Hyperuricemia in medium-chain acyl-coenzyme A dehydrogenase deficiency
- 1 March 1992
- journal article
- Published by Elsevier in The Journal of Pediatrics
- Vol. 120 (3) , 444-446
- https://doi.org/10.1016/s0022-3476(05)80918-7
Abstract
No abstract availableKeywords
This publication has 7 references indexed in Scilit:
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- Familial Reye-Like Syndrome: A Presentation of Medium-Chain Acyl-Coenzyme A Dehydrogenase DeficiencyPediatrics, 1987
- New Genetic Defects in Mitochondrial Fatty Acid Oxidation and Carnitine DeficiencyAdvances in Pediatrics, 1987
- Sudden Child Death and `Healthy' Affected Family Members With Medium-Chain Acyl-Coenzyme A Dehydrogenase DeficiencyPediatrics, 1986
- Medium-chain and long-chain acyl CoA dehydrogenase deficiency: Clinical, pathologic and ultrastructural differentiation from Reye's syndrome†Hepatology, 1986
- Recognition of medium-chain acyl-CoA dehydrogenase deficiency in asymptomatic siblings of children dying of sudden infant death or Reye-like syndromesThe Journal of Pediatrics, 1986