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Pediatric Pathology|May 1, 1991
Postmortem recognition of fatty acid oxidation disordersM J Bennett, D E Hale, P M Coates, 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.Clinical Cardiology|March 1, 1996
Endocardial fibroelastosis and primary carnitine deficiency due to a defect in the plasma membrane carnitine transporterM J Bennett, D E Hale, R J Pollitt, et al.Current Opinion in Pediatrics|August 1, 1994
Genetic disorders of mitochondrial fatty acid oxidationC A Stanley, D E HaleNew Jersey Medicine : the Journal of the Medical Society of New Jersey|September 1, 1992
Medium chain acyl-coenzyme A dehydrogenase deficiencyM J Bennett, D E HaleThe Journal of Clinical Investigation|September 1, 1988
Relationship between unusual hepatic acyl coenzyme A profiles and the pathogenesis of Reye syndromeB E Corkey, D E Hale, M C Glennon, et al.Pediatric Research|July 1, 1985
Long-chain acyl coenzyme A dehydrogenase deficiency: an inherited cause of nonketotic hypoglycemiaD E Hale, M L Batshaw, P M Coates, et al.Pediatric Research|July 1, 1993
Renal handling of carnitine in secondary carnitine deficiency disordersC A Stanley, G T Berry, M J Bennett, et al.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.Pageof 40