Neugeborenenscreening auf Endokrinopathien-Reference-Cited by-同舟云学术

Neugeborenenscreening auf Endokrinopathien

Published:2009-11-29 Issue:12 Volume:157 Page:1215-1221
ISSN:0026-9298
Container-title:Monatsschrift Kinderheilkunde
language:de
Short-container-title:Monatsschr Kinderheilkd

Author:

Zabransky S.

Publisher

Springer Science and Business Media LLC

Subject

Surgery,Pediatrics, Perinatology and Child Health

Link

http://link.springer.com/content/pdf/10.1007/s00112-009-2043-5.pdf

Reference29 articles.

1. Bongers-Schokking JJ (2001) Pre- and postnatal brain development in neonates with congenital hypothyroidism. J Pediatr Endocrinol Metab [Suppl 6] 14:1463–1468

2. Caulfield MP, Lynn T, Gottschalk ME et al (2002) The diagnosis of congenital adrenal hyperplasia in the newborn by gas chromatography/mass spectrometry analysis of random urine specimens. J Clin Endocrinol Metab 87:3682–3690

3. Chiesa A, Gruneiro de Papendieck L, Keselman A et al (1994) Growth follow-up in 100 children with congenital hypothyroidism before and during treatment. J Pediatr Endocrinol 7(3):211–217

4. Clayton PE, Miller WL, Oberfield SE et al; ESPE/ LWPES CAH Working Group (2002) Consensus statement on 21-hydroxylase deficiency from the European Society for Paediatric Endocrinology and the Lawson Wilkins Pediatric Endocrine Society. Horm Res 58:188–195

5. Dussault JH, Coulombe P, Laberge C et al (1975) Preliminary report on a mass screening program for neonatal hypothyroidism. J Pediatr 86:670–674

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1. Neugeborenenscreening auf Endokrinopathien und Stoffwechselstörungen/Newborn screening for endocrine and metabolic disorders;LaboratoriumsMedizin;2012-01-01