Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Philippe Moulin

Showing results (121-130 of 188) with videos related to

Pageof 19
Sort By:
Atherosclerosis|November 9, 2025
Synergic combination of the monogenic ANGPTL3 p.H343R variant and a polygenic predisposition in a family with hypobetalipoproteinemiaManon Levy, Alexandre Janin, Oriane Marmontel, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|December 29, 2022
Maternal Inheritance of Familial Hypercholesterolemia Gene Mutation Predisposes to Coronary Atherosclerosis as Assessed by Calcium Score in AdulthoodFlorian Mourre, Roch Giorgi, Antonio Gallo, et al.
Clinical Chemistry and Laboratory Medicine|June 13, 2023
Interest of minigene splicing reporter assay in familial hypobetalipoproteinemia genetic diagnosis: the example of the missense mutation <i>APOB</i> c.1468C>TZoé Henry, Alexandre Janin, Séverine Nony, et al.
The Journal of Clinical Endocrinology and Metabolism|August 6, 2011
GPIHBP1 C89F neomutation and hydrophobic C-terminal domain G175R mutation in two pedigrees with severe hyperchylomicronemiaSybil Charrière, Noël Peretti, Sophie Bernard, et al.
European Journal of Preventive Cardiology|February 22, 2021
Lipid goal achievements after acute myocardial infarction: the gap between real-life and ESC 2019 guidelinesThéo Cambet, Thomas Bochaton, Floriane Bel, et al.
Clinical Genetics|November 25, 2024
Mobile Element Insertion in the APOB Exon 3 Coding Sequence: A New Challenge in Hypobetalipoproteinemia DiagnosisLaurie Surles, Alexandre Janin, Corentin Molitor, et al.
Orphanet Journal of Rare Diseases|October 6, 2010
Guidelines for the diagnosis and management of chylomicron retention disease based on a review of the literature and the experience of two centersNoel Peretti, Agnès Sassolas, Claude C Roy, et al.
The British Journal of Nutrition|September 29, 2009
A controlled study of consumption of beta-glucan-enriched soups for 2 months by type 2 diabetic free-living subjectsChristine Cugnet-Anceau, Julie-Anne Nazare, Maria Biorklund, et al.
Journal of the American Society of Echocardiography : Official Publication of the American Society of Echocardiography|October 12, 2010
Impaired myocardial radial function in asymptomatic patients with type 2 diabetes mellitus: a speckle-tracking imaging studyLaura Ernande, Ernst R Rietzschel, Cyrille Bergerot, et al.
European Journal of Preventive Cardiology|May 6, 2025
Cascade screening in familial hypercholesterolaemia is associated with earlier statin initiation and fewer cardiovascular events than opportunistic screeningFlorian Mourre, Roch Giorgi, Lauranne Cattieuw, et al.
Pageof 19

Showing results (121-130 of 188) with videos related to

Sort By:
Pageof 19
Atherosclerosis|November 9, 2025
Synergic combination of the monogenic ANGPTL3 p.H343R variant and a polygenic predisposition in a family with hypobetalipoproteinemiaManon Levy, Alexandre Janin, Oriane Marmontel, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|December 29, 2022
Maternal Inheritance of Familial Hypercholesterolemia Gene Mutation Predisposes to Coronary Atherosclerosis as Assessed by Calcium Score in AdulthoodFlorian Mourre, Roch Giorgi, Antonio Gallo, et al.
Clinical Chemistry and Laboratory Medicine|June 13, 2023
Interest of minigene splicing reporter assay in familial hypobetalipoproteinemia genetic diagnosis: the example of the missense mutation <i>APOB</i> c.1468C>TZoé Henry, Alexandre Janin, Séverine Nony, et al.
The Journal of Clinical Endocrinology and Metabolism|August 6, 2011
GPIHBP1 C89F neomutation and hydrophobic C-terminal domain G175R mutation in two pedigrees with severe hyperchylomicronemiaSybil Charrière, Noël Peretti, Sophie Bernard, et al.
European Journal of Preventive Cardiology|February 22, 2021
Lipid goal achievements after acute myocardial infarction: the gap between real-life and ESC 2019 guidelinesThéo Cambet, Thomas Bochaton, Floriane Bel, et al.
Clinical Genetics|November 25, 2024
Mobile Element Insertion in the APOB Exon 3 Coding Sequence: A New Challenge in Hypobetalipoproteinemia DiagnosisLaurie Surles, Alexandre Janin, Corentin Molitor, et al.
Orphanet Journal of Rare Diseases|October 6, 2010
Guidelines for the diagnosis and management of chylomicron retention disease based on a review of the literature and the experience of two centersNoel Peretti, Agnès Sassolas, Claude C Roy, et al.
The British Journal of Nutrition|September 29, 2009
A controlled study of consumption of beta-glucan-enriched soups for 2 months by type 2 diabetic free-living subjectsChristine Cugnet-Anceau, Julie-Anne Nazare, Maria Biorklund, et al.
Journal of the American Society of Echocardiography : Official Publication of the American Society of Echocardiography|October 12, 2010
Impaired myocardial radial function in asymptomatic patients with type 2 diabetes mellitus: a speckle-tracking imaging studyLaura Ernande, Ernst R Rietzschel, Cyrille Bergerot, et al.
European Journal of Preventive Cardiology|May 6, 2025
Cascade screening in familial hypercholesterolaemia is associated with earlier statin initiation and fewer cardiovascular events than opportunistic screeningFlorian Mourre, Roch Giorgi, Lauranne Cattieuw, et al.
Pageof 19