Volume 8, Issue 4

December 2016
(1) Review, (12) Original Research, (5) Case Report, (1) Brief Report, (1) Letter to the Editor, (3) Other

Cover

Cover Page


Review

Current Status of Childhood Hyperinsulinemic Hypoglycemia in Turkey
  • Zeynep Şıklar
  • Merih Berberoğlu
J Clin Res Pediatr Endocrinol 2016; 8: 375-380 DOI: 10.4274/jcrpe.2991 PMID:27181376

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
J Clin Res Pediatr Endocrinol 2016; 8: 381-391 DOI: 10.4274/jcrpe.2720 PMID:27217155
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
J Clin Res Pediatr Endocrinol 2016; 8: 392-398 DOI: 10.4274/jcrpe.3091 PMID:27215137
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
J Clin Res Pediatr Endocrinol 2016; 8: 399-404 DOI: 10.4274/jcrpe.3082 PMID:27353561
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
J Clin Res Pediatr Endocrinol 2016; 8: 405-410 DOI: 10.4274/jcrpe.2784 PMID:27217259
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
J Clin Res Pediatr Endocrinol 2016; 8: 411-418 DOI: 10.4274/jcrpe.3171 PMID:27353948
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
J Clin Res Pediatr Endocrinol 2016; 8: 419-424 DOI: 10.4274/jcrpe.3260 PMID:27354200
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
J Clin Res Pediatr Endocrinol 2016; 8: 425-431 DOI: 10.4274/jcrpe.2504 PMID:27476441
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
J Clin Res Pediatr Endocrinol 2016; 8: 432-438 DOI: 10.4274/jcrpe.2743 PMID:27467896
The Effect of Congenital and Postnatal Hypothyroidism on Depression-Like Behaviors in Juvenile Rats
  • Erdoğan Özgür
  • Börte Gürbüz Özgür
  • Hatice Aksu
  • Gökhan Cesur
J Clin Res Pediatr Endocrinol 2016; 8: 439-444 DOI: 10.4274/jcrpe.3498 PMID:27611926
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
J Clin Res Pediatr Endocrinol 2016; 8: 445-451 DOI: 10.4274/jcrpe.3474 PMID:27550850
Effect of Cytokine Signaling 3 Gene Polymorphisms in Childhood Obesity
  • Mehmet Boyraz
  • Ediz Yeşilkaya
  • Fatih Ezgü
  • Aysun Bideci
  • Haldun Doğan
  • Korkut Ulucan
  • Peyami Cinaz
J Clin Res Pediatr Endocrinol 2016; 8: 452-460 DOI: 10.4274/jcrpe.3167 PMID:27611604
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
J Clin Res Pediatr Endocrinol 2016; 8: 461-467 DOI: 10.4274/jcrpe.3301 PMID:27476528

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
J Clin Res Pediatr Endocrinol 2016; 8: 468-471 DOI: 10.4274/jcrpe.2539 PMID:27087023
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
J Clin Res Pediatr Endocrinol 2016; 8: 472-477 DOI: 10.4274/jcrpe.2717 PMID:27087618
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
J Clin Res Pediatr Endocrinol 2016; 8: 478-481 DOI: 10.4274/jcrpe.2773 PMID:27181099
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
J Clin Res Pediatr Endocrinol 2016; 8: 482-483 DOI: 10.4274/jcrpe.3021 PMID:27217304
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
J Clin Res Pediatr Endocrinol 2016; 8: 484-489 DOI: 10.4274/jcrpe.3128 PMID:27353739

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
J Clin Res Pediatr Endocrinol 2016; 8: 490-495 DOI: 10.4274/jcrpe.3209 PMID:27354120

Letter to the Editor

Wolcott-Rallison Syndrome with Novel EIF2AK3 Gene Mutation
  • Fatih Gürbüz
  • Bilgin Yüksel
  • Ali Kemal Topaloğlu
J Clin Res Pediatr Endocrinol 2016; 8: 496-497 DOI: 10.4274/jcrpe.3065

Other

2016 Referee Index
J Clin Res Pediatr Endocrinol 2016; 8: 0-0
2016 Author Index
J Clin Res Pediatr Endocrinol 2016; 8: 0-0
2016 Subject Index
J Clin Res Pediatr Endocrinol 2016; 8: 0-0

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