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P M Coates

Showing results (71-80 of 86) with videos related to

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Journal of Lipid Research|February 1, 1987
Kinetics of chylomicron remnant clearance in normal and in hyperlipoproteinemic subjectsJ A Cortner, P M Coates, N A Le, et al.
The Journal of Pediatrics|December 1, 1978
Neonatal presentation of I-cell diseaseR A Sprigz, R A Doughty, T J Spackman, et al.
The Journal of Clinical Investigation|September 1, 1988
Relationship between unusual hepatic acyl coenzyme A profiles and the pathogenesis of Reye syndromeB E Corkey, D E Hale, M C Glennon, et al.
Pediatric Research|July 1, 1985
Long-chain acyl coenzyme A dehydrogenase deficiency: an inherited cause of nonketotic hypoglycemiaD E Hale, M L Batshaw, P M Coates, et al.
Progress in Clinical and Biological Research|January 1, 1990
The L-3-hydroxyacyl-CoA dehydrogenase deficiencyD E Hale, C Thorpe, K Braat, et al.
Hepatology (Baltimore, Md.)|November 1, 1986
Medium-chain and long-chain acyl CoA dehydrogenase deficiency: clinical, pathologic and ultrastructural differentiation from Reye's syndromeW R Treem, C A Witzleben, D A Piccoli, et al.
American Journal of Medical Genetics|March 1, 1987
Cholesteryl ester storage disease: pathologic changes in an affected fetusP K Desai, K H Astrin, S N Thung, et al.
Journal of Inherited Metabolic Disease|January 1, 1990
Analysis of abnormal urinary metabolites in the newborn period in medium-chain acyl-CoA dehydrogenase deficiencyM J Bennett, P M Coates, D E Hale, et al.
Lancet (London, England)|February 21, 1987
Prenatal diagnosis of medium-chain acyl-CoA dehydrogenase deficiency in family with sudden infant deathM J Bennett, F Allison, R J Pollitt, et al.
The Journal of Pediatrics|October 1, 1992
Atypical features of the hepatic form of carnitine palmitoyltransferase deficiency in a Hutterite familyJ C Haworth, F Demaugre, F A Booth, et al.
Pageof 9

Showing results (71-80 of 86) with videos related to

Sort By:
Pageof 9
Journal of Lipid Research|February 1, 1987
Kinetics of chylomicron remnant clearance in normal and in hyperlipoproteinemic subjectsJ A Cortner, P M Coates, N A Le, et al.
The Journal of Pediatrics|December 1, 1978
Neonatal presentation of I-cell diseaseR A Sprigz, R A Doughty, T J Spackman, et al.
The Journal of Clinical Investigation|September 1, 1988
Relationship between unusual hepatic acyl coenzyme A profiles and the pathogenesis of Reye syndromeB E Corkey, D E Hale, M C Glennon, et al.
Pediatric Research|July 1, 1985
Long-chain acyl coenzyme A dehydrogenase deficiency: an inherited cause of nonketotic hypoglycemiaD E Hale, M L Batshaw, P M Coates, et al.
Progress in Clinical and Biological Research|January 1, 1990
The L-3-hydroxyacyl-CoA dehydrogenase deficiencyD E Hale, C Thorpe, K Braat, et al.
Hepatology (Baltimore, Md.)|November 1, 1986
Medium-chain and long-chain acyl CoA dehydrogenase deficiency: clinical, pathologic and ultrastructural differentiation from Reye's syndromeW R Treem, C A Witzleben, D A Piccoli, et al.
American Journal of Medical Genetics|March 1, 1987
Cholesteryl ester storage disease: pathologic changes in an affected fetusP K Desai, K H Astrin, S N Thung, et al.
Journal of Inherited Metabolic Disease|January 1, 1990
Analysis of abnormal urinary metabolites in the newborn period in medium-chain acyl-CoA dehydrogenase deficiencyM J Bennett, P M Coates, D E Hale, et al.
Lancet (London, England)|February 21, 1987
Prenatal diagnosis of medium-chain acyl-CoA dehydrogenase deficiency in family with sudden infant deathM J Bennett, F Allison, R J Pollitt, et al.
The Journal of Pediatrics|October 1, 1992
Atypical features of the hepatic form of carnitine palmitoyltransferase deficiency in a Hutterite familyJ C Haworth, F Demaugre, F A Booth, et al.
Pageof 9