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D E HALE

Showing results (41-50 of 85) with videos related to

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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.
Journal of Inherited Metabolic Disease|January 1, 1991
Atypical riboflavin-responsive glutaric aciduria, and deficient peroxisomal glutaryl-CoA oxidase activity: a new peroxisomal disorderM J Bennett, R J Pollitt, S I Goodman, et al.
American Journal of Medical Genetics|September 5, 1997
Growth hormone insufficiency associated with haploinsufficiency at 18q23J D Cody, D E Hale, Z Brkanac, et al.
European Journal of Pediatrics|November 1, 1993
A new case of short-chain acyl-CoA dehydrogenase deficiency with isolated ethylmalonic aciduriaA C Sewell, J Herwig, H Böhles, et al.
Brain Research. Developmental Brain Research|October 16, 1999
Molecular, morphometric and functional analyses demonstrate that the growth hormone deficient little mouse is not hypomyelinatedD M Lehman, D E Hale, J T Cody, et al.
The New England Journal of Medicine|November 17, 1988
Primary carnitine deficiency due to a failure of carnitine transport in kidney, muscle, and fibroblastsW R Treem, C A Stanley, D N Finegold, et al.
Diabetes Care|May 20, 1999
Diabetes risk factors in low-income Mexican-American childrenR P Treviño, R M Marshall, D E Hale, 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 Research|November 1, 1993
Expression and characterization of human mutant (glutamic acid304) medium-chain acyl-coenzyme A dehydrogenase in mammalian cellsA J Whelan, A W Strauss, D E Hale, 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.
Pageof 9

Showing results (41-50 of 85) with videos related to

Sort By:
Pageof 9
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.
Journal of Inherited Metabolic Disease|January 1, 1991
Atypical riboflavin-responsive glutaric aciduria, and deficient peroxisomal glutaryl-CoA oxidase activity: a new peroxisomal disorderM J Bennett, R J Pollitt, S I Goodman, et al.
American Journal of Medical Genetics|September 5, 1997
Growth hormone insufficiency associated with haploinsufficiency at 18q23J D Cody, D E Hale, Z Brkanac, et al.
European Journal of Pediatrics|November 1, 1993
A new case of short-chain acyl-CoA dehydrogenase deficiency with isolated ethylmalonic aciduriaA C Sewell, J Herwig, H Böhles, et al.
Brain Research. Developmental Brain Research|October 16, 1999
Molecular, morphometric and functional analyses demonstrate that the growth hormone deficient little mouse is not hypomyelinatedD M Lehman, D E Hale, J T Cody, et al.
The New England Journal of Medicine|November 17, 1988
Primary carnitine deficiency due to a failure of carnitine transport in kidney, muscle, and fibroblastsW R Treem, C A Stanley, D N Finegold, et al.
Diabetes Care|May 20, 1999
Diabetes risk factors in low-income Mexican-American childrenR P Treviño, R M Marshall, D E Hale, 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 Research|November 1, 1993
Expression and characterization of human mutant (glutamic acid304) medium-chain acyl-coenzyme A dehydrogenase in mammalian cellsA J Whelan, A W Strauss, D E Hale, 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.
Pageof 9