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Showing results (71-80 of 88) with videos related to

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Biochemical Society Transactions|February 15, 2001
The multigenic family of monogalactosyl diacylglycerol synthasesE Maréchal, K Awai, M A Block, et al.
International Journal of Obesity and Related Metabolic Disorders : Journal of the International Association for the Study of Obesity|May 1, 1995
The insulin resistance-dyslipidemic syndrome: contribution of visceral obesity and therapeutic implicationsJ P Després, S Lemieux, B Lamarche, et al.
Arteriosclerosis (Dallas, Tex.)|March 1, 1989
Homozygous familial hypercholesterolemia among French Canadians in Québec ProvinceS Moorjani, M Roy, C Gagné, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|February 1, 1989
Hypertriglyceridemia and lower LDL cholesterol concentration in relation to apolipoprotein E phenotypes in myotonic dystrophyS Moorjani, D Gaudet, C Laberge, et al.
Atherosclerosis|September 27, 1996
Heterozygous familial hypercholesterolemia in children: low-density lipoprotein receptor mutational analysis and variation in the expression of plasma lipoprotein-lipid concentrationsA L Torres, S Moorjani, M C Vohl, et al.
The Canadian Journal of Cardiology|June 1, 1993
Comparison of the short term efficacy and tolerability of lovastatin and simvastatin in the management of primary hypercholesterolemiaJ Frohlich, L D Brun, D Blank, et al.
International Journal of Obesity and Related Metabolic Disorders : Journal of the International Association for the Study of Obesity|October 1, 1992
Adipose cell size and distribution in familial lipoprotein lipase deficiencyE Peeva, L D Brun, M R Ven Murthy, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|June 20, 1998
Association of specific LDL receptor gene mutations with differential plasma lipoprotein response to simvastatin in young French Canadians with heterozygous familial hypercholesterolemiaP Couture, L D Brun, F Szots, et al.
The Journal of Clinical Endocrinology and Metabolism|March 1, 1991
A hepatic lipase gene mutation associated with heritable lipolytic deficiencyR A Hegele, C Vezina, S Moorjani, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|July 1, 1992
[Double-blind clinical and echocardiographic study of oral enoximone versus placebo in severe cardiac insufficiency]G Delorme, O Dubourg, G Jondeau, et al.
Pageof 9

Showing results (71-80 of 88) with videos related to

Sort By:
Pageof 9
Biochemical Society Transactions|February 15, 2001
The multigenic family of monogalactosyl diacylglycerol synthasesE Maréchal, K Awai, M A Block, et al.
International Journal of Obesity and Related Metabolic Disorders : Journal of the International Association for the Study of Obesity|May 1, 1995
The insulin resistance-dyslipidemic syndrome: contribution of visceral obesity and therapeutic implicationsJ P Després, S Lemieux, B Lamarche, et al.
Arteriosclerosis (Dallas, Tex.)|March 1, 1989
Homozygous familial hypercholesterolemia among French Canadians in Québec ProvinceS Moorjani, M Roy, C Gagné, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|February 1, 1989
Hypertriglyceridemia and lower LDL cholesterol concentration in relation to apolipoprotein E phenotypes in myotonic dystrophyS Moorjani, D Gaudet, C Laberge, et al.
Atherosclerosis|September 27, 1996
Heterozygous familial hypercholesterolemia in children: low-density lipoprotein receptor mutational analysis and variation in the expression of plasma lipoprotein-lipid concentrationsA L Torres, S Moorjani, M C Vohl, et al.
The Canadian Journal of Cardiology|June 1, 1993
Comparison of the short term efficacy and tolerability of lovastatin and simvastatin in the management of primary hypercholesterolemiaJ Frohlich, L D Brun, D Blank, et al.
International Journal of Obesity and Related Metabolic Disorders : Journal of the International Association for the Study of Obesity|October 1, 1992
Adipose cell size and distribution in familial lipoprotein lipase deficiencyE Peeva, L D Brun, M R Ven Murthy, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|June 20, 1998
Association of specific LDL receptor gene mutations with differential plasma lipoprotein response to simvastatin in young French Canadians with heterozygous familial hypercholesterolemiaP Couture, L D Brun, F Szots, et al.
The Journal of Clinical Endocrinology and Metabolism|March 1, 1991
A hepatic lipase gene mutation associated with heritable lipolytic deficiencyR A Hegele, C Vezina, S Moorjani, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|July 1, 1992
[Double-blind clinical and echocardiographic study of oral enoximone versus placebo in severe cardiac insufficiency]G Delorme, O Dubourg, G Jondeau, et al.
Pageof 9