Diagnosis of malignant hyperphenylalaninaemia.
Open Access
- 1 May 1979
- journal article
- research article
- Published by BMJ in Archives of Disease in Childhood
- Vol. 54 (5) , 329-330
- https://doi.org/10.1136/adc.54.5.329
Abstract
No abstract availableThis publication has 9 references indexed in Scilit:
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- Tetrahydrobiopterin therapy of atypical phenylketonuria due to defective dihydrobiopterin biosynthesis.Archives of Disease in Childhood, 1978
- Pteridines and phenylketonuria report of a workshop: Introductory commentsJournal of Inherited Metabolic Disease, 1978
- Malignant hyperphenylalaninaemia—Current status (June 1977)Journal of Inherited Metabolic Disease, 1978
- A disorder of biogenic amines in dihydropteridine reductase deficiencyAnnals of Neurology, 1978
- VARIANT FORMS OF PHENYLKETONURIAThe Lancet, 1976
- L-DOPA AND 5-HYDROXYTRYPTOPHAN THERAPY IN PHENYLKETONURIA WITH NORMAL PHENYLALANINE-HYDROXYLASE ACTIVITYThe 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