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Validation of an echocardiographic multiparametric strategy to increase responders patients after cardiac resynchronization: a multicentre study

European heart journal, 2009-12, Vol.30 (23), p.2880-2887

2009

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Altered two-dimensional strain measures of the right and left ventricle in patients with arrhythmogenic right ventricular cardiomyopathy and their first degree relatives

European heart journal, 2013-08, Vol.34 (suppl 1), p.P2918-P2918

2013

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Syndrome dysautonomique avec gastroparésie sévère : une manifestation inaugurale rare de l’amylose AL

La revue de medecine interne, 2024-06, Vol.45, p.A175-A176

2024

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Predicting mortality factors in advanced cardiac AL Amyloidosis: Prospective cohort study to improve cardiac stratification

Archives of cardiovascular diseases, 2024-01, Vol.117 (1), p.S49

2024

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13 - Hypertrophic Cardiomyopathy or Athlete’s Heart?

Archives of Cardiovascular Diseases Supplements, 2017-06, Vol.9 (3), p.243-243

2017

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Systolic and early diastolic left ventricular velocities assessed by tissue Doppler imaging in 65 top-level Athletes

Archives of cardiovascular diseases supplements, 2017-06, Vol.9 (3), p.255

2017

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38 - Systolic and early diastolic left ventricular velocities assessed by tissue Doppler imaging in 65 top-level Athletes

Archives of Cardiovascular Diseases Supplements, 2017-06, Vol.9 (3), p.255-255

2017

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Characterization of right atrial function and dimension in top-level athletes: an echocardiographic study

Archives of cardiovascular diseases supplements, 2017-06, Vol.9 (3), p.255-256

2017

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39 - Characterization of right atrial function and dimension in top-level athletes: an echocardiographic study

Archives of Cardiovascular Diseases Supplements, 2017-06, Vol.9 (3), p.255-256

2017

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Hypertrophic Cardiomyopathy or Athlete’s Heart?

Archives of cardiovascular diseases supplements, 2017-06, Vol.9 (3), p.243

2017

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Prevalence and prognosis of cardiac and extra-cardiac disorders in older and geriatric patients with transthyretin cardiomyopathy

Archives of cardiovascular diseases, 2024-01, Vol.117 (1), p.S37-S38

2024

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Amylose cardiaque à transthyrétine une maladie du XXIe siècle : du diagnostic au traitement

Bulletin de l'Académie nationale de médecine, 2023-05, Vol.207 (5), p.576-582

2023

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Matrix metalloproteainase-3 polymorphism association with hypertrophic cardiomyopathy

European heart journal, 2020-11, Vol.41 (Supplement_2)

2020

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Amylo-AFFECT-QOL, a self-reported questionnaire to assess health-related quality of life and to determine the prognosis in cardiac amyloidosis

Archives of cardiovascular diseases, 2024-01, Vol.117 (1), p.S39-S40

2024

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Penicillin therapy effect on MMP-2 and TIMP-2 levels in mitral restenosis after percutaneous mitral commissurotomy

Archives of cardiovascular diseases, 2024-01, Vol.117 (1), p.S82

2024

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Amylose cardiaque sénile et rétrécissement aortique: l’œuf et la poule

La revue de medecine interne, 2021-12, Vol.42, p.A344-A344

2021

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Contribution of the left atrioventricular coupling index in the prediction of atrial fibrillation in cardiac amyloidosis ATTR

Archives of cardiovascular diseases, 2024-01, Vol.117 (1), p.S51

2024

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Echographic factors of atrial arrhythmia in patients with arrythmogenic right ventricular dysplasia

European journal of heart failure, 2017-05, Vol.19 (1, SI)

2017

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Evaluation of left ventricular function by two-dimensional echocardiography and three-dimensional speckle-tracking echocardiography in noncompaction cardiomyopathy and dilated myocardiopathy

Archives of Cardiovascular Diseases Supplements, 2018-01, Vol.10 (1), p.43-44

2018

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Traitements cardiologiques et spécifiques de l’amylose cardiaque

Archives des maladies du coeur et des vaisseaux. Pratique, 2022-02, Vol.2022 (305), p.18-22

2022

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Prevalence and prognostic value of autonomic neuropathy assessed by Sudoscan® in transthyretin wild‐type cardiac amyloidosis

ESC Heart Failure, 2021-04, Vol.8 (2), p.1656-1665

2021

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381 - Arrhythmogenic right ventricular cardiomyopathy or athlete’s heart adaptations?

Archives of Cardiovascular Diseases Supplements, 2017-01, Vol.9 (1), p.102-103

2017

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Arrhythmogenic right ventricular cardiomyopathy or athlete’s heart adaptations?

Archives of cardiovascular diseases supplements, 2017-01, Vol.9 (1), p.102-103

2017

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Prognostic value of collagen biomarkers on left atrial remodeling and arrhythmia on hypertrophic cardiomyopathy

Archives of Cardiovascular Diseases Supplements, 2018-01, Vol.10 (1), p.30-30

2018

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Correlation between MYBPC3 mutation and Circulating concentrations of a marker of type I collagen metabolism on hypertrophic cardiomyopathy

Archives of Cardiovascular Diseases Supplements, 2018-01, Vol.10 (1), p.115-116

2018

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Validation of an echocardiographic multiparametric strategy to increase responders patients after cardiac resynchronization: a multicentre study

Altered two-dimensional strain measures of the right and left ventricle in patients with arrhythmogenic right ventricular cardiomyopathy and their first degree relatives

Syndrome dysautonomique avec gastroparésie sévère : une manifestation inaugurale rare de l’amylose AL

Predicting mortality factors in advanced cardiac AL Amyloidosis: Prospective cohort study to improve cardiac stratification

13 - Hypertrophic Cardiomyopathy or Athlete’s Heart?

Systolic and early diastolic left ventricular velocities assessed by tissue Doppler imaging in 65 top-level Athletes

38 - Systolic and early diastolic left ventricular velocities assessed by tissue Doppler imaging in 65 top-level Athletes

Characterization of right atrial function and dimension in top-level athletes: an echocardiographic study

39 - Characterization of right atrial function and dimension in top-level athletes: an echocardiographic study

Hypertrophic Cardiomyopathy or Athlete’s Heart?

Prevalence and prognosis of cardiac and extra-cardiac disorders in older and geriatric patients with transthyretin cardiomyopathy

Amylose cardiaque à transthyrétine une maladie du XXIe siècle : du diagnostic au traitement

Matrix metalloproteainase-3 polymorphism association with hypertrophic cardiomyopathy

Amylo-AFFECT-QOL, a self-reported questionnaire to assess health-related quality of life and to determine the prognosis in cardiac amyloidosis

Penicillin therapy effect on MMP-2 and TIMP-2 levels in mitral restenosis after percutaneous mitral commissurotomy

Amylose cardiaque sénile et rétrécissement aortique: l’œuf et la poule

Contribution of the left atrioventricular coupling index in the prediction of atrial fibrillation in cardiac amyloidosis ATTR

Echographic factors of atrial arrhythmia in patients with arrythmogenic right ventricular dysplasia

Evaluation of left ventricular function by two-dimensional echocardiography and three-dimensional speckle-tracking echocardiography in noncompaction cardiomyopathy and dilated myocardiopathy

Traitements cardiologiques et spécifiques de l’amylose cardiaque

Prevalence and prognostic value of autonomic neuropathy assessed by Sudoscan® in transthyretin wild‐type cardiac amyloidosis

381 - Arrhythmogenic right ventricular cardiomyopathy or athlete’s heart adaptations?

Arrhythmogenic right ventricular cardiomyopathy or athlete’s heart adaptations?

Prognostic value of collagen biomarkers on left atrial remodeling and arrhythmia on hypertrophic cardiomyopathy

Correlation between MYBPC3 mutation and Circulating concentrations of a marker of type I collagen metabolism on hypertrophic cardiomyopathy

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