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Mathilde Varret

Showing results (21-30 of 55) with videos related to

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Molecular and Cellular Probes|September 21, 2014
PCSK9 polymorphism in a Tunisian cohort: identification of a new allele, L8, and association of allele L10 with reduced coronary heart disease riskAfef Slimani, Mohamed Yahia Hrira, Mohamed Najah, et al.
Metabolites|June 23, 2022
Circulating PCSK9 Linked to Dyslipidemia in Lebanese SchoolchildrenYara Azar, Marie-Hélène Gannagé-Yared, Elie Naous, et al.
Atherosclerosis|October 2, 2018
High burden of recurrent cardiovascular events in heterozygous familial hypercholesterolemia: The French Familial Hypercholesterolemia RegistrySophie Béliard, Franck Boccara, Bertrand Cariou, et al.
The Journal of Rheumatology|January 10, 2009
Angiotensin-converting enzyme gene does not contribute to genetic susceptibility to systemic sclerosis in European CaucasiansJulien Wipff, Guillaume Gallier, Philippe Dieude, et al.
Human Mutation|March 26, 2009
The molecular basis of familial hypercholesterolemia in Lebanon: spectrum of LDLR mutations and role of PCSK9 as a modifier geneMarianne Abifadel, Jean-Pierre Rabès, Sélim Jambart, et al.
Journal of Human Genetics|May 6, 2003
Familial hypercholesterolemia in Morocco: first report of mutations in the LDL receptor geneMariame El Messal, Karima Aït Chihab, Rachid Chater, et al.
Human Mutation|October 8, 2005
Novel mutations of the PCSK9 gene cause variable phenotype of autosomal dominant hypercholesterolemiaDelphine Allard, Sabine Amsellem, Marianne Abifadel, et al.
Journal of Clinical Lipidology|December 8, 2018
Postprandial lipid absorption in seven heterozygous carriers of deleterious variants of MTTP in two abetalipoproteinemic familiesMathilde Di Filippo, Mathilde Varret, Vanessa Boehm, et al.
Human Mutation|September 3, 2010
Molecular spectrum of autosomal dominant hypercholesterolemia in FranceMarie Marduel, Alain Carrié, Agnes Sassolas, et al.
Atherosclerosis|March 16, 2012
Effect of mutations in LDLR and PCSK9 genes on phenotypic variability in Tunisian familial hypercholesterolemia patientsAfef Slimani, Awatef Jelassi, Imen Jguirim, et al.
Pageof 6

Showing results (21-30 of 55) with videos related to

Sort By:
Pageof 6
Molecular and Cellular Probes|September 21, 2014
PCSK9 polymorphism in a Tunisian cohort: identification of a new allele, L8, and association of allele L10 with reduced coronary heart disease riskAfef Slimani, Mohamed Yahia Hrira, Mohamed Najah, et al.
Metabolites|June 23, 2022
Circulating PCSK9 Linked to Dyslipidemia in Lebanese SchoolchildrenYara Azar, Marie-Hélène Gannagé-Yared, Elie Naous, et al.
Atherosclerosis|October 2, 2018
High burden of recurrent cardiovascular events in heterozygous familial hypercholesterolemia: The French Familial Hypercholesterolemia RegistrySophie Béliard, Franck Boccara, Bertrand Cariou, et al.
The Journal of Rheumatology|January 10, 2009
Angiotensin-converting enzyme gene does not contribute to genetic susceptibility to systemic sclerosis in European CaucasiansJulien Wipff, Guillaume Gallier, Philippe Dieude, et al.
Human Mutation|March 26, 2009
The molecular basis of familial hypercholesterolemia in Lebanon: spectrum of LDLR mutations and role of PCSK9 as a modifier geneMarianne Abifadel, Jean-Pierre Rabès, Sélim Jambart, et al.
Journal of Human Genetics|May 6, 2003
Familial hypercholesterolemia in Morocco: first report of mutations in the LDL receptor geneMariame El Messal, Karima Aït Chihab, Rachid Chater, et al.
Human Mutation|October 8, 2005
Novel mutations of the PCSK9 gene cause variable phenotype of autosomal dominant hypercholesterolemiaDelphine Allard, Sabine Amsellem, Marianne Abifadel, et al.
Journal of Clinical Lipidology|December 8, 2018
Postprandial lipid absorption in seven heterozygous carriers of deleterious variants of MTTP in two abetalipoproteinemic familiesMathilde Di Filippo, Mathilde Varret, Vanessa Boehm, et al.
Human Mutation|September 3, 2010
Molecular spectrum of autosomal dominant hypercholesterolemia in FranceMarie Marduel, Alain Carrié, Agnes Sassolas, et al.
Atherosclerosis|March 16, 2012
Effect of mutations in LDLR and PCSK9 genes on phenotypic variability in Tunisian familial hypercholesterolemia patientsAfef Slimani, Awatef Jelassi, Imen Jguirim, et al.
Pageof 6