NEWBORN SCREENING FOR CONGENITAL ADRENAL HYPERPLASIA
- 1 March 2001
- journal article
- review article
- Published by Elsevier BV in Endocrinology and Metabolism Clinics of North America
- Vol. 30 (1), 15-30
- https://doi.org/10.1016/s0889-8529(08)70017-3
Abstract
No abstract availableKeywords
This publication has 22 references indexed in Scilit:
- Improved precision of newborn screening for congenital adrenal hyperplasia using weight-adjusted criteria for 17-hydroxyprogesterone levelsThe Journal of Pediatrics, 1997
- Reference ranges for serum cortisol and 17-hydroxyprogesterone levels in preterm infantsThe Journal of Pediatrics, 1995
- Normal newborn 17-hydroxyprogesterone level in an infant with congenital adrenal hyperplasia due to 11β-hydroxylase deficiencyScreening, 1994
- Improving the efficacy of newborn screening for congenital adrenal hyperplasia by adjusting the cut-off level of 17α-hydroxyprogesterone to gestational ageScreening, 1994
- Congenital adrenal hyperplasia due to 21-hydroxylase deficiency: Newborn screening and its relationship to the diagnosis and treatment of the disorderScreening, 1993
- Screening of half a million Swedish newborn infants for congenital adrenal hyperplasiaScreening, 1992
- U.S. newborn screening system guidelines: Statement of the council of regional networks for genetic servicesScreening, 1992
- Neonatal Screening Program for Congenital Adrenal Hyperplasia in a Homogeneous Caucasian PopulationAnnals of the New York Academy of Sciences, 1985
- Elevated 17-Hydroxyprogesterone and Testosterone in a Newborn with 3-Beta-Hydroxysteroid Dehydrogenase DeficiencyNew England Journal of Medicine, 1985
- An unusually high incidence of salt-losing congenital adrenal hyperplasia in the Alaskan EskimoThe Journal of Pediatrics, 1969