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P M Coates

Showing results (61-70 of 86) with videos related to

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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.
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.
European Journal of Clinical Investigation|March 1, 1992
Determinants of fasting plasma triglyceride levels: metabolism of hepatic and intestinal lipoproteinsJ A Cortner, N A Le, P M Coates, et al.
Nursing Research|September 1, 1988
Type A behavior and physiological cardiovascular risk factors in school-age twin childrenL L Hayman, J C Meininger, E E Stashinko, 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.
Journal of Lipid Research|May 1, 1986
Direct measurement of apolipoprotein B synthesis in human very low density lipoprotein using stable isotopes and mass spectrometryD R Cryer, T Matsushima, J B Marsh, et al.
Biomedical & Environmental Mass Spectrometry|August 1, 1990
Measurement of (C13)arginine incorporation into apolipoprotein B-100 in very low density lipoproteins and low density lipoproteins in normal subjects using (13C)sodium bicarbonate infusion and isotope ratio mass spectrometryM J Bennett, D R Cryer, M Yudkoff, et al.
Journal of Medical Genetics|July 1, 1994
Rapid detection of medium chain acyl-CoA dehydrogenase gene mutations by non-radioactive, single strand conformation polymorphism minigelsA Iolascon, T Parrella, S Perrotta, et al.
The American Journal of Clinical Nutrition|November 14, 1997
Effects of family history of heart disease, apolipoprotein E phenotype, and lipoprotein(a) on the response of children's plasma lipids to change in dietary lipidsL B Dixon, B M Shannon, A M Tershakovec, et al.
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.
Pageof 9

Showing results (61-70 of 86) with videos related to

Sort By:
Pageof 9
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.
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.
European Journal of Clinical Investigation|March 1, 1992
Determinants of fasting plasma triglyceride levels: metabolism of hepatic and intestinal lipoproteinsJ A Cortner, N A Le, P M Coates, et al.
Nursing Research|September 1, 1988
Type A behavior and physiological cardiovascular risk factors in school-age twin childrenL L Hayman, J C Meininger, E E Stashinko, 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.
Journal of Lipid Research|May 1, 1986
Direct measurement of apolipoprotein B synthesis in human very low density lipoprotein using stable isotopes and mass spectrometryD R Cryer, T Matsushima, J B Marsh, et al.
Biomedical & Environmental Mass Spectrometry|August 1, 1990
Measurement of (C13)arginine incorporation into apolipoprotein B-100 in very low density lipoproteins and low density lipoproteins in normal subjects using (13C)sodium bicarbonate infusion and isotope ratio mass spectrometryM J Bennett, D R Cryer, M Yudkoff, et al.
Journal of Medical Genetics|July 1, 1994
Rapid detection of medium chain acyl-CoA dehydrogenase gene mutations by non-radioactive, single strand conformation polymorphism minigelsA Iolascon, T Parrella, S Perrotta, et al.
The American Journal of Clinical Nutrition|November 14, 1997
Effects of family history of heart disease, apolipoprotein E phenotype, and lipoprotein(a) on the response of children's plasma lipids to change in dietary lipidsL B Dixon, B M Shannon, A M Tershakovec, et al.
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.
Pageof 9