Volume 9, Issue 3

September 2017
(10) Original Research, (1) Short Communication, (5) Case Report

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Original Research

Clinicopathological Characteristics of Papillary Thyroid Cancer in Children with Emphasis on Pubertal Status and Association with BRAFV600E Mutation
  • Şükran Poyrazoğlu
  • Rüveyde Bundak
  • Firdevs Baş
  • Gülçin Yeğen
  • Yasemin Şanlı
  • Feyza Darendeliler
J Clin Res Pediatr Endocrinol 2017; 9: 185-193 DOI: 10.4274/jcrpe.3873 PMID:28077340
Congenital Hyperinsulinism in China: A Review of Chinese Literature Over the Past 15 Years
  • Wei-Yan Wang
  • Yi Sun
  • Wen-Ting Zhao
  • Tai Wu
  • Liang Wang
  • Tian-Ming Yuan
  • Hui-Min Yu
J Clin Res Pediatr Endocrinol 2017; 9: 194-201 DOI: 10.4274/jcrpe.3934 PMID:28270372
The Relationship Between Glycemic Variability and Inflammatory Markers in Obese Children with Insulin Resistance and Metabolic Syndrome
  • Abdurrahman Kaya
  • Cemil Koçyiğit
  • Gönül Çatlı
  • Elif Büşra Özkan
  • Bumin Nuri Dündar
J Clin Res Pediatr Endocrinol 2017; 9: 202-207 DOI: 10.4274/jcrpe.4031 PMID:28163257
Treatment of Pre-pubertal Patients with Growth Hormone Deficiency: Patterns in Growth Hormone Dosage and Insulin-like Growth Factor-I Z-scores
  • Megan Oberle
  • Adda Grimberg
  • Vaneeta Bamba
J Clin Res Pediatr Endocrinol 2017; 9: 208-215 DOI: 10.4274/jcrpe.4125 PMID:28150584
Melanocortin-4 Receptor Gene Mutations in a Group of Turkish Obese Children and Adolescents
  • Selma Tunç
  • Korcan Demir
  • Fatma Ajlan Tükün
  • Cihan Topal
  • Filiz Hazan
  • Burcu Sağlam
  • Özlem Nalbantoğlu
  • Melek Yıldız
  • Behzat Özkan
J Clin Res Pediatr Endocrinol 2017; 9: 216-221 DOI: 10.4274/jcrpe.4225 PMID:28218067
Management of Childhood Thyroid Nodules: Surgical and Endocrinological Findings in a Large Group of Cases
  • Emre Divarcı
  • Ülgen Çeltik
  • Zafer Dökümcü
  • Orkan Ergün
  • Geylani Özok
  • Samim Özen
  • Damla Gökşen Şimşek
  • Şükran Darcan
  • Nazan Çetingül
  • Aylin Oral
  • Yeşim Ertan
  • Bengü Demirağ
  • Ahmet Çelik
J Clin Res Pediatr Endocrinol 2017; 9: 222-228 DOI: 10.4274/jcrpe.4272 PMID:28387647
Clinical and Genetic Findings of Turkish Hypophosphatasia Cases
  • Halil Sağlam
  • Şahin Erdöl
  • Sevil Dorum
J Clin Res Pediatr Endocrinol 2017; 9: 229-236 DOI: 10.4274/jcrpe.4549 PMID:28663156
The Relationship of Disordered Eating Attitudes with Stress Level, Bone Turnover Markers, and Bone Mineral Density in Obese Adolescents
  • Aslı Okbay Güneş
  • Müjgan Alikaşifoğlu
  • Ezgi Şen Demirdöğen
  • Ethem Erginöz
  • Türkay Demir
  • Mine Kucur
  • Oya Ercan
J Clin Res Pediatr Endocrinol 2017; 9: 237-245 DOI: 10.4274/jcrpe.3794 PMID:28196789
Phenotype Heterogeneity in Glucokinase–Maturity-Onset Diabetes of the Young (GCK-MODY) Patients
  • Anna Wedrychowicz
  • Ewa Tobór
  • Magdalena Wilk
  • Ewa Ziólkowska-Ledwith
  • Anna Rams
  • Katarzyna Wzorek
  • Barbara Sabal
  • Malgorzata Stelmach
  • Jerzy B. Starzyk
J Clin Res Pediatr Endocrinol 2017; 9: 246-252 DOI: 10.4274/jcrpe.4461 PMID:28663157
The Relationship Between Perceived Family Climate and Glycemic Control in Type 1 Diabetes Mellitus Adolescent Patients
  • Şafak Eray
  • Halit Necmi Uçar
  • Fatma Çetinkaya
  • Erdal Eren
  • Pınar Vural
J Clin Res Pediatr Endocrinol 2017; 9: 253-259 DOI: 10.4274/jcrpe.3825 PMID:28218068

Short Communication

An ABCC8 Nonsense Mutation Causing Neonatal Diabetes Through Altered Transcript Expression
  • Sarah E. Flanagan
  • Vu Chí Dung
  • Jayne A. L. Houghton
  • Elisa De Franco
  • Can Thi Bich Ngoc
  • Annet Damhuis
  • Frances M. Ashcroft
  • Lorna W. Harries
  • Sian Ellard
J Clin Res Pediatr Endocrinol 2017; 9: 260-264 DOI: 10.4274/jcrpe.4624 PMID:28663158

Case Report

Pituitary Adenoma Apoplexy in an Adolescent: A Case Report and Review of the Literature
  • Hero Zijlker
  • Sebastian Schagen
  • Jan Maarten Wit
  • Nienke Biermasz
  • Wouter van Furth
  • Wilma Oostdijk
J Clin Res Pediatr Endocrinol 2017; 9: 265-273 DOI: 10.4274/jcrpe.4420 PMID:28588003
Pancreatic Agenesis due to Compound Heterozygosity for a Novel Enhancer and Truncating Mutation in the PTF1A Gene
  • Monica Gabbay
  • Sian Ellard
  • Elisa De Franco
  • Regina S. Moisés
J Clin Res Pediatr Endocrinol 2017; 9: 274-277 DOI: 10.4274/jcrpe.4494 PMID:28663161
Congenital Central Hypothyroidism Caused by a Novel Thyroid-Stimulating Hormone-Beta Subunit Gene Mutation in Two Siblings
  • Bayram Özhan
  • Özlem Boz Anlaş
  • Bilge Sarıkepe
  • Burcu Albuz
  • Nur Semerci Gündüz
J Clin Res Pediatr Endocrinol 2017; 9: 278-282 DOI: 10.4274/jcrpe.4595 PMID:28515030
Long-Term Follow-up of a Case with Proprotein Convertase 1/3 Deficiency: Transient Diabetes Mellitus with Intervening Diabetic Ketoacidosis During Growth Hormone Therapy
  • E. Nazlı Gönç
  • Alev Özön
  • Ayfer Alikaşifoğlu
  • Nurgün Kandemir
J Clin Res Pediatr Endocrinol 2017; 9: 283-287 DOI: 10.4274/jcrpe.3986 PMID:28588004
Tolvaptan Treatment in Children with Chronic Hyponatremia due to Inappropriate Antidiuretic Hormone Secretion: A Report of Three Cases
  • Gerdi Tuli
  • Daniele Tessaris
  • Silvia Einaudi
  • Luisa De Sanctis
  • Patrizia Matarazzo
J Clin Res Pediatr Endocrinol 2017; 9: 288-292 DOI: 10.4274/jcrpe.4531 PMID:28515029

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