PERSISTENT HYPERPHENYLALANINEMIA
- 1 May 1972
- journal article
- Published by Wiley in Acta Paediatrica
- Vol. 61 (3) , 321-328
- https://doi.org/10.1111/j.1651-2227.1972.tb16107.x
Abstract
No abstract availableKeywords
This publication has 15 references indexed in Scilit:
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- Atypical Phenylketonuria: An Approach to Diagnosis and ManagementArchives of Disease in Childhood, 1970
- Two Siblings of Hyperphenylalaninemia: Suggestion to a Genetic Variant of PhenylketonuriaThe Tohoku Journal of Experimental Medicine, 1970
- Effect of elevated plasma phenylalanine levels on other amino acids in phenylketonuric and normal subjectsThe Journal of Pediatrics, 1969
- Causes for High Phenylalanine With Normal TyrosineAmerican Journal of Diseases of Children, 1969
- Transient hyperphenylalaninemiaThe Journal of Pediatrics, 1968
- PHENYLALANINE-HYDROXYLASE ACTIVITY IN HYPERPHENYLALANINÆMIAThe Lancet, 1967
- Diagnostic and therapeutic implications of persistent hyperphenylalaninemia in an infant heterozygous for the gene of phenylketonuriaThe Journal of Pediatrics, 1966
- Atypical phenylketonuric heterozygoteThe Journal of Pediatrics, 1966
- ATYPICAL PHENYLKETONURIA IN SISTERS WITH NORMAL OFFSPRINGThe Lancet, 1961