Use of sapropterin dihydrochloride in maternal phenylketonuria. A European experience of eight cases-Reference-Cited by-同舟云学术

Use of sapropterin dihydrochloride in maternal phenylketonuria. A European experience of eight cases

Published:2014-05-01 Issue:5 Volume:37 Page:753-762
ISSN:0141-8955
Container-title:Journal of Inherited Metabolic Disease
language:en
Short-container-title:J Inherit Metab Dis

Author:

Feillet François,Muntau Ania C.,Debray François-Guillaume,Lotz-Havla Amelie S.,Puchwein-Schwepcke Alexandra,Fofou-Caillierez Ma’atem Béatrice,van Spronsen Francjan,Trefz Fritz Friedrich

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/s10545-014-9716-5

Reference31 articles.

1. Blau N (2013) Sapropterin dihydrochloride for the treatment of hyperphenylalaninemias. Expert Opin Drug Metab Toxicol 9:1207–1218

2. Cipcic-Schmidt S, Trefz FK, Funders B, Seidlitz G, Ullrich K (1996) German Maternal Phenylketonuria Study. Eur J Pediatr 155(Suppl 1):S173–S176

3. de Groot CJ, Hoeksma M, Reijngoud DJ et al (2013) Phenylketonuria: reduced tyrosine brain influx relates to reduced cerebral protein synthesis. Orphanet J Rare Dis 8:133–142

4. Dhondt JL, Hayte JM (2002) [Screening of tetrahydrobiopterin deficiency among hyperphenylalaninemic patients]. Ann Biol Clin (Paris) 60:165–171

5. EMA. 2009. http://www.ema.europa.eu/docs/en_GB/document_library/EPAR_-_Product_Information/human/000943/WC500045038.pdf

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