Neonatal screening for congenital adrenal hyperplasia
Author:
Publisher
Springer Science and Business Media LLC
Subject
Endocrinology,Endocrinology, Diabetes and Metabolism
Link
http://www.nature.com/articles/nrendo.2009.148.pdf
Reference68 articles.
1. White, P. C. & Speiser, P. W. Congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Endocr. Rev. 21, 245–291 (2000).
2. Speiser, P. W. & White, P. C. Congenital adrenal hyperplasia. N. Engl. J. Med. 349, 776–788 (2003).
3. Joint LWPES/ESPE CAH Working Group. Consensus statement on 21-hydroxylase deficiency from the Lawson Wilkins Pediatric Endocrine Society and the European Society for Paediatric Endocrinology. J. Clin. Endocrinol. Metab. 87, 4048–4053 (2002).
4. Pang, S. & Shook, M. K. Current status of neonatal screening for congenital adrenal hyperplasia. Curr. Opin. Pediatr. 9, 419–423 (1997).
5. Therrell, B. L. Newborn screening for congenital adrenal hyperplasia. Endocrinol. Metab. Clin. North Am. 30, 15–30 (2001).
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