Volume 12, Issue 1

March 2020
(4) Case Report, (2) Review, (9) Original Article, (1) Letter to the Editor, (1) Erratum

Cover

Cover Page


Review

Syndromic Disorders Caused by Disturbed Human Imprinting
  • Diana Carli
  • Evelise Riberi
  • Giovanni Battista Ferrero
  • Alessandro Mussa
J Clin Res Pediatr Endocrinol 2020; 12: 1-16 DOI: 10.4274/jcrpe.galenos.2019.2018.0249 PMID:30968677
Current Diagnosis, Treatment and Clinical Challenges in the Management of Lipodystrophy Syndromes in Children and Young People
  • Samim Özen
  • Barış Akıncı
  • Elif A. Oral
J Clin Res Pediatr Endocrinol 2020; 12: 17-28 DOI: 10.4274/jcrpe.galenos.2019.2019.0124 PMID:31434462

Original Article

Can Nesfatin-1 Predict Hypertension in Obese Children?
  • Hatice Güneş
  • Filiz Alkan Baylan
  • Hakan Güneş
  • Fatih Temiz
J Clin Res Pediatr Endocrinol 2020; 12: 29-36 DOI: 10.4274/jcrpe.galenos.2019.2019.0072 PMID:31339256
Treatment with Depot Leuprolide Acetate in Girls with Idiopathic Precocious Puberty: What Parameter should be Used in Deciding on the Initial Dose?
  • Doğuş Vurallı
  • Ayfer Alikaşifoğlu
  • İrem İyigün
  • Dicle Canoruç
  • Alev Ozon
  • Nazlı Gönç
  • Nurgün Kandemir
J Clin Res Pediatr Endocrinol 2020; 12: 37-44 DOI: 10.4274/jcrpe.galenos.2019.2019.0060 PMID:31347350
The Significance of Thiol/Disulfide Homeostasis and Ischemia-modified Albumin Levels in Assessing Oxidative Stress in Obese Children and Adolescents
  • Eda Mengen
  • Seyit Ahmet Uçaktürk
  • Pınar Kocaay
  • Özlem Kaymaz
  • Salim Neşelioğlu
  • Özcan Erel
J Clin Res Pediatr Endocrinol 2020; 12: 45-54 DOI: 10.4274/jcrpe.galenos.2019.2019.0039 PMID:31414586
Prevalence of Obesity and Metabolic Syndrome in Children with Type 1 Diabetes: A Comparative Assessment Based on Criteria Established by the International Diabetes Federation, World Health Organisation and National Cholesterol Education Program
  • Özlem Yayıcı Köken
  • Cengiz Kara
  • Gülay Can Yılmaz
  • Hasan Murat Aydın
J Clin Res Pediatr Endocrinol 2020; 12: 55-62 DOI: 10.4274/jcrpe.galenos.2019.2019.0048 PMID:31434460
Macular Variability in Children and Adolescents with Metabolic Syndrome: A Cross-sectional Study Examining the Associations with Anthropometric Measurements, Metabolic Parameters and Inflammatory Markers
  • Hakan Öztürk
  • Bediz Özen
  • Gönül Çatlı
  • Bumin N. Dündar
J Clin Res Pediatr Endocrinol 2020; 12: 63-70 DOI: 10.4274/jcrpe.galenos.2019.2019.0082 PMID:31434461
Growth and Adult Height during Human Growth Hormone Treatment in Chinese Children with Multiple Pituitary Hormone Deficiency Caused by Pituitary Stalk Interruption Syndrome: A Single Centre Study
  • Fengxue Wang
  • Jinyan Han
  • Zengmin Wang
  • Xiaohong Shang
  • Guimei Li
J Clin Res Pediatr Endocrinol 2020; 12: 71-78 DOI: 10.4274/jcrpe.galenos.2019.2019.0086 PMID:31475508
Effects of 5-Hydroxymethylfurfural on Pubertal Development of Female Wistar Rats
  • Selin Elmaoğulları
  • Elçin Kadan
  • Elvan Anadol
  • Ayris Gökçeoğlu
  • Semra Çetinkaya
  • Gül Fatma Yarım
  • Seyit Ahmet Uçaktürk
  • Zehra Aycan
J Clin Res Pediatr Endocrinol 2020; 12: 79-85 DOI: 10.4274/jcrpe.galenos.2019.2019.0080 PMID:31475510
Assessment of Bisphenol A Levels in Preschool Children: Results of a Human Biomonitoring Study in Ankara, Turkey
  • İsmet Çok
  • Özlem Toprak İkidağ
  • Dilek Battal
  • Ayça Aktaş
J Clin Res Pediatr Endocrinol 2020; 12: 86-94 DOI: 10.4274/jcrpe.galenos.2019.2019.0087 PMID:31475509
Evaluation of Turner Syndrome Knowledge among Physicians and Parents
  • Berna Eroğlu Filibeli
  • Nesrin Havare
  • Huriye Erbak Yılmaz
  • Jülide Gülizar Yıldırım
  • Gönül Çatlı
  • Bumin N. Dündar
J Clin Res Pediatr Endocrinol 2020; 12: 95-103 DOI: 10.4274/jcrpe.galenos.2019.2019.0041 PMID:31486330

Case Report

Hypophosphatasia: A Novel Mutation Associated with an Atypical Newborn Presentation
  • Roger Esmel-Vilomara
  • Susana Hernández
  • Ariadna Campos-Martorel
  • Eva González-Roca
  • Diego Yeste
  • Félix Castillo
J Clin Res Pediatr Endocrinol 2020; 12: 104-108 DOI: 10.4274/jcrpe.galenos.2019.2018.0263 PMID:30929401
Aromatase Deficiency in Two Siblings with 46,XX Karyotype Raised as Different Genders: A Novel Mutation (p.R115X) in the CYP19A1 Gene
  • Samim Özen
  • Tahir Atik
  • Özlem Korkmaz
  • Hüseyin Onay
  • Damla Gökşen
  • Ferda Özkınay
  • Özgür Çoğulu
  • Şükran Darcan
J Clin Res Pediatr Endocrinol 2020; 12: 109-112 DOI: 10.4274/jcrpe.galenos.2019.2018.0198 PMID:30968679
A Neurofibromatosis Noonan Syndrome Patient Presenting with Abnormal External Genitalia
  • Esra Işık
  • Hüseyin Onay
  • Tahir Atik
  • Aslı Ece Solmaz
  • Samim Özen
  • Özgür Çoğulu
  • Şükran Darcan
  • Ferda Özkınay
J Clin Res Pediatr Endocrinol 2020; 12: 113-116 DOI: 10.4274/jcrpe.galenos.2019.2019.0023 PMID:31088041
An Unusual Presentation of Carney Complex
  • Aydilek Dağdeviren Çakır
  • Hande Turan
  • Tiraje Celkan
  • Nil Çomunoğlu
  • Oya Ercan
  • Olcay Evliyaoğlu
J Clin Res Pediatr Endocrinol 2020; 12: 117-121 DOI: 10.4274/jcrpe.galenos.2019.2019.0043 PMID:31117334

Letter to the Editor

An Iranian Patient with Maroteaux Type Acromesomelic Dysplasia, Showing no Involvement of Distal Lower Limbs
  • Hossein Moravej
  • Mozhagn Moghtaderi
  • Sara Mostafavi
J Clin Res Pediatr Endocrinol 2020; 12: 122-123 DOI: 10.4274/jcrpe.galenos.2019.2019.0090 PMID:31339259

Erratum

Erratum
J Clin Res Pediatr Endocrinol 2020; 12: 124-124 DOI: 10.4274/jcrpe.galenos.2020.e001 PMID:32191422

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