Malignant hyperphenylalaninaemia—Current status (June 1977)
- 1 June 1978
- journal article
- research article
- Published by Wiley in Journal of Inherited Metabolic Disease
- Vol. 1 (2) , 49-53
- https://doi.org/10.1007/bf01801843
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
- Metabolism and metabolic roles of 6-polyhydroxyalkylpterinsJournal of Inherited Metabolic Disease, 1978
- Dihydroxanthopterinuria in phenylketonuria and lethal hyperphenylalaninemia patientsClinica Chimica Acta; International Journal of Clinical Chemistry, 1977
- Atypical Phenylketonuria With Normal Phenylalanine Hydroxylase and Dihydropteridine Reductase Activity in VitroPediatrics, 1977
- HYPERPHENYLALANINEMIA DUE TO PHENYLALANINE HYDROXYLASE COFACTOR DEFICIENCYPediatric Research, 1977
- Hyperphenylalaninemia due to dihydropteridine reductase deficiencyThe Journal of Pediatrics, 1976
- Biopterin derivatives in normal and phenylketonuric patients after oral loads of L-phenylalanine, L-tyrosine, and L-tryptophan.Archives of Disease in Childhood, 1976
- VARIANT FORMS OF PHENYLKETONURIAThe Lancet, 1976
- TETRAHYDROBIOPTERIN TREATMENT OF VARIANT FORM OF PHENYLKETONURIAThe Lancet, 1975
- Phenylketonuria Due to a Deficiency of Dihydropteridine ReductaseNew England Journal of Medicine, 1975
- NEW VARIANT OF PHENYLKETONURIA WITH PROGRESSIVE NEUROLOGICAL ILLNESS UNRESPONSIVE TO PHENYLALANINE RESTRICTIONThe Lancet, 1975