Sudden infant death syndrome and multiple acyl-coenzyme A dehydrogenase deficiency, ethylmalonic-adipic aciduria, or systemic carnitine deficiency
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology, and Child Health
Reference10 articles.
1. Multiple acyl-CoA dehydrogenase deficiency occurring in pregnancy and caused by a defect in riboflavin metabolism in the mother;Harpey;J Pediatr,1983
2. Ethylmalonic-adipic aciduria: in vivo and in vitro studies indicating deficiency of activities of multiple acyl-CoA dehydrogenases;Mantagos;J Clin Invest,1979
3. Systemic carnitine deficiency presenting as familial endocardial fibroelastosis: a treatable cardiomyopathy;Tripp;N Engl J Med,1981
4. Recognition of medium-chain acyl-CoA dehydrogenase deficiency in asymptomatic siblings of children dying of sudden infant death or Reye-like syndromes;Roe;J Pediatr,1986
5. Defects of metabolism of fatty acids in the sudden infant death syndrome;Howat;Br Med J,1985
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