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QJM : Monthly Journal of the Association of Physicians|March 1, 1997
Genetic testing for familial hypercholesterolaemia: practical and ethical issuesS E Humphries, D Galton, P NichollsAtherosclerosis|August 1, 1988
DNA polymorphisms of the apolipoprotein genes--their use in the investigation of the genetic component of hyperlipidaemia and atherosclerosisS E HumphriesTrends in Cardiovascular Medicine|January 20, 2011
The genetic contribution to the risk of thrombosis and cardiovascular diseaseS E HumphriesClinical Genetics|August 15, 2008
Multiplex MassARRAY spectrometry (iPLEX) produces a fast and economical test for 56 familial hypercholesterolaemia-causing mutationsW T Wright, S V Heggarty, I S Young, et al.Genes and Immunity|January 12, 2007
Interleukin-18 genetics and inflammatory disease susceptibilityS R Thompson, S E HumphriesCurrent Opinion in Lipidology|June 1, 1997
Apolipoprotein C-III gene variation and dyslipidaemiaP J Talmud, S E HumphriesBailliere'S Best Practice & Research. Clinical Haematology|June 17, 2000
Genetic determinants of arterial thrombosisP J Grant, S E HumphriesCurrent Opinion in Lipidology|August 1, 1995
Hyperlipidaemia associated with genetic variation in the apolipoprotein B geneS E Humphries, P J TalmudAtherosclerosis|October 1, 1992
Familial defective apolipoprotein B-100: a single mutation that causes hypercholesterolemia and premature coronary artery diseaseA Tybjaerg-Hansen, S E HumphriesPageof 60