Tetrahydrobiopterin responsiveness in a large series of phenylketonuria patients

Journal of Inherited Metabolic Disease

Volumn 25, Issue 4, 2002, Pages 321-322

  Weglage, J ^a   Grenzebach, M ^a   Teeffelen Heithoff, A V ^a   Marquardt, T ^a   Feldmann, R ^a   Denecke, J ^a   Godde D ^a   Koch, H G ^a  

^a UNIVERSITY HOSPITAL MÜNSTER   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

PHENYLALANINE; TETRAHYDROBIOPTERIN;

AMINO ACID BLOOD LEVEL; ARTICLE; CASE REPORT; DIET SUPPLEMENTATION; DRUG RESPONSE; FEMALE; HUMAN; HYPERPHENYLALANINEMIA; MALE; NEWBORN; PHENYLKETONURIA;

BIOPTERIN; FEMALE; HUMANS; INFANT, NEWBORN; MALE; NEONATAL SCREENING; PHENYLALANINE; PHENYLALANINE HYDROXYLASE; PHENYLKETONURIAS; RETROSPECTIVE STUDIES;

EID: 0036691053     PISSN: 01418955     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1016514727870     Document Type: Article

References (3)

1. Tetrahydrobiopterin-responsive phenylalanine hydroxylase deficiency
2. Tetrahydrobiopterin responsiveness in phenylketonuria differs between patients with the same genotype
3. Successful treatment of phenylketonuria with tetrahydrobiopterin