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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 Study
Miriam Larouche, Olivier Bluteau, Alain Carrié, et al.
Epigenetics
|
August 22, 2012
IGF2 DNA methylation is a modulator of newborn's fetal growth and development
Julie St-Pierre, Marie-France Hivert, Patrice Perron, et al.
Journal of Medical Economics
|
February 23, 2013
Medical resource use and costs associated with chylomicronemia
Daniel 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 1
Cynthia 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 deficiency
Daniel Gaudet, Janneke de Wal, Karine Tremblay, et al.
Diabetes Care
|
August 21, 2010
Leptin gene epigenetic adaptation to impaired glucose metabolism during pregnancy
Luigi 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 mellitus
Julie 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 myopathy
Andrew 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 hypercholesterolaemia
Joost 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 cholesterol
Guillaume Pare, David Serre, Diane Brisson, et al.
Page
of 10
Search research articles
Search
Showing results (51-60 of 95) with videos related to
Sort By:
Page
of 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 Study
Miriam Larouche, Olivier Bluteau, Alain Carrié, et al.
Epigenetics
|
August 22, 2012
IGF2 DNA methylation is a modulator of newborn's fetal growth and development
Julie St-Pierre, Marie-France Hivert, Patrice Perron, et al.
Journal of Medical Economics
|
February 23, 2013
Medical resource use and costs associated with chylomicronemia
Daniel 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 1
Cynthia 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 deficiency
Daniel Gaudet, Janneke de Wal, Karine Tremblay, et al.
Diabetes Care
|
August 21, 2010
Leptin gene epigenetic adaptation to impaired glucose metabolism during pregnancy
Luigi 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 mellitus
Julie 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 myopathy
Andrew 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 hypercholesterolaemia
Joost 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 cholesterol
Guillaume Pare, David Serre, Diane Brisson, et al.
Page
of 10