Agnes Sassolas
Lyon, France
Last Updated: 09/26/2026
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Found 10 publications
Efficacy of two vitamin E formulations in patients with abetalipoproteinemia and chylomicron retention disease.
Journal: Journal of lipid research
Published: May 28, 2018
Lipid profile and cardiovascular risk factors in pediatric liver transplant recipients.
Journal: Pediatric transplantation
Published: November 23, 2015
Homozygous familial hypercholesterolemia in childhood: Genotype-phenotype description, established therapies and perspectives.
Journal: Atherosclerosis
Published: April 02, 2015
Post-heparin LPL activity measurement using VLDL as a substrate: a new robust method for routine assessment of plasma triglyceride lipolysis defects.
Journal: PloS one
Published: June 03, 2014
Post-heparin LPL activity measurement using VLDL as a substrate: a new robust method for routine assessment of plasma triglyceride lipolysis defects.
Journal: PloS one
Published: November 08, 2013
Homozygous MTTP and APOB mutations may lead to hepatic steatosis and fibrosis despite metabolic differences in congenital hypocholesterolemia.
Journal: Journal of hepatology
Published: November 05, 2013
An APOA5 3' UTR variant associated with plasma triglycerides triggers APOA5 downregulation by creating a functional miR-485-5p binding site.
Journal: American journal of human genetics
Published: July 26, 2013
Molecular characterization of Tunisian families with abetalipoproteinemia and identification of a novel mutation in MTTP gene.
Journal: Diagnostic pathology
Published: December 06, 2012
Molecular and functional analysis of two new MTTP gene mutations in an atypical case of abetalipoproteinemia.
Journal: Journal of lipid research
Published: January 13, 2012
Showing 1-10 of 10
Last Updated: 09/26/2026