Volume 8, Issue 2

June 2016
(1) Review, (14) Original Research, (7) Case Report, (1) Editor’s Note

Cover

Cover Page


Editor’s Note

Editor’s Note
  • Feyza Darendeliler
J Clin Res Pediatr Endocrinol 2016; 8: 0-0

Review

Maternal Obesity and its Short- and Long-Term Maternal and Infantile Effects
  • Levent Korkmaz
  • Osman Baştuğ
  • Selim Kurtoğlu
J Clin Res Pediatr Endocrinol 2016; 8: 114-124 DOI: 10.4274/jcrpe.2127 PMID:26758575

Original Research

Idiopathic Hypogonadotropic Hypogonadism Caused by Inactivating Mutations in SRA1
  • Leman Damla Kotan
  • Charlton Cooper
  • Şükran Darcan
  • Ian M. Carr
  • Samim Özen
  • Yi Yan
  • Mohammad K. Hamedani
  • Fatih Gürbüz
  • Eda Mengen
  • İhsan Turan
  • Ayça Ulubay
  • Gamze Akkuş
  • Bilgin Yüksel
  • A. Kemal Topaloğlu
  • Etienne Leygue
J Clin Res Pediatr Endocrinol 2016; 8: 125-134 DOI: 10.4274/jcrpe.3248 PMID:27086651
Association of DENND1A Gene Polymorphisms with Polycystic Ovary Syndrome: A Meta-Analysis
  • Shan Bao
  • Jun-Hong Cai
  • Shu-Ying Yang
  • Yongchao Ren
  • Tian Feng
  • Tianbo Jin
  • Zhuo-Ri Li
J Clin Res Pediatr Endocrinol 2016; 8: 135-143 DOI: 10.4274/jcrpe.2259 PMID:26757598
Investigation of SHOX Gene Mutations in Turkish Patients with Idiopathic Short Stature
  • Kenan Delil
  • Halil Gürhan Karabulut
  • Bülent Hacıhamdioğlu
  • Zeynep Şıklar
  • Merih Berberoğlu
  • Gönül Öçal
  • Ajlan Tükün
  • Hatice Ilgın Ruhi
J Clin Res Pediatr Endocrinol 2016; 8: 144-149 DOI: 10.4274/jcrpe.2307 PMID:26758084
Effects of Thyroid Autoimmunity on Early Atherosclerosis in Euthyroid Girls with Hashimoto’s Thyroiditis
  • Pınar İşgüven
  • Yasemin Gündüz
  • Mukaddes Kılıç
J Clin Res Pediatr Endocrinol 2016; 8: 150-156 DOI: 10.4274/jcrpe.2145 PMID:26761929
Thyroid Function and Thyroid Autoimmunity in Relation to Weight Status and Cardiovascular Risk Factors in Children and Adolescents: A Population-Based Study
  • Emilio García-García
  • María A. Vázquez-López
  • Eduardo García-Fuentes
  • Rafael Galera-Martínez
  • Carolina Gutiérrez-Repiso
  • Icíar García-Escobar
  • Antonio Bonillo-Perales
J Clin Res Pediatr Endocrinol 2016; 8: 157-162 DOI: 10.4274/jcrpe.2687 PMID:26761948
Bone Mineral Density in Adolescent Girls with Hypogonadotropic and Hypergonadotropic Hypogonadism
  • Mehmet Nuri Özbek
  • Hüseyin Demirbilek
  • Rıza Taner Baran
  • Ahmet Baran
J Clin Res Pediatr Endocrinol 2016; 8: 163-169 DOI: 10.4274/jcrpe.2228 PMID:27087454
Transient Congenital Hypothyroidism in Turkey: An Analysis on Frequency and Natural Course
  • Cengiz Kara
  • Figen Günindi
  • Gülay Can Yılmaz
  • Murat Aydın
J Clin Res Pediatr Endocrinol 2016; 8: 170-179 DOI: 10.4274/jcrpe.2345 PMID:27086592
Cellular Trace Element Changes in Type 1 Diabetes Patients
  • Vahap Uğurlu
  • Çiğdem Binay
  • Enver Şimşek
  • Cengiz Bal
J Clin Res Pediatr Endocrinol 2016; 8: 180-186 DOI: 10.4274/jcrpe.2449 PMID:27086726
Neonatal Thyroid-Stimulating Hormone Screening as a Monitoring Tool for Iodine Deficiency in Turkey
  • Nilgün Çaylan
  • Başak Tezel
  • Sema Özbaş
  • Nuran Şahin
  • Şirin Aydın
  • Deniz Acıcan
  • Bekir Keskinkılıç
J Clin Res Pediatr Endocrinol 2016; 8: 187-191 DOI: 10.4274/jcrpe.2526 PMID:27086874
Menstrual Characteristics of Pubertal Girls: A Questionnaire-Based Study in Turkey
  • İhsan Esen
  • Baran Oğuz
  • Hepsen Mine Serin
J Clin Res Pediatr Endocrinol 2016; 8: 192-196 DOI: 10.4274/jcrpe.2026 PMID:26758209
Clinical and Genetic Characteristics, Management and Long-Term Follow-Up of Turkish Patients with Congenital Hyperinsulinism
  • Ayla Güven
  • Ayşe Nurcan Cebeci
  • Sian Ellard
  • Sarah E. Flanagan
J Clin Res Pediatr Endocrinol 2016; 8: 197-204 DOI: 10.4274/jcrpe.2408 PMID:26758964
A Novel Null Mutation in P450 Aromatase Gene (CYP19A1) Associated with Development of Hypoplastic Ovaries in Humans
  • Sema Akçurin
  • Doğa Türkkahraman
  • Woo-Young Kim
  • Erdem Durmaz
  • Jae-Gook Shin
  • Su-Jun Lee
J Clin Res Pediatr Endocrinol 2016; 8: 205-210 DOI: 10.4274/jcrpe.2761 PMID:27086564
Gonadotropin-Releasing Hormone Analogue Treatment in Females with Moderately Early Puberty: No Effect on Final Height
  • Şenay Savaş-Erdeve
  • Zeynep Şıklar
  • Bülent Hacıhamdioğlu
  • Pınar Kocaay
  • Emine Çamtosun
  • Gönül Öcal
  • Merih Berberoğlu
J Clin Res Pediatr Endocrinol 2016; 8: 211-217 DOI: 10.4274/jcrpe.2356 PMID:26758571
Homozygous Ala65Pro Mutation with V89L Polymorphism in SRD5A2 Deficiency
  • Erdal Eren
  • Tuba Edgünlü
  • Emre Asut
  • Sevim Karakaş Çelik
J Clin Res Pediatr Endocrinol 2016; 8: 218-223 DOI: 10.4274/jcrpe.2495 PMID:26761946

Case Report

A Novel c.554+5C>T Mutation in the DUOXA2 Gene Combined with p.R885Q Mutation in the DUOX2 Gene Causing Congenital Hypothyroidism
  • Xiao Zheng
  • Shao-Gang Ma
  • Ya-Li Qiu
  • Man-Li Guo
  • Xiao-Juan Shao
J Clin Res Pediatr Endocrinol 2016; 8: 224-227 DOI: 10.4274/jcrpe.2380 PMID:26758695
Early Presentation of Hyperinsulinism/Hyperammonemia Syndrome in Three Serbian Patients
  • Adrijan Sarajlija
  • Tatjana Milenkovic
  • Maja Djordjevic
  • Katarina Mitrovic
  • Sladjana Todorovic
  • Bozica Kecman
  • Khalid Hussain
J Clin Res Pediatr Endocrinol 2016; 8: 228-231 DOI: 10.4274/jcrpe.2436 PMID:26759084
A Novel Mutation in Human Androgen Receptor Gene Causing Partial Androgen Insensitivity Syndrome in a Patient Presenting with Gynecomastia at Puberty
  • Cemil Koçyiğit
  • Serdar Sarıtaş
  • Gönül Çatlı
  • Hüseyin Onay
  • Bumin Nuri Dündar
J Clin Res Pediatr Endocrinol 2016; 8: 232-235 DOI: 10.4274/jcrpe.2637 PMID:27087292
Phenotype, Sex of Rearing, Gender Re-Assignment, and Response to Medical Treatment in Extended Family Members with a Novel Mutation in the SRD5A2 Gene
  • Asma Deeb
  • Hana Al Suwaidi
  • Fakunle Ibukunoluwa
  • Salima Attia
J Clin Res Pediatr Endocrinol 2016; 8: 236-240 DOI: 10.4274/jcrpe.2782 PMID:27086719
A Novel Mutation in Thyroid Peroxidase Gene Causing Congenital Goitrous Hypothyroidism in a German-Thai Patient
  • Chutintorn Sriphrapradang
  • Yotsapon Thewjitcharoen
  • Suwannee Chanprasertyothin
  • Soontaree Nakasatien
  • Thep Himathongkam
  • Objoon Trachoo
J Clin Res Pediatr Endocrinol 2016; 8: 241-245 DOI: 10.4274/jcrpe.2503 PMID:26761947
A Newly-Discovered Mutation in the RFX6 Gene of the Rare Mitchell-Riley Syndrome
  • Nusrat Khan
  • Waleed Dandan
  • Noura Al Hassani
  • Suha Hadi
J Clin Res Pediatr Endocrinol 2016; 8: 246-249 DOI: 10.4274/jcrpe.2387 PMID:26761945
Long-term Outcome after Robotic-assisted Gastroplication in Adolescents: Hunger Hormone and Food Preference Changes Two Case Reports
  • Valeria Calcaterra
  • Hellas Cena
  • Maria Luisa Fonte
  • Mara De Amici
  • Matteo Vandoni
  • Michela Albanesi
  • Gloria Pelizzo
J Clin Res Pediatr Endocrinol 2016; 8: 250-256 DOI: 10.4274/jcrpe.2283 PMID:26757831

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