Volume 9, Issue 1

March 2017
(1) Review, (9) Original Article, (5) Case Report

Cover

Cover Page


Review

Non-Classical Congenital Adrenal Hyperplasia in Childhood
  • Selim Kurtoglu
  • Nihal Hatipoglu
J Clin Res Pediatr Endocrinol 2017; 9: 1-7 DOI: 10.4274/jcrpe.3378 PMID:27354284

Original Article

Subclinical Hypothyroidism in Danish Lean and Obese Children and Adolescents
  • Maria Dahl
  • Johanne Dam Ohrt
  • Cilius Esmann Fonvig
  • Julie Tonsgaard Kloppenborg
  • Oluf Pedersen
  • Torben Hansen
  • Jens-Christian Holm
J Clin Res Pediatr Endocrinol 2017; 9: 8-16 DOI: 10.4274/jcrpe.3319 PMID:27611730
Neck Circumference to Assess Obesity in Preschool Children
  • Meda Kondolot
  • Duygu Horoz
  • Serpil Poyrazoglu
  • Arda Borlu
  • Ahmet Öztürk
  • Selim Kurtoglu
  • Mümtaz M. Mazicioglu
J Clin Res Pediatr Endocrinol 2017; 9: 17-23 DOI: 10.4274/jcrpe.3525 PMID:27660068
Role of Versican and ADAMTS-1 in Polycystic Ovary Syndrome
  • Sibel Özler
  • Efser Öztaş
  • Aytekin Tokmak
  • Merve Ergin
  • Meryem Kuru Pekcan
  • Basak Gümüs Güler
  • Halil Ibrahim Yakut
  • Nafiye Yilmaz
J Clin Res Pediatr Endocrinol 2017; 9: 24-30 DOI: 10.4274/jcrpe.3414 PMID:27908842
The Relationship between Serum Zonulin Level and Clinical and Laboratory Parameters of Childhood Obesity
  • Tuncay Küme
  • Sezer Acar
  • Hale Tuhan
  • Gönül Çatlı
  • Ahmet Anık
  • Özlem Gürsoy Çalan
  • Ece Böber
  • Ayhan Abacı
J Clin Res Pediatr Endocrinol 2017; 9: 31-38 DOI: 10.4274/jcrpe.3682 PMID:28008865
Comparison of Updated Weight and Height Percentiles with Previous References in 6-17-Year-Old Children in Kayseri, Turkey
  • Gökmen Zararsiz
  • Betül Çiçek
  • Meda Kondolot
  • M. Mümtaz Mazicioglu
  • Ahmet Öztürk
  • Selim Kurtoglu
J Clin Res Pediatr Endocrinol 2017; 9: 39-47 DOI: 10.4274/jcrpe.3482 PMID:27507256
Association Between Endocrine Diseases and Serous Otitis Media in Children
  • Murat Koçyigit
  • Taliye Çakabay
  • Safiye G. Örtekin
  • Teoman Akçay
  • Güven Özkaya
  • Selin Üstün Bezgin
  • Melek Yildiz
  • Mustafa Kemal Adali
J Clin Res Pediatr Endocrinol 2017; 9: 48-51 DOI: 10.4274/jcrpe.3585 PMID:27612192
Clinical and Mutational Features of Three Chinese Children with Congenital Generalized Lipodystrophy
  • Xueying Su
  • Ruizhu Lin
  • Yonglan Huang
  • Huiying Sheng
  • Xiaofei Li
  • Tzer Hwu Ting
  • Li Liu
  • Xiuzhen Li
J Clin Res Pediatr Endocrinol 2017; 9: 52-57 DOI: 10.4274/jcrpe.3556 PMID:27612026
Age-Specific Frequencies and Characteristics of Ovarian Cysts in Children and Adolescents
  • Hamdi Cihan Emeksiz
  • Oksan Derinöz
  • Esra Betül Akkoyun
  • Faruk Güçlü Pinarli
  • Aysun Bideci
J Clin Res Pediatr Endocrinol 2017; 9: 58-62 DOI: 10.4274/jcrpe.3781 PMID:28044991
Safety and Efficacy of Stosstherapy in Nutritional Rickets
  • Daipayan Chatterjee
  • Mathad K. S. Swamy
  • Vikas Gupta
  • Vasu Sharma
  • Akshat Sharma
  • Krishti Chatterjee
J Clin Res Pediatr Endocrinol 2017; 9: 63-69 DOI: 10.4274/jcrpe.3557 PMID:27550890

Case Report

Uniparental Isodisomy of Chromosome 1 Unmasking an Autosomal Recessive 3-Beta Hydroxysteroid Dehydrogenase Type II-Related Congenital Adrenal Hyperplasia
  • Karin Panzer
  • Osayame A. Ekhaguere
  • Benjamin Darbro
  • Jennifer Cook
  • Oleg A. Shchelochkov
J Clin Res Pediatr Endocrinol 2017; 9: 70-73 DOI: 10.4274/jcrpe.3680 PMID:27796263
Follow-up Findings in a Turkish Girl with Pseudohypoparathyroidism Type Ia Caused by a Novel Heterozygous Mutation in the GNAS Gene
  • Sezgin Sahin
  • Olaf Hiort
  • Susanne Thiele
  • Olcay Evliyaoglu
  • Beyhan Tüysüz
J Clin Res Pediatr Endocrinol 2017; 9: 74-79 DOI: 10.4274/jcrpe.3191 PMID:27425121
Clinical and Molecular Genetic Analysis in Three Children with Wolfram Syndrome: A Novel WFS1 Mutation (c.2534T>A)
  • Gamze Çelmeli
  • Doga Türkkahraman
  • Yusuf Çürek
  • Jayne Houghton
  • Sema Akçurin
  • Iffet Bircan
J Clin Res Pediatr Endocrinol 2017; 9: 80-84 DOI: 10.4274/jcrpe.2894 PMID:27468121
Testicular Adrenal Rest Tumor in Two Brothers with a Novel Mutation in the 3-Beta-Hydroxysteroid Dehydrogenase-2 Gene
  • Ayla Güven
  • Seher Polat
J Clin Res Pediatr Endocrinol 2017; 9: 85-90 DOI: 10.4274/jcrpe.3306 PMID:27476613
A Rare Cause of Short Stature: 3M Syndrome in a Patient with Novel Mutation in OBSL1 Gene
  • Meliksah Keskin
  • Nursel Muratoglu Sahin
  • Erdal Kurnaz
  • Elvan Bayramoglu
  • Senay Savas Erdeve
  • Zehra Aycan
  • Semra Çetinkaya
J Clin Res Pediatr Endocrinol 2017; 9: 91-94 DOI: 10.4274/jcrpe.3238 PMID:27796265

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