Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Edip Ünal"'
Publikováno v:
JCRPE, Vol 16, Iss 1, Pp 76-83 (2024)
INTRODUCTION: Noonan syndrome (NS) is characterized by dysmorphic facial features, short stature, congenital heart defects, and varying levels of developmental delays. It is a genetic, multisystem disorder with autosomal dominant inheritance and is t
Externí odkaz:
https://doaj.org/article/6bf50421226a4fad894e64571fd939a4
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:
Aysel Taktak, Mehtap Akbalık Kara, Neslihan Çiçek, Caner Alparslan, Edip Ünal, Mehmet Ağın, Mehmet Nuri Özbek
Publikováno v:
Turkish Journal of Nephrology, Vol 32, Iss 3, Pp 249-254 (2023)
Externí odkaz:
https://doaj.org/article/ffbcb11ee2ca44c5995f200643c19b95
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:
Damla Gökşen, Ediz Yeşilkaya, Samim Özen, Yılmaz Kor, Erdal Eren, Özlem Korkmaz, Merih Berberoğlu, Gülay Karagüzel, Eren Er, Ayhan Abacı, Olcay Evliyaoğlu, Emine Demet Akbaş, Edip Ünal, Semih Bolu, Özlem Nalbantoğlu, Ahmet Anık, Meltem Tayfun, Muammer Büyükinan, Saygın Abalı, Gülay Can Yılmaz, Deniz Kör, Elif Söbü, Zeynep Şıklar, Recep Polat, Şükran Darcan
Publikováno v:
JCRPE, Vol 13, Iss 4, Pp 433-438 (2021)
Objective:Monogenic diabetes is a heterogeneous disease that causes functional problems in pancreatic beta cells and hyperglycemia. The aim of this study was to determine the clinical and laboratory features, the admission characteristics and distrib
Externí odkaz:
https://doaj.org/article/d246cab85ec94663b4edadd4a7d45387
Autor:
Zeynep Şıklar, Serap Turan, Abdullah Bereket, Firdevs Baş, Tülay Güran, Azad Akberzade, Ayhan Abacı, Korcan Demir, Ece Böber, Mehmet Nuri Özbek, Cengiz Kara, Şükran Poyrazoğlu, Murat Aydın, Aslı Kardelen, Ömer Tarım, Erdal Eren, Nihal Hatipoğlu, Muammer Büyükinan, Nesibe Akyürek, Semra Çetinkaya, Elvan Bayramoğlu, Beray Selver Eklioğlu, Ahmet Uçaktürk, Saygın Abalı, Damla Gökşen, Yılmaz Kor, Edip Ünal, İhsan Esen, Ruken Yıldırım, Onur Akın, Atilla Çayır, Emine Dilek, Birgül Kırel, Ahmet Anık, Gönül Çatlı, Merih Berberoğlu
Publikováno v:
JCRPE, Vol 12, Iss 2, Pp 150-159 (2020)
Objective:Hypophosphatemic rickets (HR) is a rare renal phosphate-wasting disorder, which is usually X-linked and is commonly caused by PHEX mutations. The treatment and follow-up of HR is challenging due to imperfect treatment options.Methods:Here w
Externí odkaz:
https://doaj.org/article/57157ae9f20b435fb128022ec51d0c16
Autor:
Erdal Eren, Ayça Törel Ergür, Şükriye Pınar İşgüven, Eda Çelebi Bitkin, Merih Berberoğlu, Zeynep Şıklar, Firdevs Baş, Servet Yel, Serpil Baş, Elif Söbü, Abdullah Bereket, Serap Turan, Halil Sağlam, Zeynep Atay, Oya Ercan, Tülay Güran, Mehmet Emre Atabek, Hüseyin Anıl Korkmaz, Aylin Kılınç Uğurlu, Ayşehan Akıncı, Esra Döğer, Enver Şimşek, Emine Demet Akbaş, Ayhan Abacı, Ülkü Gül, Sezer Acar, Eda Mengen Uçaktürk, Melek Yıldız, Edip Ünal, Ömer Tarım
Publikováno v:
JCRPE, Vol 11, Iss 2, Pp 149-156 (2019)
Objective:We aimed to report the characteristics at admission, diagnosis, treatment, and follow-up of cases of pediatric hyperprolactinemia in a large multicenter study.Methods:We reviewed the records of 233 hyperprolactinemic patients, under 18 year
Externí odkaz:
https://doaj.org/article/bfc431f9dff74272a2b6236d033334a3
Autor:
İhsan Esen, Elvan Bayramoğlu, Melek Yıldız, Murat Aydın, Esin Karakılıç Özturhan, Zehra Aycan, Semih Bolu, Hasan Önal, Yılmaz Kör, Deniz Ökdemir, Edip Ünal, Aşan Önder, Olcay Evliyaoğlu, Atilla Çayır, Mehmet Taştan, Ayşegül Yüksel, Aylin Kılınç, Muammer Büyükinan, Bahar Özcabı, Onur Akın, Çiğdem Binay, Suna Kılınç, Ruken Yıldırım, Emel Hatun Aytaç, Elif Sağsak
Publikováno v:
JCRPE, Vol 11, Iss 2, Pp 164-172 (2019)
Objective:To determine the demographic and biochemical features of childhood and juvenile thyrotoxicosis and treatment outcome.Methods:We reviewed the records of children from 22 centers in Turkey who were diagnosed with thyrotoxicosis between 2007 t
Externí odkaz:
https://doaj.org/article/96ed27a3391b46649c54ada49a6403e7
Publikováno v:
Güncel Pediatri. 20:373-378
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::20f3cd597ae50108839c057ca2e7d4e1
https://doi.org/10.4274/jcp.2022.66564
https://doi.org/10.4274/jcp.2022.66564
Publikováno v:
Güncel Pediatri. 20:174-180
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::667fd9876d9169de9d9e396244b277df
https://doi.org/10.4274/jcp.2022.54280
https://doi.org/10.4274/jcp.2022.54280