10 Neonatal screening for inborn errors of amino acid metabolism
- 1 March 1974
- journal article
- research article
- Published by Elsevier in Clinics in Endocrinology and Metabolism
- Vol. 3 (1), 153-166
- https://doi.org/10.1016/s0300-595x(74)80031-9
Abstract
No abstract availableKeywords
This publication has 17 references indexed in Scilit:
- Genetic Difference between Hyperphenyl-Alaninemia and PhenylketonuriaNeuropediatrics, 1972
- False-Positive Test for Branched-Chain KetonuriaNew England Journal of Medicine, 1971
- D-Methioninuria Due to DL-Methionine IngestionAmerican Journal of Diseases of Children, 1969
- Hypermethioninemia With Other HyperaminoacidemiasAmerican Journal of Diseases of Children, 1969
- Newborn Phenylketonuria Detection Program in MassachusettsAmerican Journal of Public Health and the Nations Health, 1964
- APPLICATION OF A SIMPLE MICROMETHOD TO THE SCREENING OF PLASMA FOR A VARIETY OF AMINOACIDOPATHIESThe Lancet, 1964
- A Simple Chromatographic Screening Test for the Detection of Disorders of Amino Acid MetabolismNew England Journal of Medicine, 1964
- Blood Screening for PhenylketonuriaJAMA, 1961
- Preliminary CommunicationThe Lancet, 1953
- DETECTION OF AMINO-ACIDS IN URINE AND OTHER FLUIDSThe Lancet, 1946