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D E HALE

Showing results (31-40 of 85) with videos related to

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The Journal of Pediatrics|October 1, 1984
Systemic carnitine deficiency simulating Reye syndromeP M Coates, D E Hale, C A Stanley, et al.
Progress in Clinical and Biological Research|January 1, 1992
The molecular basis of medium chain acyl-CoA dehydrogenase deficiency: survey and evolution of 985A----G transition, and identification of five rare types of mutation within the medium chain acyl-CoA dehydrogenase geneI Yokota, P M Coates, D E Hale, et al.
American Journal of Human Genetics|December 1, 1991
Molecular survey of a prevalent mutation, 985A-to-G transition, and identification of five infrequent mutations in the medium-chain Acyl-CoA dehydrogenase (MCAD) gene in 55 patients with MCAD deficiencyI Yokota, P M Coates, D E Hale, et al.
Pediatric Research|January 1, 1992
Immunochemical characterization of variant medium-chain acyl-CoA dehydrogenase in fibroblasts from patients with medium-chain acyl-CoA dehydrogenase deficiencyP M Coates, Y Indo, D Young, et al.
Journal of Inherited Metabolic Disease|January 1, 1993
Marked elevation of urinary 3-hydroxydecanedioic acid in a malnourished infant with glycogen storage disease, mimicking long-chain L-3-hydroxyacyl-CoA dehydrogenase deficiencyJ Bergoffen, P Kaplan, D E Hale, et al.
Pediatric Research|September 1, 1986
Biosynthesis of variant medium chain acyl-CoA dehydrogenase in cultured fibroblasts from patients with medium chain acyl-CoA dehydrogenase deficiencyY Ikeda, D E Hale, S M Keese, et al.
Human Genetics|July 29, 2000
Genetic basis of acanthosis nigricans in Mexican Americans and its association with phenotypes related to type 2 diabetesJ P Burke, R Duggirala, D E Hale, et al.
The Journal of Clinical Investigation|January 1, 1988
Genetic deficiency of short-chain acyl-coenzyme A dehydrogenase in cultured fibroblasts from a patient with muscle carnitine deficiency and severe skeletal muscle weaknessP M Coates, D E Hale, G Finocchiaro, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Fatal outcome in a patient with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiencyA Ribes, E Riudor, C Navarro, et al.
American Family Physician|May 1, 1989
Medium-chain acyl-CoA dehydrogenase deficiencyR J Egidio, G L Francis, P M Coates, et al.
Pageof 9

Showing results (31-40 of 85) with videos related to

Sort By:
Pageof 9
The Journal of Pediatrics|October 1, 1984
Systemic carnitine deficiency simulating Reye syndromeP M Coates, D E Hale, C A Stanley, et al.
Progress in Clinical and Biological Research|January 1, 1992
The molecular basis of medium chain acyl-CoA dehydrogenase deficiency: survey and evolution of 985A----G transition, and identification of five rare types of mutation within the medium chain acyl-CoA dehydrogenase geneI Yokota, P M Coates, D E Hale, et al.
American Journal of Human Genetics|December 1, 1991
Molecular survey of a prevalent mutation, 985A-to-G transition, and identification of five infrequent mutations in the medium-chain Acyl-CoA dehydrogenase (MCAD) gene in 55 patients with MCAD deficiencyI Yokota, P M Coates, D E Hale, et al.
Pediatric Research|January 1, 1992
Immunochemical characterization of variant medium-chain acyl-CoA dehydrogenase in fibroblasts from patients with medium-chain acyl-CoA dehydrogenase deficiencyP M Coates, Y Indo, D Young, et al.
Journal of Inherited Metabolic Disease|January 1, 1993
Marked elevation of urinary 3-hydroxydecanedioic acid in a malnourished infant with glycogen storage disease, mimicking long-chain L-3-hydroxyacyl-CoA dehydrogenase deficiencyJ Bergoffen, P Kaplan, D E Hale, et al.
Pediatric Research|September 1, 1986
Biosynthesis of variant medium chain acyl-CoA dehydrogenase in cultured fibroblasts from patients with medium chain acyl-CoA dehydrogenase deficiencyY Ikeda, D E Hale, S M Keese, et al.
Human Genetics|July 29, 2000
Genetic basis of acanthosis nigricans in Mexican Americans and its association with phenotypes related to type 2 diabetesJ P Burke, R Duggirala, D E Hale, et al.
The Journal of Clinical Investigation|January 1, 1988
Genetic deficiency of short-chain acyl-coenzyme A dehydrogenase in cultured fibroblasts from a patient with muscle carnitine deficiency and severe skeletal muscle weaknessP M Coates, D E Hale, G Finocchiaro, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Fatal outcome in a patient with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiencyA Ribes, E Riudor, C Navarro, et al.
American Family Physician|May 1, 1989
Medium-chain acyl-CoA dehydrogenase deficiencyR J Egidio, G L Francis, P M Coates, et al.
Pageof 9