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of 10
pro vyhledávání: '"Nilgun Tanriverdi"'
Autor:
Nilgun Tanriverdi, Ayfer Pazarbasi, Dilara Karahan, Ayse Avci, Aysegul Yolga Tahiroglu, Erdal Tunc, Osman Demirhan
Publikováno v:
Çukurova Üniversitesi Tıp Fakültesi Dergisi, Vol 38, Iss 1, Pp 108-113 (2013)
Aggressive behavior and hyperactivity are neurodevelopmental diseases with unknown pathogenesis. Pericentric inv(10)(p11.2;q21.2) mutation is frequently encountered in cytogenetic laboratories. This mutation is accepted as a polymorphic variant and i
Externí odkaz:
https://doaj.org/article/1c432abcc9974dfcb0286a04fa4e9e94
Autor:
Onur Ozer, Osman Demirhan, Erdal Tunc, Huseyin Bagci, Dilara Karahan, Nilgun Tanriverdi, Bertan Yilmaz, Ali Irfan Guzel, Ibrahim Keser
Publikováno v:
Çukurova Üniversitesi Tıp Fakültesi Dergisi, Vol 37, Iss 2, Pp 76-83 (2012)
Objective: Fragile X syndrome (FXS) is the most common cause of inherited mental retardation and is due to a mutation in the X-linked FMR1 gene. Molecular genetic testing and chromosome analysis are indicated for this disorder. In this context, we tr
Externí odkaz:
https://doaj.org/article/44ac9314a44146dbb00df46b0f64088c
Autor:
Nilgun Tanriverdi, Ayfer Pazarbasi, Dilara Suleymanova Karahan, Ilker Guney, Deniz Tastemir, Erdal Tunc, Osman Demirhan, Ozlem Herguner
Publikováno v:
Çukurova Üniversitesi Tıp Fakültesi Dergisi, Vol 38, Iss 3, Pp 540-542 (2013)
Purpose: Mental retardation is a common handicap (2-3% of the general population) with an unknown cause in more than 50% of mentally retarded patients. Important causes are chromosome abnormalities which are detectable in 4-28% of cases, depending on
Externí odkaz:
https://doaj.org/article/9f7ca2f54fa54a7a90e73809fd60357d
Akademický článek
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Autor:
Onur Ozer, Osman Demirhan, Erdal Tunc, Huseyin Bagci, Dilara Karahan, Nilgun Tanriverdi, Bertan Yilmaz, Ali Irfan Guzel, Ibrahim Keser
Publikováno v:
Volume: 37, Issue: 2 76-83
Cukurova Medical Journal
Çukurova Üniversitesi Tıp Fakültesi Dergisi, Vol 37, Iss 2, Pp 76-83 (2012)
Cukurova Medical Journal
Çukurova Üniversitesi Tıp Fakültesi Dergisi, Vol 37, Iss 2, Pp 76-83 (2012)
Objective: Fragile X syndrome (FXS) is the most common cause of inherited mental retardation and is due to a mutation in the X-linked FMR1 gene. Molecular genetic testing and chromosome analysis are indicated for this disorder. In this context, we tr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::882032da7e3d08b6e8a85bce2ed649c1
https://dergipark.org.tr/tr/pub/cumj/issue/4199/55372
https://dergipark.org.tr/tr/pub/cumj/issue/4199/55372
Autor:
Osman, Demirhan, Ayfer, Pazarbasi, Dilara, Suleymanova-Karahan, Nilgun, Tanriverdi, Yurdanur, Kilinc
Publikováno v:
Saudi medical journal. 29(7)
To describe the history of 157 carriers of pericentric inversions on chromosome 9 [inv9] with karyotype analyses and evaluate the significance of these findings.We studied the incidence, clinical significance, and genetic counseling of inv9 p11;q12,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6b7770e5673a1b20cae3dc8092ca1a81
https://pubmed.ncbi.nlm.nih.gov/18626518
https://pubmed.ncbi.nlm.nih.gov/18626518
Autor:
Nilgun Tanriverdi MD
Publikováno v:
Acta Psychiatrica Scandinavica. 104:315-316
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f145d38c8ed700a6f1b46f64b789d8a2
https://doi.org/10.1034/j.1600-0447.2001.00001-2.x
https://doi.org/10.1034/j.1600-0447.2001.00001-2.x
Autor:
Nilgün TANRIVERDİ, Ayfer PAZARBAŞI, Dilara Süleymanova KARAHAN, İlker GÜNEY, Deniz TAŞTEMİR, Erdal TUNÇ, Osman DEMİRHAN, Özlem HERGÜNER
Publikováno v:
Cukurova Medical Journal, Vol 38, Iss 3, Pp 540-545 (2013)
Giriş: Zeka geriliği, genel populasyonda %2-3 gibi oldukça yüksek bir oranda bulunan ve vakaların %50"sinden fazlasında sebebi bulunamayan bir sağlık problemidir. En önemli nedenlerinden birisi kromozom düzensizlikleri olup hasta seçimi ve
Externí odkaz:
https://doaj.org/article/e82f085f51e243bc8969ec56328fc47b
Autor:
Nilgün TANRIVERDİ, Ayfer PAZARBAŞI, Dilara KARAHAN, Ayşe AVCI, Ayşegül Yolga TAHİROĞLU, Erdal TUNÇ, Osman DEMİRHAN
Publikováno v:
Cukurova Medical Journal, Vol 38, Iss 1, Pp 108-113 (2013)
Agresif davranış ve hiperaktivite, nedeni ve patogenezi bilinmeyen genetik nörogelişimsel hastalıklardır. Perisentrik inv(10)(p11.2;q21.2) mutasyonu sitogenetik laboratuarlarında sıklıkla tanımlanmaktadır. Bu olgu fenotipik olarak sessizdi
Externí odkaz:
https://doaj.org/article/8454f5d16a0643cdb5a77939147b62a7
Autor:
Onur ÖZER, Osman DEMİRHAN, Erdal TUNC, Hüseyin BAĞCI, Dilara KARAHAN, Nilgün TANRİVERDİ, Bertan YILMAZ, Ali İrfan GÜZEL, İbrahim KESER
Publikováno v:
Cukurova Medical Journal, Vol 37, Iss 2, Pp 76-83 (2012)
Amaç: Kalıtımla geçen mental retardasyonun en yaygın nedeni Frajil X sendromudur (FXS). X kromozomu üzerinde bulunan FMR1 geninde meydana gelen bir mutasyon, bu sendroma yol açmaktadır. Tanı için kromozom analizi ve moleküler genetik testl
Externí odkaz:
https://doaj.org/article/9f6b80c6b3034f3a92f9803dc181e9e1