Late Manifesting Variant of Branched-Chain Ketoaciduria (Maple Syrup Urine Disease)
- 1 July 1964
- journal article
- research article
- Published by Wiley in Acta Paediatrica
- Vol. 53 (4), 356-364
- https://doi.org/10.1111/j.1651-2227.1964.tb07789.x
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- Dietary Treatment of a Child with Maple Syrup Urine Disease (Branched-chain Ketoaciduria)Archives of Disease in Childhood, 1963
- THE DIAGNOSIS OF MAPLE SYRUP URINE DISEASE (Branched-chain Ketoaciduria)Published by American Academy of Pediatrics (AAP) ,1963
- CLINICAL AND BIOCHEMICAL OBSERVATIONS ON AN APPARENTLY NONFATAL VARIANT OF BRANCHEDCHAIN KETOACIDURIA (MAPLE SYRUP URINE DISEASE)Published by American Academy of Pediatrics (AAP) ,1961
- Studies in Maple Syrup Urine DiseaseArchives of Disease in Childhood, 1961
- MAPLE SYRUP DISEASEPublished by American Academy of Pediatrics (AAP) ,1959
- The quantitative estimation of pyruvic and α-oxyglutaric acids by paper chromatography in blood, urine and cerebrospinal fluidBiochemical Journal, 1957
- Chromatography of α-Keto Acid 2,4-Dinitrophenylhydrazones and Their Hydrogenation ProductsAnalytical Chemistry, 1956