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Pediatric Pathology|May 1, 1991
Postmortem recognition of fatty acid oxidation disordersM J Bennett, D E Hale, P M Coates, 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.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.American Journal of Human Genetics|December 1, 1991
Molecular survey of a prevalent mutation, 985A-to-G transition, and identification of five infrequent mutations in the medium-chain Acyl-CoA dehydrogenase (MCAD) gene in 55 patients with MCAD deficiencyI Yokota, P M Coates, D E Hale, et al.Biochimica Et Biophysica Acta|February 26, 1979
Acid lipase activity of human lymphocytesP M Coates, J A Cortner, G M Hoffman, et al.Pediatric Research|September 1, 1986
Biosynthesis of variant medium chain acyl-CoA dehydrogenase in cultured fibroblasts from patients with medium chain acyl-CoA dehydrogenase deficiencyY Ikeda, D E Hale, S M Keese, et al.Clinical Nephrology|October 1, 1980
Hydrocarbon exposure and glomerulonephritisR Finn, A G Fennerty, R AhmadNeuroscience|July 30, 2014
Strain-dependent brain defects in mouse models of primary ciliary dyskinesia with mutations in Pcdp1 and Spef2R Finn, C C Evans, L LeeBlood Purification|January 1, 1989
Management of patients with renal failure complicated by cerebral oedemaA Davenport, R Finn, H J GoldsmithPageof 29