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Left and right ventricular functions may be impaired in children diagnosed with subclinical hypothyroidism 

Akın, Alper; Ünal, Edip; Yıldırım, Ruken; Türe, Mehmet; Balık, Hasan; Haspolat, Yusuf Kenan (Nature Research, 2020)
Subclinical hypothyroidism (SH) may infuence both ventricular functions. The aim of this study was to evaluation the fndings of Tissue Doppler Imaging (TDI) and other echocardiography modalities in children with SH. We ...
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Nationwide Turkish cohort study of hypophosphatemic rickets 

Şıklar, Zeynep; Turan, Serap; Bereket, Abdullah; Baş, Firdevs; Güran, Tülay; Akberzade, Azad; Abacı, Ayhan; Demir, Korcan; Böber, Ece; Özbek, Mehmet Nuri; Kara, Cengiz; Poyrazǒglu, Şükran; Aydın, Murat; Kardelen, Aslı Derya; Tarım, Ömer Faruk; Eren, Erdal; Hatipoǧlu, Nihal; Büyükinan, Muammer; Akyürek, Nesibe; Çetinkaya, Semra Çaǧlar; Bayramoǧlu, Elvan; Eklioǧlu, Beray Selver; Uçaktürk, Ahmet; Abali, Saygin; Gökşen, Damla; Kör, Yilmaz; Ünal, Edip; Esen, İhsan; Yıldırım, Ruken; Akın, Önur; Çayır, Atilla; Dilek, Emine; Kırel, Birgül; Anık, Ahmet; Çatlι, Gönül; Berberoǧlu, Merih (Galenos Yayincilik, 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 ...
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Novel markers in predicting non-alcoholic liver fatty and metabolic syndrome in obese children and adolescents: Atherogenic index of plasma and monocyte / high-density lipoprotein cholesterol ratio 

Ünal, Edip; Haspolat, Yusuf Kenan (2020)
Aim: The aim of this study is to investigate the relationship between metabolic syndrome (MetS), insulin resistance, waist circumference (WC) and non-alcoholic fatty liver disease (NAFLD) with atherogenic index of plasma ...
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A different perspective of elevated lactace in pediatric patients with diabetic ketoacidosis 

Ünal, Edip; Pirinççioğlu, Ayfer Gözü; Yanmaz, Sercan Yücel; Yılmaz, Kamil; Taşkesen, Mustafa; Haspolat, Yusuf Kenan (Romanian Academy, 2020)
Objective: This study aims to determine the frequency and prognostic significance of lactic acidosis in children with diabetic ketoacidosis (DKA) admitted to the pediatric intensive care unit. Methods: The study was ...
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A novel variant in LCHGR gene in 3 siblings with type 1 leydig cell hypoplasia 

Karakaya, Amine Aktar; Ünal, Edip; Beştaş, Aslı; Taş, Funda; Onay, Hüseyin; Haspolat, Yusuf Kenan (Taylor & Francis Group, 2020)
Introduction: Leydig cell hypoplasia (LCH) is an autosomal recessive disease that causes 46, XY sex development disorder. The patients with LCH are usually in the female phenotype and are presented with the complaints of ...
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A rare cause of delayed puberty in two cases with 46,XX and 46,XY karyotype: 17 α-hydroxylase deficiency due to a novel variant in CYP17A1 gene 

Ünal, Edip; Yıldırım, Ruken; Taş, Funda Feryal; Tekin, Suat; Ceylaner, Serdar; Haspolat, Yusuf Kenan (Taylor & Francis Group, 2020)
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 ...
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YIPF5 mutations cause neonatal diabetes and microcephaly through endoplasmic reticulum stress 

de Franco, Elisa; Lytrivi, Maria; Ibrahim, Hazem; Montaser, Hossam; Wakeling, Matthew Neil; Fantuzzi, Federica; Patel, Kashyap A.; Demarez, Céline; Cai, Ying; Igoillo-Esteve, Mariana; Cosentino, Cristina; Lithovius, Väinö; Vihinen, Helena; Jokitalo, Eija; Laver, Thomas William; Johnson, Matthew B.; Sawatani, Toshiaki; Shakeri, Hadis; Pachera, Nathalie; Haliloǧlu, Belma; Özbek, Mehmet Nuri; Ünal, Edip; Yıldırım, Ruken; Godbole, Tushar R.; Yıldız, Melek; Aydın, Banu Küçükemre; Bilheu, Angéline; Suzuki, Ikuo K. (American Society for Clinical Investigation, 2020)
Neonatal diabetes is caused by single gene mutations reducing pancreatic β cell number or impairing β cell function. Understanding the genetic basis of rare diabetes subtypes highlights fundamental biological processes in ...



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Ünal, Edip (7)
Haspolat, Yusuf Kenan (5)Yıldırım, Ruken (4)Özbek, Mehmet Nuri (2)Abacı, Ayhan (1)Abali, Saygin (1)Akberzade, Azad (1)Akyürek, Nesibe (1)Akın, Alper (1)Akın, Önur (1)... View MoreSubjectChildren (2)Primary amenorrhea (2)17α-hydroxylase (1)Adolescents (1)Atherogenic index of plasma (1)Brain edema (1)Cardiac-function (1)Cell line (1)CYP17A1 gene (1)Delayed puberty (1)... View MoreDate Issued
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