Family with intermittent maple syrup urine disease

Author:

Valman H. B.,Patrick A. D.,Seakins J. W. T.,Platt J. W.,Gompertz D.

Publisher

BMJ

Subject

Pediatrics, Perinatology and Child Health

Reference21 articles.

1. Biotin-responsive propionicacidaemia;Barnes, N.D.; Hull, D.; Balgobin, L.; Gompertz, D.;Lancet,1970

2. La variante intermittente de la leucinose;Boisse, J.; Saudubray, J.M.; Pham-Huu-Trung, Charpentier; C., Castets; M., Lemonnier; A., Jerome; H.; Mozziconacci, P.;Archives Franfaises de Pediatrie,1971

3. Branched chain a-keto acid metabolism. II. Evidence for the common identity of a-ketoisocaproic acid and a-keto-3 methylvaleric acid dehydrogenases;Bowden, J.A.; Connelly, J.L.;journal of Biological Chemistry,1968

4. Leigh's subacute necrotizing encephalopathy: clinical and biochemical study, with special reference to therapy with lipoate;Clayton, B.E.; Dobbs, R.H.; Patrick, A.D.;Archives of Disease in Childhood,1967

5. Intermittent branched chain ketonuria. In Amino Acid Metabolism and Genetic Variation;Dancis, J.,1967

Cited by 9 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Expanded Newborn Screening for Inborn Errors of Metabolism;Advances in Pediatrics;2012-01

2. References;Metabolic and Degenerative Diseases of the Central Nervous System;1995

3. Cardiac Abnormalities in One Case of Maple Syrup Urine Disease;Echocardiography;1994-03

4. Thiamine-responsive intermittent branched-chain ketoaciduria;The Journal of Pediatrics;1979-04

5. Modification of genetic expression in phagocytes;Inborn Errors of Immunity and Phagocytosis;1979

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