Screening of half a million Swedish newborn infants for congenital adrenal hyperplasia
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology and Child Health
Reference15 articles.
1. Neonatal screening for congenital adrenal hyperplasia using a microfilter paper method for 17-α-hydroxyprogesterone radioimmunoassay;Cacciari;Horm Res,1982
2. Congenital adrenal hyperplasia due to 21-hydroxylase deficiency;Cutler;New Engl J Med,1990
3. Prenatal treatment of congenital adrenal hyperplasia resulting from 21-hydroxylase deficiency;David;Pediatrics,1984
4. Dépistage néonatal de l'hyperplasie congénitale des surrénales par déficit en 21-hydroxylase. Réalités et perspectives;Farriaux;Arch Fr Pédiatr,1987
5. Plasma 17OH-progesterone concentrations in newborn infants;Hughes;Arch Dis Childhood,1979
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2. Cutoff Levels of 17-α-Hydroxyprogesterone in Neonatal Screening for Congenital Adrenal Hyperplasia Should Be Based on Gestational Age Rather Than on Birth Weight;The Journal of Clinical Endocrinology & Metabolism;2005-07-01
3. Newborn Screening for Congenital Adrenal Hyperplasia inthe Netherlands;Pediatrics;2001-12-01
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5. Benefits of Neonatal Screening for Congenital Adrenal Hyperplasia (21-Hydroxylase Deficiency) in Sweden;Pediatrics;1998-04-01
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