Congenital adrenal hyperplasias
- 31 March 2001
- journal article
- review article
- Published by Elsevier in Best Practice & Research Clinical Endocrinology & Metabolism
- Vol. 15 (1) , 17-41
- https://doi.org/10.1053/beem.2000.0117
Abstract
No abstract availableKeywords
This publication has 64 references indexed in Scilit:
- Congenital Adrenal Hyperplasia due to 21-Hydroxylase DeficiencyEndocrine Reviews, 2000
- Effect of Newborn Screening for Congenital Adrenal HyperplasiaArchives of Pediatrics & Adolescent Medicine, 1999
- Results of Screening 1.9 Million Texas Newborns for 21-Hydroxylase-Deficient Congenital Adrenal HyperplasiaPediatrics, 1998
- Benefits of Neonatal Screening for Congenital Adrenal Hyperplasia (21-Hydroxylase Deficiency) in SwedenPediatrics, 1998
- Improved precision of newborn screening for congenital adrenal hyperplasia using weight-adjusted criteria for 17-hydroxyprogesterone levelsThe Journal of Pediatrics, 1997
- The Pathophysiology and Genetics of Congenital Lipoid Adrenal HyperplasiaNew England Journal of Medicine, 1996
- 17α-Hydroxylase/17,20-lyase defectsThe Journal of Steroid Biochemistry and Molecular Biology, 1995
- Role of Steroidogenic Acute Regulatory Protein in Adrenal and Gonadal SteroidogenesisScience, 1995
- Disorders of steroid 11 beta-hydroxylase isozymesEndocrine Reviews, 1994
- 17α-Hydroxylase/17,20-Lyase Deficiency: From Clinical Investigation to Molecular Definition*Endocrine Reviews, 1991