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Hepatology (Baltimore, Md.)|November 1, 1986
Medium-chain and long-chain acyl CoA dehydrogenase deficiency: clinical, pathologic and ultrastructural differentiation from Reye's syndromeW R Treem, C A Witzleben, D A Piccoli, et al.Pediatrics|March 1, 1991
Hypoglycemia, hypotonia, and cardiomyopathy: the evolving clinical picture of long-chain acyl-CoA dehydrogenase deficiencyW R Treem, C A Stanley, D E Hale, et al.Pediatric Pathology|May 1, 1991
Postmortem recognition of fatty acid oxidation disordersM J Bennett, D E Hale, P M Coates, et al.Pediatrics|June 1, 1989
Massive hepatomegaly, steatosis, and secondary plasma carnitine deficiency in an infant with cystic fibrosisW R Treem, C A StanleyPediatric Research|July 1, 1993
Renal handling of carnitine in secondary carnitine deficiency disordersC A Stanley, G T Berry, M J Bennett, et al.Pediatric Research|July 1, 1985
Genetic deficiency of medium-chain acyl coenzyme A dehydrogenase: studies in cultured skin fibroblasts and peripheral mononuclear leukocytesP M Coates, D E Hale, C A Stanley, et al.The New England Journal of Medicine|November 17, 1988
Medium-chain acyl-CoA dehydrogenase deficiency. Diagnosis by stable-isotope dilution measurement of urinary n-hexanoylglycine and 3-phenylpropionylglycineP Rinaldo, J J O'Shea, P M Coates, et al.Journal of Inherited Metabolic Disease|January 1, 1989
Medium-chain acyl-CoA dehydrogenase deficiency: metabolic effects and therapeutic efficacy of long-term L-carnitine supplementationW R Treem, C A Stanley, S I GoodmanHepatology (Baltimore, Md.)|February 1, 1994
Acute fatty liver of pregnancy and long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiencyW R Treem, P Rinaldo, D E Hale, et al.Current Opinion in Pediatrics|August 1, 1994
Genetic disorders of mitochondrial fatty acid oxidationC A Stanley, D E HalePageof 23