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C A Stanley

Showing results (41-50 of 106) with videos related to

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Biochemical and Biophysical Research Communications|December 5, 1998
The structure and organization of the human carnitine/acylcarnitine translocase (CACT1) gene2V Iacobazzi, M A Naglieri, C A Stanley, et al.
Journal of Molecular Biology|March 20, 2001
Structures of bovine glutamate dehydrogenase complexes elucidate the mechanism of purine regulationT J Smith, P E Peterson, T Schmidt, et al.
Pediatrics|July 1, 1980
Decreased oxygenation and hyperlipemia during intravenous fat infusions in premature infantsG R Periera, W W Fox, C A Stanley, et al.
The New England Journal of Medicine|October 23, 1997
Fasting hypoketotic coma in a child with deficiency of mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthaseG N Thompson, B Y Hsu, J J Pitt, et al.
The Journal of Pediatrics|October 1, 1993
Short- and long-term use of octreotide in the treatment of congenital hyperinsulinismP S Thornton, C A Alter, L E Katz, 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.
The Journal of Pediatrics|August 1, 1997
Sudden neonatal death in carnitine transporter deficiencyP Rinaldo, C A Stanley, B Y Hsu, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 1, 1976
Sex differences in binding of human growth hormone to isolated rat hepatocytesM B Ranke, C A Stanley, D Rodbard, 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.
Journal of Inherited Metabolic Disease|January 1, 1995
Glycine and L-carnitine therapy in 3-methylcrotonyl-CoA carboxylase deficiencyS L Rutledge, G T Berry, C A Stanley, et al.
Pageof 11

Showing results (41-50 of 106) with videos related to

Sort By:
Pageof 11
Biochemical and Biophysical Research Communications|December 5, 1998
The structure and organization of the human carnitine/acylcarnitine translocase (CACT1) gene2V Iacobazzi, M A Naglieri, C A Stanley, et al.
Journal of Molecular Biology|March 20, 2001
Structures of bovine glutamate dehydrogenase complexes elucidate the mechanism of purine regulationT J Smith, P E Peterson, T Schmidt, et al.
Pediatrics|July 1, 1980
Decreased oxygenation and hyperlipemia during intravenous fat infusions in premature infantsG R Periera, W W Fox, C A Stanley, et al.
The New England Journal of Medicine|October 23, 1997
Fasting hypoketotic coma in a child with deficiency of mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthaseG N Thompson, B Y Hsu, J J Pitt, et al.
The Journal of Pediatrics|October 1, 1993
Short- and long-term use of octreotide in the treatment of congenital hyperinsulinismP S Thornton, C A Alter, L E Katz, 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.
The Journal of Pediatrics|August 1, 1997
Sudden neonatal death in carnitine transporter deficiencyP Rinaldo, C A Stanley, B Y Hsu, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 1, 1976
Sex differences in binding of human growth hormone to isolated rat hepatocytesM B Ranke, C A Stanley, D Rodbard, 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.
Journal of Inherited Metabolic Disease|January 1, 1995
Glycine and L-carnitine therapy in 3-methylcrotonyl-CoA carboxylase deficiencyS L Rutledge, G T Berry, C A Stanley, et al.
Pageof 11