Dietary Treatment of a Child with Maple Syrup Urine Disease (Branched-chain Ketoaciduria)-Reference-Cited by-同舟云学术

Dietary Treatment of a Child with Maple Syrup Urine Disease (Branched-chain Ketoaciduria)

Published:1963-10-01 Issue:201 Volume:38 Page:485-491
ISSN:0003-9888
Container-title:Archives of Disease in Childhood
language:en
Short-container-title:Archives of Disease in Childhood

Author:

Westall R. G.

Publisher

BMJ

Subject

Pediatrics, Perinatology, and Child Health

Reference14 articles.

1. Bloxam H. R., Day, M. G., Gibbs, N. K. and Woolf, L. I. (1960).

2. Maple syrup urine disease.;Dancis, J.; Levitz, M.; Miller, S.; Westall, R.G.;Brit. med. J,1959

3. Studies in maple syrup urine disease;Dent, C.E.; Westall, R.G.;Arch. Dis. Childh,1961

4. Metabolism of amino acids and related compounds in vivo;Gullino, P.; Winitz, M.; Birnbaum, S.M.; Cornfield, J.; Otey, M.C.; Greenstein, J.P.,1956

5. Toxicity of essential amino acids, individually and in mixtures, and the protective effect of Larginine;Holt, Jr., L.E.; Snyderman, S.E.; Dancis, J.; Norton, P.M.;Arch. Biochem; The treatment of a case of maple syrup urine disease,1960

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