Quantitation of urinary carnitine esters in a patient with medium-chain acyl-coenzyme A dehydrogenase deficiency: Effect of metabolic state and l-carnitine therapy-Reference-Cited by-同舟云学术

Quantitation of urinary carnitine esters in a patient with medium-chain acyl-coenzyme A dehydrogenase deficiency: Effect of metabolic state and l-carnitine therapy

Published:1989-10 Issue:4 Volume:115 Page:577-582
ISSN:0022-3476
Container-title:The Journal of Pediatrics
language:en
Short-container-title:The Journal of Pediatrics

Author:

Schmidt-Sommerfeld Eberhard,Penn Duna,Kerner Janos,Bieber Loran L.,Rossi Thomas M.,Lebenthal Emanuel

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology, and Child Health

Reference24 articles.

1. In vitro fibroblast studies in a patient with C6–C10 dicarboxylic aciduria: evidence for a defect in general acyl-CoA dehydrogenase;Kolvraa;Clin Chim Acta,1982

2. Familial Reye-like syndrome: a presentation of medium-chain acyl-coenzyme A dehydrogenase deficiency;Taubman;Pediatrics,1987

3. Deficiency of medium-chain fatty acylcoenzyme A dehydrogenase presenting as the sudden infant death syndrome;Howat;Br Med J,1984

4. Acylcoenzyme A dehydrogenase deficiency in heart tissue from infants who died unexpectedly with fatty change in the liver;Allison;Br Med J,1988

5. Genetic deficiency of medium-chain acyl coenzyme A dehydrogenase: studies in cultured skin fibroblasts and peripheral mononuclear leukocytes;Coates;Pediatr Res,1985

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