Phenylalaninemia
- 1 May 1968
- journal article
- review article
- Published by Elsevier in Pediatric Clinics of North America
- Vol. 15 (2), 313-323
- https://doi.org/10.1016/s0031-3955(16)32124-1
Abstract
No abstract availableThis publication has 12 references indexed in Scilit:
- Phenylketonuria 1967Developmental Medicine and Child Neurology, 1967
- Diagnosis of Phenylketonuria (Phenylalanine Hydroxylase Deficiency, Temporary and Permanent)BMJ, 1967
- PHENYLALANINE-HYDROXYLASE ACTIVITY IN HYPERPHENYLALANINÆMIAThe Lancet, 1967
- Conference on treatment of phenylketonuriaThe Journal of Pediatrics, 1967
- Aminoacidemia of PrematurityAmerican Journal of Diseases of Children, 1966
- Cystathioninuria: Nature of the DefectScience, 1965
- GENETIC MECHANISMS PRODUCING MULTIPLE ENZYME DEFECTS A REVIEW OF UNEXPLAINED CASES AND A NEW HYPOTHESISThe American Journal of the Medical Sciences, 1965
- Delayed maturation of tyrosine metabolism in a full-term sibling of a child with phenylketonuriaThe Journal of Pediatrics, 1963
- Serum Phenylalanine and Tyrosine Levels in the Newborn InfantNew England Journal of Medicine, 1962
- Identification of heterozygotes with phenylketonuria on basis of blood tyrosine responsesThe Journal of Pediatrics, 1962