Review

Steroid Assays in Paediatric Endocrinology
  • John W. Honour
J Clin Res Pediatr Endocrinol 2010; 2: 1-16 DOI: 10.4274/jcrpe.v2i1.1 PMID:21274330
Diagnosis of Diseases of Steroid Hormone Production, Metabolism and Action
  • John W. Honour
J Clin Res Pediatr Endocrinol 2009; 1: 209-226 DOI: 10.4274/jcrpe.v1i5.209 PMID:21274298

Case Report

Uniparental Isodisomy of Chromosome 1 Unmasking an Autosomal Recessive 3-Beta Hydroxysteroid Dehydrogenase Type II-Related Congenital Adrenal Hyperplasia
  • Karin Panzer
  • Osayame A. Ekhaguere
  • Benjamin Darbro
  • Jennifer Cook
  • Oleg A. Shchelochkov
J Clin Res Pediatr Endocrinol 2017; 9: 70-73 DOI: 10.4274/jcrpe.3680 PMID:27796263
Testicular Adrenal Rest Tumor in Two Brothers with a Novel Mutation in the 3-Beta-Hydroxysteroid Dehydrogenase-2 Gene
  • Ayla Güven
  • Seher Polat
J Clin Res Pediatr Endocrinol 2017; 9: 85-90 DOI: 10.4274/jcrpe.3306 PMID:27476613

Case Report

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
Iatrogenic Cushing’s Syndrome Following Short-Term Intranasal Steroid Use
  • Deep Dutta
  • Shivaprasad KS
  • Sujoy Ghosh
  • Satinath Mukhopadhyay
  • Subhankar Chowdhury
J Clin Res Pediatr Endocrinol 2012; 4: 157-159 DOI: 10.4274/Jcrpe.726 PMID:22985615
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

Case Report

Fetal Adrenal Suppression Due to Maternal Corticosteroid Use: Case Report
  • Selim Kurtoğlu
  • Dilek Sarıcı
  • Mustafa Ali Akın
  • Ghaniya Daar
  • Levent Korkmaz
  • Şeyma Memur
J Clin Res Pediatr Endocrinol 2011; 3: 160-162 DOI: 10.4274/jcrpe.v3i3.31 PMID:21911331

Other

A New Mutation on the SFR1 (NR5A1) Gene in a 46 XY Sexual Development Disorder Case without the Adrenal Deficiency
  • Ahmet Anık
  • Gönül Çatlı
  • Ayhan Abacı
  • Hale Ünver Tuhan
  • Hüseyin Onay
  • Ayça Aykut
  • Ece Böber
J Clin Res Pediatr Endocrinol 2015; 7: 57-57

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