Review

Achieving Optimal Short- and Long-term Responses to Paediatric Growth Hormone Therapy
  • Jan M. Wit
  • Asma Deeb
  • Bassam Bin-Abbas
  • Angham Al Mutair
  • Ekaterina Koledova
  • Martin O. Savage
J Clin Res Pediatr Endocrinol 2019; 11: 329-340 DOI: 10.4274/jcrpe.galenos.2019.2019.0088 PMID:31284701

Original Article

Novel Mutations in Obesity-related Genes in Turkish Children with Non-syndromic Early Onset Severe Obesity: A Multicentre Study
  • Ayşehan Akıncı
  • Doğa Türkkahraman
  • İbrahim Tekedereli
  • Leyla Özer
  • Bahri Evren
  • İbrahim Şahin
  • Tarkan Kalkan
  • Yusuf Çürek
  • Emine Çamtosun
  • Esra Döğer
  • Aysun Bideci
  • Ayla Güven
  • Erdal Eren
  • Özlem Sangün
  • Atilla Çayır
  • Pelin Bilir
  • Ayça Törel Ergür
  • Oya Ercan
J Clin Res Pediatr Endocrinol 2019; 11: 341-349 DOI: 10.4274/jcrpe.galenos.2019.2019.0021 PMID:30991789
Glucose Metabolism Evaluated by Glycated Hemoglobin and Insulin Sensitivity Indices in Children Treated with Recombinant Human Growth Hormone
  • Maria Chiara Pellegrin
  • Daria Michelon
  • Elena Faleschini
  • Claudio Germani
  • Egidio Barbi
  • Gianluca Tornese
J Clin Res Pediatr Endocrinol 2019; 11: 350-357 DOI: 10.4274/jcrpe.galenos.2019.2019.0281 PMID:30819016
Impact of Socioeconomic Characteristics on Metabolic Control in Children with Type 1 Diabetes in a Developing Country
  • Abeer Alassaf
  • Rasha Odeh
  • Lubna Gharaibeh
  • Sarah Ibrahim
  • Kamel Ajlouni
J Clin Res Pediatr Endocrinol 2019; 11: 358-365 DOI: 10.4274/jcrpe.galenos.2019.2019.0014 PMID:30991788
Accuracy of Tri-ponderal Mass Index and Body Mass Index in Estimating Insulin Resistance, Hyperlipidemia, Impaired Liver Enzymes or Thyroid Hormone Function and Vitamin D Levels in Children and Adolescents
  • Neşe Akcan
  • Rüveyde Bundak
J Clin Res Pediatr Endocrinol 2019; 11: 366-373 DOI: 10.4274/jcrpe.galenos.2019.2018.0279 PMID:30991791
Serum Neuron-specific Enolase and S100 Calcium-binding Protein B in Pediatric Diabetic Ketoacidosis
  • Hatem Hamed Elshorbagy
  • Naglaa Fathy Barseem
  • Akram Elshafey Elsadek
  • Ashraf Hamed Al-shokary
  • Yehia Hamed Abdel Maksoud
  • Sameh Elsayed Abdulsamea
  • Iman M. Talaat
  • Hany Abdelaziz Suliman
  • Naglaa M. Kamal
  • Waleed E. Abdelghani
  • Sanaa Mohammed Azab
  • Dalia Mohamed Nour El Din
J Clin Res Pediatr Endocrinol 2019; 11: 374-387 DOI: 10.4274/jcrpe.galenos.2019.2018.0280 PMID:31067852
Clinical and Biochemical Phenotype of Adolescent Males with Gynecomastia
  • Miłosz Lorek
  • Dominika Tobolska-Lorek
  • Barbara Kalina-Faska
  • Aleksandra Januszek-Trzciakowska
  • Aneta Gawlik
J Clin Res Pediatr Endocrinol 2019; 11: 388-394 DOI: 10.4274/jcrpe.galenos.2019.2019.0027 PMID:31117335
Liver Biochemical Abnormalities in Adolescent Patients with Turner Syndrome
  • Małgorzata Wójcik
  • Anna Ruszała
  • Dominika Januś
  • Jerzy B. Starzyk
J Clin Res Pediatr Endocrinol 2019; 11: 395-399 DOI: 10.4274/jcrpe.galenos.2019.2018.0271 PMID:31117336
Clinical Management and Gene Mutation Analysis of Children with Congenital Hyperinsulinism in South China
  • Aijing Xu
  • Jing Cheng
  • Huiying Sheng
  • Zhe Wen
  • Yunting Lin
  • Zhihong Zhou
  • Chunhua Zeng
  • Yongxian Shao
  • Cuiling Li
  • Li Liu
  • Xiuzhen Li
J Clin Res Pediatr Endocrinol 2019; 11: 400-409 DOI: 10.4274/jcrpe.galenos.2019.2019.0046 PMID:31208162
Subclinical Myocardial Dysfunction Demonstrated by Speckle Tracking Echocardiography in Children with Euthyroid Hashimoto’s Thyroiditis
  • Emine Azak
  • Seyit Ahmet Uçaktürk
  • İbrahim İlker Çetin
  • Hazım Alper Gürsu
  • Eda Mengen
  • Utku Pamuk
J Clin Res Pediatr Endocrinol 2019; 11: 410-418 DOI: 10.4274/jcrpe.galenos.2019.2018.0273 PMID:31218876

Case Report

A Novel Nonsense Mutation of PHF6 in a Female with Extended Phenotypes of Borjeson-Forssman-Lehmann Syndrome
  • Xia Zhang
  • Yanjie Fan
  • Xiaomin Liu
  • Ming-Ang Zhu
  • Yu Sun
  • Hui Yan
  • Yunjuan He
  • Xiantao Ye
  • Xuefan Gu
  • Yongguo Yu
J Clin Res Pediatr Endocrinol 2019; 11: 419-425 DOI: 10.4274/jcrpe.galenos.2019.2018.0220 PMID:30630810
Isolated Growth Hormone Deficiency Type 2 due to a novel GH1 Mutation: A Case Report
  • Ahmad Kautsar
  • Jan M. Wit
  • Aman Pulungan
J Clin Res Pediatr Endocrinol 2019; 11: 426-431 DOI: 10.4274/jcrpe.galenos.2019.2018.0305 PMID:30678423
A Novel Homozygous Mutation of the Acid-Labile Subunit (IGFALS) Gene in a Male Adolescent
  • Şükran Poyrazoğlu
  • Vivian Hwa
  • Firdevs Baş
  • Andrew Dauber
  • Ron Rosenfeld
  • Feyza Darendeliler
J Clin Res Pediatr Endocrinol 2019; 11: 432-438 DOI: 10.4274/jcrpe.galenos.2019.2018.0301 PMID:30717585
A Case of Autosomal Dominant Osteopetrosis Type 2 with a CLCN7 Gene Mutation
  • Sol Kang
  • Young Kyung Kang
  • Jun Ah Lee
  • Dong Ho Kim
  • Jung Sub Lim
J Clin Res Pediatr Endocrinol 2019; 11: 439-443 DOI: 10.4274/jcrpe.galenos.2019.2018.0229 PMID:30759959
Three Siblings with Idiopathic Hypogonadotropic Hypogonadism in a Nonconsanguineous Family: A Novel KISS1R/GPR54 Loss-of-Function Mutation
  • Özlem Nalbantoğlu
  • Gülçin Arslan
  • Özge Köprülü
  • Filiz Hazan
  • Semra Gürsoy
  • Behzat Özkan
J Clin Res Pediatr Endocrinol 2019; 11: 444-448 DOI: 10.4274/jcrpe.galenos.2019.2018.0230 PMID:30905142

Erratum

Erratum
J Clin Res Pediatr Endocrinol 2019; 11: 451-451 DOI: 10.4274/jcrpe.galenos.2019.e002 PMID:31760732

Other

2019 Referee Index
J Clin Res Pediatr Endocrinol 2019; 11: 0-0
2019 Author Index
J Clin Res Pediatr Endocrinol 2019; 11: 0-0
2019 Subject Index
J Clin Res Pediatr Endocrinol 2019; 11: 0-0

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