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Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|July 8, 2024
Internalisation of immunoglobulin light chains by cardiomyocytes in AL amyloidosis: what can biopsies tell us?Mélanie Bézard, Amira Zaroui, Mounira Kharoubi, et al.JACC. Heart Failure|February 7, 2021
The Impact of Patients With Cardiac Amyloidosis in HFpEF TrialsSilvia Oghina, Wulfran Bougouin, Mélanie Bézard, et al.Scientific Reports|February 5, 2025
Amyloidogenic immunoglobulin light chains disturb contractile function and calcium transients in a human cardiac spheroid model of light chain (AL) amyloidosisMélanie Bézard, Jean-Sébastien Vartanian-Grimaldi, Julien Henri, et al.International Journal of Cardiology|November 9, 2024
A phenotypic comparison of the Romanian and French ATTRv cohorts: Glu54Gln founder pathogenic variant vs the most common variants in Western EuropeGabriela Neculae, Amira Zaroui, Mounira Kharoubi, et al.Journal of the American College of Cardiology|November 26, 2021
Assessing Cardiac Amyloidosis Subtypes by Unsupervised Phenotype Clustering AnalysisLouis Bonnefous, Mounira Kharoubi, Mélanie Bézard, et al.Journal of Clinical Medicine|November 13, 2021
Prognostic Value of N-Terminal Pro-Brain Natriuretic Peptide and High-Sensitivity Troponin T Levels in the Natural History of Transthyretin Amyloid Cardiomyopathy and Their Evolution after Tafamidis TreatmentSilvia Oghina, Constant Josse, Mélanie Bézard, et al.Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|May 27, 2025
Men and women differ with regard to the prevalence, phenotype, and prognosis of wild-type transthyretin amyloid cardiomyopathyAmira Zaroui, Charlotte Lafont, Mounira Kharoubi, et al.Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|June 28, 2023
Comparison of cardiac involvement, extracardiac manifestations and outcomes between homozygote and heterozygote transthyretin p.Val142Ile (V122I) variant in patients with hereditary transthyretin amyloidosis: a cohort studyGrégoire Albenque, Mélanie Bézard, Mounira Kharoubi, et al.ESC Heart Failure|December 23, 2020
Prevalence and prognostic value of autonomic neuropathy assessed by Sudoscan® in transthyretin wild-type cardiac amyloidosisMounira Kharoubi, Fréderic Roche, Mélanie Bézard, et al.Plos One|September 15, 2021
Dexamethasone is associated with early deaths in light chain amyloidosis patients with severe cardiac involvementMélanie Bézard, Silvia Oghina, Damien Vitiello, et al.Pageof 2