Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Ciğdem Binay"'
Publikováno v:
JCRPE, Vol 14, Iss 1, Pp 69-75 (2022)
INTRODUCTION: Advances in knowledge of neurotrophic factors are now revealing the complex control of energy homeostasis and appetite, as well as the crucial role these factors play in nervous system function. The aim of this study was to assess serum
Externí odkaz:
https://doaj.org/article/d6a06a27a61947f1aec1095c70dcf7bd
Publikováno v:
Case Reports in Endocrinology, Vol 2017 (2017)
Horner syndrome (HS), caused by an interruption in the oculosympathetic pathway, is characterised by myosis, ipsilateral blepharoptosis, enophthalmos, facial anhydrosis, and vascular dilation of the lateral part of the face. HS is a rare complication
Externí odkaz:
https://doaj.org/article/a43c3b098ff84e5cae1a7e17500588dc
Autor:
Enver Şimşek, Oğuz Çilingir, Tülay Şimşek, Sinem Kocagil, Ebru Erzurumluoğlu Gökalp, Meliha Demiral, Çiğdem Binay
Publikováno v:
JCRPE, Vol 16, Iss 2, Pp 137-145 (2024)
INTRODUCTION: Maturity-onset diabetes of the young (MODY) is the most common type of monogenic diabetes. To date, mutations have been identified in 14 different genes of patients with a clinical diagnosis of MODY. This study screened mutations in 14
Externí odkaz:
https://doaj.org/article/dc998513a3bb459ca58f77550f1024b7
Autor:
Selis Gülseven Güven, Çiğdem Binay
Publikováno v:
JCRPE, Vol 15, Iss 2, Pp 127-137 (2023)
INTRODUCTION: Type 1 diabetes (T1D), one of the most common childhood diseases worldwide, can cause hearing loss through systemic effects. Diabetes-induced hearing loss is considered a progressive sensorineural hearing loss with a gradual onset, typi
Externí odkaz:
https://doaj.org/article/88363fd10a294d7286bea5a9974cffe9
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:
İstanbul Kuzey Klinikleri, Vol 5, Iss 4, Pp 277-281 (2018)
INTRODUCTION[|]The granulocyte colony-stimulating factor (G-CSF) is the most commonly used hematopoietic growth factor recombinant DNA technology. It affects bone metabolism by modulating both osteoclast and osteoblast functions. The aim of the prese
Externí odkaz:
https://doaj.org/article/cb16b01491214b6c8b8d25112544e93f
Publikováno v:
International Journal of Endocrinology, Vol 2014 (2014)
Background. Nonclassic congenital adrenal hyperplasia (NCAH), caused by mutations in the gene encoding 21-hydroxylase, is a common autosomal recessive disorder. In the present work, our aim was to determine the prevalence of NCAH presenting as premat
Externí odkaz:
https://doaj.org/article/8707a38d075d4b4c8a08fb748582a7a1