Cover

Cover Page

Review

Current Status of Childhood Hyperinsulinemic Hypoglycemia in Turkey

• Zeynep Şıklar
• Merih Berberoğlu

Original Research

Breast-Milk Iodine Concentrations, Iodine Status, and Thyroid Function of Breastfed Infants Aged 2-4 Months and Their Mothers Residing in a South African Township

• Jennifer Osei
• Maria Andersson
• Olivia van der Reijden
• Susanne Dold
• Cornelius M. Smuts
• Jeannine Baumgartner

Luteinizing Hormone Secretion during Gonadotropin-Releasing Hormone Stimulation Tests in Obese Girls with Central Precocious Puberty

• Hae Sang Lee
• Jong Seo Yoon
• Jin Soon Hwang

The Role of Osteopontin in the Pathogenesis and Complications of Type 1 Diabetes Mellitus in Children

• Mohamed A. Talat
• Laila Metwaly Sherief
• Hosam Fathy El-Saadany
• Anwar Ahmed Rass
• Rabab M. Saleh
• Maha Mahmoud Hamed Sakr

Association between Common Genetic Variants and Polycystic Ovary Syndrome Risk in a Chinese Han Population

• Ying Sun
• Yi Yuan
• Hua Yang
• Jingjie Li
• Tian Feng
• Yongri Ouyang
• Tianbo Jin
• Ming Liu

Development and Validation of a Pediatric Endocrine Knowledge Assessment Questionnaire: Impact of ac Pediatric Endocrine Knowledge Assessment Questionnaire Intervention Study

• Nidhi Gupta
• Marwan Zidan
• Kathleen Moltz
• Amita Adhikari
• Colleen Buggs-Saxton
• Hanaa Zidan
• Dania Abushanab
• Aida Lteif
• Chandra Edwin

The 13C-Glucose Breath Test for Insulin Resistance Assessment in Adolescents: Comparison with Fasting and Post-Glucose Stimulus Surrogate Markers of Insulin Resistance

• Jorge Maldonado-Hernández
• Azucena Martínez-Basila
• Alejandra Salas-Fernández
• José R. Navarro-Betancourt
• Mónica I. Piña-Aguero
• Mariela Bernabe-García

Lower Plasma Ghrelin Levels are Found in Women with Diabetes-Complicated Pregnancies

• Rita Angélica Gómez-Díaz
• Monica P. Gómez-Medina
• Eleazar Ramírez-Soriano
• Lucio López-Robles
• Carlos A. Aguilar-Salinas
• Renata Saucedo
• Arturo Zarate
• Adan Valladares-Salgado
• Niels H. Wacher

Pseudohypoparathyroidism Type 1A-Subclinical Hypothyroidism and Rapid Weight Gain as Early Clinical Signs: A Clinical Review of 10 Cases

• Simon Kayemba-Kay’s
• Cedric Tripon
• Anne Heron
• Peter Hindmarsh

The Effect of Congenital and Postnatal Hypothyroidism on Depression-Like Behaviors in Juvenile Rats

• Erdoğan Özgür
• Börte Gürbüz Özgür
• Hatice Aksu
• Gökhan Cesur

Vitamin D Deficiency in Pediatric Fracture Patients: Prevalence, Risk Factors, and Vitamin D Supplementation

• Erwin A. Gorter
• Wilma Oostdijk
• Abraham Felius
• Pieta Krijnen
• Inger B. Schipper

Effect of Cytokine Signaling 3 Gene Polymorphisms in Childhood Obesity

• Mehmet Boyraz
• Ediz Yeşilkaya
• Fatih Ezgü
• Aysun Bideci
• Haldun Doğan
• Korkut Ulucan
• Peyami Cinaz

Prevalence of Vitamin D Deficiency and Calcium Homeostasis in Saudi Children

• Adnan M. Al Shaikh
• Bahaa Abaalkhail
• Ashraf Soliman
• Ibrahim Kaddam
• Khalid Aseri
• Yousef Al Saleh
• Ali Al Qarni
• Ahmed Al Shuaibi
• Waleed Al Tamimi
• Abdel Moniem Mukhtar

Case Report

Complex Glycerol Kinase Deficiency and Adrenocortical Insufficiency in Two Neonates

• Sabriye Korkut
• Osman Baştuğ
• Margarita Raygada
• Nihal Hatipoğlu
• Selim Kurtoğlu
• Mustafa Kendirci
• Charalampos Lyssikatos
• Constantine A. Stratakis

A Novel Missense Mutation in the CLPP Gene Causing Perrault Syndrome Type 3 in a Turkish Family

• Fatma Dursun
• Hussein Sheikh Ali Mohamoud
• Noreen Karim
• Muhammad Naeem
• Musharraf Jelani
• Heves Kırmızıbekmez

A Novel Homozygous Mutation in the KCNJ11 Gene of a Neonate with Congenital Hyperinsulinism and Successful Management with Sirolimus

• Sevim Ünal
• Deniz Gönülal
• Ahmet Uçaktürk
• Betül Siyah Bilgin
• Sarah E. Flanagan
• Fatih Gürbüz
• Meltem Tayfun
• Selin Elmaoğulları
• Aslıhan Araslı
• Fatma Demirel
• Sian Ellard
• Khalid Hussain

A p.(Glu809Lys) Mutation in the WFS1 Gene Associated with Wolfram-like Syndrome: A Case Report

• Dagmar Prochazkova
• Zuzana Hruba
• Petra Konecna
• Jarmila Skotakova
• Lenka Fajkusova

A Case of Vitamin D-Dependent Rickets Type 1A with a Novel Mutation in the Uzbek Population

• Bahar Özcabı
• Feride Tahmiscioğlu Bucak
• Sevinç Jaferova
• Çiğdem Oruç
• Amra Adrovic
• Serdar Ceylaner
• Oya Ercan
• Olcay Evliyaoğlu

Brief Report

A Critical Appraisal of Growth Hormone Therapy in Growth Hormone Deficiency and Turner Syndrome Patients in Turkey

• Zehra Yavaş Abalı
• Feyza Darendeliler
• Olcay Neyzi

Letter to the Editor

Wolcott-Rallison Syndrome with Novel EIF2AK3 Gene Mutation

• Fatih Gürbüz
• Bilgin Yüksel
• Ali Kemal Topaloğlu

Other

2016 Referee Index

2016 Author Index

2016 Subject Index