Related references
Note: Only part of the references are listed.Revisiting Classical 3β-hydroxysteroid Dehydrogenase 2 Deficiency: Lessons from 31 Pediatric Cases
Tulay Guran et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2020)
11-Oxygenated androgens in health and disease
Adina F. Turcu et al.
NATURE REVIEWS ENDOCRINOLOGY (2020)
Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
Deborah P. Merke et al.
NEW ENGLAND JOURNAL OF MEDICINE (2020)
17α-HYDROXYLASE DEFICIENCY IS AN UNDERDIAGNOSED DISEASE: HIGH FREQUENCY OF MISDIAGNOSES IN A LARGE COHORT OF BRAZILIAN PATIENTS
Rafaela Fontenele et al.
ENDOCRINE PRACTICE (2018)
Steroid 17-hydroxylase and 17,20-lyase deficiencies, genetic and pharmacologic
Richard J. Auchus
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY (2017)
Successful Live Birth in a Woman With 17 α-Hydroxylase Deficiency Through IVF Frozen-Thawed Embryo Transfer
Paulo Homem de Mello Bianchi et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2016)
THE CLASSIC AND NONCLASSIC CONCENITAL ADRENAL HYPERPLASIAS
Richard J. Auchus
ENDOCRINE PRACTICE (2015)
A Diagnosis Not to Be Missed: Nonclassic Steroid 11β-Hydroxylase Deficiency Presenting With Premature Adrenarche and Hirsutism
Nicole Reisch et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2013)
Genotype-Phenotype Analysis in Congenital Adrenal Hyperplasia due to P450 Oxidoreductase Deficiency
Nils Krone et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2012)
Superior discriminating value of ACTH-stimulated serum 21-deoxycortisol in identifying heterozygote carriers for 21-hydroxylase deficiency
Flavia A. Costa-Barbosa et al.
CLINICAL ENDOCRINOLOGY (2010)
Gonadal Function, First Cases of Pregnancy, and Child Delivery in a Woman with Lipoid Congenital Adrenal Hyperplasia
Khalil Khoury et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2009)
Nonclassic congenital lipoid adrenal hyperplasia: A new disorder of the steroidogenic acute regulatory protein with very late presentation and normal male genitalia
Bo Y. Baker et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2006)
Urine steroid hormone profile analysis in cytochrome P450 oxidoreductase deficiency: Implication for the backdoor pathway to dihydrotestosterone
Keiko Homma et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2006)
Diversity and function of mutations in p450 oxidoreductase in patients with Antley-Bixler Syndrome and disordered steroidogenesis
NW Huang et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2005)
Mutant P450 oxidoreductase causes disordered steroidogenesis with and without Antley-Bixler syndrome
CE Flück et al.
NATURE GENETICS (2004)
Two prevalent CYP17 mutations and genotype-phenotype correlations in 24 Brazilian patients with 17-hydroxylase deficiency
M Costa-Santos et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2004)