Impact of Socioeconomic Characteristics on Metabolic Control in Children with Type 1 Diabetes in a Developing Country

Abeer ALASSAF, Rasha ODEH, Lubna GHARAIBEH, Sarah IBRAHIM, Kamel AJLOUNI

Serum Neuron-specific Enolase and S100 Calcium-binding Protein B in Pediatric Diabetic Ketoacidosis

Hatem Hamed ELSHORBAGY, Naglaa Fathy BARSEEM, Akram Elshafey ELSADEK, Ashraf Hamed AL SHOKARY, Yehia Hamed Abdel MAKSOUD, Sameh Elsayed ABDULSAMEA, Iman M. TALAAT, Hany Abdelaziz SULIMAN, Naglaa M KAMAL, Waleed E. ABDELGHANI, Sanaa Mohammed AZAB, Dalia Mohamed Nour EL DIN

Clinical Management and Gene Mutation Analysis of Children with Congenital Hyperinsulinism in South China

Aijing XU, Jing CHENG, Huiying SHENG, Zhe WEN, Yunting LIN, Zhihong ZHOU, Chunhua ZENG, Yongxian SHAO, Cuiling LI, Li LIU, Xiuzhen Lİ

A Novel Nonsense Mutation of PHF6 in a Female with Extended Phenotypes of Borjeson-Forssman-Lehmann Syndrome

Xia ZHANG, Yanjie FAN, Xiaomin LIU, Ming-Ang ZHU, Yu SUN, Hui YAN, Yunjuan HE, Xiantao YE, Xuefan GU, Yongguo YU

A Novel Homozygous Mutation of the Acid-Labile Subunit (IGFALS) Gene in a Male Adolescent

ŞÜKRAN POYRAZOĞLU, Vivian HWA, Andrew DAUBER, Ron ROSENFELD, FATMA FEYZA DARENDELİLER

Catch-up Growth at Term Equivalence in Extremely Premature Small for Gestational Age Infants Compared with Extremely Premature Appropriate for Gestational Age Infants

Hüseyin Anıl KORKMAZ

Novel Mutations in Obesity-related Genes in Turkish Children with Non-syndromic Early Onset Severe Obesity: A Multicentre Study

Ayşehan AKINCI, Doğa TÜRKKAHRAMAN, İbrahim TEKEDERELİ, Leyla ÖZER, Bahri EVREN, İbrahim ŞAHİN, Tarkan KALKAN, Yusuf ÇÜREK, Emine ÇAMTOSUN, Esra DÖĞER, Aysun BİDECİ, Ayla GÜVEN, Erdal EREN, Özlem SANGÜN, Atilla ÇAYIR, Pelin BİLİR, Ayça ERGÜR, OYA ERCAN

Glucose Metabolism Evaluated by Glycated Hemoglobin and Insulin Sensitivity Indices in Children Treated with Recombinant Human Growth Hormone

Maria Chiara PELLEGRIN, Daria MICHELON, Elena FALESCHINI, Claudio GERMANI, Egidio BARBI, Gianluca TORNESE

Clinical and Biochemical Phenotype of Adolescent Males with Gynecomastia

Miłosz LOREK, Dominika TOBOLSKA LOREK, Barbara KALINA FASKA, Aleksandra JANUSZEK TRZCIAKOWSKA, Aneta GAWLIK

A Case of Autosomal Dominant Osteopetrosis Type 2 with a CLCN7 Gene Mutation

Sol KANG, Young Kyung KANG, Jun Ah LEE, Dong Ho KIM, Jung Sub LIM

Three Siblings with Idiopathic Hypogonadotropic Hypogonadism in a Nonconsanguineous Family: A Novel KISS1R/GPR54 Loss-ofFunction Mutation

Özlem NALBANTOĞLU, Gülçin ARSLAN, Özge KÖPRÜLÜ, Filiz HAZAN, Semra GÜRSOY, BEHZAT ÖZKAN

Achieving Optimal Short- and Long-term Responses to Paediatric Growth Hormone Therapy

Jan M. WIT, Asma DEEB, Bassam BIN ABBAS, Angham AL MUTAIR, Ekaterina KOLEDOVA, Martin O. SAVAGE

Accuracy of Tri-ponderal Mass Index and Body Mass Index in Estimating Insulin Resistance, Hyperlipidemia, Impaired Liver Enzymes or Thyroid Hormone Function and Vitamin D Levels in Children and Adolescents

Neşe AKCAN, Rüveyde BUNDAK

Liver Biochemical Abnormalities in Adolescent Patients with Turner Syndrome

Małgorzata WOJCIK, Anna RUSZALA, Dominika JANUS, Jerzy B. STARZYK

Subclinical Myocardial Dysfunction Demonstrated by Speckle Tracking Echocardiography in Children with Euthyroid Hashimoto’s Thyroiditis

Emine AZAK, Seyit Ahmet UÇAKTÜRK, İBRAHİM İLKER ÇETİN, HAZIM ALPER GÜRSU, Eda MENGEN, Utku PAMUK

Isolated Growth Hormone Deficiency Type 2 due to a novel GH1 Mutation: A Case Report

Ahmad KAUTSAR, Jan M. WIT, Aman PULUNGAN