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The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|November 1, 1984
Distribution of apolipoprotein E phenotypes in Friedreich's ataxiaD Bouthillier, A C Nestruck, R Milne, et al.
Clinical and Investigative Medicine. Medecine Clinique Et Experimentale|April 1, 1992
The relation between triglyceride synthesis in peripheral tissues and postprandial plasma triglyceride levels: preliminary evidence of a role for acylation stimulating proteinK M Cianflone, A D Sniderman, J Dallongeville, et al.
Human Genetics|March 1, 1992
Molecular genetic evidence for a founder effect in familial hypercholesterolemia among French CanadiansC Bétard, A M Kessling, M Roy, et al.
Biochimica Et Biophysica Acta|July 20, 1977
The effect of portacaval shunt on plasma lipids and lipoproteins in swineA C Nestruck, S Lussier-Cacan, M Bergseth, et al.
The Journal of Clinical Investigation|March 1, 1984
Isolation and characterization of apolipoprotein B-48 and B-100 very low density lipoproteins from type III hyperlipoproteinemic subjectsR W Milne, P K Weech, L Blanchette, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|May 1, 1979
Erythrocyte membrane lipids in Friedreich's ataxiaP Draper, Y S Huang, D Shapcott, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|January 1, 1996
Lp(a) levels and atherosclerotic vascular disease in a sample of patients with familial hypercholesterolemia sharing the same gene defectR Carmena, S Lussier-Cacan, M Roy, et al.
Metabolism: Clinical and Experimental|August 1, 1991
Cyclic fluctuations in human serum lipid and apolipoprotein levels during the normal menstrual cycle: comparison with changes occurring during oral contraceptive therapyS Lussier-Cacan, M Xhignesse, J L Desmarais, et al.
The American Journal of Medicine|November 27, 1987
Effect of fenofibrate treatment on type III hyperlipoproteinemiaJ C Fruchart, J Davignon, J M Bard, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|August 1, 1995
Severe familial HDL deficiency in French-Canadian kindreds. Clinical, biochemical, and molecular characterizationM Marcil, B Boucher, L Krimbou, et al.
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