Dihydrolipoyl dehydrogenase deficiency: a therapeutic trial with branched-chain amino acid restriction-Reference-Cited by-同舟云学术

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Dihydrolipoyl dehydrogenase deficiency: a therapeutic trial with branched-chain amino acid restriction

Published:1986-09 Issue:4 Volume:145 Page:271-274
ISSN:0340-6199
Container-title:European Journal of Pediatrics
language:en
Short-container-title:Eur J Pediatr

Author:

Sakaguchi Y.,Yoshino M.,Aramaki S.,Yoshida I.,Yamashita F.,Kuhara T.,Matsumoto I.,Hayashi T.

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology, and Child Health

Link

http://link.springer.com/content/pdf/10.1007/BF00439399.pdf

Reference14 articles.

1. Blass JP, Avigan J, Uhlendorf BW (1970) A defect in pyruvate decarboxylase in a child with an intermittent movement disorder. J Clin Invest 49:423?432

2. Blass JP, Schulman JD, Young DS, Hom E (1972) An inherited defect affecting the tricarboxylic acid cycle in a patient with congenital lactic acidosis. J Clin Invest 51:1845?1851

3. Hayashi T, Tsuchiya H, Todoriki H, Naruse H (1982) High-performance liquid chromatographic determination of ?-ketoacids in human urine and plasma. Anal Biochem 122:173?179

4. Kornberg A (1955) Lactate dehydrogenase of muscle. Methods Enzymol 1:441?443

5. Kuhara T, Shinka T, Inoue Y, Matsumoto M, Yoshino M, Sakaguchi Y, Matsumoto I (1983) Studies of organic acid profiles of a patient with dihydrolipoyl dehydrogenase deficiency. Clin Chim Acta 133:133?140

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