Sandy Elbitar
Paris, France
Last Updated: 09/26/2026
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Found 14 publications
Low circulating PCSK9 levels in LPL homozygous children with chylomicronemia syndrome in a syrian refugee family in Lebanon.
Journal: Frontiers in genetics
Published: June 03, 2022
Circulating PCSK9 Linked to Dyslipidemia in Lebanese Schoolchildren.
Journal: Metabolites
Published: April 26, 2022
Pathogenic variants in THSD4, encoding the ADAMTS-like 6 protein, predispose to inherited thoracic aortic aneurysm.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: June 03, 2020
Identification of the first Tangier disease patient in Lebanon carrying a new pathogenic variant in ABCA1.
Journal: Journal of clinical lipidology
Published: May 17, 2018
High prevalence of ventricular repolarization abnormalities in people carrying TGFβR2 mutations.
Journal: Scientific reports
Published: February 02, 2018
PCSK9 Mutations in Familial Hypercholesterolemia: from a Groundbreaking Discovery to Anti-PCSK9 Therapies.
Journal: Current atherosclerosis reports
Published: October 18, 2017
New Sequencing technologies help revealing unexpected mutations in Autosomal Dominant Hypercholesterolemia.
Journal: Scientific reports
Published: October 18, 2017
Plasma proprotein-convertase-subtilisin/kexin type 9 (PCSK9) and cardiovascular events in type 2 diabetes.
Journal: Diabetes, obesity & metabolism
Published: September 10, 2017
Usefulness of the genetic risk score to identify phenocopies in families with familial hypercholesterolemia?
Journal: European journal of human genetics : EJHG
Published: June 05, 2017
Proprotein convertase subtilisin / kexin 9 (PCSK9) inhibitors and the future of dyslipidemia therapy: an updated patent review (2011-2015).
Journal: Expert opinion on therapeutic patents
Published: July 01, 2016
Last Updated: 09/26/2026