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Diane Brisson

Showing results (51-60 of 95) with videos related to

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Journal of Clinical Medicine|October 16, 2024
Clinical Expression of Familial Hypercholesterolemia in Patients from France and French Canada Carrying Identical-by-Descent Pathogenic <i>LDLR</i> Gene Variants: A Proof-of-Concept StudyMiriam Larouche, Olivier Bluteau, Alain Carrié, et al.
Epigenetics|August 22, 2012
IGF2 DNA methylation is a modulator of newborn's fetal growth and developmentJulie St-Pierre, Marie-France Hivert, Patrice Perron, et al.
Journal of Medical Economics|February 23, 2013
Medical resource use and costs associated with chylomicronemiaDaniel Gaudet, James Signorovitch, Elyse Swallow, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|December 20, 2012
Prevalence of lifestyle risk factors in myotonic dystrophy type 1Cynthia Gagnon, Maud-Christine Chouinard, Luc Laberge, et al.
Atherosclerosis. Supplements|April 30, 2010
Review of the clinical development of alipogene tiparvovec gene therapy for lipoprotein lipase deficiencyDaniel Gaudet, Janneke de Wal, Karine Tremblay, et al.
Diabetes Care|August 21, 2010
Leptin gene epigenetic adaptation to impaired glucose metabolism during pregnancyLuigi Bouchard, Stéphanie Thibault, Simon-Pierre Guay, et al.
The American Journal of Cardiology|January 31, 2007
Relation of the "hypertriglyceridemic waist" phenotype to earlier manifestations of coronary artery disease in patients with glucose intolerance and type 2 diabetes mellitusJulie St-Pierre, Isabelle Lemieux, Patrice Perron, et al.
Arthritis Care & Research|March 17, 2012
Increased frequency of DRB1*11:01 in anti-hydroxymethylglutaryl-coenzyme A reductase-associated autoimmune myopathyAndrew L Mammen, Daniel Gaudet, Diane Brisson, et al.
European Heart Journal|April 6, 2016
Selection of individuals for genetic testing for familial hypercholesterolaemia: development and external validation of a prediction model for the presence of a mutation causing familial hypercholesterolaemiaJoost Besseling, Johannes B Reitsma, Daniel Gaudet, et al.
American Journal of Human Genetics|March 16, 2007
Genetic analysis of 103 candidate genes for coronary artery disease and associated phenotypes in a founder population reveals a new association between endothelin-1 and high-density lipoprotein cholesterolGuillaume Pare, David Serre, Diane Brisson, et al.
Pageof 10

Showing results (51-60 of 95) with videos related to

Sort By:
Pageof 10
Journal of Clinical Medicine|October 16, 2024
Clinical Expression of Familial Hypercholesterolemia in Patients from France and French Canada Carrying Identical-by-Descent Pathogenic <i>LDLR</i> Gene Variants: A Proof-of-Concept StudyMiriam Larouche, Olivier Bluteau, Alain Carrié, et al.
Epigenetics|August 22, 2012
IGF2 DNA methylation is a modulator of newborn's fetal growth and developmentJulie St-Pierre, Marie-France Hivert, Patrice Perron, et al.
Journal of Medical Economics|February 23, 2013
Medical resource use and costs associated with chylomicronemiaDaniel Gaudet, James Signorovitch, Elyse Swallow, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|December 20, 2012
Prevalence of lifestyle risk factors in myotonic dystrophy type 1Cynthia Gagnon, Maud-Christine Chouinard, Luc Laberge, et al.
Atherosclerosis. Supplements|April 30, 2010
Review of the clinical development of alipogene tiparvovec gene therapy for lipoprotein lipase deficiencyDaniel Gaudet, Janneke de Wal, Karine Tremblay, et al.
Diabetes Care|August 21, 2010
Leptin gene epigenetic adaptation to impaired glucose metabolism during pregnancyLuigi Bouchard, Stéphanie Thibault, Simon-Pierre Guay, et al.
The American Journal of Cardiology|January 31, 2007
Relation of the "hypertriglyceridemic waist" phenotype to earlier manifestations of coronary artery disease in patients with glucose intolerance and type 2 diabetes mellitusJulie St-Pierre, Isabelle Lemieux, Patrice Perron, et al.
Arthritis Care & Research|March 17, 2012
Increased frequency of DRB1*11:01 in anti-hydroxymethylglutaryl-coenzyme A reductase-associated autoimmune myopathyAndrew L Mammen, Daniel Gaudet, Diane Brisson, et al.
European Heart Journal|April 6, 2016
Selection of individuals for genetic testing for familial hypercholesterolaemia: development and external validation of a prediction model for the presence of a mutation causing familial hypercholesterolaemiaJoost Besseling, Johannes B Reitsma, Daniel Gaudet, et al.
American Journal of Human Genetics|March 16, 2007
Genetic analysis of 103 candidate genes for coronary artery disease and associated phenotypes in a founder population reveals a new association between endothelin-1 and high-density lipoprotein cholesterolGuillaume Pare, David Serre, Diane Brisson, et al.
Pageof 10