ISSN: 1308-5727 | E-ISSN: 1308-5735
Volume : 8 Issue : 1 Year : 2024
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Abstracting & Indexing
Turkish Society for Pediatric Endocrinology and Diabetes
JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY - J Clin Res Pediatr Endocrinol: 8 (1)
Volume: 8  Suppl: 1 - 2016
1.Cover

Pages I - XI

2.Current Perspectives on Pseudohypoparathyroidism-New Classification
Serap Turan
Pages 1 - 2
Abstract |Full Text PDF

3.Disorders/Differences of Sex Development: A World of Uncertainty
Eric Vilain
Page 3
Abstract |Full Text PDF

4.Automating Glycemic Management in Diabetes Mellitus with a Bionic Pancreas
Steven Jon Russell
Page 4
Abstract |Full Text PDF

5.Use of Next Generation Sequencing in Clinical Practice: The Example of Disorders/Differences of Sex Development
Eric Vilain
Page 5
Abstract |Full Text PDF

6.Long-acting Growth Hormone Formulations: Structure and Activity
Alan D. Rogol
Page 6
Abstract |Full Text PDF

7.The Genetics of Growth and Growth Disorders: From the Hypothalamus to the Epiphysis
Mitchell E. Geffner
Pages 7 - 8
Abstract |Full Text PDF

8.Turner Syndrome: Care Through the Ages
Alan D. Rogol
Page 9
Abstract |Full Text PDF

9.Efficacy and Safety of Long-Acting Gonadotropin Releasing Hormone Analogs
Mitchell E. Geffner
Page 10
Abstract |Full Text PDF

10.Genetic Defects Affecting Adrenal Development
Allen Lipson, Eric Vilain
Page 11
Abstract |Full Text PDF

11.Congenital Adrenal Hyperplasia: Consensus Guidelines and Beyond
Mitchell E. Geffner
Pages 12 - 13
Abstract |Full Text PDF

12.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
Page 14

13.Pseudohypoparathyroisidm Type 1a: A Case Report
Murat Dogan, Selami Kocaman, Keziban Asli Bala, Sultan Kaba, Servet Yel, Askin Sen
Page 15

14.A Diabetic Infant with Homozygous LRBA Mutation: The Youngest Patient Reported
Ayla Güven, Matthew Jonhson, Elisa De Franco
Page 16

15.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
Page 17

16.Editorial
Korcan Demir
Page 18
Abstract |Full Text PDF

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