Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Ahmet Okay Çağlayan"'
Autor:
Hilal Akköprü, Alper Alnak, Zeynep Nur Karadoğan, Ahmet Okay Çağlayan, Mustafa Özçetin, Murat Coşkun
Publikováno v:
Psychiatry and Clinical Psychopharmacology, Vol 33, Iss 1, Pp 14-19 (2023)
Externí odkaz:
https://doaj.org/article/88f72bd0cf4a4be79c52f18d2a251046
Publikováno v:
Psychiatry and Clinical Psychopharmacology, Vol 31, Iss 3, Pp 261-268 (2021)
Externí odkaz:
https://doaj.org/article/098fc880b5484d199961a19b18203602
Autor:
Tayfun Cinleti, Ali Gülen, Beria Sönmez, Semra Gürsoy, Özge Kangalli Boyacioğlu, Suna Asilsoy, Ayfer Ulgenalp, Özlem Giray Bozkaya, Ahmet Okay Çağlayan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7672510d1eb1b9a48c410b27aef67775
https://avesis.deu.edu.tr/publication/details/6394efc0-6d18-4302-afff-c1f02f964f75/oai
https://avesis.deu.edu.tr/publication/details/6394efc0-6d18-4302-afff-c1f02f964f75/oai
Autor:
Aylin Yüksel Ülker, Dilek Uludağ Alkaya, Ahmet Okay Çağlayan, Esra Usluer, Ayça Aykut, Ayça Aslanger, Mehmet Vural, Beyhan Tüysüz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ad0174ce25e0b9d47408a7ded67e7dca
https://avesis.deu.edu.tr/publication/details/079fd9bb-1a6d-44c8-8eb6-f38a6f9e25e1/oai
https://avesis.deu.edu.tr/publication/details/079fd9bb-1a6d-44c8-8eb6-f38a6f9e25e1/oai
Hemoglobin A(1C) can differentiate subjects with GCK mutations among patients suspected to have MODY
Autor:
Ceren Yılmaz Uzman, İbrahim Mert Erbaş, Özlem Giray Bozkaya, Ahu Paketçi, Ahmet Okay Çağlayan, Ayhan Abacı, Melike Ataseven Kulalı, Ece Böber, Arda Kekilli, Tayfun Çinleti, Murat Derya Erçal, Korcan Demir
Objectives The aim of this study is to determine the clinical and molecular characteristics enabling differential diagnosis in a group of Turkish children clinically diagnosed with MODY and identify the cut-off value of HbA1c, which can distinguish p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b53469bb9fa3e5092aeb1399f5506326
https://avesis.deu.edu.tr/publication/details/92b0ebf1-e738-44fc-bc9d-723ab8e0ecf3/oai
https://avesis.deu.edu.tr/publication/details/92b0ebf1-e738-44fc-bc9d-723ab8e0ecf3/oai
Autor:
Ceren, Yılmaz Uzman, İbrahim Mert, Erbaş, Özlem, Giray Bozkaya, Ahu, Paketçi, Ahmet Okay, Çağlayan, Ayhan, Abacı, Melike Ataseven, Kulalı, Ece, Böber, Arda, Kekilli, Tayfun, Çinleti, Murat Derya, Erçal, Korcan, Demir
Publikováno v:
Journal of pediatric endocrinologymetabolism : JPEMReferences. 35(12)
The aim of this study is to determine the clinical and molecular characteristics enabling differential diagnosis in a group of Turkish children clinically diagnosed with MODY and identify the cut-off value of HbAThe study included 49 patients from 48
Autor:
Selcan Öztürk, Ayten Güleç, Murat Erdoğan, Mikail Demir, Mehmet Canpolat, Hakan Gümüş, Ahmet Okay Çağlayan, Munis Dündar, Hüseyin Per
Publikováno v:
Pediatric neurology. 136
© 2022 Elsevier Inc.Background: Congenital myasthenic syndromes (CMS) are composed of numerous hereditary disorders involving genetic mutations in proteins essential to the integrity of neuromuscular transmission. The symptoms of CMS vary according
Constitutional mismatch repair deficiency (CMMRD) is one of the rare cancer predisposition syndromes. The aim of this study was to evaluate the cerebral developmental venous anomalies in children with central nervous system tumors associated with CMM
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d8e489bf85a73d50b3ded768bf0b2527
https://avesis.deu.edu.tr/publication/details/f849019b-0120-41ab-9b04-f061d850ef83/oai
https://avesis.deu.edu.tr/publication/details/f849019b-0120-41ab-9b04-f061d850ef83/oai
Autor:
Nurettin, Bayram, Ayşe Kaçar, Bayram, Hüseyin, Per, Hakan, Gümüş, Cemal, Ozsaygili, Mehmet Said, Doğan, Ahmet Okay, Çağlayan
Publikováno v:
European journal of ophthalmology. 32(5)
Walker-Warburg syndrome (WWS) is a rare autosomal recessive disorder characterized by congenital muscular dystrophy and severe brain and eye malformations. This study aims to analyze genotype-phenotype correlations in WWS with a novel cytidine diphos
Autor:
Ahmet Okay Çağlayan
Publikováno v:
Istanbul Bilim University Florence Nightingale Journal of Medicine. 1:52-57
Intellectual disability (ID) refers to a diverse group of disorders with marked heterogeneity in both clinical presentation and genetic etiology. Some cases of ID are associated with distinctive clinical findings that can lead to specific clinical an