Dietary Treatment of a Child with Maple Syrup Urine Disease (Branched-chain Ketoaciduria)
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Open Access
- 1 October 1963
- journal article
- research article
- Published by BMJ in Archives of Disease in Childhood
- Vol. 38 (201) , 485-491
Abstract
No abstract availableKeywords
This publication has 12 references indexed in Scilit:
- A NEW FINDING IN MAPLE-SYRUP-URINE DISEASEThe Lancet, 1962
- Studies in Maple Syrup Urine DiseaseArchives of Disease in Childhood, 1961
- An inborn defect in the metabolism of tyrosine in infants on a normal dietBiochemical Journal, 1960
- A modified procedure for the automatic analysis of amino acidsAnalytical Biochemistry, 1960
- "Maple Syrup Urine Disease"BMJ, 1959
- "Maple Syrup Urine Disease"BMJ, 1959
- Automatic Recording Apparatus for Use in Chromatography of Amino AcidsAnalytical Chemistry, 1958
- Studies on the metabolism of amino acids and related compounds in vivo. I. Toxicity of essential amino acids, individually and in mixtures, and the protective effect of l-arginineArchives of Biochemistry and Biophysics, 1956
- A NEW SYNDROME: PROGRESSIVE FAMILIAL INFANTILE CEREBRAL DYSFUNCTION ASSOCIATED WITH AN UNUSUAL URINARY SUBSTANCEPediatrics, 1954
- A DEFECT IN THE METABOLISM OF TYROSINE AND PHENYLALANINE IN PREMATURE INFANTS. II. SPONTANEOUS OCCURRENCE AND ERADICATION BY VITAMIN C 12Journal of Clinical Investigation, 1941