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Atherosclerosis
|
February 6, 2026
The hidden burden of kidney damage in chylomicronemia syndromes
Laura D'Erasmo, Daniele Tramontano, Alessia Di Costanzo, et al.
Obesity (Silver Spring, Md.)
|
March 21, 2017
Genetic determinants of adiponectin regulation revealed by pregnancy
Marie-France Hivert, Denise M Scholtens, Catherine Allard, et al.
Human Gene Therapy
|
July 15, 2016
Long-Term Retrospective Analysis of Gene Therapy with Alipogene Tiparvovec and Its Effect on Lipoprotein Lipase Deficiency-Induced Pancreatitis
Daniel Gaudet, Erik S Stroes, Julie Méthot, et al.
The Canadian Journal of Cardiology
|
November 14, 2021
Influence of the LDL-Receptor Genotype on Statin Response in Heterozygous Familial Hypercholesterolemia: Insights From the Canadian FH Registry
Gabrielle Roy, Patrick Couture, Jacques Genest, et al.
Atherosclerosis
|
February 5, 2026
Assessment of LDL receptor-dependent lipid lowering therapies in patients with homozygous familial hypercholesterolemia according to functional genotype
G B John Mancini, Arnold Ryomoto, Isabelle Ruel, et al.
The New England Journal of Medicine
|
July 30, 2015
Antisense Inhibition of Apolipoprotein C-III in Patients with Hypertriglyceridemia
Daniel Gaudet, Veronica J Alexander, Brenda F Baker, et al.
Atherosclerosis
|
November 23, 2025
Imputation of untreated LDL-C in treated subjects with homozygous familial hypercholesterolaemia: An international collaboration
G B John Mancini, Arnold Ryomoto, Isabelle Ruel, et al.
Clinical Chemistry
|
October 18, 2017
Imputation of Baseline LDL Cholesterol Concentration in Patients with Familial Hypercholesterolemia on Statins or Ezetimibe
Isabelle Ruel, Sumayah Aljenedil, Iman Sadri, et al.
Journal of Clinical Lipidology
|
December 5, 2024
Extreme LDL-C concentration is associated with increased cardiovascular disease in women with homozygous familial hypercholesterolemia
Martine Paquette, Isabelle Ruel, Simon-Pierre Guay, et al.
European Journal of Human Genetics : EJHG
|
September 7, 2007
Identification of a chromosome 8p locus for early-onset coronary heart disease in a French Canadian population
James C Engert, Mathieu Lemire, Janet Faith, et al.
Page
of 10
Search research articles
Search
Showing results (81-90 of 95) with videos related to
Sort By:
Page
of 10
Atherosclerosis
|
February 6, 2026
The hidden burden of kidney damage in chylomicronemia syndromes
Laura D'Erasmo, Daniele Tramontano, Alessia Di Costanzo, et al.
Obesity (Silver Spring, Md.)
|
March 21, 2017
Genetic determinants of adiponectin regulation revealed by pregnancy
Marie-France Hivert, Denise M Scholtens, Catherine Allard, et al.
Human Gene Therapy
|
July 15, 2016
Long-Term Retrospective Analysis of Gene Therapy with Alipogene Tiparvovec and Its Effect on Lipoprotein Lipase Deficiency-Induced Pancreatitis
Daniel Gaudet, Erik S Stroes, Julie Méthot, et al.
The Canadian Journal of Cardiology
|
November 14, 2021
Influence of the LDL-Receptor Genotype on Statin Response in Heterozygous Familial Hypercholesterolemia: Insights From the Canadian FH Registry
Gabrielle Roy, Patrick Couture, Jacques Genest, et al.
Atherosclerosis
|
February 5, 2026
Assessment of LDL receptor-dependent lipid lowering therapies in patients with homozygous familial hypercholesterolemia according to functional genotype
G B John Mancini, Arnold Ryomoto, Isabelle Ruel, et al.
The New England Journal of Medicine
|
July 30, 2015
Antisense Inhibition of Apolipoprotein C-III in Patients with Hypertriglyceridemia
Daniel Gaudet, Veronica J Alexander, Brenda F Baker, et al.
Atherosclerosis
|
November 23, 2025
Imputation of untreated LDL-C in treated subjects with homozygous familial hypercholesterolaemia: An international collaboration
G B John Mancini, Arnold Ryomoto, Isabelle Ruel, et al.
Clinical Chemistry
|
October 18, 2017
Imputation of Baseline LDL Cholesterol Concentration in Patients with Familial Hypercholesterolemia on Statins or Ezetimibe
Isabelle Ruel, Sumayah Aljenedil, Iman Sadri, et al.
Journal of Clinical Lipidology
|
December 5, 2024
Extreme LDL-C concentration is associated with increased cardiovascular disease in women with homozygous familial hypercholesterolemia
Martine Paquette, Isabelle Ruel, Simon-Pierre Guay, et al.
European Journal of Human Genetics : EJHG
|
September 7, 2007
Identification of a chromosome 8p locus for early-onset coronary heart disease in a French Canadian population
James C Engert, Mathieu Lemire, Janet Faith, et al.
Page
of 10