Publications by authors named "Sandy Elbitar"

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Low circulating PCSK9 levels in homozygous children with chylomicronemia syndrome in a syrian refugee family in Lebanon.
Carine Ayoub, Yara Azar, Dina Maddah, Youmna Ghaleb, Sandy Elbitar

Front Genet· August 2022

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Circulating PCSK9 Linked to Dyslipidemia in Lebanese Schoolchildren.
Yara Azar, Marie-Hélène Gannagé-Yared, Elie Naous, Carine Ayoub, Yara Abou Khalil, Sandy Elbitar

Metabolites· May 2022

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Whole Exome/Genome Sequencing Joint Analysis of a Family with Oligogenic Familial Hypercholesterolemia.
Youmna Ghaleb, Sandy Elbitar, Anne Philippi, Petra El Khoury, Yara Azar

Metabolites· March 2022

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Identification of a Variant in Gene as a Major Cause of Hypobetalipoproteinemia in Lebanese Families.
Carine Ayoub, Yara Azar, Yara Abou-Khalil, Youmna Ghaleb, Sandy Elbitar

Metabolites· August 2021

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Pathogenic variants in THSD4, encoding the ADAMTS-like 6 protein, predispose to inherited thoracic aortic aneurysm.
Sandy Elbitar, Marjolijn Renard, Pauline Arnaud, Nadine Hanna, Marie-Paule Jacob

Genet Med· January 2021

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Identification of the first Tangier disease patient in Lebanon carrying a new pathogenic variant in ABCA1.
Petra El Khoury, Philippe Couvert, Sandy Elbitar, Youmna Ghaleb, Yara Abou-Khalil

J Clin Lipidol· October 2019

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Extraocular Muscle Metastasis from Esophageal Carcinoma: an Atypical and Rare Presentation.
Nishitha Thumallapally, Sandy El-Bitar, Farhan Mohammad, Jean Paul Atallah

J Gastrointest Cancer· June 2018

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Plasma proprotein-convertase-subtilisin/kexin type 9 (PCSK9) and cardiovascular events in type 2 diabetes.
Petra El Khoury, Ronan Roussel, Frederic Fumeron, Yara Abou-Khalil, Gilberto Velho, Sandy Elbitar

Diabetes Obes Metab· April 2018

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Usefulness of the genetic risk score to identify phenocopies in families with familial hypercholesterolemia?
Youmna Ghaleb, Sandy Elbitar, Petra El Khoury, Eric Bruckert, Valérie Carreau

Eur J Hum Genet· April 2018

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New Sequencing technologies help revealing unexpected mutations in Autosomal Dominant Hypercholesterolemia.
Sandy Elbitar, Delia Susan-Resiga, Youmna Ghaleb, Petra El Khoury, Gina Peloso

Sci Rep· January 2018

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PCSK9 Mutations in Familial Hypercholesterolemia: from a Groundbreaking Discovery to Anti-PCSK9 Therapies.
Petra El Khoury, Sandy Elbitar, Youmna Ghaleb, Yara Abou Khalil, Mathilde Varret

Curr Atheroscler Rep· October 2017

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Proprotein convertase subtilisin / kexin 9 (PCSK9) inhibitors and the future of dyslipidemia therapy: an updated patent review (2011-2015).
Sandy Elbitar, Petra El Khoury, Youmna Ghaleb, Jean-Pierre Rabès, Mathilde Varret

Expert Opin Ther Pat· December 2016

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[Anti-PCSK9 in coronary artery disease: genetic progress, therapeutic approaches].
Marianne Abifadel, Youmna Ghaleb, Sandy Elbitar, Petra El Khoury, Jean-Pierre Rabès

Rev Prat· March 2015

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Living the PCSK9 adventure: from the identification of a new gene in familial hypercholesterolemia towards a potential new class of anticholesterol drugs.
Marianne Abifadel, Sandy Elbitar, Petra El Khoury, Youmna Ghaleb, Mélody Chémaly

Curr Atheroscler Rep· September 2014

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