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D E HALE

Showing results (61-70 of 85) with videos related to

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European Journal of Pediatrics|May 1, 1990
Early diagnosis and treatment of neonatal medium-chain acyl-CoA dehydrogenase deficiency: report of two siblingsC Catzeflis, C Bachmann, D E Hale, et al.
The 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.
Journal of Inherited Metabolic Disease|January 1, 1992
Molecular basis of inherited medium-chain acyl-CoA dehydrogenase deficiency causing sudden child deathD P Kelly, D E Hale, S L Rutledge, et al.
The Journal of Pediatrics|May 1, 1991
Progressive neuropathy and recurrent myoglobinuria in a child with long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiencyC Dionisi Vici, A B Burlina, E Bertini, 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.
Annals of Neurology|September 1, 1991
Short-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency in muscle: a new cause for recurrent myoglobinuria and encephalopathyI Tein, D C De Vivo, D E Hale, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 7, 1995
Molecular basis of human mitochondrial very-long-chain acyl-CoA dehydrogenase deficiency causing cardiomyopathy and sudden death in childhoodA W Strauss, C K Powell, D E Hale, et al.
Pediatric Obesity|March 31, 2012
Cardiovascular risk factors in multi-ethnic middle school students: the HEALTHY primary prevention trialS M Willi, K Hirst, R Jago, et al.
Pediatric Research|September 1, 1996
Maternal acute fatty liver of pregnancy associated with fetal trifunctional protein deficiency: molecular characterization of a novel maternal mutant alleleJ D Isaacs, H F Sims, C K Powell, et al.
Progress in Clinical and Biological Research|January 1, 1990
The L-3-hydroxyacyl-CoA dehydrogenase deficiencyD E Hale, C Thorpe, K Braat, et al.
Pageof 9

Showing results (61-70 of 85) with videos related to

Sort By:
Pageof 9
European Journal of Pediatrics|May 1, 1990
Early diagnosis and treatment of neonatal medium-chain acyl-CoA dehydrogenase deficiency: report of two siblingsC Catzeflis, C Bachmann, D E Hale, et al.
The 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.
Journal of Inherited Metabolic Disease|January 1, 1992
Molecular basis of inherited medium-chain acyl-CoA dehydrogenase deficiency causing sudden child deathD P Kelly, D E Hale, S L Rutledge, et al.
The Journal of Pediatrics|May 1, 1991
Progressive neuropathy and recurrent myoglobinuria in a child with long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiencyC Dionisi Vici, A B Burlina, E Bertini, 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.
Annals of Neurology|September 1, 1991
Short-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency in muscle: a new cause for recurrent myoglobinuria and encephalopathyI Tein, D C De Vivo, D E Hale, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 7, 1995
Molecular basis of human mitochondrial very-long-chain acyl-CoA dehydrogenase deficiency causing cardiomyopathy and sudden death in childhoodA W Strauss, C K Powell, D E Hale, et al.
Pediatric Obesity|March 31, 2012
Cardiovascular risk factors in multi-ethnic middle school students: the HEALTHY primary prevention trialS M Willi, K Hirst, R Jago, et al.
Pediatric Research|September 1, 1996
Maternal acute fatty liver of pregnancy associated with fetal trifunctional protein deficiency: molecular characterization of a novel maternal mutant alleleJ D Isaacs, H F Sims, C K Powell, et al.
Progress in Clinical and Biological Research|January 1, 1990
The L-3-hydroxyacyl-CoA dehydrogenase deficiencyD E Hale, C Thorpe, K Braat, et al.
Pageof 9