Phenylketonuria and Its Variants
- 1 January 1983
- book chapter
- Published by Springer Nature
- Vol. 13, 217-297
- https://doi.org/10.1007/978-1-4615-8342-4_5
Abstract
No abstract availableKeywords
This publication has 190 references indexed in Scilit:
- Studies on the molecular defect in phenylketonuria and hyperphenylalaninaemia using antibodies against phenylalanine hydroxylaseJournal of Inherited Metabolic Disease, 1982
- Neurotransmitter defects and treatment of disorders of hyperphenylalaninemiaThe Journal of Pediatrics, 1981
- Intelligence and phenylketonuria: Effects of diet terminationThe Journal of Pediatrics, 1979
- Modification of the multiple forms of rat hepatic phenylalanine hydroxylase by in vitro phosphorylationBiochemical and Biophysical Research Communications, 1977
- Studies of the isoenzymes of phenylalanine hydroxylase in humansBiochemical Medicine, 1977
- Hyperphenylalaninemia due to dihydropteridine reductase deficiencyThe Journal of Pediatrics, 1976
- Production of antibodies to sheep liver dihydropteridine reductase: Characterization and use to study the enzyme defect in a variant form of phenylketonuriaBiochemical and Biophysical Research Communications, 1975
- Phenylketonuria: Mental development, behavior, and termination of low phenylalanine dietThe Journal of Pediatrics, 1968
- Legislation and advances in medical knowledge—acceleration or inhibition?The Journal of Pediatrics, 1966
- The role of tetrahydropteridines in the enzymatic conversion of tyrosine to 3,4-dihydroxyphenylalanineBiochemical and Biophysical Research Communications, 1964