ISSN:1308-5727 E-ISSN:1308-5735

Case Reports

Insulin Oedema in Newly Diagnosed Type 1 Diabetes Mellitus
  • Veysel Nijat Baş
  • Semra Çetinkaya
  • Sebahat Yılmaz Ağladıoğlu
  • Havva Nur Peltek Kendirici
  • Hatice Bilgili
  • Nurdan Yıldırım
  • Zehra Aycan
J Clin Res Pediatr Endocrinol 2010; 2: 46-48 DOI: 10.4274/jcrpe.v2i1.46 PMID:21274337
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A Patient with 22q11.2 Deletion Syndrome: Case Report
  • Sema Kabataş Eryılmaz
  • Firdevs Baş
  • Ali Satan
  • Feyza Darendeliler
  • Rüveyde Bundak
  • Hülya Günöz
  • Nurçin Saka
J Clin Res Pediatr Endocrinol 2009; 1: 151-154 DOI: 10.4008/jcrpe.v1i3.46 PMID:21274400
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Case Report

A Patient with Proopiomelanocortin Deficiency: An Increasingly Important Diagnosis to Make
  • Semra Çetinkaya
  • Tülay Güran
  • Erdal Kurnaz
  • Melikşah Keskin
  • Elif Sağsak
  • Senay Savaş Erdeve
  • Jenifer P. Suntharalingham
  • Federica Buonocore
  • John C. Achermann
  • Zehra Aycan
J Clin Res Pediatr Endocrinol 2018; 10: 68-73 DOI: 10.4274/jcrpe.4638 PMID:28739551
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46,XY Disorder of Sex Development due to 17-Beta Hydroxysteroid Dehydrogenase Type 3 Deficiency in an Infant of Greek Origin
  • Assimina Galli Tsinopoulou
  • Anastasios Serbis
  • Eleni P. Kotanidou
  • Eleni Litou
  • Vaia Dokousli
  • Konstantina Mouzaki
  • Pavlos Fanis
  • Vassos Neocleous
  • Nicos Skordis
J Clin Res Pediatr Endocrinol 2018; 10: 74-78 DOI: 10.4274/jcrpe.4829 PMID:28739554
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An Unusual Presentation of 46,XY Pure Gonadal Dysgenesis: Spontaneous Breast Development and Menstruation
  • Gönül Çatlı
  • Caner Alparslan
  • P. Şule Can
  • Sinem Akbay
  • Sefa Kelekçi
  • Tahir Atik
  • Berk Özyılmaz
  • Bumin N. Dündar
J Clin Res Pediatr Endocrinol 2015; 7: 159-162 DOI: 10.4274/jcrpe.1919 PMID:26316442
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Severe Undervirilisation in a 46,XY Case Due to a Novel Mutation in HSD17B3 Gene
  • Ayfer Alikaşifoğlu
  • Doğuş Vurallı
  • Olaf Hiort
  • Nazlı Gönç
  • Alev Özön
  • Nurgün Kandemir
J Clin Res Pediatr Endocrinol 2015; 7: 249-252 DOI: 10.4274/jcrpe.2069 PMID:26831562
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46,XX Male Disorder of Sexual Development: A Case Report
  • Ahmet Anık
  • Gönül Çatlı
  • Ayhan Abacı
  • Ece Böber
J Clin Res Pediatr Endocrinol 2013; 5: 258-260 DOI: 10.4274/Jcrpe.1098 PMID:24379036
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Gonadoblastoma with Dysgerminoma in a Phenotypically Turner-Like Girl with 45,X/46,XY Karyotype
  • Özge Yüce
  • Esra Döğer
  • Nurullah Çelik
  • Hamdi Cihan Emeksiz
  • Mahmut Orhun Çamurdan
  • Aysun Bideci
  • Peyami Cinaz
J Clin Res Pediatr Endocrinol 2015; 7: 336-339 DOI: 10.4274/jcrpe.2022 PMID:26777047
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Review

A Review of the Principles of Radiological Assessment of Skeletal Dysplasias
  • Yasemin Alanay
  • Ralph S. Lachman
J Clin Res Pediatr Endocrinol 2011; 3: 163-178 DOI: 10.4274/jcrpe.463 PMID:22155458
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Original Research

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
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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
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Letter to Editor

Letter to the Editor regarding “Testotoxicosis: Report of Two Cases, One with a Novel Mutation in Luteinizing Hormone/Choriogonadotropin Receptor Gene”
  • Doğa Türkkahraman
J Clin Res Pediatr Endocrinol 2015; 7: 355-355 DOI: 10.4274/jcrpe.2461
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Latest Update: 19.08.2019
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