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P M Coates

Showing results (1-10 of 86) with videos related to

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European Journal of Pediatrics|January 1, 1994
New developments in the diagnosis and investigation of mitochondrial fatty acid oxidation disordersP M Coates
Biofactors (Oxford, England)|May 6, 1998
Fatty acid metabolism in mitochondria: defects and geneticsP M Coates
Progress in Clinical and Biological Research|January 1, 1992
Historical perspective of medium-chain acyl-CoA dehydrogenase deficiency: a decade of discoveryP M Coates
American Journal of Human Genetics|August 1, 1995
Very-long-chain acyl-CoA dehydrogenase deficiency: molecular genetics of a mitochondrial membrane enzymeP M Coates
Journal of Lipid Research|August 1, 1992
Molecular basis of mitochondrial fatty acid oxidation defectsP M Coates, K Tanaka
Lancet (London, England)|January 22, 1977
Plasma exchange in myasthenia gravisR Finn, P M Coates
Annals of Human Genetics|July 1, 1986
Genetic polymorphism of esterase B3 in human leukocytesP M Coates, J A Cortner
Science (New York, N.Y.)|March 31, 1972
Genetic variation in human erythrocyte acetylcholinesteraseP M Coates, N E Simpson
Progress in Liver Diseases|January 1, 1992
Inherited disorders of mitochondrial fatty acid oxidationP M Coates, C A Stanley
Metabolism: Clinical and Experimental|January 1, 1984
Effect of diabetes and insulin therapy on human mononuclear leukocyte lysosomal acid lipase activityD N Finegold, P M Coates
Pageof 9

Showing results (1-10 of 86) with videos related to

Sort By:
Pageof 9
European Journal of Pediatrics|January 1, 1994
New developments in the diagnosis and investigation of mitochondrial fatty acid oxidation disordersP M Coates
Biofactors (Oxford, England)|May 6, 1998
Fatty acid metabolism in mitochondria: defects and geneticsP M Coates
Progress in Clinical and Biological Research|January 1, 1992
Historical perspective of medium-chain acyl-CoA dehydrogenase deficiency: a decade of discoveryP M Coates
American Journal of Human Genetics|August 1, 1995
Very-long-chain acyl-CoA dehydrogenase deficiency: molecular genetics of a mitochondrial membrane enzymeP M Coates
Journal of Lipid Research|August 1, 1992
Molecular basis of mitochondrial fatty acid oxidation defectsP M Coates, K Tanaka
Lancet (London, England)|January 22, 1977
Plasma exchange in myasthenia gravisR Finn, P M Coates
Annals of Human Genetics|July 1, 1986
Genetic polymorphism of esterase B3 in human leukocytesP M Coates, J A Cortner
Science (New York, N.Y.)|March 31, 1972
Genetic variation in human erythrocyte acetylcholinesteraseP M Coates, N E Simpson
Progress in Liver Diseases|January 1, 1992
Inherited disorders of mitochondrial fatty acid oxidationP M Coates, C A Stanley
Metabolism: Clinical and Experimental|January 1, 1984
Effect of diabetes and insulin therapy on human mononuclear leukocyte lysosomal acid lipase activityD N Finegold, P M Coates
Pageof 9