In Vivo residual activities of the phenylalanine hydroxylating system in phenylketonuria and variants
- 1 December 1981
- journal article
- Published by Wiley in Journal of Inherited Metabolic Disease
- Vol. 4 (1), 101-102
- https://doi.org/10.1007/bf02263611
Abstract
No abstract availableKeywords
This publication has 6 references indexed in Scilit:
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- Atypical phenylketonuria due to tetrahydrobiopterin deficiency. Diagnosis and treatment with tetrahydrobiopterin, dihydrobiopterin and sepiapterinClinica Chimica Acta; International Journal of Clinical Chemistry, 1979
- Determination of deuterium-labeled phenylalanine and tyrosine in human plasma with high pressure liquid chromatography and mass spectrometryClinica Chimica Acta; International Journal of Clinical Chemistry, 1976
- Determination of Phenylalanine Hydroxylase Activity in Patients with Phenylketonuria and HyperphenylalaninemiaPediatric Research, 1975
- Determination of Phenylalanine Hydroxylase Activity in Patients with Phenylketonuria and HyperphenylalaninemiaPediatric Research, 1975
- Phenylalaninaemia: Differential diagnosisArchives of Disease in Childhood, 1974