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European Journal of Clinical Investigation|September 1, 1992
Severe type III hyperlipoproteinemia associated with unusual apolipoprotein E1 phenotype and epsilon 1/'null' genotypeG Feussner, H Funke, W Weng, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|May 1, 1995
Reverse cholesterol transport in plasma of patients with different forms of familial HDL deficiencyA von Eckardstein, Y Huang, S Wu, et al.
Journal of Lipid Research|February 1, 1997
The molecular pathology of lecithin:cholesterol acyltransferase (LCAT) deficiency syndromesJ A Kuivenhoven, H Pritchard, J Hill, et al.
The Journal of Clinical Investigation|May 1, 1991
Apolipoprotein C-III(Lys58----Glu). Identification of an apolipoprotein C-III variant in a family with hyperalphalipoproteinemiaA von Eckardstein, H Holz, M Sandkamp, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|June 20, 1998
Relationship between plasma viscosity and the severity of coronary heart diseaseR Junker, J Heinrich, H Ulbrich, et al.
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