Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

P M Coates

Showing results (41-50 of 86) with videos related to

Pageof 9
Sort By:
Nursing Research|September 1, 1995
Nongenetic influences of obesity on risk factors for cardiovascular disease during two phases of developmentL L Hayman, J C Meininger, P M Coates, et al.
The Journal of Pediatrics|August 1, 1993
Familial combined hyperlipidemia in children: clinical expression, metabolic defects, and managementJ A Cortner, P M Coates, C A Liacouras, et al.
Pediatric Pathology|May 1, 1991
Postmortem recognition of fatty acid oxidation disordersM J Bennett, D E Hale, P M Coates, et al.
Progress in Clinical and Biological Research|January 1, 1990
A genetic defect in carnitine transport causing primary carnitine deficiencyC A Stanley, W R Treem, D E Hale, et al.
Biochimica Et Biophysica Acta|May 1, 1979
Increase in liver acid lipase of thyroidectomized rats by thyroid hormones and its inhibition by actinomycin DP M Coates, H Lau, L Krulich, et al.
American Journal of Diseases of Children (1960)|April 1, 1986
Metabolic disorder possible cause of Reye's syndromeR I Kelley, P M Coates, D E Hale, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 29, 1994
Mutations at the lysosomal acid cholesteryl ester hydrolase gene locus in Wolman diseaseR A Anderson, R S Byrum, P M Coates, et al.
Nursing Research|March 21, 1998
Genetic and environmental influences on cardiovascular disease risk factors in adolescentsJ C Meininger, L L Hayman, P M Coates, et al.
The Journal of Pediatrics|October 1, 1984
Systemic carnitine deficiency simulating Reye syndromeP M Coates, D E Hale, C A Stanley, et al.
Progress in Clinical and Biological Research|January 1, 1992
The molecular basis of medium chain acyl-CoA dehydrogenase deficiency: survey and evolution of 985A----G transition, and identification of five rare types of mutation within the medium chain acyl-CoA dehydrogenase geneI Yokota, P M Coates, D E Hale, et al.
Pageof 9

Showing results (41-50 of 86) with videos related to

Sort By:
Pageof 9
Nursing Research|September 1, 1995
Nongenetic influences of obesity on risk factors for cardiovascular disease during two phases of developmentL L Hayman, J C Meininger, P M Coates, et al.
The Journal of Pediatrics|August 1, 1993
Familial combined hyperlipidemia in children: clinical expression, metabolic defects, and managementJ A Cortner, P M Coates, C A Liacouras, et al.
Pediatric Pathology|May 1, 1991
Postmortem recognition of fatty acid oxidation disordersM J Bennett, D E Hale, P M Coates, et al.
Progress in Clinical and Biological Research|January 1, 1990
A genetic defect in carnitine transport causing primary carnitine deficiencyC A Stanley, W R Treem, D E Hale, et al.
Biochimica Et Biophysica Acta|May 1, 1979
Increase in liver acid lipase of thyroidectomized rats by thyroid hormones and its inhibition by actinomycin DP M Coates, H Lau, L Krulich, et al.
American Journal of Diseases of Children (1960)|April 1, 1986
Metabolic disorder possible cause of Reye's syndromeR I Kelley, P M Coates, D E Hale, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 29, 1994
Mutations at the lysosomal acid cholesteryl ester hydrolase gene locus in Wolman diseaseR A Anderson, R S Byrum, P M Coates, et al.
Nursing Research|March 21, 1998
Genetic and environmental influences on cardiovascular disease risk factors in adolescentsJ C Meininger, L L Hayman, P M Coates, et al.
The Journal of Pediatrics|October 1, 1984
Systemic carnitine deficiency simulating Reye syndromeP M Coates, D E Hale, C A Stanley, et al.
Progress in Clinical and Biological Research|January 1, 1992
The molecular basis of medium chain acyl-CoA dehydrogenase deficiency: survey and evolution of 985A----G transition, and identification of five rare types of mutation within the medium chain acyl-CoA dehydrogenase geneI Yokota, P M Coates, D E Hale, et al.
Pageof 9