E-ISSN: 1308-5735
ISSN: 1308-5727
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Volume 8, Issue 4
December 2016
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Review
1
Original Research
12
Case Report
5
Brief Report
1
Letter to the Editor
1
Other
3
Review
Current Status of Childhood Hyperinsulinemic Hypoglycemia in Turkey
Zeynep Şıklar
Merih Berberoğlu
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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
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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
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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
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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
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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
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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
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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
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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
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The Effect of Congenital and Postnatal Hypothyroidism on Depression-Like Behaviors in Juvenile Rats
Erdoğan Özgür
Börte Gürbüz Özgür
Hatice Aksu
Gökhan Cesur
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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
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Effect of Cytokine Signaling 3 Gene Polymorphisms in Childhood Obesity
Mehmet Boyraz
Ediz Yeşilkaya
Fatih Ezgü
Aysun Bideci
Haldun Doğan
Korkut Ulucan
Peyami Cinaz
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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
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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
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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
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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
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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
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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
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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
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Letter to the Editor
Wolcott-Rallison Syndrome with Novel EIF2AK3 Gene Mutation
Fatih Gürbüz
Bilgin Yüksel
Ali Kemal Topaloğlu
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Date of Foundation
Jan 2008
Abbreviation
J Clin Res Pediatr Endocrinol
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