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C A Stanley

Showing results (51-60 of 106) with videos related to

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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.
The American Journal of Physiology|March 1, 1997
Carnitine effects on coenzyme A profiles in rat liver with hypoglycin inhibition of multiple dehydrogenasesY K Lieu, B Y Hsu, W A Price, 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.
The Journal of Pediatrics|May 1, 1993
Detection of inborn errors of fatty acid oxidation from acylcarnitine analysis of plasma and blood spots with the radioisotopic exchange-high-performance liquid chromatographic methodE Schmidt-Sommerfeld, D Penn, M Duran, 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.
European Journal of Pediatrics|January 1, 1993
Impairment of calcium mobilization in phagocytic cells in glycogen storage disease type 1bH M Korchak, B Z Garty, C A Stanley, et al.
The Journal of Pediatrics|April 1, 1997
A syndrome of congenital hyperinsulinism and hyperammonemiaS A Weinzimer, C A Stanley, G T Berry, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Elevated plasma carnitine in the hepatic form of carnitine palmitoyltransferase-1 deficiencyC A Stanley, F Sunaryo, D E Hale, et al.
The New England Journal of Medicine|July 2, 1992
Brief report: a deficiency of carnitine-acylcarnitine translocase in the inner mitochondrial membraneC A Stanley, D E Hale, G T Berry, et al.
Endocrinology|October 1, 1976
Characterization of somatogenic and lactogenic binding sites in isolated rat hepatocytesM B Ranke, C A Stanley, A Tenore, et al.
Pageof 11

Showing results (51-60 of 106) with videos related to

Sort By:
Pageof 11
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.
The American Journal of Physiology|March 1, 1997
Carnitine effects on coenzyme A profiles in rat liver with hypoglycin inhibition of multiple dehydrogenasesY K Lieu, B Y Hsu, W A Price, 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.
The Journal of Pediatrics|May 1, 1993
Detection of inborn errors of fatty acid oxidation from acylcarnitine analysis of plasma and blood spots with the radioisotopic exchange-high-performance liquid chromatographic methodE Schmidt-Sommerfeld, D Penn, M Duran, 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.
European Journal of Pediatrics|January 1, 1993
Impairment of calcium mobilization in phagocytic cells in glycogen storage disease type 1bH M Korchak, B Z Garty, C A Stanley, et al.
The Journal of Pediatrics|April 1, 1997
A syndrome of congenital hyperinsulinism and hyperammonemiaS A Weinzimer, C A Stanley, G T Berry, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Elevated plasma carnitine in the hepatic form of carnitine palmitoyltransferase-1 deficiencyC A Stanley, F Sunaryo, D E Hale, et al.
The New England Journal of Medicine|July 2, 1992
Brief report: a deficiency of carnitine-acylcarnitine translocase in the inner mitochondrial membraneC A Stanley, D E Hale, G T Berry, et al.
Endocrinology|October 1, 1976
Characterization of somatogenic and lactogenic binding sites in isolated rat hepatocytesM B Ranke, C A Stanley, A Tenore, et al.
Pageof 11