Hyperphenylalaninaemias
- 1 January 1995
- book chapter
- Published by Springer Nature
Abstract
No abstract availableKeywords
This publication has 16 references indexed in Scilit:
- Recommendations on the dietary management of phenylketonuria. Report of Medical Research Council Working Party on Phenylketonuria.Archives of Disease in Childhood, 1993
- Phenylketonuria due to phenylalanine hydroxylase deficiency: an unfolding story. Medical Research Council Working Party on Phenylketonuria.BMJ, 1993
- Reduced plasma C-20 and C-22 polyunsaturated fatty acids in children with phenylketonuria during dietary interventionThe Journal of Pediatrics, 1991
- Prevalence of congenital heart disease in patients with phenylketonuriaThe Journal of Pediatrics, 1991
- Review of neonatal screening programme for phenylketonuria.BMJ, 1991
- Molecular Basis of Phenotypic Heterogeneity in PhenylketonuriaNew England Journal of Medicine, 1991
- Bony changes of PKU neonates unrelated to phenylalanine levelsJournal of Inherited Metabolic Disease, 1991
- Regional distribution of the phenylalanine‐sensitive ATP‐sulphurylase in brainJournal of Inherited Metabolic Disease, 1986
- Problems related to diet management of maternal phenylketonuriaJournal of Inherited Metabolic Disease, 1986
- The hyperphenylalaninaemiasPublished by Elsevier ,1985