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 12-cytogenetyka
[url] => /12-cytogenetyka
)
)
[artykuly] => Array
(
)
)
)
)
[sort] => 1
[status_code] => active
[authors] => Array
(
[0] => dr n. med., prof IMiD Monika Gos
)
[authors_data] => Array
(
[0] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => dr n. med., prof IMiD Monika Gos
[firstname] => Monika
[lastname] => Gos
[title] => dr n. med., prof IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-monika_gos
[url] => eksperci/13-monika_gos
)
)
[authors_ids] => Array
(
[0] => 13
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
[3] => 14
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 154-rdzeniowy_zanik_miesni___od_mutacji_do_terapii
[url] => wideo/154-rdzeniowy_zanik_miesni___od_mutacji_do_terapii
[short_name] => Rdzeniowy zanik mięśni - od mutacji do terapii
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
[14] => Array
(
[id] => 14
[site_id] => 1
[status_id] => 5
[name] => choroby rzadkie
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 14-choroby_rzadkie
[url] => /14-choroby_rzadkie
)
)
[artykuly] => Array
(
)
[logotypy] => Array
(
)
[pliki] => Array
(
[123] => Array
(
[id] => 123
[site_id] => 1
[status_id] => 5
[entity_key] => material
[entity_id] => 154
[name] => Rdzeniowy zanik mięśni - od mutacji do terapii
[file] => resources/data/pliki/material/154/25.06_w2sma_mg_materialy.pdf
[sort] => 120
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
[155] => Array
(
[id] => 155
[name] => Niepełnosprawność intelektualna – badania molekularne
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/155/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
[linked] => Array
(
[144] => Array
(
[id] => 144
[site_id] => 1
[status_id] => 5
[name] => Badania molekularne. Od kliniki do interpretacji wyniku.
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/144/postergen_i_geno.png
[video] => resources/data/material/144/5_badania_molekularne_–_od_kliniki_do_interpretacji_wyniku_dr_hab._dorota_hoffmanzacharska.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
[3] => 14
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 144-badania_molekularne_od_kliniki_do_interpretacji_wyniku
[url] => wideo/144-badania_molekularne_od_kliniki_do_interpretacji_wyniku
[short_name] => Badania molekularne. Od kliniki do interpretacji w...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
[14] => Array
(
[id] => 14
[site_id] => 1
[status_id] => 5
[name] => choroby rzadkie
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 14-choroby_rzadkie
[url] => /14-choroby_rzadkie
)
)
[artykuly] => Array
(
)
)
[145] => Array
(
[id] => 145
[site_id] => 1
[status_id] => 5
[name] => Choroba Huntingtona
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/145/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 145-choroba_huntingtona
[url] => wideo/145-choroba_huntingtona
[short_name] => Choroba Huntingtona
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[146] => Array
(
[id] => 146
[site_id] => 1
[status_id] => 5
[name] => Wspólne drogi zaburzeń neurorozwojowych
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/146/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 146-wspolne_drogi_zaburzen_neurorozwojowych
[url] => wideo/146-wspolne_drogi_zaburzen_neurorozwojowych
[short_name] => Wspólne drogi zaburzeń neurorozwojowych
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[147] => Array
(
[id] => 147
[site_id] => 1
[status_id] => 5
[name] => Genetyka chorób neurologicznych o późnym początku
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/147/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Maciej Geremek
)
[authors_data] => Array
(
[0] => Array
(
[id] => 69
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Maciej Geremek
[firstname] => Maciej
[lastname] => Geremek
[title] => dr n. med.
[affiliation] => Zakład genetyki Medycznej IMiD
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 69-maciej_geremek
[url] => eksperci/69-maciej_geremek
)
)
[authors_ids] => Array
(
[0] => 69
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 147-genetyka_chorob_neurologicznych_o_poznym_poczatku
[url] => wideo/147-genetyka_chorob_neurologicznych_o_poznym_poczatku
[short_name] => Genetyka chorób neurologicznych o późnym początku
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[148] => Array
(
[id] => 148
[site_id] => 1
[status_id] => 5
[name] => Neurogenetyka molekularna
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/148/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 148-neurogenetyka_molekularna
[url] => wideo/148-neurogenetyka_molekularna
[short_name] => Neurogenetyka molekularna
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[149] => Array
(
[id] => 149
[site_id] => 1
[status_id] => 5
[name] => Poradnictwo genetyczne w odniesieniu do chorób neurologicznych
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/149/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Ewa Obersztyn
)
[authors_data] => Array
(
[0] => Array
(
[id] => 14
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Ewa Obersztyn
[firstname] => Ewa
[lastname] => Obersztyn
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 14-ewa_obersztyn
[url] => eksperci/14-ewa_obersztyn
)
)
[authors_ids] => Array
(
[0] => 14
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 149-poradnictwo_genetyczne_w_odniesieniu_do_chorob_neurologicznych
[url] => wideo/149-poradnictwo_genetyczne_w_odniesieniu_do_chorob_neurologicznych
[short_name] => Poradnictwo genetyczne w odniesieniu do chorób neu...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[150] => Array
(
[id] => 150
[site_id] => 1
[status_id] => 5
[name] => Niepełnosprawność intelektualna –badania cytogenetyczne.
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/150/postergen_i_geno.png
[video] => resources/data/material/150/5_niepelnosprawnosc_intelektualna_–_badania_molekularne_dr_sylwia_rzonca.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => mgr Kamila Ziemkiewicz
)
[authors_data] => Array
(
[0] => Array
(
[id] => 11
[site_id] => 1
[status_id] => 5
[name] => mgr Kamila Ziemkiewicz
[firstname] => Kamila
[lastname] => Ziemkiewicz
[title] => mgr
[affiliation] =>
[avatar] => resources/data/eksperci/11/kziemkiewicz.png
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 11-kamila_ziemkiewicz
[url] => eksperci/11-kamila_ziemkiewicz
)
)
[authors_ids] => Array
(
[0] => 11
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 12
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 150-niepelnosprawnosc_intelektualna_badania_cytogenetyczne
[url] => wideo/150-niepelnosprawnosc_intelektualna_badania_cytogenetyczne
[short_name] => Niepełnosprawność intelektualna –badania cytogenet...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[12] => Array
(
[id] => 12
[site_id] => 1
[status_id] => 5
[name] => cytogenetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 12-cytogenetyka
[url] => /12-cytogenetyka
)
)
[artykuly] => Array
(
)
)
[151] => Array
(
[id] => 151
[site_id] => 1
[status_id] => 5
[name] => Techniki cytogenetyczne w diagnostyce chorób układu nerwowego.
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/151/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => mgr Kamila Ziemkiewicz
)
[authors_data] => Array
(
[0] => Array
(
[id] => 11
[site_id] => 1
[status_id] => 5
[name] => mgr Kamila Ziemkiewicz
[firstname] => Kamila
[lastname] => Ziemkiewicz
[title] => mgr
[affiliation] =>
[avatar] => resources/data/eksperci/11/kziemkiewicz.png
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 11-kamila_ziemkiewicz
[url] => eksperci/11-kamila_ziemkiewicz
)
)
[authors_ids] => Array
(
[0] => 11
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 12
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 151-techniki_cytogenetyczne_w_diagnostyce_chorob_ukladu_nerwowego
[url] => wideo/151-techniki_cytogenetyczne_w_diagnostyce_chorob_ukladu_nerwowego
[short_name] => Techniki cytogenetyczne w diagnostyce chorób układ...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[12] => Array
(
[id] => 12
[site_id] => 1
[status_id] => 5
[name] => cytogenetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 12-cytogenetyka
[url] => /12-cytogenetyka
)
)
[artykuly] => Array
(
)
)
[152] => Array
(
[id] => 152
[site_id] => 1
[status_id] => 5
[name] => Choroby nerwów obwodowych
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/152/postergen_i_geno.png
[video] => resources/data/material/152/5_choroby_nerwowobwodowych_potulska.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab. n. med. Anna Potulska-Chromik
)
[authors_data] => Array
(
[0] => Array
(
[id] => 70
[site_id] => 1
[status_id] => 5
[name] => dr hab. n. med. Anna Potulska-Chromik
[firstname] => Anna
[lastname] => Potulska-Chromik
[title] => dr hab. n. med.
[affiliation] => Klinika Neurologii WUM
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 70-anna_potulska_chromik
[url] => eksperci/70-anna_potulska_chromik
)
)
[authors_ids] => Array
(
[0] => 70
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 152-choroby_nerwow_obwodowych
[url] => wideo/152-choroby_nerwow_obwodowych
[short_name] => Choroby nerwów obwodowych
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[153] => Array
(
[id] => 153
[site_id] => 1
[status_id] => 5
[name] => Choroby nerwowo-mięśniowe
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/153/postergen_i_geno.png
[video] => resources/data/material/153/5_choroby_nerwowomiesniowe_dr_hab._monika_gos.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med., prof IMiD Monika Gos
)
[authors_data] => Array
(
[0] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => dr n. med., prof IMiD Monika Gos
[firstname] => Monika
[lastname] => Gos
[title] => dr n. med., prof IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-monika_gos
[url] => eksperci/13-monika_gos
)
)
[authors_ids] => Array
(
[0] => 13
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 153-choroby_nerwowo_miesniowe
[url] => wideo/153-choroby_nerwowo_miesniowe
[short_name] => Choroby nerwowo-mięśniowe
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[154] => Array
(
[id] => 154
[site_id] => 1
[status_id] => 5
[name] => Rdzeniowy zanik mięśni - od mutacji do terapii
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/154/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med., prof IMiD Monika Gos
)
[authors_data] => Array
(
[0] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => dr n. med., prof IMiD Monika Gos
[firstname] => Monika
[lastname] => Gos
[title] => dr n. med., prof IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-monika_gos
[url] => eksperci/13-monika_gos
)
)
[authors_ids] => Array
(
[0] => 13
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
[3] => 14
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 154-rdzeniowy_zanik_miesni___od_mutacji_do_terapii
[url] => wideo/154-rdzeniowy_zanik_miesni___od_mutacji_do_terapii
[short_name] => Rdzeniowy zanik mięśni - od mutacji do terapii
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
[14] => Array
(
[id] => 14
[site_id] => 1
[status_id] => 5
[name] => choroby rzadkie
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 14-choroby_rzadkie
[url] => /14-choroby_rzadkie
)
)
[artykuly] => Array
(
)
)
[156] => Array
(
[id] => 156
[site_id] => 1
[status_id] => 5
[name] => Choroby neurologiczne o późnym wieku zachorowania - wyzwania diagnostyki i poradnictwa
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/156/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 156-choroby_neurologiczne_o_poznym_wieku_zachorowania___wyzwania_diagnostyki_i_poradnictwa
[url] => wideo/156-choroby_neurologiczne_o_poznym_wieku_zachorowania___wyzwania_diagnostyki_i_poradnictwa
[short_name] => Choroby neurologiczne o późnym wieku zachorowania ...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[158] => Array
(
[id] => 158
[site_id] => 1
[status_id] => 5
[name] => Badania cytogenetyczne – od kliniki do interpretacji wyniku
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/158/postergen_i_geno.png
[video] => resources/data/material/158/5_badania_cytogenetyczne_–_od_kliniki_do_interpretacji_wyniku.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med.,prof IMiD Beata Nowakowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 9
[site_id] => 1
[status_id] => 5
[name] => dr n. med.,prof IMiD Beata Nowakowska
[firstname] => Beata
[lastname] => Nowakowska
[title] => dr n. med.,prof IMiD
[affiliation] => Zakład Genetyki Medycznej, Zespół Pracowni Cytogenetyki, IMID
[avatar] => resources/data/eksperci/9/dr_nowakowska_v2.jpg
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 9-beata_nowakowska
[url] => eksperci/9-beata_nowakowska
)
)
[authors_ids] => Array
(
[0] => 9
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 12
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 158-badania_cytogenetyczne__od_kliniki_do_interpretacji_wyniku
[url] => wideo/158-badania_cytogenetyczne__od_kliniki_do_interpretacji_wyniku
[short_name] => Badania cytogenetyczne – od kliniki do interpretac...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[12] => Array
(
[id] => 12
[site_id] => 1
[status_id] => 5
[name] => cytogenetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 12-cytogenetyka
[url] => /12-cytogenetyka
)
)
[artykuly] => Array
(
)
)
)
)
[sort] => 1
[status_code] => active
[authors] => Array
(
[0] => dr n. med. Sylwia Rzońca
)
[authors_data] => Array
(
[0] => Array
(
[id] => 10
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Sylwia Rzońca
[firstname] => Sylwia
[lastname] => Rzońca
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 10-sylwia_rzonca
[url] => eksperci/10-sylwia_rzonca
)
)
[authors_ids] => Array
(
[0] => 10
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 155-niepelnosprawnosc_intelektualna__badania_molekularne
[url] => wideo/155-niepelnosprawnosc_intelektualna__badania_molekularne
[short_name] => Niepełnosprawność intelektualna – badania molekula...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
[logotypy] => Array
(
)
[pliki] => Array
(
[124] => Array
(
[id] => 124
[site_id] => 1
[status_id] => 5
[entity_key] => material
[entity_id] => 155
[name] => Niepełnosprawność intelektualna – badania molekularne
[file] => resources/data/pliki/material/155/24.06_w5_srzn_materialy.pdf
[sort] => 121
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
[156] => Array
(
[id] => 156
[name] => Choroby neurologiczne o późnym wieku zachorowania - wyzwania diagnostyki i poradnictwa
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/156/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
[linked] => Array
(
[144] => Array
(
[id] => 144
[site_id] => 1
[status_id] => 5
[name] => Badania molekularne. Od kliniki do interpretacji wyniku.
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/144/postergen_i_geno.png
[video] => resources/data/material/144/5_badania_molekularne_–_od_kliniki_do_interpretacji_wyniku_dr_hab._dorota_hoffmanzacharska.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
[3] => 14
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 144-badania_molekularne_od_kliniki_do_interpretacji_wyniku
[url] => wideo/144-badania_molekularne_od_kliniki_do_interpretacji_wyniku
[short_name] => Badania molekularne. Od kliniki do interpretacji w...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
[14] => Array
(
[id] => 14
[site_id] => 1
[status_id] => 5
[name] => choroby rzadkie
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 14-choroby_rzadkie
[url] => /14-choroby_rzadkie
)
)
[artykuly] => Array
(
)
)
[145] => Array
(
[id] => 145
[site_id] => 1
[status_id] => 5
[name] => Choroba Huntingtona
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/145/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 145-choroba_huntingtona
[url] => wideo/145-choroba_huntingtona
[short_name] => Choroba Huntingtona
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[146] => Array
(
[id] => 146
[site_id] => 1
[status_id] => 5
[name] => Wspólne drogi zaburzeń neurorozwojowych
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/146/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 146-wspolne_drogi_zaburzen_neurorozwojowych
[url] => wideo/146-wspolne_drogi_zaburzen_neurorozwojowych
[short_name] => Wspólne drogi zaburzeń neurorozwojowych
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[147] => Array
(
[id] => 147
[site_id] => 1
[status_id] => 5
[name] => Genetyka chorób neurologicznych o późnym początku
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/147/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Maciej Geremek
)
[authors_data] => Array
(
[0] => Array
(
[id] => 69
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Maciej Geremek
[firstname] => Maciej
[lastname] => Geremek
[title] => dr n. med.
[affiliation] => Zakład genetyki Medycznej IMiD
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 69-maciej_geremek
[url] => eksperci/69-maciej_geremek
)
)
[authors_ids] => Array
(
[0] => 69
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 147-genetyka_chorob_neurologicznych_o_poznym_poczatku
[url] => wideo/147-genetyka_chorob_neurologicznych_o_poznym_poczatku
[short_name] => Genetyka chorób neurologicznych o późnym początku
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[148] => Array
(
[id] => 148
[site_id] => 1
[status_id] => 5
[name] => Neurogenetyka molekularna
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/148/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 148-neurogenetyka_molekularna
[url] => wideo/148-neurogenetyka_molekularna
[short_name] => Neurogenetyka molekularna
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[149] => Array
(
[id] => 149
[site_id] => 1
[status_id] => 5
[name] => Poradnictwo genetyczne w odniesieniu do chorób neurologicznych
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/149/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Ewa Obersztyn
)
[authors_data] => Array
(
[0] => Array
(
[id] => 14
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Ewa Obersztyn
[firstname] => Ewa
[lastname] => Obersztyn
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 14-ewa_obersztyn
[url] => eksperci/14-ewa_obersztyn
)
)
[authors_ids] => Array
(
[0] => 14
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 149-poradnictwo_genetyczne_w_odniesieniu_do_chorob_neurologicznych
[url] => wideo/149-poradnictwo_genetyczne_w_odniesieniu_do_chorob_neurologicznych
[short_name] => Poradnictwo genetyczne w odniesieniu do chorób neu...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[150] => Array
(
[id] => 150
[site_id] => 1
[status_id] => 5
[name] => Niepełnosprawność intelektualna –badania cytogenetyczne.
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/150/postergen_i_geno.png
[video] => resources/data/material/150/5_niepelnosprawnosc_intelektualna_–_badania_molekularne_dr_sylwia_rzonca.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => mgr Kamila Ziemkiewicz
)
[authors_data] => Array
(
[0] => Array
(
[id] => 11
[site_id] => 1
[status_id] => 5
[name] => mgr Kamila Ziemkiewicz
[firstname] => Kamila
[lastname] => Ziemkiewicz
[title] => mgr
[affiliation] =>
[avatar] => resources/data/eksperci/11/kziemkiewicz.png
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 11-kamila_ziemkiewicz
[url] => eksperci/11-kamila_ziemkiewicz
)
)
[authors_ids] => Array
(
[0] => 11
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 12
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 150-niepelnosprawnosc_intelektualna_badania_cytogenetyczne
[url] => wideo/150-niepelnosprawnosc_intelektualna_badania_cytogenetyczne
[short_name] => Niepełnosprawność intelektualna –badania cytogenet...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[12] => Array
(
[id] => 12
[site_id] => 1
[status_id] => 5
[name] => cytogenetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 12-cytogenetyka
[url] => /12-cytogenetyka
)
)
[artykuly] => Array
(
)
)
[151] => Array
(
[id] => 151
[site_id] => 1
[status_id] => 5
[name] => Techniki cytogenetyczne w diagnostyce chorób układu nerwowego.
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/151/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => mgr Kamila Ziemkiewicz
)
[authors_data] => Array
(
[0] => Array
(
[id] => 11
[site_id] => 1
[status_id] => 5
[name] => mgr Kamila Ziemkiewicz
[firstname] => Kamila
[lastname] => Ziemkiewicz
[title] => mgr
[affiliation] =>
[avatar] => resources/data/eksperci/11/kziemkiewicz.png
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 11-kamila_ziemkiewicz
[url] => eksperci/11-kamila_ziemkiewicz
)
)
[authors_ids] => Array
(
[0] => 11
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 12
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 151-techniki_cytogenetyczne_w_diagnostyce_chorob_ukladu_nerwowego
[url] => wideo/151-techniki_cytogenetyczne_w_diagnostyce_chorob_ukladu_nerwowego
[short_name] => Techniki cytogenetyczne w diagnostyce chorób układ...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[12] => Array
(
[id] => 12
[site_id] => 1
[status_id] => 5
[name] => cytogenetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 12-cytogenetyka
[url] => /12-cytogenetyka
)
)
[artykuly] => Array
(
)
)
[152] => Array
(
[id] => 152
[site_id] => 1
[status_id] => 5
[name] => Choroby nerwów obwodowych
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/152/postergen_i_geno.png
[video] => resources/data/material/152/5_choroby_nerwowobwodowych_potulska.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab. n. med. Anna Potulska-Chromik
)
[authors_data] => Array
(
[0] => Array
(
[id] => 70
[site_id] => 1
[status_id] => 5
[name] => dr hab. n. med. Anna Potulska-Chromik
[firstname] => Anna
[lastname] => Potulska-Chromik
[title] => dr hab. n. med.
[affiliation] => Klinika Neurologii WUM
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 70-anna_potulska_chromik
[url] => eksperci/70-anna_potulska_chromik
)
)
[authors_ids] => Array
(
[0] => 70
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 152-choroby_nerwow_obwodowych
[url] => wideo/152-choroby_nerwow_obwodowych
[short_name] => Choroby nerwów obwodowych
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[153] => Array
(
[id] => 153
[site_id] => 1
[status_id] => 5
[name] => Choroby nerwowo-mięśniowe
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/153/postergen_i_geno.png
[video] => resources/data/material/153/5_choroby_nerwowomiesniowe_dr_hab._monika_gos.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med., prof IMiD Monika Gos
)
[authors_data] => Array
(
[0] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => dr n. med., prof IMiD Monika Gos
[firstname] => Monika
[lastname] => Gos
[title] => dr n. med., prof IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-monika_gos
[url] => eksperci/13-monika_gos
)
)
[authors_ids] => Array
(
[0] => 13
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 153-choroby_nerwowo_miesniowe
[url] => wideo/153-choroby_nerwowo_miesniowe
[short_name] => Choroby nerwowo-mięśniowe
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[154] => Array
(
[id] => 154
[site_id] => 1
[status_id] => 5
[name] => Rdzeniowy zanik mięśni - od mutacji do terapii
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/154/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med., prof IMiD Monika Gos
)
[authors_data] => Array
(
[0] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => dr n. med., prof IMiD Monika Gos
[firstname] => Monika
[lastname] => Gos
[title] => dr n. med., prof IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-monika_gos
[url] => eksperci/13-monika_gos
)
)
[authors_ids] => Array
(
[0] => 13
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
[3] => 14
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 154-rdzeniowy_zanik_miesni___od_mutacji_do_terapii
[url] => wideo/154-rdzeniowy_zanik_miesni___od_mutacji_do_terapii
[short_name] => Rdzeniowy zanik mięśni - od mutacji do terapii
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
[14] => Array
(
[id] => 14
[site_id] => 1
[status_id] => 5
[name] => choroby rzadkie
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 14-choroby_rzadkie
[url] => /14-choroby_rzadkie
)
)
[artykuly] => Array
(
)
)
[155] => Array
(
[id] => 155
[site_id] => 1
[status_id] => 5
[name] => Niepełnosprawność intelektualna – badania molekularne
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/155/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Sylwia Rzońca
)
[authors_data] => Array
(
[0] => Array
(
[id] => 10
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Sylwia Rzońca
[firstname] => Sylwia
[lastname] => Rzońca
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 10-sylwia_rzonca
[url] => eksperci/10-sylwia_rzonca
)
)
[authors_ids] => Array
(
[0] => 10
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 155-niepelnosprawnosc_intelektualna__badania_molekularne
[url] => wideo/155-niepelnosprawnosc_intelektualna__badania_molekularne
[short_name] => Niepełnosprawność intelektualna – badania molekula...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[158] => Array
(
[id] => 158
[site_id] => 1
[status_id] => 5
[name] => Badania cytogenetyczne – od kliniki do interpretacji wyniku
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/158/postergen_i_geno.png
[video] => resources/data/material/158/5_badania_cytogenetyczne_–_od_kliniki_do_interpretacji_wyniku.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med.,prof IMiD Beata Nowakowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 9
[site_id] => 1
[status_id] => 5
[name] => dr n. med.,prof IMiD Beata Nowakowska
[firstname] => Beata
[lastname] => Nowakowska
[title] => dr n. med.,prof IMiD
[affiliation] => Zakład Genetyki Medycznej, Zespół Pracowni Cytogenetyki, IMID
[avatar] => resources/data/eksperci/9/dr_nowakowska_v2.jpg
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 9-beata_nowakowska
[url] => eksperci/9-beata_nowakowska
)
)
[authors_ids] => Array
(
[0] => 9
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 12
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 158-badania_cytogenetyczne__od_kliniki_do_interpretacji_wyniku
[url] => wideo/158-badania_cytogenetyczne__od_kliniki_do_interpretacji_wyniku
[short_name] => Badania cytogenetyczne – od kliniki do interpretac...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[12] => Array
(
[id] => 12
[site_id] => 1
[status_id] => 5
[name] => cytogenetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 12-cytogenetyka
[url] => /12-cytogenetyka
)
)
[artykuly] => Array
(
)
)
)
)
[sort] => 1
[status_code] => active
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 156-choroby_neurologiczne_o_poznym_wieku_zachorowania___wyzwania_diagnostyki_i_poradnictwa
[url] => wideo/156-choroby_neurologiczne_o_poznym_wieku_zachorowania___wyzwania_diagnostyki_i_poradnictwa
[short_name] => Choroby neurologiczne o późnym wieku zachorowania ...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
[logotypy] => Array
(
)
[pliki] => Array
(
[125] => Array
(
[id] => 125
[site_id] => 1
[status_id] => 5
[entity_key] => material
[entity_id] => 156
[name] => Choroby neurologiczne o późnym wieku zachorowania - wyzwania diagnostyki i poradnictwa
[file] => resources/data/pliki/material/156/neurodeg_11.2020_.pdf
[sort] => 122
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
[158] => Array
(
[id] => 158
[name] => Badania cytogenetyczne – od kliniki do interpretacji wyniku
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/158/postergen_i_geno.png
[video] => resources/data/material/158/5_badania_cytogenetyczne_–_od_kliniki_do_interpretacji_wyniku.mp4
[content] =>
[ext] => Array
(
[files_header] =>
[linked] => Array
(
[144] => Array
(
[id] => 144
[site_id] => 1
[status_id] => 5
[name] => Badania molekularne. Od kliniki do interpretacji wyniku.
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/144/postergen_i_geno.png
[video] => resources/data/material/144/5_badania_molekularne_–_od_kliniki_do_interpretacji_wyniku_dr_hab._dorota_hoffmanzacharska.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
[3] => 14
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 144-badania_molekularne_od_kliniki_do_interpretacji_wyniku
[url] => wideo/144-badania_molekularne_od_kliniki_do_interpretacji_wyniku
[short_name] => Badania molekularne. Od kliniki do interpretacji w...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
[14] => Array
(
[id] => 14
[site_id] => 1
[status_id] => 5
[name] => choroby rzadkie
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 14-choroby_rzadkie
[url] => /14-choroby_rzadkie
)
)
[artykuly] => Array
(
)
)
[145] => Array
(
[id] => 145
[site_id] => 1
[status_id] => 5
[name] => Choroba Huntingtona
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/145/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 145-choroba_huntingtona
[url] => wideo/145-choroba_huntingtona
[short_name] => Choroba Huntingtona
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[146] => Array
(
[id] => 146
[site_id] => 1
[status_id] => 5
[name] => Wspólne drogi zaburzeń neurorozwojowych
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/146/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 146-wspolne_drogi_zaburzen_neurorozwojowych
[url] => wideo/146-wspolne_drogi_zaburzen_neurorozwojowych
[short_name] => Wspólne drogi zaburzeń neurorozwojowych
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[147] => Array
(
[id] => 147
[site_id] => 1
[status_id] => 5
[name] => Genetyka chorób neurologicznych o późnym początku
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/147/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Maciej Geremek
)
[authors_data] => Array
(
[0] => Array
(
[id] => 69
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Maciej Geremek
[firstname] => Maciej
[lastname] => Geremek
[title] => dr n. med.
[affiliation] => Zakład genetyki Medycznej IMiD
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 69-maciej_geremek
[url] => eksperci/69-maciej_geremek
)
)
[authors_ids] => Array
(
[0] => 69
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 147-genetyka_chorob_neurologicznych_o_poznym_poczatku
[url] => wideo/147-genetyka_chorob_neurologicznych_o_poznym_poczatku
[short_name] => Genetyka chorób neurologicznych o późnym początku
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[148] => Array
(
[id] => 148
[site_id] => 1
[status_id] => 5
[name] => Neurogenetyka molekularna
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/148/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 148-neurogenetyka_molekularna
[url] => wideo/148-neurogenetyka_molekularna
[short_name] => Neurogenetyka molekularna
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[149] => Array
(
[id] => 149
[site_id] => 1
[status_id] => 5
[name] => Poradnictwo genetyczne w odniesieniu do chorób neurologicznych
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/149/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Ewa Obersztyn
)
[authors_data] => Array
(
[0] => Array
(
[id] => 14
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Ewa Obersztyn
[firstname] => Ewa
[lastname] => Obersztyn
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 14-ewa_obersztyn
[url] => eksperci/14-ewa_obersztyn
)
)
[authors_ids] => Array
(
[0] => 14
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 149-poradnictwo_genetyczne_w_odniesieniu_do_chorob_neurologicznych
[url] => wideo/149-poradnictwo_genetyczne_w_odniesieniu_do_chorob_neurologicznych
[short_name] => Poradnictwo genetyczne w odniesieniu do chorób neu...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[150] => Array
(
[id] => 150
[site_id] => 1
[status_id] => 5
[name] => Niepełnosprawność intelektualna –badania cytogenetyczne.
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/150/postergen_i_geno.png
[video] => resources/data/material/150/5_niepelnosprawnosc_intelektualna_–_badania_molekularne_dr_sylwia_rzonca.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => mgr Kamila Ziemkiewicz
)
[authors_data] => Array
(
[0] => Array
(
[id] => 11
[site_id] => 1
[status_id] => 5
[name] => mgr Kamila Ziemkiewicz
[firstname] => Kamila
[lastname] => Ziemkiewicz
[title] => mgr
[affiliation] =>
[avatar] => resources/data/eksperci/11/kziemkiewicz.png
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 11-kamila_ziemkiewicz
[url] => eksperci/11-kamila_ziemkiewicz
)
)
[authors_ids] => Array
(
[0] => 11
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 12
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 150-niepelnosprawnosc_intelektualna_badania_cytogenetyczne
[url] => wideo/150-niepelnosprawnosc_intelektualna_badania_cytogenetyczne
[short_name] => Niepełnosprawność intelektualna –badania cytogenet...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[12] => Array
(
[id] => 12
[site_id] => 1
[status_id] => 5
[name] => cytogenetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 12-cytogenetyka
[url] => /12-cytogenetyka
)
)
[artykuly] => Array
(
)
)
[151] => Array
(
[id] => 151
[site_id] => 1
[status_id] => 5
[name] => Techniki cytogenetyczne w diagnostyce chorób układu nerwowego.
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/151/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => mgr Kamila Ziemkiewicz
)
[authors_data] => Array
(
[0] => Array
(
[id] => 11
[site_id] => 1
[status_id] => 5
[name] => mgr Kamila Ziemkiewicz
[firstname] => Kamila
[lastname] => Ziemkiewicz
[title] => mgr
[affiliation] =>
[avatar] => resources/data/eksperci/11/kziemkiewicz.png
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 11-kamila_ziemkiewicz
[url] => eksperci/11-kamila_ziemkiewicz
)
)
[authors_ids] => Array
(
[0] => 11
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 12
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 151-techniki_cytogenetyczne_w_diagnostyce_chorob_ukladu_nerwowego
[url] => wideo/151-techniki_cytogenetyczne_w_diagnostyce_chorob_ukladu_nerwowego
[short_name] => Techniki cytogenetyczne w diagnostyce chorób układ...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[12] => Array
(
[id] => 12
[site_id] => 1
[status_id] => 5
[name] => cytogenetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 12-cytogenetyka
[url] => /12-cytogenetyka
)
)
[artykuly] => Array
(
)
)
[152] => Array
(
[id] => 152
[site_id] => 1
[status_id] => 5
[name] => Choroby nerwów obwodowych
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/152/postergen_i_geno.png
[video] => resources/data/material/152/5_choroby_nerwowobwodowych_potulska.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab. n. med. Anna Potulska-Chromik
)
[authors_data] => Array
(
[0] => Array
(
[id] => 70
[site_id] => 1
[status_id] => 5
[name] => dr hab. n. med. Anna Potulska-Chromik
[firstname] => Anna
[lastname] => Potulska-Chromik
[title] => dr hab. n. med.
[affiliation] => Klinika Neurologii WUM
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 70-anna_potulska_chromik
[url] => eksperci/70-anna_potulska_chromik
)
)
[authors_ids] => Array
(
[0] => 70
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 152-choroby_nerwow_obwodowych
[url] => wideo/152-choroby_nerwow_obwodowych
[short_name] => Choroby nerwów obwodowych
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[153] => Array
(
[id] => 153
[site_id] => 1
[status_id] => 5
[name] => Choroby nerwowo-mięśniowe
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/153/postergen_i_geno.png
[video] => resources/data/material/153/5_choroby_nerwowomiesniowe_dr_hab._monika_gos.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med., prof IMiD Monika Gos
)
[authors_data] => Array
(
[0] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => dr n. med., prof IMiD Monika Gos
[firstname] => Monika
[lastname] => Gos
[title] => dr n. med., prof IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-monika_gos
[url] => eksperci/13-monika_gos
)
)
[authors_ids] => Array
(
[0] => 13
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 153-choroby_nerwowo_miesniowe
[url] => wideo/153-choroby_nerwowo_miesniowe
[short_name] => Choroby nerwowo-mięśniowe
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[154] => Array
(
[id] => 154
[site_id] => 1
[status_id] => 5
[name] => Rdzeniowy zanik mięśni - od mutacji do terapii
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/154/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med., prof IMiD Monika Gos
)
[authors_data] => Array
(
[0] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => dr n. med., prof IMiD Monika Gos
[firstname] => Monika
[lastname] => Gos
[title] => dr n. med., prof IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-monika_gos
[url] => eksperci/13-monika_gos
)
)
[authors_ids] => Array
(
[0] => 13
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
[3] => 14
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 154-rdzeniowy_zanik_miesni___od_mutacji_do_terapii
[url] => wideo/154-rdzeniowy_zanik_miesni___od_mutacji_do_terapii
[short_name] => Rdzeniowy zanik mięśni - od mutacji do terapii
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
[14] => Array
(
[id] => 14
[site_id] => 1
[status_id] => 5
[name] => choroby rzadkie
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 14-choroby_rzadkie
[url] => /14-choroby_rzadkie
)
)
[artykuly] => Array
(
)
)
[155] => Array
(
[id] => 155
[site_id] => 1
[status_id] => 5
[name] => Niepełnosprawność intelektualna – badania molekularne
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/155/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Sylwia Rzońca
)
[authors_data] => Array
(
[0] => Array
(
[id] => 10
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Sylwia Rzońca
[firstname] => Sylwia
[lastname] => Rzońca
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 10-sylwia_rzonca
[url] => eksperci/10-sylwia_rzonca
)
)
[authors_ids] => Array
(
[0] => 10
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 13
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 155-niepelnosprawnosc_intelektualna__badania_molekularne
[url] => wideo/155-niepelnosprawnosc_intelektualna__badania_molekularne
[short_name] => Niepełnosprawność intelektualna – badania molekula...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[13] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => wady wrodzone
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-wady_wrodzone
[url] => /13-wady_wrodzone
)
)
[artykuly] => Array
(
)
)
[156] => Array
(
[id] => 156
[site_id] => 1
[status_id] => 5
[name] => Choroby neurologiczne o późnym wieku zachorowania - wyzwania diagnostyki i poradnictwa
[type_id] => 1
[group_id] => 19
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/156/postergen_i_geno.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 156-choroby_neurologiczne_o_poznym_wieku_zachorowania___wyzwania_diagnostyki_i_poradnictwa
[url] => wideo/156-choroby_neurologiczne_o_poznym_wieku_zachorowania___wyzwania_diagnostyki_i_poradnictwa
[short_name] => Choroby neurologiczne o późnym wieku zachorowania ...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
)
)
[sort] => 1
[status_code] => active
[authors] => Array
(
[0] => dr n. med.,prof IMiD Beata Nowakowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 9
[site_id] => 1
[status_id] => 5
[name] => dr n. med.,prof IMiD Beata Nowakowska
[firstname] => Beata
[lastname] => Nowakowska
[title] => dr n. med.,prof IMiD
[affiliation] => Zakład Genetyki Medycznej, Zespół Pracowni Cytogenetyki, IMID
[avatar] => resources/data/eksperci/9/dr_nowakowska_v2.jpg
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 9-beata_nowakowska
[url] => eksperci/9-beata_nowakowska
)
)
[authors_ids] => Array
(
[0] => 9
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 12
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 158-badania_cytogenetyczne__od_kliniki_do_interpretacji_wyniku
[url] => wideo/158-badania_cytogenetyczne__od_kliniki_do_interpretacji_wyniku
[short_name] => Badania cytogenetyczne – od kliniki do interpretac...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 19
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika chorób neurologicznych
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 19-genetyka_i_genomika_chorob_neurologicznych
[url] => kursy/19-genetyka_i_genomika_chorob_neurologicznych
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[12] => Array
(
[id] => 12
[site_id] => 1
[status_id] => 5
[name] => cytogenetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 12-cytogenetyka
[url] => /12-cytogenetyka
)
)
[artykuly] => Array
(
)
[logotypy] => Array
(
)
[pliki] => Array
(
[127] => Array
(
[id] => 127
[site_id] => 1
[status_id] => 5
[entity_key] => material
[entity_id] => 158
[name] => Badania cytogenetyczne – od kliniki do interpretacji wyniku
[file] => resources/data/pliki/material/158/_w7_nowakowska.pdf
[sort] => 124
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
)
[quiz_questions] => Array
(
[235] => Array
(
[id] => 235
[site_id] => 1
[status_id] => 5
[group_id] => 19
[type_id] => 1
[name] => Celem analizy rodowodu jest: (poniższe stwierdzenia są prawidłowe oprócz)
[ext] =>
[sort] => 0
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[type_name] => pojedyncza odpowiedź
[type_code] => single
[answers] => Array
(
[850] => Array
(
[id] => 850
[site_id] => 1
[status_id] => 5
[question_id] => 235
[name] => a. ocena zróżnicowanej ekspresji choroby u różnych członków rodziny
[correct] => 0
[ext] =>
[sort] => 843
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[851] => Array
(
[id] => 851
[site_id] => 1
[status_id] => 5
[question_id] => 235
[name] => b. określenie toku dziedziczenia choroby
[correct] => 0
[ext] =>
[sort] => 844
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[852] => Array
(
[id] => 852
[site_id] => 1
[status_id] => 5
[question_id] => 235
[name] => c. wykluczenie genetycznego uwarunkowania choroby
[correct] => 1
[ext] =>
[sort] => 845
[correct_yesno] => Tak
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[853] => Array
(
[id] => 853
[site_id] => 1
[status_id] => 5
[question_id] => 235
[name] => d. planowanie badań diagnostycznych w rodzinie
[correct] => 0
[ext] =>
[sort] => 846
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
[237] => Array
(
[id] => 237
[site_id] => 1
[status_id] => 5
[group_id] => 19
[type_id] => 2
[name] => Najistotniejszym czynnikiem ryzyka choroby Alzheimera jest:
[ext] =>
[sort] => 0
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[type_name] => wielokrotna odpowiedź
[type_code] => multi
[answers] => Array
(
[854] => Array
(
[id] => 854
[site_id] => 1
[status_id] => 5
[question_id] => 237
[name] => a. Allel e4 genu ApoE
[correct] => 0
[ext] =>
[sort] => 847
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[855] => Array
(
[id] => 855
[site_id] => 1
[status_id] => 5
[question_id] => 237
[name] => b. Pozytywny wywiad rodzinny
[correct] => 0
[ext] =>
[sort] => 848
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[856] => Array
(
[id] => 856
[site_id] => 1
[status_id] => 5
[question_id] => 237
[name] => c. Wariant G2019S w genie LRRK2
[correct] => 0
[ext] =>
[sort] => 849
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[857] => Array
(
[id] => 857
[site_id] => 1
[status_id] => 5
[question_id] => 237
[name] => d. Wiek
[correct] => 1
[ext] =>
[sort] => 850
[correct_yesno] => Tak
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
[238] => Array
(
[id] => 238
[site_id] => 1
[status_id] => 5
[group_id] => 19
[type_id] => 1
[name] => Podstawowym badaniem genetycznym wykonywanym w przypadku podejrzenia dystrofii miotonicznej typu I jest:
[ext] =>
[sort] => 0
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[type_name] => pojedyncza odpowiedź
[type_code] => single
[answers] => Array
(
[858] => Array
(
[id] => 858
[site_id] => 1
[status_id] => 5
[question_id] => 238
[name] => a. Analiza genu DMPK pod kątem obecności delecji obejmujących jeden lub więcej eksonów z wykorzystaniem techniki MLPA
[correct] => 0
[ext] =>
[sort] => 851
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[859] => Array
(
[id] => 859
[site_id] => 1
[status_id] => 5
[question_id] => 238
[name] => b. Analiza genu DMPK pod kątem obecności ekspansji sekwencji CTG (>50 powtórzeń) z zastosowaniem techniki TP-PCR
[correct] => 1
[ext] =>
[sort] => 852
[correct_yesno] => Tak
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[860] => Array
(
[id] => 860
[site_id] => 1
[status_id] => 5
[question_id] => 238
[name] => c. Analiza sekwencji kodującej genu DMPK w celu identyfikacji mutacji punktowych powodujących utratę funkcji białka
[correct] => 0
[ext] =>
[sort] => 853
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[861] => Array
(
[id] => 861
[site_id] => 1
[status_id] => 5
[question_id] => 238
[name] => d. Sekwencjonowanie następnej generacji obejmujące panel genów związanych z chorobami nerwowo-mięśniowymi
[correct] => 0
[ext] =>
[sort] => 854
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
[239] => Array
(
[id] => 239
[site_id] => 1
[status_id] => 5
[group_id] => 19
[type_id] => 1
[name] => U dwojga dzieci 40 letniego zdrowego mężczyzny występują objawy tej samej choroby dziedziczonej autosomalnie dominująco. Ojciec mężczyzny również wykazuje objawy tej samej choroby co jego wnuki. U wszystkich osób zidentyfikowano obecność tej samej heterozygotycznej patogennej mutacji. Proszę podać, która z poniższych możliwości najlepiej definiuje zaistniałą sytuację?
[ext] =>
[sort] => 0
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[type_name] => pojedyncza odpowiedź
[type_code] => single
[answers] => Array
(
[862] => Array
(
[id] => 862
[site_id] => 1
[status_id] => 5
[question_id] => 239
[name] => a. Zróżnicowany, wewnątrzrodzinny stopień ekspresji klinicznej choroby
[correct] => 0
[ext] =>
[sort] => 855
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[863] => Array
(
[id] => 863
[site_id] => 1
[status_id] => 5
[question_id] => 239
[name] => b. Heterogenność alleliczna
[correct] => 0
[ext] =>
[sort] => 856
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[864] => Array
(
[id] => 864
[site_id] => 1
[status_id] => 5
[question_id] => 239
[name] => c. Brak penetracji mutacji u 40 letniego mężczyzny, ojca chorych dzieci
[correct] => 1
[ext] =>
[sort] => 857
[correct_yesno] => Tak
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[865] => Array
(
[id] => 865
[site_id] => 1
[status_id] => 5
[question_id] => 239
[name] => d. Mozaikowość germinalna
[correct] => 0
[ext] =>
[sort] => 858
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
[240] => Array
(
[id] => 240
[site_id] => 1
[status_id] => 5
[group_id] => 19
[type_id] => 1
[name] => Wykonanie testów predykcyjnych u osoby 25-cio letniej, która ma bliskiego krewnego z chorobą Huntingtona (wskaż błędne stwierdzenie):
[ext] =>
[sort] => 0
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[type_name] => pojedyncza odpowiedź
[type_code] => single
[answers] => Array
(
[866] => Array
(
[id] => 866
[site_id] => 1
[status_id] => 5
[question_id] => 240
[name] => a. umożliwia określenie ryzyka wystąpienia choroby w wieku późniejszym
[correct] => 0
[ext] =>
[sort] => 859
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[867] => Array
(
[id] => 867
[site_id] => 1
[status_id] => 5
[question_id] => 240
[name] => b. stwierdzenie mutacji oznacza, że objawy choroby mogą, ale nie muszą wystąpić w przyszłości
[correct] => 1
[ext] =>
[sort] => 860
[correct_yesno] => Tak
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[868] => Array
(
[id] => 868
[site_id] => 1
[status_id] => 5
[question_id] => 240
[name] => c. stwierdzenie mutacji oznacza, że objawy choroby na pewno wystąpią, jest to kwestia czasu
[correct] => 0
[ext] =>
[sort] => 861
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[869] => Array
(
[id] => 869
[site_id] => 1
[status_id] => 5
[question_id] => 240
[name] => d. powinno być poprzedzone poradą genetyczna oraz konsultacja psychologiczną
[correct] => 0
[ext] =>
[sort] => 862
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
[241] => Array
(
[id] => 241
[site_id] => 1
[status_id] => 5
[group_id] => 19
[type_id] => 1
[name] => Które z badań nie ma zastosowania w diagnostyce chorób nerwów obwodowych:
[ext] =>
[sort] => 0
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[type_name] => pojedyncza odpowiedź
[type_code] => single
[answers] => Array
(
[870] => Array
(
[id] => 870
[site_id] => 1
[status_id] => 5
[question_id] => 241
[name] => a. EMG
[correct] => 0
[ext] =>
[sort] => 863
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[871] => Array
(
[id] => 871
[site_id] => 1
[status_id] => 5
[question_id] => 241
[name] => b. Badanie genetyczne
[correct] => 0
[ext] =>
[sort] => 864
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[872] => Array
(
[id] => 872
[site_id] => 1
[status_id] => 5
[question_id] => 241
[name] => c. Rezonans magnetyczny mózgu
[correct] => 0
[ext] =>
[sort] => 865
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[873] => Array
(
[id] => 873
[site_id] => 1
[status_id] => 5
[question_id] => 241
[name] => d. EEG
[correct] => 1
[ext] =>
[sort] => 866
[correct_yesno] => Tak
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
[242] => Array
(
[id] => 242
[site_id] => 1
[status_id] => 5
[group_id] => 19
[type_id] => 1
[name] => Zespół łamliwego chromosomu X:
[ext] =>
[sort] => 0
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[type_name] => pojedyncza odpowiedź
[type_code] => single
[answers] => Array
(
[874] => Array
(
[id] => 874
[site_id] => 1
[status_id] => 5
[question_id] => 242
[name] => a. jest chorobą nie sprzężoną z płcią
[correct] => 0
[ext] =>
[sort] => 867
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[875] => Array
(
[id] => 875
[site_id] => 1
[status_id] => 5
[question_id] => 242
[name] => b. za chorobę odpowiada mutacja dynamiczna w genie FMR1
[correct] => 1
[ext] =>
[sort] => 868
[correct_yesno] => Tak
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[876] => Array
(
[id] => 876
[site_id] => 1
[status_id] => 5
[question_id] => 242
[name] => c. za chorobę odpowiada premutacja w genie FMR1
[correct] => 0
[ext] =>
[sort] => 869
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[877] => Array
(
[id] => 877
[site_id] => 1
[status_id] => 5
[question_id] => 242
[name] => d. wszystkie odpowiedzi są prawidłowe
[correct] => 0
[ext] =>
[sort] => 870
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
[243] => Array
(
[id] => 243
[site_id] => 1
[status_id] => 5
[group_id] => 19
[type_id] => 1
[name] => Neuropatia z nadwrażliwością na ucisk (HNPP) spowodowane jest:
[ext] =>
[sort] => 0
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[type_name] => pojedyncza odpowiedź
[type_code] => single
[answers] => Array
(
[878] => Array
(
[id] => 878
[site_id] => 1
[status_id] => 5
[question_id] => 243
[name] => a. Delecją w genie PMP22
[correct] => 1
[ext] =>
[sort] => 871
[correct_yesno] => Tak
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[879] => Array
(
[id] => 879
[site_id] => 1
[status_id] => 5
[question_id] => 243
[name] => b. Duplikacją genu PMP22
[correct] => 0
[ext] =>
[sort] => 872
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[880] => Array
(
[id] => 880
[site_id] => 1
[status_id] => 5
[question_id] => 243
[name] => c. Może być obrazem przewlekłej neuropatii zapalnej
[correct] => 0
[ext] =>
[sort] => 873
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[881] => Array
(
[id] => 881
[site_id] => 1
[status_id] => 5
[question_id] => 243
[name] => d. Mutacja genu LITA
[correct] => 0
[ext] =>
[sort] => 874
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
[244] => Array
(
[id] => 244
[site_id] => 1
[status_id] => 5
[group_id] => 19
[type_id] => 2
[name] => Zaznacz zdanie nieprawdziwe:
[ext] =>
[sort] => 0
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[type_name] => wielokrotna odpowiedź
[type_code] => multi
[answers] => Array
(
[882] => Array
(
[id] => 882
[site_id] => 1
[status_id] => 5
[question_id] => 244
[name] => a. Niepełnosprawność intelektualną definiuje się jako istotne obniżenie ogólnego funkcjonowania intelektualnego oraz deficyty w zakresie zachowań adaptacyjnych.
[correct] => 0
[ext] =>
[sort] => 875
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[883] => Array
(
[id] => 883
[site_id] => 1
[status_id] => 5
[question_id] => 244
[name] => b. Uważa się, że około 50% przypadków niepełnosprawności intelektualnej w stopniu umiarkowanym i znacznym ma podłoże genetyczne.
[correct] => 0
[ext] =>
[sort] => 876
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[884] => Array
(
[id] => 884
[site_id] => 1
[status_id] => 5
[question_id] => 244
[name] => c. Najczęstszą przyczyną niepełnosprawności intelektualnej są mutacje w pojedynczych genach
[correct] => 1
[ext] =>
[sort] => 877
[correct_yesno] => Tak
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[885] => Array
(
[id] => 885
[site_id] => 1
[status_id] => 5
[question_id] => 244
[name] => d. Zastosowanie w diagnostyce niepełnosprawności intelektualnej wysokoprzepustowych metod analizy (m.in. NGS) pozwoliło na uzyskanie ponad 60% skuteczności diagnostycznej w tej grupie chorób.
[correct] => 0
[ext] =>
[sort] => 878
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
[245] => Array
(
[id] => 245
[site_id] => 1
[status_id] => 5
[group_id] => 19
[type_id] => 1
[name] => Chorobą nerwowo-mięśniową, w której stwierdza się zaburzenia działania połączeń nerwowo-mięśniowych jest:
[ext] =>
[sort] => 0
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[type_name] => pojedyncza odpowiedź
[type_code] => single
[answers] => Array
(
[886] => Array
(
[id] => 886
[site_id] => 1
[status_id] => 5
[question_id] => 245
[name] => a. Rdzeniowy zanik mięśni
[correct] => 0
[ext] =>
[sort] => 879
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[887] => Array
(
[id] => 887
[site_id] => 1
[status_id] => 5
[question_id] => 245
[name] => b. Zespół synaptyczny
[correct] => 1
[ext] =>
[sort] => 880
[correct_yesno] => Tak
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[888] => Array
(
[id] => 888
[site_id] => 1
[status_id] => 5
[question_id] => 245
[name] => c. Dystrofia mięśniowa Beckera
[correct] => 0
[ext] =>
[sort] => 881
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[889] => Array
(
[id] => 889
[site_id] => 1
[status_id] => 5
[question_id] => 245
[name] => d. Dystrofia miotoniczna typu I
[correct] => 0
[ext] =>
[sort] => 882
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
[246] => Array
(
[id] => 246
[site_id] => 1
[status_id] => 5
[group_id] => 19
[type_id] => 1
[name] => Sekwencjonowanie następnej generacji (NGS) stało się ostatnio metodą wykorzystywaną zarówno w diagnostyce jaki identyfikacji nowych genów stanowiących podłoże molekularne chorób genetycznych o dziedziczeniu mendlowskim. W przypadku ciężkich postaci niepełnosprawności intelektualnej i encefalopatii padaczkowych, występujących zazwyczaj sporadycznie. Przy założeniu, że mutacje patogenne mają charakter dominujący i występują de novo często stosuje się tzw. analizę triosów (pacjent + rodzice). Jakie warianty DNA należy brać tu pod uwagę przy rozpatrywaniu mutacji potencjalnie patogennych:
[ext] =>
[sort] => 0
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[type_name] => pojedyncza odpowiedź
[type_code] => single
[answers] => Array
(
[890] => Array
(
[id] => 890
[site_id] => 1
[status_id] => 5
[question_id] => 246
[name] => a. warianty heterozygotyczne występujące w rodzinie pacjenta
[correct] => 0
[ext] =>
[sort] => 883
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[891] => Array
(
[id] => 891
[site_id] => 1
[status_id] => 5
[question_id] => 246
[name] => b. warianty heterozygotyczne złożone (lub homozygotyczne), z których jeden został odziedziczony od rodzica
[correct] => 0
[ext] =>
[sort] => 884
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[892] => Array
(
[id] => 892
[site_id] => 1
[status_id] => 5
[question_id] => 246
[name] => c. warianty heterozygotyczne występujące tylko u chorego dziecka, nie stwierdzane u rodziców
[correct] => 1
[ext] =>
[sort] => 885
[correct_yesno] => Tak
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[893] => Array
(
[id] => 893
[site_id] => 1
[status_id] => 5
[question_id] => 246
[name] => d. wszystkie warianty występujące w genach powiązanych z danym fenotypem
[correct] => 0
[ext] =>
[sort] => 886
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
[247] => Array
(
[id] => 247
[site_id] => 1
[status_id] => 5
[group_id] => 19
[type_id] => 1
[name] => Warianty CNV mające wpływ na wystąpienie zaburzeń ze spektrum autyzmu, zaburzeń zachowania oraz schizofrenii, to zmiany:
[ext] =>
[sort] => 0
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[type_name] => pojedyncza odpowiedź
[type_code] => single
[answers] => Array
(
[894] => Array
(
[id] => 894
[site_id] => 1
[status_id] => 5
[question_id] => 247
[name] => a. zawsze patogenne
[correct] => 0
[ext] =>
[sort] => 887
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[895] => Array
(
[id] => 895
[site_id] => 1
[status_id] => 5
[question_id] => 247
[name] => b. o niepełnej penetracji
[correct] => 0
[ext] =>
[sort] => 888
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[896] => Array
(
[id] => 896
[site_id] => 1
[status_id] => 5
[question_id] => 247
[name] => c. o zmiennej ekspresji
[correct] => 0
[ext] =>
[sort] => 889
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[897] => Array
(
[id] => 897
[site_id] => 1
[status_id] => 5
[question_id] => 247
[name] => d. o niepełnej penetracji i zmiennej ekspresji
[correct] => 1
[ext] =>
[sort] => 890
[correct_yesno] => Tak
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
[248] => Array
(
[id] => 248
[site_id] => 1
[status_id] => 5
[group_id] => 19
[type_id] => 1
[name] => W rodzinie w trzech pokoleniach występuje delecja na chromosomie 1 pary. Jednak nie wszyscy nosiciele tej samej zmiany mają nieprawidłowy fenotyp. Jak należy zakwalifikować delecję:
[ext] =>
[sort] => 0
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[type_name] => pojedyncza odpowiedź
[type_code] => single
[answers] => Array
(
[898] => Array
(
[id] => 898
[site_id] => 1
[status_id] => 5
[question_id] => 248
[name] => a. Jako wariant łagodny
[correct] => 0
[ext] =>
[sort] => 891
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[899] => Array
(
[id] => 899
[site_id] => 1
[status_id] => 5
[question_id] => 248
[name] => b. Jako zmiana o zmiennej ekspresji
[correct] => 0
[ext] =>
[sort] => 892
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[900] => Array
(
[id] => 900
[site_id] => 1
[status_id] => 5
[question_id] => 248
[name] => c. Jako zmiana o niepełnej penetracji
[correct] => 1
[ext] =>
[sort] => 893
[correct_yesno] => Tak
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[901] => Array
(
[id] => 901
[site_id] => 1
[status_id] => 5
[question_id] => 248
[name] => d. Jako zmiana o nieznanym znaczeniu klinicznym
[correct] => 0
[ext] =>
[sort] => 894
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
[249] => Array
(
[id] => 249
[site_id] => 1
[status_id] => 5
[group_id] => 19
[type_id] => 1
[name] => Warianty o zmiennej ekspresji:
[ext] =>
[sort] => 0
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[type_name] => pojedyncza odpowiedź
[type_code] => single
[answers] => Array
(
[902] => Array
(
[id] => 902
[site_id] => 1
[status_id] => 5
[question_id] => 249
[name] => a. Mogą objawiać się zróżnicowanym obrazem klinicznym, ale wszyscy nosiciele tej zmiany mają nieprawidłowy fenotyp.
[correct] => 1
[ext] =>
[sort] => 895
[correct_yesno] => Tak
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[903] => Array
(
[id] => 903
[site_id] => 1
[status_id] => 5
[question_id] => 249
[name] => b. Mogą objawiać się zróżnicowanym obrazem klinicznym, ale część nosicieli tej zmiany ma prawidłowy fenotyp.
[correct] => 0
[ext] =>
[sort] => 896
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[904] => Array
(
[id] => 904
[site_id] => 1
[status_id] => 5
[question_id] => 249
[name] => c. U wszystkich nosicieli powodują taki sam obraz kliniczny.
[correct] => 0
[ext] =>
[sort] => 897
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
[905] => Array
(
[id] => 905
[site_id] => 1
[status_id] => 5
[question_id] => 249
[name] => d. U większości nosicieli nie powodują nieprawidłowego fenotypu.
[correct] => 0
[ext] =>
[sort] => 898
[correct_yesno] => Nie
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
)
[quiz_active] => 0
[materials_count] => 14
)
[20] => Array
(
[id] => 20
[block_id] => 5
[name] => Genetyka i genomika w codziennej praktyce lekarskiej.
[sort] => 1
[status_code] => active
[authors] => Array
(
[0] => dr n. med. Sylwia Rzońca
)
[authors_data] => Array
(
[0] => Array
(
[id] => 10
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Sylwia Rzońca
[firstname] => Sylwia
[lastname] => Rzońca
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 10-sylwia_rzonca
[url] => eksperci/10-sylwia_rzonca
)
)
[authors_ids] => Array
(
[0] => 10
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
[url] => kursy/20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
[materials] => Array
(
[400] => Array
(
[id] => 400
[name] => Heterogenność podłoża genetycznego chorób mitochondrialnych.
[type_id] => 1
[group_id] => 20
[problem_id] => 0
[date_publish] => 2023-01-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/400/posterprakt_lek.png
[video] => resources/data/material/400/7_3_heterogennosc_podloza_molekularnego_k.tonska.mp4
[content] =>
[ext] => Array
(
[files_header] =>
[linked] => Array
(
[159] => Array
(
[id] => 159
[site_id] => 1
[status_id] => 5
[name] => Zmienność kliniczna i genetyczna niepełnosprawności intelektualnej
[type_id] => 1
[group_id] => 20
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/159/posterprakt_lek.png
[video] => resources/data/material/159/zmiennosc_kliniczna_i_genetyczna_niepelnosprawnosci_intelektualnej_rzonca.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Sylwia Rzońca
)
[authors_data] => Array
(
[0] => Array
(
[id] => 10
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Sylwia Rzońca
[firstname] => Sylwia
[lastname] => Rzońca
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 10-sylwia_rzonca
[url] => eksperci/10-sylwia_rzonca
)
)
[authors_ids] => Array
(
[0] => 10
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 159-zmiennosc_kliniczna_i_genetyczna_niepelnosprawnosci_intelektualnej
[url] => wideo/159-zmiennosc_kliniczna_i_genetyczna_niepelnosprawnosci_intelektualnej
[short_name] => Zmienność kliniczna i genetyczna niepełnosprawnośc...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 20
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika w codziennej praktyce lekarskiej.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Sylwia Rzońca
)
[authors_data] => Array
(
[0] => Array
(
[id] => 10
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Sylwia Rzońca
[firstname] => Sylwia
[lastname] => Rzońca
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 10-sylwia_rzonca
[url] => eksperci/10-sylwia_rzonca
)
)
[authors_ids] => Array
(
[0] => 10
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
[url] => kursy/20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[160] => Array
(
[id] => 160
[site_id] => 1
[status_id] => 5
[name] => Podłoże molekularne neurofibromatozy typu I –możliwości diagnostyczne
[type_id] => 1
[group_id] => 20
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/160/posterprakt_lek.png
[video] => resources/data/material/160/6_2_podloze_molekularne_neurofibromatozy_a.abramowicz.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => mgr Anna Abramowicz
)
[authors_data] => Array
(
[0] => Array
(
[id] => 71
[site_id] => 1
[status_id] => 5
[name] => mgr Anna Abramowicz
[firstname] => Anna
[lastname] => Abramowicz
[title] => mgr
[affiliation] => Zakład Genetyki Medycznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 71-anna_abramowicz
[url] => eksperci/71-anna_abramowicz
)
)
[authors_ids] => Array
(
[0] => 71
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 160-podloze_molekularne_neurofibromatozy_typu_i_mozliwosci_diagnostyczne
[url] => wideo/160-podloze_molekularne_neurofibromatozy_typu_i_mozliwosci_diagnostyczne
[short_name] => Podłoże molekularne neurofibromatozy typu I –możli...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 20
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika w codziennej praktyce lekarskiej.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Sylwia Rzońca
)
[authors_data] => Array
(
[0] => Array
(
[id] => 10
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Sylwia Rzońca
[firstname] => Sylwia
[lastname] => Rzońca
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 10-sylwia_rzonca
[url] => eksperci/10-sylwia_rzonca
)
)
[authors_ids] => Array
(
[0] => 10
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
[url] => kursy/20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[162] => Array
(
[id] => 162
[site_id] => 1
[status_id] => 5
[name] => Choroby neurodegeneracyjne wieku późnego - idiopatyczne i genetyczne
[type_id] => 1
[group_id] => 20
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/162/posterprakt_lek.png
[video] => resources/data/material/162/5_choroby_neurologiczne_o_poznym_wieku_zachorowania_d.hoffman.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 162-choroby_neurodegeneracyjne_wieku_poznego___idiopatyczne_i_genetyczne
[url] => wideo/162-choroby_neurodegeneracyjne_wieku_poznego___idiopatyczne_i_genetyczne
[short_name] => Choroby neurodegeneracyjne wieku późnego - idiopat...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 20
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika w codziennej praktyce lekarskiej.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Sylwia Rzońca
)
[authors_data] => Array
(
[0] => Array
(
[id] => 10
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Sylwia Rzońca
[firstname] => Sylwia
[lastname] => Rzońca
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 10-sylwia_rzonca
[url] => eksperci/10-sylwia_rzonca
)
)
[authors_ids] => Array
(
[0] => 10
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
[url] => kursy/20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[163] => Array
(
[id] => 163
[site_id] => 1
[status_id] => 5
[name] => Mukowiscydoza i nie tylko. Choroby uwarunkowane mutacjami genu CFTR.
[type_id] => 1
[group_id] => 20
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/163/posterprakt_lek.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 14
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 163-mukowiscydoza_i_nie_tylko_choroby_uwarunkowane_mutacjami_genu_cftr
[url] => wideo/163-mukowiscydoza_i_nie_tylko_choroby_uwarunkowane_mutacjami_genu_cftr
[short_name] => Mukowiscydoza i nie tylko. Choroby uwarunkowane mu...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 20
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika w codziennej praktyce lekarskiej.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Sylwia Rzońca
)
[authors_data] => Array
(
[0] => Array
(
[id] => 10
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Sylwia Rzońca
[firstname] => Sylwia
[lastname] => Rzońca
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 10-sylwia_rzonca
[url] => eksperci/10-sylwia_rzonca
)
)
[authors_ids] => Array
(
[0] => 10
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
[url] => kursy/20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[14] => Array
(
[id] => 14
[site_id] => 1
[status_id] => 5
[name] => choroby rzadkie
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 14-choroby_rzadkie
[url] => /14-choroby_rzadkie
)
)
[artykuly] => Array
(
)
)
[164] => Array
(
[id] => 164
[site_id] => 1
[status_id] => 5
[name] => Genetyka klasyczna - wzory dziedziczenia
[type_id] => 1
[group_id] => 20
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/164/posterprakt_lek.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 164-genetyka_klasyczna___wzory_dziedziczenia
[url] => wideo/164-genetyka_klasyczna___wzory_dziedziczenia
[short_name] => Genetyka klasyczna - wzory dziedziczenia
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 20
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika w codziennej praktyce lekarskiej.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Sylwia Rzońca
)
[authors_data] => Array
(
[0] => Array
(
[id] => 10
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Sylwia Rzońca
[firstname] => Sylwia
[lastname] => Rzońca
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 10-sylwia_rzonca
[url] => eksperci/10-sylwia_rzonca
)
)
[authors_ids] => Array
(
[0] => 10
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
[url] => kursy/20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[165] => Array
(
[id] => 165
[site_id] => 1
[status_id] => 5
[name] => Genetyka molekularna -zmienność materiału genetycznego
[type_id] => 1
[group_id] => 20
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/165/posterprakt_lek.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med., prof IMiD Monika Gos
)
[authors_data] => Array
(
[0] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => dr n. med., prof IMiD Monika Gos
[firstname] => Monika
[lastname] => Gos
[title] => dr n. med., prof IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-monika_gos
[url] => eksperci/13-monika_gos
)
)
[authors_ids] => Array
(
[0] => 13
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 165-genetyka_molekularna__zmiennosc_materialu_genetycznego
[url] => wideo/165-genetyka_molekularna__zmiennosc_materialu_genetycznego
[short_name] => Genetyka molekularna -zmienność materiału genetycz...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 20
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika w codziennej praktyce lekarskiej.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Sylwia Rzońca
)
[authors_data] => Array
(
[0] => Array
(
[id] => 10
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Sylwia Rzońca
[firstname] => Sylwia
[lastname] => Rzońca
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 10-sylwia_rzonca
[url] => eksperci/10-sylwia_rzonca
)
)
[authors_ids] => Array
(
[0] => 10
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
[url] => kursy/20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
)
)
[sort] => 0
[status_code] => active
[authors] => Array
(
[0] => dr hab. Katarzyna Tońska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 95
[site_id] => 1
[status_id] => 5
[name] => dr hab. Katarzyna Tońska
[firstname] => Katarzyna
[lastname] => Tońska
[title] => dr hab.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 95-katarzyna_tonska
[url] => eksperci/95-katarzyna_tonska
)
)
[authors_ids] => Array
(
[0] => 95
)
[topics] => Array
(
[0] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 400-heterogennosc_podloza_genetycznego_chorob_mitochondrialnych
[url] => wideo/400-heterogennosc_podloza_genetycznego_chorob_mitochondrialnych
[short_name] => Heterogenność podłoża genetycznego chorób mitochon...
[date_publish_pl] => 4 stycznia 2023 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 20
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika w codziennej praktyce lekarskiej.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Sylwia Rzońca
)
[authors_data] => Array
(
[0] => Array
(
[id] => 10
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Sylwia Rzońca
[firstname] => Sylwia
[lastname] => Rzońca
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 10-sylwia_rzonca
[url] => eksperci/10-sylwia_rzonca
)
)
[authors_ids] => Array
(
[0] => 10
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
[url] => kursy/20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
)
[topics_data] => Array
(
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
[logotypy] => Array
(
)
[pliki] => Array
(
)
)
[159] => Array
(
[id] => 159
[name] => Zmienność kliniczna i genetyczna niepełnosprawności intelektualnej
[type_id] => 1
[group_id] => 20
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/159/posterprakt_lek.png
[video] => resources/data/material/159/zmiennosc_kliniczna_i_genetyczna_niepelnosprawnosci_intelektualnej_rzonca.mp4
[content] =>
[ext] => Array
(
[files_header] =>
[linked] => Array
(
[400] => Array
(
[id] => 400
[site_id] => 1
[status_id] => 5
[name] => Heterogenność podłoża genetycznego chorób mitochondrialnych.
[type_id] => 1
[group_id] => 20
[problem_id] => 0
[date_publish] => 2023-01-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/400/posterprakt_lek.png
[video] => resources/data/material/400/7_3_heterogennosc_podloza_molekularnego_k.tonska.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 0
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab. Katarzyna Tońska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 95
[site_id] => 1
[status_id] => 5
[name] => dr hab. Katarzyna Tońska
[firstname] => Katarzyna
[lastname] => Tońska
[title] => dr hab.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 95-katarzyna_tonska
[url] => eksperci/95-katarzyna_tonska
)
)
[authors_ids] => Array
(
[0] => 95
)
[topics] => Array
(
[0] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 400-heterogennosc_podloza_genetycznego_chorob_mitochondrialnych
[url] => wideo/400-heterogennosc_podloza_genetycznego_chorob_mitochondrialnych
[short_name] => Heterogenność podłoża genetycznego chorób mitochon...
[date_publish_pl] => 4 stycznia 2023 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 20
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika w codziennej praktyce lekarskiej.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Sylwia Rzońca
)
[authors_data] => Array
(
[0] => Array
(
[id] => 10
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Sylwia Rzońca
[firstname] => Sylwia
[lastname] => Rzońca
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 10-sylwia_rzonca
[url] => eksperci/10-sylwia_rzonca
)
)
[authors_ids] => Array
(
[0] => 10
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
[url] => kursy/20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
)
[topics_data] => Array
(
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[160] => Array
(
[id] => 160
[site_id] => 1
[status_id] => 5
[name] => Podłoże molekularne neurofibromatozy typu I –możliwości diagnostyczne
[type_id] => 1
[group_id] => 20
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/160/posterprakt_lek.png
[video] => resources/data/material/160/6_2_podloze_molekularne_neurofibromatozy_a.abramowicz.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => mgr Anna Abramowicz
)
[authors_data] => Array
(
[0] => Array
(
[id] => 71
[site_id] => 1
[status_id] => 5
[name] => mgr Anna Abramowicz
[firstname] => Anna
[lastname] => Abramowicz
[title] => mgr
[affiliation] => Zakład Genetyki Medycznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 71-anna_abramowicz
[url] => eksperci/71-anna_abramowicz
)
)
[authors_ids] => Array
(
[0] => 71
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 160-podloze_molekularne_neurofibromatozy_typu_i_mozliwosci_diagnostyczne
[url] => wideo/160-podloze_molekularne_neurofibromatozy_typu_i_mozliwosci_diagnostyczne
[short_name] => Podłoże molekularne neurofibromatozy typu I –możli...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 20
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika w codziennej praktyce lekarskiej.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Sylwia Rzońca
)
[authors_data] => Array
(
[0] => Array
(
[id] => 10
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Sylwia Rzońca
[firstname] => Sylwia
[lastname] => Rzońca
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 10-sylwia_rzonca
[url] => eksperci/10-sylwia_rzonca
)
)
[authors_ids] => Array
(
[0] => 10
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
[url] => kursy/20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[162] => Array
(
[id] => 162
[site_id] => 1
[status_id] => 5
[name] => Choroby neurodegeneracyjne wieku późnego - idiopatyczne i genetyczne
[type_id] => 1
[group_id] => 20
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/162/posterprakt_lek.png
[video] => resources/data/material/162/5_choroby_neurologiczne_o_poznym_wieku_zachorowania_d.hoffman.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 162-choroby_neurodegeneracyjne_wieku_poznego___idiopatyczne_i_genetyczne
[url] => wideo/162-choroby_neurodegeneracyjne_wieku_poznego___idiopatyczne_i_genetyczne
[short_name] => Choroby neurodegeneracyjne wieku późnego - idiopat...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 20
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika w codziennej praktyce lekarskiej.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Sylwia Rzońca
)
[authors_data] => Array
(
[0] => Array
(
[id] => 10
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Sylwia Rzońca
[firstname] => Sylwia
[lastname] => Rzońca
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 10-sylwia_rzonca
[url] => eksperci/10-sylwia_rzonca
)
)
[authors_ids] => Array
(
[0] => 10
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
[url] => kursy/20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[163] => Array
(
[id] => 163
[site_id] => 1
[status_id] => 5
[name] => Mukowiscydoza i nie tylko. Choroby uwarunkowane mutacjami genu CFTR.
[type_id] => 1
[group_id] => 20
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/163/posterprakt_lek.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 14
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 163-mukowiscydoza_i_nie_tylko_choroby_uwarunkowane_mutacjami_genu_cftr
[url] => wideo/163-mukowiscydoza_i_nie_tylko_choroby_uwarunkowane_mutacjami_genu_cftr
[short_name] => Mukowiscydoza i nie tylko. Choroby uwarunkowane mu...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 20
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika w codziennej praktyce lekarskiej.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Sylwia Rzońca
)
[authors_data] => Array
(
[0] => Array
(
[id] => 10
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Sylwia Rzońca
[firstname] => Sylwia
[lastname] => Rzońca
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 10-sylwia_rzonca
[url] => eksperci/10-sylwia_rzonca
)
)
[authors_ids] => Array
(
[0] => 10
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
[url] => kursy/20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[14] => Array
(
[id] => 14
[site_id] => 1
[status_id] => 5
[name] => choroby rzadkie
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 14-choroby_rzadkie
[url] => /14-choroby_rzadkie
)
)
[artykuly] => Array
(
)
)
[164] => Array
(
[id] => 164
[site_id] => 1
[status_id] => 5
[name] => Genetyka klasyczna - wzory dziedziczenia
[type_id] => 1
[group_id] => 20
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/164/posterprakt_lek.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 164-genetyka_klasyczna___wzory_dziedziczenia
[url] => wideo/164-genetyka_klasyczna___wzory_dziedziczenia
[short_name] => Genetyka klasyczna - wzory dziedziczenia
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 20
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika w codziennej praktyce lekarskiej.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Sylwia Rzońca
)
[authors_data] => Array
(
[0] => Array
(
[id] => 10
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Sylwia Rzońca
[firstname] => Sylwia
[lastname] => Rzońca
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 10-sylwia_rzonca
[url] => eksperci/10-sylwia_rzonca
)
)
[authors_ids] => Array
(
[0] => 10
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
[url] => kursy/20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[165] => Array
(
[id] => 165
[site_id] => 1
[status_id] => 5
[name] => Genetyka molekularna -zmienność materiału genetycznego
[type_id] => 1
[group_id] => 20
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/165/posterprakt_lek.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med., prof IMiD Monika Gos
)
[authors_data] => Array
(
[0] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => dr n. med., prof IMiD Monika Gos
[firstname] => Monika
[lastname] => Gos
[title] => dr n. med., prof IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-monika_gos
[url] => eksperci/13-monika_gos
)
)
[authors_ids] => Array
(
[0] => 13
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 165-genetyka_molekularna__zmiennosc_materialu_genetycznego
[url] => wideo/165-genetyka_molekularna__zmiennosc_materialu_genetycznego
[short_name] => Genetyka molekularna -zmienność materiału genetycz...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 20
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika w codziennej praktyce lekarskiej.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Sylwia Rzońca
)
[authors_data] => Array
(
[0] => Array
(
[id] => 10
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Sylwia Rzońca
[firstname] => Sylwia
[lastname] => Rzońca
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 10-sylwia_rzonca
[url] => eksperci/10-sylwia_rzonca
)
)
[authors_ids] => Array
(
[0] => 10
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
[url] => kursy/20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
)
)
[sort] => 1
[status_code] => active
[authors] => Array
(
[0] => dr n. med. Sylwia Rzońca
)
[authors_data] => Array
(
[0] => Array
(
[id] => 10
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Sylwia Rzońca
[firstname] => Sylwia
[lastname] => Rzońca
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 10-sylwia_rzonca
[url] => eksperci/10-sylwia_rzonca
)
)
[authors_ids] => Array
(
[0] => 10
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 159-zmiennosc_kliniczna_i_genetyczna_niepelnosprawnosci_intelektualnej
[url] => wideo/159-zmiennosc_kliniczna_i_genetyczna_niepelnosprawnosci_intelektualnej
[short_name] => Zmienność kliniczna i genetyczna niepełnosprawnośc...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 20
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika w codziennej praktyce lekarskiej.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Sylwia Rzońca
)
[authors_data] => Array
(
[0] => Array
(
[id] => 10
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Sylwia Rzońca
[firstname] => Sylwia
[lastname] => Rzońca
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 10-sylwia_rzonca
[url] => eksperci/10-sylwia_rzonca
)
)
[authors_ids] => Array
(
[0] => 10
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
[url] => kursy/20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
[logotypy] => Array
(
)
[pliki] => Array
(
[128] => Array
(
[id] => 128
[site_id] => 1
[status_id] => 5
[entity_key] => material
[entity_id] => 159
[name] => Zmienność kliniczna i genetyczna niepełnosprawności intelektualnej
[file] => resources/data/pliki/material/159/23.06_mat_w3_srzn.pdf
[sort] => 125
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
[160] => Array
(
[id] => 160
[name] => Podłoże molekularne neurofibromatozy typu I –możliwości diagnostyczne
[type_id] => 1
[group_id] => 20
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/160/posterprakt_lek.png
[video] => resources/data/material/160/6_2_podloze_molekularne_neurofibromatozy_a.abramowicz.mp4
[content] =>
[ext] => Array
(
[files_header] =>
[linked] => Array
(
[400] => Array
(
[id] => 400
[site_id] => 1
[status_id] => 5
[name] => Heterogenność podłoża genetycznego chorób mitochondrialnych.
[type_id] => 1
[group_id] => 20
[problem_id] => 0
[date_publish] => 2023-01-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/400/posterprakt_lek.png
[video] => resources/data/material/400/7_3_heterogennosc_podloza_molekularnego_k.tonska.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 0
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab. Katarzyna Tońska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 95
[site_id] => 1
[status_id] => 5
[name] => dr hab. Katarzyna Tońska
[firstname] => Katarzyna
[lastname] => Tońska
[title] => dr hab.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 95-katarzyna_tonska
[url] => eksperci/95-katarzyna_tonska
)
)
[authors_ids] => Array
(
[0] => 95
)
[topics] => Array
(
[0] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 400-heterogennosc_podloza_genetycznego_chorob_mitochondrialnych
[url] => wideo/400-heterogennosc_podloza_genetycznego_chorob_mitochondrialnych
[short_name] => Heterogenność podłoża genetycznego chorób mitochon...
[date_publish_pl] => 4 stycznia 2023 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 20
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika w codziennej praktyce lekarskiej.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Sylwia Rzońca
)
[authors_data] => Array
(
[0] => Array
(
[id] => 10
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Sylwia Rzońca
[firstname] => Sylwia
[lastname] => Rzońca
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 10-sylwia_rzonca
[url] => eksperci/10-sylwia_rzonca
)
)
[authors_ids] => Array
(
[0] => 10
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
[url] => kursy/20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
)
[topics_data] => Array
(
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[159] => Array
(
[id] => 159
[site_id] => 1
[status_id] => 5
[name] => Zmienność kliniczna i genetyczna niepełnosprawności intelektualnej
[type_id] => 1
[group_id] => 20
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/159/posterprakt_lek.png
[video] => resources/data/material/159/zmiennosc_kliniczna_i_genetyczna_niepelnosprawnosci_intelektualnej_rzonca.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Sylwia Rzońca
)
[authors_data] => Array
(
[0] => Array
(
[id] => 10
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Sylwia Rzońca
[firstname] => Sylwia
[lastname] => Rzońca
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 10-sylwia_rzonca
[url] => eksperci/10-sylwia_rzonca
)
)
[authors_ids] => Array
(
[0] => 10
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 159-zmiennosc_kliniczna_i_genetyczna_niepelnosprawnosci_intelektualnej
[url] => wideo/159-zmiennosc_kliniczna_i_genetyczna_niepelnosprawnosci_intelektualnej
[short_name] => Zmienność kliniczna i genetyczna niepełnosprawnośc...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 20
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika w codziennej praktyce lekarskiej.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Sylwia Rzońca
)
[authors_data] => Array
(
[0] => Array
(
[id] => 10
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Sylwia Rzońca
[firstname] => Sylwia
[lastname] => Rzońca
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 10-sylwia_rzonca
[url] => eksperci/10-sylwia_rzonca
)
)
[authors_ids] => Array
(
[0] => 10
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
[url] => kursy/20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[162] => Array
(
[id] => 162
[site_id] => 1
[status_id] => 5
[name] => Choroby neurodegeneracyjne wieku późnego - idiopatyczne i genetyczne
[type_id] => 1
[group_id] => 20
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/162/posterprakt_lek.png
[video] => resources/data/material/162/5_choroby_neurologiczne_o_poznym_wieku_zachorowania_d.hoffman.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 162-choroby_neurodegeneracyjne_wieku_poznego___idiopatyczne_i_genetyczne
[url] => wideo/162-choroby_neurodegeneracyjne_wieku_poznego___idiopatyczne_i_genetyczne
[short_name] => Choroby neurodegeneracyjne wieku późnego - idiopat...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 20
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika w codziennej praktyce lekarskiej.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Sylwia Rzońca
)
[authors_data] => Array
(
[0] => Array
(
[id] => 10
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Sylwia Rzońca
[firstname] => Sylwia
[lastname] => Rzońca
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 10-sylwia_rzonca
[url] => eksperci/10-sylwia_rzonca
)
)
[authors_ids] => Array
(
[0] => 10
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
[url] => kursy/20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[163] => Array
(
[id] => 163
[site_id] => 1
[status_id] => 5
[name] => Mukowiscydoza i nie tylko. Choroby uwarunkowane mutacjami genu CFTR.
[type_id] => 1
[group_id] => 20
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/163/posterprakt_lek.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 14
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 163-mukowiscydoza_i_nie_tylko_choroby_uwarunkowane_mutacjami_genu_cftr
[url] => wideo/163-mukowiscydoza_i_nie_tylko_choroby_uwarunkowane_mutacjami_genu_cftr
[short_name] => Mukowiscydoza i nie tylko. Choroby uwarunkowane mu...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 20
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika w codziennej praktyce lekarskiej.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Sylwia Rzońca
)
[authors_data] => Array
(
[0] => Array
(
[id] => 10
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Sylwia Rzońca
[firstname] => Sylwia
[lastname] => Rzońca
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 10-sylwia_rzonca
[url] => eksperci/10-sylwia_rzonca
)
)
[authors_ids] => Array
(
[0] => 10
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
[url] => kursy/20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[14] => Array
(
[id] => 14
[site_id] => 1
[status_id] => 5
[name] => choroby rzadkie
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 14-choroby_rzadkie
[url] => /14-choroby_rzadkie
)
)
[artykuly] => Array
(
)
)
[164] => Array
(
[id] => 164
[site_id] => 1
[status_id] => 5
[name] => Genetyka klasyczna - wzory dziedziczenia
[type_id] => 1
[group_id] => 20
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/164/posterprakt_lek.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 164-genetyka_klasyczna___wzory_dziedziczenia
[url] => wideo/164-genetyka_klasyczna___wzory_dziedziczenia
[short_name] => Genetyka klasyczna - wzory dziedziczenia
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 20
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika w codziennej praktyce lekarskiej.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Sylwia Rzońca
)
[authors_data] => Array
(
[0] => Array
(
[id] => 10
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Sylwia Rzońca
[firstname] => Sylwia
[lastname] => Rzońca
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 10-sylwia_rzonca
[url] => eksperci/10-sylwia_rzonca
)
)
[authors_ids] => Array
(
[0] => 10
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
[url] => kursy/20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[165] => Array
(
[id] => 165
[site_id] => 1
[status_id] => 5
[name] => Genetyka molekularna -zmienność materiału genetycznego
[type_id] => 1
[group_id] => 20
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/165/posterprakt_lek.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med., prof IMiD Monika Gos
)
[authors_data] => Array
(
[0] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => dr n. med., prof IMiD Monika Gos
[firstname] => Monika
[lastname] => Gos
[title] => dr n. med., prof IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-monika_gos
[url] => eksperci/13-monika_gos
)
)
[authors_ids] => Array
(
[0] => 13
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 165-genetyka_molekularna__zmiennosc_materialu_genetycznego
[url] => wideo/165-genetyka_molekularna__zmiennosc_materialu_genetycznego
[short_name] => Genetyka molekularna -zmienność materiału genetycz...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 20
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika w codziennej praktyce lekarskiej.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Sylwia Rzońca
)
[authors_data] => Array
(
[0] => Array
(
[id] => 10
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Sylwia Rzońca
[firstname] => Sylwia
[lastname] => Rzońca
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 10-sylwia_rzonca
[url] => eksperci/10-sylwia_rzonca
)
)
[authors_ids] => Array
(
[0] => 10
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
[url] => kursy/20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
)
)
[sort] => 1
[status_code] => active
[authors] => Array
(
[0] => mgr Anna Abramowicz
)
[authors_data] => Array
(
[0] => Array
(
[id] => 71
[site_id] => 1
[status_id] => 5
[name] => mgr Anna Abramowicz
[firstname] => Anna
[lastname] => Abramowicz
[title] => mgr
[affiliation] => Zakład Genetyki Medycznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 71-anna_abramowicz
[url] => eksperci/71-anna_abramowicz
)
)
[authors_ids] => Array
(
[0] => 71
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 160-podloze_molekularne_neurofibromatozy_typu_i_mozliwosci_diagnostyczne
[url] => wideo/160-podloze_molekularne_neurofibromatozy_typu_i_mozliwosci_diagnostyczne
[short_name] => Podłoże molekularne neurofibromatozy typu I –możli...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 20
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika w codziennej praktyce lekarskiej.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Sylwia Rzońca
)
[authors_data] => Array
(
[0] => Array
(
[id] => 10
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Sylwia Rzońca
[firstname] => Sylwia
[lastname] => Rzońca
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 10-sylwia_rzonca
[url] => eksperci/10-sylwia_rzonca
)
)
[authors_ids] => Array
(
[0] => 10
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
[url] => kursy/20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
[logotypy] => Array
(
)
[pliki] => Array
(
[129] => Array
(
[id] => 129
[site_id] => 1
[status_id] => 5
[entity_key] => material
[entity_id] => 160
[name] => Podłoże molekularne neurofibromatozy typu I –możliwości diagnostyczne
[file] => resources/data/pliki/material/160/23.06_mat_w7_aa_06.2020.pdf
[sort] => 126
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
[162] => Array
(
[id] => 162
[name] => Choroby neurodegeneracyjne wieku późnego - idiopatyczne i genetyczne
[type_id] => 1
[group_id] => 20
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/162/posterprakt_lek.png
[video] => resources/data/material/162/5_choroby_neurologiczne_o_poznym_wieku_zachorowania_d.hoffman.mp4
[content] =>
[ext] => Array
(
[files_header] =>
[linked] => Array
(
[400] => Array
(
[id] => 400
[site_id] => 1
[status_id] => 5
[name] => Heterogenność podłoża genetycznego chorób mitochondrialnych.
[type_id] => 1
[group_id] => 20
[problem_id] => 0
[date_publish] => 2023-01-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/400/posterprakt_lek.png
[video] => resources/data/material/400/7_3_heterogennosc_podloza_molekularnego_k.tonska.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 0
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab. Katarzyna Tońska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 95
[site_id] => 1
[status_id] => 5
[name] => dr hab. Katarzyna Tońska
[firstname] => Katarzyna
[lastname] => Tońska
[title] => dr hab.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 95-katarzyna_tonska
[url] => eksperci/95-katarzyna_tonska
)
)
[authors_ids] => Array
(
[0] => 95
)
[topics] => Array
(
[0] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 400-heterogennosc_podloza_genetycznego_chorob_mitochondrialnych
[url] => wideo/400-heterogennosc_podloza_genetycznego_chorob_mitochondrialnych
[short_name] => Heterogenność podłoża genetycznego chorób mitochon...
[date_publish_pl] => 4 stycznia 2023 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 20
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika w codziennej praktyce lekarskiej.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Sylwia Rzońca
)
[authors_data] => Array
(
[0] => Array
(
[id] => 10
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Sylwia Rzońca
[firstname] => Sylwia
[lastname] => Rzońca
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 10-sylwia_rzonca
[url] => eksperci/10-sylwia_rzonca
)
)
[authors_ids] => Array
(
[0] => 10
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
[url] => kursy/20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
)
[topics_data] => Array
(
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[159] => Array
(
[id] => 159
[site_id] => 1
[status_id] => 5
[name] => Zmienność kliniczna i genetyczna niepełnosprawności intelektualnej
[type_id] => 1
[group_id] => 20
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/159/posterprakt_lek.png
[video] => resources/data/material/159/zmiennosc_kliniczna_i_genetyczna_niepelnosprawnosci_intelektualnej_rzonca.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Sylwia Rzońca
)
[authors_data] => Array
(
[0] => Array
(
[id] => 10
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Sylwia Rzońca
[firstname] => Sylwia
[lastname] => Rzońca
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 10-sylwia_rzonca
[url] => eksperci/10-sylwia_rzonca
)
)
[authors_ids] => Array
(
[0] => 10
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 159-zmiennosc_kliniczna_i_genetyczna_niepelnosprawnosci_intelektualnej
[url] => wideo/159-zmiennosc_kliniczna_i_genetyczna_niepelnosprawnosci_intelektualnej
[short_name] => Zmienność kliniczna i genetyczna niepełnosprawnośc...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 20
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika w codziennej praktyce lekarskiej.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Sylwia Rzońca
)
[authors_data] => Array
(
[0] => Array
(
[id] => 10
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Sylwia Rzońca
[firstname] => Sylwia
[lastname] => Rzońca
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 10-sylwia_rzonca
[url] => eksperci/10-sylwia_rzonca
)
)
[authors_ids] => Array
(
[0] => 10
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
[url] => kursy/20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[160] => Array
(
[id] => 160
[site_id] => 1
[status_id] => 5
[name] => Podłoże molekularne neurofibromatozy typu I –możliwości diagnostyczne
[type_id] => 1
[group_id] => 20
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/160/posterprakt_lek.png
[video] => resources/data/material/160/6_2_podloze_molekularne_neurofibromatozy_a.abramowicz.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => mgr Anna Abramowicz
)
[authors_data] => Array
(
[0] => Array
(
[id] => 71
[site_id] => 1
[status_id] => 5
[name] => mgr Anna Abramowicz
[firstname] => Anna
[lastname] => Abramowicz
[title] => mgr
[affiliation] => Zakład Genetyki Medycznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 71-anna_abramowicz
[url] => eksperci/71-anna_abramowicz
)
)
[authors_ids] => Array
(
[0] => 71
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 160-podloze_molekularne_neurofibromatozy_typu_i_mozliwosci_diagnostyczne
[url] => wideo/160-podloze_molekularne_neurofibromatozy_typu_i_mozliwosci_diagnostyczne
[short_name] => Podłoże molekularne neurofibromatozy typu I –możli...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 20
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika w codziennej praktyce lekarskiej.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Sylwia Rzońca
)
[authors_data] => Array
(
[0] => Array
(
[id] => 10
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Sylwia Rzońca
[firstname] => Sylwia
[lastname] => Rzońca
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 10-sylwia_rzonca
[url] => eksperci/10-sylwia_rzonca
)
)
[authors_ids] => Array
(
[0] => 10
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
[url] => kursy/20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[163] => Array
(
[id] => 163
[site_id] => 1
[status_id] => 5
[name] => Mukowiscydoza i nie tylko. Choroby uwarunkowane mutacjami genu CFTR.
[type_id] => 1
[group_id] => 20
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/163/posterprakt_lek.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 14
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 163-mukowiscydoza_i_nie_tylko_choroby_uwarunkowane_mutacjami_genu_cftr
[url] => wideo/163-mukowiscydoza_i_nie_tylko_choroby_uwarunkowane_mutacjami_genu_cftr
[short_name] => Mukowiscydoza i nie tylko. Choroby uwarunkowane mu...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 20
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika w codziennej praktyce lekarskiej.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Sylwia Rzońca
)
[authors_data] => Array
(
[0] => Array
(
[id] => 10
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Sylwia Rzońca
[firstname] => Sylwia
[lastname] => Rzońca
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 10-sylwia_rzonca
[url] => eksperci/10-sylwia_rzonca
)
)
[authors_ids] => Array
(
[0] => 10
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
[url] => kursy/20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[14] => Array
(
[id] => 14
[site_id] => 1
[status_id] => 5
[name] => choroby rzadkie
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 14-choroby_rzadkie
[url] => /14-choroby_rzadkie
)
)
[artykuly] => Array
(
)
)
[164] => Array
(
[id] => 164
[site_id] => 1
[status_id] => 5
[name] => Genetyka klasyczna - wzory dziedziczenia
[type_id] => 1
[group_id] => 20
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/164/posterprakt_lek.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 164-genetyka_klasyczna___wzory_dziedziczenia
[url] => wideo/164-genetyka_klasyczna___wzory_dziedziczenia
[short_name] => Genetyka klasyczna - wzory dziedziczenia
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 20
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika w codziennej praktyce lekarskiej.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Sylwia Rzońca
)
[authors_data] => Array
(
[0] => Array
(
[id] => 10
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Sylwia Rzońca
[firstname] => Sylwia
[lastname] => Rzońca
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 10-sylwia_rzonca
[url] => eksperci/10-sylwia_rzonca
)
)
[authors_ids] => Array
(
[0] => 10
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
[url] => kursy/20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[165] => Array
(
[id] => 165
[site_id] => 1
[status_id] => 5
[name] => Genetyka molekularna -zmienność materiału genetycznego
[type_id] => 1
[group_id] => 20
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/165/posterprakt_lek.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med., prof IMiD Monika Gos
)
[authors_data] => Array
(
[0] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => dr n. med., prof IMiD Monika Gos
[firstname] => Monika
[lastname] => Gos
[title] => dr n. med., prof IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-monika_gos
[url] => eksperci/13-monika_gos
)
)
[authors_ids] => Array
(
[0] => 13
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 165-genetyka_molekularna__zmiennosc_materialu_genetycznego
[url] => wideo/165-genetyka_molekularna__zmiennosc_materialu_genetycznego
[short_name] => Genetyka molekularna -zmienność materiału genetycz...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 20
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika w codziennej praktyce lekarskiej.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Sylwia Rzońca
)
[authors_data] => Array
(
[0] => Array
(
[id] => 10
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Sylwia Rzońca
[firstname] => Sylwia
[lastname] => Rzońca
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 10-sylwia_rzonca
[url] => eksperci/10-sylwia_rzonca
)
)
[authors_ids] => Array
(
[0] => 10
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
[url] => kursy/20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
)
)
[sort] => 1
[status_code] => active
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 162-choroby_neurodegeneracyjne_wieku_poznego___idiopatyczne_i_genetyczne
[url] => wideo/162-choroby_neurodegeneracyjne_wieku_poznego___idiopatyczne_i_genetyczne
[short_name] => Choroby neurodegeneracyjne wieku późnego - idiopat...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 20
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika w codziennej praktyce lekarskiej.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Sylwia Rzońca
)
[authors_data] => Array
(
[0] => Array
(
[id] => 10
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Sylwia Rzońca
[firstname] => Sylwia
[lastname] => Rzońca
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 10-sylwia_rzonca
[url] => eksperci/10-sylwia_rzonca
)
)
[authors_ids] => Array
(
[0] => 10
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
[url] => kursy/20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
[logotypy] => Array
(
)
[pliki] => Array
(
[131] => Array
(
[id] => 131
[site_id] => 1
[status_id] => 5
[entity_key] => material
[entity_id] => 162
[name] => Choroby neurodegeneracyjne wieku późnego - idiopatyczne i genetyczne
[file] => resources/data/pliki/material/162/23.06_mat_w4_dhz_06.2020.pdf
[sort] => 128
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
[163] => Array
(
[id] => 163
[name] => Mukowiscydoza i nie tylko. Choroby uwarunkowane mutacjami genu CFTR.
[type_id] => 1
[group_id] => 20
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/163/posterprakt_lek.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
[linked] => Array
(
[400] => Array
(
[id] => 400
[site_id] => 1
[status_id] => 5
[name] => Heterogenność podłoża genetycznego chorób mitochondrialnych.
[type_id] => 1
[group_id] => 20
[problem_id] => 0
[date_publish] => 2023-01-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/400/posterprakt_lek.png
[video] => resources/data/material/400/7_3_heterogennosc_podloza_molekularnego_k.tonska.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 0
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab. Katarzyna Tońska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 95
[site_id] => 1
[status_id] => 5
[name] => dr hab. Katarzyna Tońska
[firstname] => Katarzyna
[lastname] => Tońska
[title] => dr hab.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 95-katarzyna_tonska
[url] => eksperci/95-katarzyna_tonska
)
)
[authors_ids] => Array
(
[0] => 95
)
[topics] => Array
(
[0] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 400-heterogennosc_podloza_genetycznego_chorob_mitochondrialnych
[url] => wideo/400-heterogennosc_podloza_genetycznego_chorob_mitochondrialnych
[short_name] => Heterogenność podłoża genetycznego chorób mitochon...
[date_publish_pl] => 4 stycznia 2023 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 20
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika w codziennej praktyce lekarskiej.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Sylwia Rzońca
)
[authors_data] => Array
(
[0] => Array
(
[id] => 10
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Sylwia Rzońca
[firstname] => Sylwia
[lastname] => Rzońca
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 10-sylwia_rzonca
[url] => eksperci/10-sylwia_rzonca
)
)
[authors_ids] => Array
(
[0] => 10
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
[url] => kursy/20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
)
[topics_data] => Array
(
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[159] => Array
(
[id] => 159
[site_id] => 1
[status_id] => 5
[name] => Zmienność kliniczna i genetyczna niepełnosprawności intelektualnej
[type_id] => 1
[group_id] => 20
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/159/posterprakt_lek.png
[video] => resources/data/material/159/zmiennosc_kliniczna_i_genetyczna_niepelnosprawnosci_intelektualnej_rzonca.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Sylwia Rzońca
)
[authors_data] => Array
(
[0] => Array
(
[id] => 10
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Sylwia Rzońca
[firstname] => Sylwia
[lastname] => Rzońca
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 10-sylwia_rzonca
[url] => eksperci/10-sylwia_rzonca
)
)
[authors_ids] => Array
(
[0] => 10
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 159-zmiennosc_kliniczna_i_genetyczna_niepelnosprawnosci_intelektualnej
[url] => wideo/159-zmiennosc_kliniczna_i_genetyczna_niepelnosprawnosci_intelektualnej
[short_name] => Zmienność kliniczna i genetyczna niepełnosprawnośc...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 20
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika w codziennej praktyce lekarskiej.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Sylwia Rzońca
)
[authors_data] => Array
(
[0] => Array
(
[id] => 10
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Sylwia Rzońca
[firstname] => Sylwia
[lastname] => Rzońca
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 10-sylwia_rzonca
[url] => eksperci/10-sylwia_rzonca
)
)
[authors_ids] => Array
(
[0] => 10
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
[url] => kursy/20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[160] => Array
(
[id] => 160
[site_id] => 1
[status_id] => 5
[name] => Podłoże molekularne neurofibromatozy typu I –możliwości diagnostyczne
[type_id] => 1
[group_id] => 20
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/160/posterprakt_lek.png
[video] => resources/data/material/160/6_2_podloze_molekularne_neurofibromatozy_a.abramowicz.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => mgr Anna Abramowicz
)
[authors_data] => Array
(
[0] => Array
(
[id] => 71
[site_id] => 1
[status_id] => 5
[name] => mgr Anna Abramowicz
[firstname] => Anna
[lastname] => Abramowicz
[title] => mgr
[affiliation] => Zakład Genetyki Medycznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 71-anna_abramowicz
[url] => eksperci/71-anna_abramowicz
)
)
[authors_ids] => Array
(
[0] => 71
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 160-podloze_molekularne_neurofibromatozy_typu_i_mozliwosci_diagnostyczne
[url] => wideo/160-podloze_molekularne_neurofibromatozy_typu_i_mozliwosci_diagnostyczne
[short_name] => Podłoże molekularne neurofibromatozy typu I –możli...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 20
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika w codziennej praktyce lekarskiej.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Sylwia Rzońca
)
[authors_data] => Array
(
[0] => Array
(
[id] => 10
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Sylwia Rzońca
[firstname] => Sylwia
[lastname] => Rzońca
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 10-sylwia_rzonca
[url] => eksperci/10-sylwia_rzonca
)
)
[authors_ids] => Array
(
[0] => 10
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
[url] => kursy/20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[162] => Array
(
[id] => 162
[site_id] => 1
[status_id] => 5
[name] => Choroby neurodegeneracyjne wieku późnego - idiopatyczne i genetyczne
[type_id] => 1
[group_id] => 20
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/162/posterprakt_lek.png
[video] => resources/data/material/162/5_choroby_neurologiczne_o_poznym_wieku_zachorowania_d.hoffman.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 162-choroby_neurodegeneracyjne_wieku_poznego___idiopatyczne_i_genetyczne
[url] => wideo/162-choroby_neurodegeneracyjne_wieku_poznego___idiopatyczne_i_genetyczne
[short_name] => Choroby neurodegeneracyjne wieku późnego - idiopat...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 20
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika w codziennej praktyce lekarskiej.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Sylwia Rzońca
)
[authors_data] => Array
(
[0] => Array
(
[id] => 10
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Sylwia Rzońca
[firstname] => Sylwia
[lastname] => Rzońca
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 10-sylwia_rzonca
[url] => eksperci/10-sylwia_rzonca
)
)
[authors_ids] => Array
(
[0] => 10
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
[url] => kursy/20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[164] => Array
(
[id] => 164
[site_id] => 1
[status_id] => 5
[name] => Genetyka klasyczna - wzory dziedziczenia
[type_id] => 1
[group_id] => 20
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/164/posterprakt_lek.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 164-genetyka_klasyczna___wzory_dziedziczenia
[url] => wideo/164-genetyka_klasyczna___wzory_dziedziczenia
[short_name] => Genetyka klasyczna - wzory dziedziczenia
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 20
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika w codziennej praktyce lekarskiej.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Sylwia Rzońca
)
[authors_data] => Array
(
[0] => Array
(
[id] => 10
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Sylwia Rzońca
[firstname] => Sylwia
[lastname] => Rzońca
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 10-sylwia_rzonca
[url] => eksperci/10-sylwia_rzonca
)
)
[authors_ids] => Array
(
[0] => 10
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
[url] => kursy/20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[165] => Array
(
[id] => 165
[site_id] => 1
[status_id] => 5
[name] => Genetyka molekularna -zmienność materiału genetycznego
[type_id] => 1
[group_id] => 20
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/165/posterprakt_lek.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med., prof IMiD Monika Gos
)
[authors_data] => Array
(
[0] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => dr n. med., prof IMiD Monika Gos
[firstname] => Monika
[lastname] => Gos
[title] => dr n. med., prof IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-monika_gos
[url] => eksperci/13-monika_gos
)
)
[authors_ids] => Array
(
[0] => 13
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 165-genetyka_molekularna__zmiennosc_materialu_genetycznego
[url] => wideo/165-genetyka_molekularna__zmiennosc_materialu_genetycznego
[short_name] => Genetyka molekularna -zmienność materiału genetycz...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 20
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika w codziennej praktyce lekarskiej.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Sylwia Rzońca
)
[authors_data] => Array
(
[0] => Array
(
[id] => 10
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Sylwia Rzońca
[firstname] => Sylwia
[lastname] => Rzońca
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 10-sylwia_rzonca
[url] => eksperci/10-sylwia_rzonca
)
)
[authors_ids] => Array
(
[0] => 10
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
[url] => kursy/20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
)
)
[sort] => 1
[status_code] => active
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 14
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 163-mukowiscydoza_i_nie_tylko_choroby_uwarunkowane_mutacjami_genu_cftr
[url] => wideo/163-mukowiscydoza_i_nie_tylko_choroby_uwarunkowane_mutacjami_genu_cftr
[short_name] => Mukowiscydoza i nie tylko. Choroby uwarunkowane mu...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 20
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika w codziennej praktyce lekarskiej.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Sylwia Rzońca
)
[authors_data] => Array
(
[0] => Array
(
[id] => 10
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Sylwia Rzońca
[firstname] => Sylwia
[lastname] => Rzońca
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 10-sylwia_rzonca
[url] => eksperci/10-sylwia_rzonca
)
)
[authors_ids] => Array
(
[0] => 10
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
[url] => kursy/20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[14] => Array
(
[id] => 14
[site_id] => 1
[status_id] => 5
[name] => choroby rzadkie
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 14-choroby_rzadkie
[url] => /14-choroby_rzadkie
)
)
[artykuly] => Array
(
)
[logotypy] => Array
(
)
[pliki] => Array
(
[132] => Array
(
[id] => 132
[site_id] => 1
[status_id] => 5
[entity_key] => material
[entity_id] => 163
[name] => Mukowiscydoza i nie tylko. Choroby uwarunkowane mutacjami genu CFTR.
[file] => resources/data/pliki/material/163/23.06_mat_w5_kwt_06.2020.pdf
[sort] => 129
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
[164] => Array
(
[id] => 164
[name] => Genetyka klasyczna - wzory dziedziczenia
[type_id] => 1
[group_id] => 20
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/164/posterprakt_lek.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
[linked] => Array
(
[400] => Array
(
[id] => 400
[site_id] => 1
[status_id] => 5
[name] => Heterogenność podłoża genetycznego chorób mitochondrialnych.
[type_id] => 1
[group_id] => 20
[problem_id] => 0
[date_publish] => 2023-01-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/400/posterprakt_lek.png
[video] => resources/data/material/400/7_3_heterogennosc_podloza_molekularnego_k.tonska.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 0
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab. Katarzyna Tońska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 95
[site_id] => 1
[status_id] => 5
[name] => dr hab. Katarzyna Tońska
[firstname] => Katarzyna
[lastname] => Tońska
[title] => dr hab.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 95-katarzyna_tonska
[url] => eksperci/95-katarzyna_tonska
)
)
[authors_ids] => Array
(
[0] => 95
)
[topics] => Array
(
[0] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 400-heterogennosc_podloza_genetycznego_chorob_mitochondrialnych
[url] => wideo/400-heterogennosc_podloza_genetycznego_chorob_mitochondrialnych
[short_name] => Heterogenność podłoża genetycznego chorób mitochon...
[date_publish_pl] => 4 stycznia 2023 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 20
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika w codziennej praktyce lekarskiej.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Sylwia Rzońca
)
[authors_data] => Array
(
[0] => Array
(
[id] => 10
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Sylwia Rzońca
[firstname] => Sylwia
[lastname] => Rzońca
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 10-sylwia_rzonca
[url] => eksperci/10-sylwia_rzonca
)
)
[authors_ids] => Array
(
[0] => 10
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
[url] => kursy/20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
)
[topics_data] => Array
(
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[159] => Array
(
[id] => 159
[site_id] => 1
[status_id] => 5
[name] => Zmienność kliniczna i genetyczna niepełnosprawności intelektualnej
[type_id] => 1
[group_id] => 20
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/159/posterprakt_lek.png
[video] => resources/data/material/159/zmiennosc_kliniczna_i_genetyczna_niepelnosprawnosci_intelektualnej_rzonca.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Sylwia Rzońca
)
[authors_data] => Array
(
[0] => Array
(
[id] => 10
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Sylwia Rzońca
[firstname] => Sylwia
[lastname] => Rzońca
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 10-sylwia_rzonca
[url] => eksperci/10-sylwia_rzonca
)
)
[authors_ids] => Array
(
[0] => 10
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 159-zmiennosc_kliniczna_i_genetyczna_niepelnosprawnosci_intelektualnej
[url] => wideo/159-zmiennosc_kliniczna_i_genetyczna_niepelnosprawnosci_intelektualnej
[short_name] => Zmienność kliniczna i genetyczna niepełnosprawnośc...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 20
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika w codziennej praktyce lekarskiej.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Sylwia Rzońca
)
[authors_data] => Array
(
[0] => Array
(
[id] => 10
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Sylwia Rzońca
[firstname] => Sylwia
[lastname] => Rzońca
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 10-sylwia_rzonca
[url] => eksperci/10-sylwia_rzonca
)
)
[authors_ids] => Array
(
[0] => 10
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
[url] => kursy/20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[160] => Array
(
[id] => 160
[site_id] => 1
[status_id] => 5
[name] => Podłoże molekularne neurofibromatozy typu I –możliwości diagnostyczne
[type_id] => 1
[group_id] => 20
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/160/posterprakt_lek.png
[video] => resources/data/material/160/6_2_podloze_molekularne_neurofibromatozy_a.abramowicz.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => mgr Anna Abramowicz
)
[authors_data] => Array
(
[0] => Array
(
[id] => 71
[site_id] => 1
[status_id] => 5
[name] => mgr Anna Abramowicz
[firstname] => Anna
[lastname] => Abramowicz
[title] => mgr
[affiliation] => Zakład Genetyki Medycznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 71-anna_abramowicz
[url] => eksperci/71-anna_abramowicz
)
)
[authors_ids] => Array
(
[0] => 71
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 160-podloze_molekularne_neurofibromatozy_typu_i_mozliwosci_diagnostyczne
[url] => wideo/160-podloze_molekularne_neurofibromatozy_typu_i_mozliwosci_diagnostyczne
[short_name] => Podłoże molekularne neurofibromatozy typu I –możli...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 20
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika w codziennej praktyce lekarskiej.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Sylwia Rzońca
)
[authors_data] => Array
(
[0] => Array
(
[id] => 10
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Sylwia Rzońca
[firstname] => Sylwia
[lastname] => Rzońca
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 10-sylwia_rzonca
[url] => eksperci/10-sylwia_rzonca
)
)
[authors_ids] => Array
(
[0] => 10
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
[url] => kursy/20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[162] => Array
(
[id] => 162
[site_id] => 1
[status_id] => 5
[name] => Choroby neurodegeneracyjne wieku późnego - idiopatyczne i genetyczne
[type_id] => 1
[group_id] => 20
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/162/posterprakt_lek.png
[video] => resources/data/material/162/5_choroby_neurologiczne_o_poznym_wieku_zachorowania_d.hoffman.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 162-choroby_neurodegeneracyjne_wieku_poznego___idiopatyczne_i_genetyczne
[url] => wideo/162-choroby_neurodegeneracyjne_wieku_poznego___idiopatyczne_i_genetyczne
[short_name] => Choroby neurodegeneracyjne wieku późnego - idiopat...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 20
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika w codziennej praktyce lekarskiej.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Sylwia Rzońca
)
[authors_data] => Array
(
[0] => Array
(
[id] => 10
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Sylwia Rzońca
[firstname] => Sylwia
[lastname] => Rzońca
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 10-sylwia_rzonca
[url] => eksperci/10-sylwia_rzonca
)
)
[authors_ids] => Array
(
[0] => 10
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
[url] => kursy/20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[163] => Array
(
[id] => 163
[site_id] => 1
[status_id] => 5
[name] => Mukowiscydoza i nie tylko. Choroby uwarunkowane mutacjami genu CFTR.
[type_id] => 1
[group_id] => 20
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/163/posterprakt_lek.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 14
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 163-mukowiscydoza_i_nie_tylko_choroby_uwarunkowane_mutacjami_genu_cftr
[url] => wideo/163-mukowiscydoza_i_nie_tylko_choroby_uwarunkowane_mutacjami_genu_cftr
[short_name] => Mukowiscydoza i nie tylko. Choroby uwarunkowane mu...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 20
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika w codziennej praktyce lekarskiej.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Sylwia Rzońca
)
[authors_data] => Array
(
[0] => Array
(
[id] => 10
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Sylwia Rzońca
[firstname] => Sylwia
[lastname] => Rzońca
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 10-sylwia_rzonca
[url] => eksperci/10-sylwia_rzonca
)
)
[authors_ids] => Array
(
[0] => 10
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
[url] => kursy/20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[14] => Array
(
[id] => 14
[site_id] => 1
[status_id] => 5
[name] => choroby rzadkie
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 14-choroby_rzadkie
[url] => /14-choroby_rzadkie
)
)
[artykuly] => Array
(
)
)
[165] => Array
(
[id] => 165
[site_id] => 1
[status_id] => 5
[name] => Genetyka molekularna -zmienność materiału genetycznego
[type_id] => 1
[group_id] => 20
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/165/posterprakt_lek.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med., prof IMiD Monika Gos
)
[authors_data] => Array
(
[0] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => dr n. med., prof IMiD Monika Gos
[firstname] => Monika
[lastname] => Gos
[title] => dr n. med., prof IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-monika_gos
[url] => eksperci/13-monika_gos
)
)
[authors_ids] => Array
(
[0] => 13
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 165-genetyka_molekularna__zmiennosc_materialu_genetycznego
[url] => wideo/165-genetyka_molekularna__zmiennosc_materialu_genetycznego
[short_name] => Genetyka molekularna -zmienność materiału genetycz...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 20
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika w codziennej praktyce lekarskiej.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Sylwia Rzońca
)
[authors_data] => Array
(
[0] => Array
(
[id] => 10
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Sylwia Rzońca
[firstname] => Sylwia
[lastname] => Rzońca
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 10-sylwia_rzonca
[url] => eksperci/10-sylwia_rzonca
)
)
[authors_ids] => Array
(
[0] => 10
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
[url] => kursy/20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
)
)
[sort] => 1
[status_code] => active
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 164-genetyka_klasyczna___wzory_dziedziczenia
[url] => wideo/164-genetyka_klasyczna___wzory_dziedziczenia
[short_name] => Genetyka klasyczna - wzory dziedziczenia
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 20
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika w codziennej praktyce lekarskiej.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Sylwia Rzońca
)
[authors_data] => Array
(
[0] => Array
(
[id] => 10
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Sylwia Rzońca
[firstname] => Sylwia
[lastname] => Rzońca
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 10-sylwia_rzonca
[url] => eksperci/10-sylwia_rzonca
)
)
[authors_ids] => Array
(
[0] => 10
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
[url] => kursy/20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
[logotypy] => Array
(
)
[pliki] => Array
(
[133] => Array
(
[id] => 133
[site_id] => 1
[status_id] => 5
[entity_key] => material
[entity_id] => 164
[name] => Genetyka klasyczna - wzory dziedziczenia
[file] => resources/data/pliki/material/164/23.06_mat_w1_dhz_06.2020.pdf
[sort] => 130
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
[165] => Array
(
[id] => 165
[name] => Genetyka molekularna -zmienność materiału genetycznego
[type_id] => 1
[group_id] => 20
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/165/posterprakt_lek.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
[linked] => Array
(
[400] => Array
(
[id] => 400
[site_id] => 1
[status_id] => 5
[name] => Heterogenność podłoża genetycznego chorób mitochondrialnych.
[type_id] => 1
[group_id] => 20
[problem_id] => 0
[date_publish] => 2023-01-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/400/posterprakt_lek.png
[video] => resources/data/material/400/7_3_heterogennosc_podloza_molekularnego_k.tonska.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 0
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab. Katarzyna Tońska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 95
[site_id] => 1
[status_id] => 5
[name] => dr hab. Katarzyna Tońska
[firstname] => Katarzyna
[lastname] => Tońska
[title] => dr hab.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 95-katarzyna_tonska
[url] => eksperci/95-katarzyna_tonska
)
)
[authors_ids] => Array
(
[0] => 95
)
[topics] => Array
(
[0] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 400-heterogennosc_podloza_genetycznego_chorob_mitochondrialnych
[url] => wideo/400-heterogennosc_podloza_genetycznego_chorob_mitochondrialnych
[short_name] => Heterogenność podłoża genetycznego chorób mitochon...
[date_publish_pl] => 4 stycznia 2023 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 20
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika w codziennej praktyce lekarskiej.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Sylwia Rzońca
)
[authors_data] => Array
(
[0] => Array
(
[id] => 10
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Sylwia Rzońca
[firstname] => Sylwia
[lastname] => Rzońca
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 10-sylwia_rzonca
[url] => eksperci/10-sylwia_rzonca
)
)
[authors_ids] => Array
(
[0] => 10
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
[url] => kursy/20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
)
[topics_data] => Array
(
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[159] => Array
(
[id] => 159
[site_id] => 1
[status_id] => 5
[name] => Zmienność kliniczna i genetyczna niepełnosprawności intelektualnej
[type_id] => 1
[group_id] => 20
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/159/posterprakt_lek.png
[video] => resources/data/material/159/zmiennosc_kliniczna_i_genetyczna_niepelnosprawnosci_intelektualnej_rzonca.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Sylwia Rzońca
)
[authors_data] => Array
(
[0] => Array
(
[id] => 10
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Sylwia Rzońca
[firstname] => Sylwia
[lastname] => Rzońca
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 10-sylwia_rzonca
[url] => eksperci/10-sylwia_rzonca
)
)
[authors_ids] => Array
(
[0] => 10
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 159-zmiennosc_kliniczna_i_genetyczna_niepelnosprawnosci_intelektualnej
[url] => wideo/159-zmiennosc_kliniczna_i_genetyczna_niepelnosprawnosci_intelektualnej
[short_name] => Zmienność kliniczna i genetyczna niepełnosprawnośc...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 20
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika w codziennej praktyce lekarskiej.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Sylwia Rzońca
)
[authors_data] => Array
(
[0] => Array
(
[id] => 10
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Sylwia Rzońca
[firstname] => Sylwia
[lastname] => Rzońca
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 10-sylwia_rzonca
[url] => eksperci/10-sylwia_rzonca
)
)
[authors_ids] => Array
(
[0] => 10
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
[url] => kursy/20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[160] => Array
(
[id] => 160
[site_id] => 1
[status_id] => 5
[name] => Podłoże molekularne neurofibromatozy typu I –możliwości diagnostyczne
[type_id] => 1
[group_id] => 20
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/160/posterprakt_lek.png
[video] => resources/data/material/160/6_2_podloze_molekularne_neurofibromatozy_a.abramowicz.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => mgr Anna Abramowicz
)
[authors_data] => Array
(
[0] => Array
(
[id] => 71
[site_id] => 1
[status_id] => 5
[name] => mgr Anna Abramowicz
[firstname] => Anna
[lastname] => Abramowicz
[title] => mgr
[affiliation] => Zakład Genetyki Medycznej, Instytut Matki i Dziecka
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 71-anna_abramowicz
[url] => eksperci/71-anna_abramowicz
)
)
[authors_ids] => Array
(
[0] => 71
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 160-podloze_molekularne_neurofibromatozy_typu_i_mozliwosci_diagnostyczne
[url] => wideo/160-podloze_molekularne_neurofibromatozy_typu_i_mozliwosci_diagnostyczne
[short_name] => Podłoże molekularne neurofibromatozy typu I –możli...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 20
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika w codziennej praktyce lekarskiej.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Sylwia Rzońca
)
[authors_data] => Array
(
[0] => Array
(
[id] => 10
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Sylwia Rzońca
[firstname] => Sylwia
[lastname] => Rzońca
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 10-sylwia_rzonca
[url] => eksperci/10-sylwia_rzonca
)
)
[authors_ids] => Array
(
[0] => 10
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
[url] => kursy/20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[162] => Array
(
[id] => 162
[site_id] => 1
[status_id] => 5
[name] => Choroby neurodegeneracyjne wieku późnego - idiopatyczne i genetyczne
[type_id] => 1
[group_id] => 20
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/162/posterprakt_lek.png
[video] => resources/data/material/162/5_choroby_neurologiczne_o_poznym_wieku_zachorowania_d.hoffman.mp4
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 162-choroby_neurodegeneracyjne_wieku_poznego___idiopatyczne_i_genetyczne
[url] => wideo/162-choroby_neurodegeneracyjne_wieku_poznego___idiopatyczne_i_genetyczne
[short_name] => Choroby neurodegeneracyjne wieku późnego - idiopat...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 20
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika w codziennej praktyce lekarskiej.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Sylwia Rzońca
)
[authors_data] => Array
(
[0] => Array
(
[id] => 10
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Sylwia Rzońca
[firstname] => Sylwia
[lastname] => Rzońca
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 10-sylwia_rzonca
[url] => eksperci/10-sylwia_rzonca
)
)
[authors_ids] => Array
(
[0] => 10
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
[url] => kursy/20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
[163] => Array
(
[id] => 163
[site_id] => 1
[status_id] => 5
[name] => Mukowiscydoza i nie tylko. Choroby uwarunkowane mutacjami genu CFTR.
[type_id] => 1
[group_id] => 20
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/163/posterprakt_lek.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Katarzyna Wertheim-Tysarowska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 6
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Katarzyna Wertheim-Tysarowska
[firstname] => Katarzyna
[lastname] => Wertheim-Tysarowska
[title] => dr n. med.
[affiliation] => Pracownia Badań Chorób Dziedzicznych, Zakład Genetyki Medycznej IMID
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 6-katarzyna_wertheim_tysarowska
[url] => eksperci/6-katarzyna_wertheim_tysarowska
)
)
[authors_ids] => Array
(
[0] => 6
)
[topics] => Array
(
[0] => 4
[1] => 8
[2] => 14
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 163-mukowiscydoza_i_nie_tylko_choroby_uwarunkowane_mutacjami_genu_cftr
[url] => wideo/163-mukowiscydoza_i_nie_tylko_choroby_uwarunkowane_mutacjami_genu_cftr
[short_name] => Mukowiscydoza i nie tylko. Choroby uwarunkowane mu...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 20
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika w codziennej praktyce lekarskiej.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Sylwia Rzońca
)
[authors_data] => Array
(
[0] => Array
(
[id] => 10
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Sylwia Rzońca
[firstname] => Sylwia
[lastname] => Rzońca
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 10-sylwia_rzonca
[url] => eksperci/10-sylwia_rzonca
)
)
[authors_ids] => Array
(
[0] => 10
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
[url] => kursy/20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
[14] => Array
(
[id] => 14
[site_id] => 1
[status_id] => 5
[name] => choroby rzadkie
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 14-choroby_rzadkie
[url] => /14-choroby_rzadkie
)
)
[artykuly] => Array
(
)
)
[164] => Array
(
[id] => 164
[site_id] => 1
[status_id] => 5
[name] => Genetyka klasyczna - wzory dziedziczenia
[type_id] => 1
[group_id] => 20
[problem_id] => 0
[date_publish] => 2022-07-04
[hp_type] => 0
[hp_new] => 0
[lead] =>
[thumb] => resources/data/material/164/posterprakt_lek.png
[video] =>
[content] =>
[ext] => Array
(
[files_header] =>
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
)
[authors_data] => Array
(
[0] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => dr hab., prof. IMiD Dorota Hoffman-Zacharska
[firstname] => Dorota
[lastname] => Hoffman-Zacharska
[title] => dr hab., prof. IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-dorota_hoffman_zacharska
[url] => eksperci/8-dorota_hoffman_zacharska
)
)
[authors_ids] => Array
(
[0] => 8
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 164-genetyka_klasyczna___wzory_dziedziczenia
[url] => wideo/164-genetyka_klasyczna___wzory_dziedziczenia
[short_name] => Genetyka klasyczna - wzory dziedziczenia
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 20
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika w codziennej praktyce lekarskiej.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Sylwia Rzońca
)
[authors_data] => Array
(
[0] => Array
(
[id] => 10
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Sylwia Rzońca
[firstname] => Sylwia
[lastname] => Rzońca
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 10-sylwia_rzonca
[url] => eksperci/10-sylwia_rzonca
)
)
[authors_ids] => Array
(
[0] => 10
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
[url] => kursy/20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
)
)
)
[sort] => 1
[status_code] => active
[authors] => Array
(
[0] => dr n. med., prof IMiD Monika Gos
)
[authors_data] => Array
(
[0] => Array
(
[id] => 13
[site_id] => 1
[status_id] => 5
[name] => dr n. med., prof IMiD Monika Gos
[firstname] => Monika
[lastname] => Gos
[title] => dr n. med., prof IMiD
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 13-monika_gos
[url] => eksperci/13-monika_gos
)
)
[authors_ids] => Array
(
[0] => 13
)
[topics] => Array
(
[0] => 4
[1] => 8
)
[type_data] => Array
(
[id] => 1
[site_id] => 1
[name] => Wideo
[ext] => Array
(
[video] => 1
[files] => 1
[authors] => 1
[lead] => 1
)
[active] => 1
[status_name] =>
[status_code] =>
[status_admin] => #0
[url] =>
)
[one_url] => 165-genetyka_molekularna__zmiennosc_materialu_genetycznego
[url] => wideo/165-genetyka_molekularna__zmiennosc_materialu_genetycznego
[short_name] => Genetyka molekularna -zmienność materiału genetycz...
[date_publish_pl] => 4 lipca 2022 r.
[type_name] => Wideo
[problem_data] =>
[group_data] => Array
(
[id] => 20
[site_id] => 1
[status_id] => 5
[block_id] => 5
[name] => Genetyka i genomika w codziennej praktyce lekarskiej.
[ext] => Array
(
[quiz] => Array
(
[active] => 1
[questions] =>
[passed_threshold] => 50
)
[certificate] => Array
(
[file] =>
)
)
[sort] => 1
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[authors] => Array
(
[0] => dr n. med. Sylwia Rzońca
)
[authors_data] => Array
(
[0] => Array
(
[id] => 10
[site_id] => 1
[status_id] => 5
[name] => dr n. med. Sylwia Rzońca
[firstname] => Sylwia
[lastname] => Rzońca
[title] => dr n. med.
[affiliation] =>
[avatar] =>
[bio] =>
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 10-sylwia_rzonca
[url] => eksperci/10-sylwia_rzonca
)
)
[authors_ids] => Array
(
[0] => 10
)
[block_data] => Array
(
[id] => 5
[name] => KURSY Z ZAKRESU GENOMIKI
[ext] =>
[sort] => 3
[one_url] => 5-kursy_z_zakresu_genomiki
[url] => bloki/5-kursy_z_zakresu_genomiki
[status_code] => active
)
[one_url] => 20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
[url] => kursy/20-genetyka_i_genomika_w_codziennej_praktyce_lekarskiej
)
[topics_data] => Array
(
[4] => Array
(
[id] => 4
[site_id] => 1
[status_id] => 5
[name] => diagnostyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 4-diagnostyka
[url] => /4-diagnostyka
)
[8] => Array
(
[id] => 8
[site_id] => 1
[status_id] => 5
[name] => genetyka
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[one_url] => 8-genetyka
[url] => /8-genetyka
)
)
[artykuly] => Array
(
)
[logotypy] => Array
(
)
[pliki] => Array
(
[134] => Array
(
[id] => 134
[site_id] => 1
[status_id] => 5
[entity_key] => material
[entity_id] => 165
[name] => Genetyka molekularna - zmienność materiału genetycznego
[file] => resources/data/pliki/material/165/23.06_mat_w2_mg.pdf
[sort] => 131
[ext] =>
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
)
)
)
)
[quiz_questions] => Array
(
[185] => Array
(
[id] => 185
[site_id] => 1
[status_id] => 5
[group_id] => 20
[type_id] => 2
[name] => Wskaż zdanie prawdziwe:
[ext] =>
[sort] => 0
[status_name] => Aktywny
[status_code] => active
[status_admin] => #1Aktywny
[type_name] => wielokrotna odpowiedź
[type_code] => multi
