Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Funda Feryal Taş"'
Autor:
Şervan Özalkak, Meliha Demiral, Edip Ünal, Funda Feryal Taş, Hüseyin Onay, Hüseyin Demirbilek, Mehmet Nuri Ozbek
Publikováno v:
JCRPE, Vol 15, Iss 3, Pp 329-333 (2023)
Congenital generalized lipodystrophy (CGL) is a rare, autosomal recessive disorder characterized by an almost complete absence of body fat. In CGL, patients may have hyperphagia due to leptin deficiency. Recombinant human leptin (metreleptin) has bee
Externí odkaz:
https://doaj.org/article/b651e69acbc8494fac0c0d6b3485c796
Autor:
Şervan Özalkak, Ruken Yıldırım, Selma Tunç, Edip Ünal, Funda Feryal Taş, Hüseyin Demirbilek, Mehmet Nuri Özbek
Publikováno v:
JCRPE, Vol 14, Iss 2, Pp 172-178 (2022)
INTRODUCTION: Objective: The incidence of type 1 diabetes mellitus (T1D) in children has an increasing trend globally, with a variable rate depending on region and ethnicity. Our group first reported T1D incidence in Diyarbakır in 2011. The aim of
Externí odkaz:
https://doaj.org/article/c47d4ecb51e04c26b855b01bbd4a87c8
Autor:
Çağlar Ödek, Halise Akça, Mehmet Erol, Remezan Demir, Melek Tunç, Ahmet Aydınalp, Funda Feryal Taş, Serhat Samancı
Publikováno v:
Journal of Pediatric Emergency and Intensive Care Medicine, Vol 6, Iss 2, Pp 72-78 (2019)
Introduction:The aim of this study was to investigate demographic, epidemiologic, and clinical characteristics of cases admitted to pediatric intensive care unit (PICU) for poisoning.Methods:Cases with poisoning admitted to PICU between January 1, 20
Externí odkaz:
https://doaj.org/article/fa5db9c030ff480abb10ffd2eb9eddbe
Autor:
Çağlar Ödek, Mehmet Erol, Remezan Demir, Melek Tunç, Ahmet Aydınalp, Funda Feryal Taş, Muhammet Köşker, Serhat Samancı
Publikováno v:
Journal of Pediatric Emergency and Intensive Care Medicine, Vol 5, Iss 3, Pp 107-112 (2018)
Introduction:Subacute sclerosing panencephalitis (SSPE) is a chronic, progressive, and degenerative infection of the central nervous system caused by measles virus. The first aim of this study was to assess the demographic and epidemiological charact
Externí odkaz:
https://doaj.org/article/8c5e67aa63ae467bbfb6ded2dab81128
Autor:
Ruken Yıldırım, Edip Unal, Aysel Tekmenuray-Unal, Funda Feryal Taş, Şervan Özalkak, Atilla Çayır, Mehmet Nuri Özbek
Publikováno v:
Endocrine. 79:376-383
Triple-A Syndrome (TAS) is a rare autosomal recessive disorder characterized by adrenal insufficiency, achalasia, and alacrimia. This disorder is caused by mutations in the AAAS gene. The aim of this study is to discuss the clinical, laboratory and m
Autor:
ruken yıldırım, Edip Unal, Aysel Unal, Funda Feryal Taş, Şervan Özalkak, Atilla Çayır, Mehmet Nuri Özbek
Aim Triple-A Syndrome(TAS) is a rare autosomal recessive disorder characterized by adrenal insufficiency, achalasia, and alacrimia. This disorder is caused by mutations in the AAAS gene. The aim of this study is to discuss the clinical, laboratory an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::115fca7dfc93ce95adbdbc7c90801a6d
https://doi.org/10.21203/rs.3.rs-1933587/v1
https://doi.org/10.21203/rs.3.rs-1933587/v1
Autor:
Şervan, Özalkak, Meliha, Demiral, Edip, Ünal, Funda Feryal, Taş, Hüseyin, Onay, Hüseyin, Demirbilek, Mehmet Nuri, Özbek
Publikováno v:
Journal of clinical research in pediatric endocrinology.
Congenital generalized lipodystrophy (CGL) is a rare autosomal recessive disorder characterized by an almost complete absence of body fat. In CGL, patients may have hyperphagia due to leptin deficiency. Recombinant human leptin (metreleptin) has been
Autor:
Funda Feryal Taş, Serdar Ceylaner, Ruken Yıldırım, Suat Tekin, Yusuf Kenan Haspolat, Edip Unal
Publikováno v:
Gynecological Endocrinology. 36:739-742
Aims: 17α-hydroxylase deficiency is a rare form of congenital adrenal hyperplasia (CAH) which is inherited autosomal recessive. It occurs result of a mutations in gene cytochrome (CYP)17A1, which encodes both 17α-hydroxylase and 17,20-lyase enzymes
Publikováno v:
Güncel Pediatri. 17:412-423
Publikováno v:
Abstracts.