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Orphanet Journal of Rare Diseases|July 10, 2008
Abetalipoproteinemia: two case reports and literature reviewRola Zamel, Razi Khan, Rebecca L Pollex, et al.
Lipids in Health and Disease|March 23, 2007
Genetic determinants of statin intoleranceJisun Oh, Matthew R Ban, Brooke A Miskie, et al.
Journal of Diabetes and Its Complications|May 12, 2007
Peroxisome proliferator-activated receptor gamma polymorphism Pro12Ala is associated with nephropathy in type 2 diabetesRebecca L Pollex, Mary Mamakeesick, Bernard Zinman, et al.
Cardiovascular Diabetology|November 9, 2005
Methylenetetrahydrofolate reductase polymorphism 677C>T is associated with peripheral arterial disease in type 2 diabetesRebecca L Pollex, Mary Mamakeesick, Bernard Zinman, et al.
Atherosclerosis|May 5, 2005
Metabolic syndrome in aboriginal Canadians: prevalence and genetic associationsRebecca L Pollex, Anthony J G Hanley, Bernard Zinman, et al.
Nature Clinical Practice. Cardiovascular Medicine|September 10, 2008
APOA5 genetic variants are markers for classic hyperlipoproteinemia phenotypes and hypertriglyceridemiaJian Wang, Matthew R Ban, Brooke A Kennedy, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|August 25, 2007
Resequencing genomic DNA of patients with severe hypertriglyceridemia (MIM 144650)Jian Wang, Henian Cao, Matthew R Ban, et al.
Cardiovascular Ultrasound|June 17, 2005
A comparison of ultrasound measurements to assess carotid atherosclerosis development in subjects with and without type 2 diabetesRebecca L Pollex, J David Spence, Andrew A House, et al.
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