Volume 8, Issue 1 (Supplement)

June 2016
(1) Editorial, (16) Other

Cover

Cover Page


Editorial

Editorial
  • Assoc. Prof. Dr. Korcan Demir
J Clin Res Pediatr Endocrinol 2016; 8: 0-0

Other

Current Perspectives on Pseudohypoparathyroidism-New Classification
  • Serap Turan
J Clin Res Pediatr Endocrinol 2016; 8: 1-2
Disorders/Differences of Sex Development: A World of Uncertainty
  • Eric Vilain
J Clin Res Pediatr Endocrinol 2016; 8: 3-3
Automating Glycemic Management in Diabetes Mellitus with a Bionic Pancreas
  • Steven Jon Russell
J Clin Res Pediatr Endocrinol 2016; 8: 4-4
Use of Next Generation Sequencing in Clinical Practice: The Example of Disorders/Differences of Sex Development
  • Eric Vilain
J Clin Res Pediatr Endocrinol 2016; 8: 5-5
Long-acting Growth Hormone Formulations: Structure and Activity
  • Alan D. Rogol
J Clin Res Pediatr Endocrinol 2016; 8: 6-6
The Genetics of Growth and Growth Disorders: From the Hypothalamus to the Epiphysis
  • Mitchell E. Geffner
J Clin Res Pediatr Endocrinol 2016; 8: 7-8
Turner Syndrome: Care Through the Ages
  • Alan D. Rogol
J Clin Res Pediatr Endocrinol 2016; 8: 9-9
Efficacy and Safety of Long-Acting Gonadotropin Releasing Hormone Analogs
  • Mitchell E. Geffner
J Clin Res Pediatr Endocrinol 2016; 8: 10-10
Genetic Defects Affecting Adrenal Development
  • Allen Lipson
  • Eric Vilain
J Clin Res Pediatr Endocrinol 2016; 8: 11-11
Congenital Adrenal Hyperplasia: Consensus Guidelines and Beyond
  • Mitchell E. Geffner
J Clin Res Pediatr Endocrinol 2016; 8: 12-13
Premature Pubarche, Hyperinsulinemia, Hypothyroxinemia and Hyperintensities in Basal Ganglia: All Caused by a Single Congenital Defect
  • Serpil Bas
  • Tülay Güran
  • Zeynep Atay
  • Belma Haliloglu
  • Saygin Abali
  • Serap Turan
  • Abdullah Bereket
J Clin Res Pediatr Endocrinol 2016; 8: 14-14
A Case Report of Xp21 Contiguous Gene Syndrome: Adrenal Hypoplasia Congenita, Glycerol Kinase Deficiency, and Duchenne Muscular Dystrophy
  • Cengiz Kara
  • Gülay Can Yilmaz
  • Eda Çelebi Bitkin
  • Murat Aydin
J Clin Res Pediatr Endocrinol 2016; 8: 14-15
Pseudohypoparathyroisidm Type 1a: A Case Report
  • Murat Dogan
  • Selami Kocaman
  • Keziban Asli Bala
  • Sultan Kaba
  • Servet Yel
  • Askin Sen
J Clin Res Pediatr Endocrinol 2016; 8: 15-15
A Diabetic Infant with Homozygous LRBA Mutation: The Youngest Patient Reported
  • Ayla Güven
  • Matthew Jonhson
  • Elisa De Franco
J Clin Res Pediatr Endocrinol 2016; 8: 16-16
Idiopathic Hypogonadotrophic Hypogonadism Caused by Inactivating Mutations in SRA1
  • Ayça Ulubay
  • L. Damla Kotan
  • Charlton Cooper
  • Sükran Darcan
  • Ian M. Carr
  • Samim Özen
  • Yi Yan
  • Mohammad K. Hamedani
  • Fatih Gürbüz
  • Eda Mengen
  • Ihsan Turan
  • Gamze Akkus
  • Bilgin Yüksel
  • Etienne Leygue
  • A. Kemal Topaloglu
J Clin Res Pediatr Endocrinol 2016; 8: 17-17
A Novel Missense Mutation in HSD17B3 Gene in Two 46,XY Siblings with Female External Gelitalia
  • Hale Tuhan
  • Ahmet Anik
  • Gönül Çatli
  • Serdar Ceylaner
  • Bumin Dündar
  • Ece Böber
  • Korcan Demir
  • Sezer Acar
  • Derya Erçal
  • Ayhan Abaci
J Clin Res Pediatr Endocrinol 2016; 8: 17-17

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