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. 1961 Jun;36(187):259–268. doi: 10.1136/adc.36.187.259

Studies in Maple Syrup Urine Disease

C E Dent, R G Westall
PMCID: PMC2012780  PMID: 13721928

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. ARMSTRONG M. D., TYLER F. H. Studies on phenylketonuria. I. Restricted phenylalanine intake in phenylketonuria. J Clin Invest. 1955 Apr;34(4):565–580. doi: 10.1172/JCI103105. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. BICKEL H., GERRARD J., HICKMANS E. M. The influence of phenylalanine intake on the chemistry and behaviour of a phenyl-ketonuric child. Acta Paediatr. 1954 Jan;43(1):64–77. doi: 10.1111/j.1651-2227.1954.tb04000.x. [DOI] [PubMed] [Google Scholar]
  3. CROME L., DUTTON G., ROSS C. F. Maple syrup urine disease. J Pathol Bacteriol. 1961 Apr;81:379–384. doi: 10.1002/path.1700810209. [DOI] [PubMed] [Google Scholar]
  4. DANCIS J., LEVITZ M., MILLER S., WESTALL R. G. Maple syrup urine disease. Br Med J. 1959 Jan 10;1(5114):91–93. doi: 10.1136/bmj.1.5114.91. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. DENT C. E., WALSHE J. M. Amino-acid metabolism. Br Med Bull. 1954;10(3):247–250. doi: 10.1093/oxfordjournals.bmb.a069430. [DOI] [PubMed] [Google Scholar]
  6. MACKENZIE D. Y., WOOLF L. I. Maple syrup urine disease; an inborn error of the metabolism of valine, leucine, and isoleucine associated with gross mental deficiency. Br Med J. 1959 Jan 10;1(5114):90–91. doi: 10.1136/bmj.1.5114.90. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. MCARDLE B. The quantitative estimation of pyruvic and alpha-oxoglutaric acids by paper chromatography in blood, urine and cerebrospinal fluid. Biochem J. 1957 May;66(1):144–148. doi: 10.1042/bj0660144. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. MENKES J. H., HURST P. L., CRAIG J. M. A new syndrome: progressive familial infantile cerebral dysfunction associated with an unusual urinary substance. Pediatrics. 1954 Nov;14(5):462–467. [PubMed] [Google Scholar]
  9. MENKES J. H. Maple syrup disease; isolation and identification of organic acids in the urine. Pediatrics. 1959 Feb;23(2):348–353. [PubMed] [Google Scholar]
  10. MOORE S., STEIN W. H. Procedures for the chromatographic determination of amino acids on four per cent cross-linked sulfonated polystyrene resins. J Biol Chem. 1954 Dec;211(2):893–906. [PubMed] [Google Scholar]
  11. PATRICK A. D. Maple syrup urine disease. Arch Dis Child. 1961 Jun;36:269–272. doi: 10.1136/adc.36.187.269. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Partridge S. M. Displacement chromatography on synthetic ion-exchange resins. 3. Fractionation of a protein hydrolysate. Biochem J. 1949;44(5):521–527. [PMC free article] [PubMed] [Google Scholar]

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