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Philippe Charron

Showing results (131-140 of 167) with videos related to

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European Journal of Heart Failure|November 28, 2012
Gender-specific differences in major cardiac events and mortality in lamin A/C mutation carriersIngrid A W van Rijsingen, Eline A Nannenberg, Eloisa Arbustini, et al.
Open Heart|June 28, 2019
Heritability in genetic heart disease: the role of genetic backgroundJoeri A Jansweijer, Karin Y van Spaendonck-Zwarts, Michael W T Tanck, et al.
Journal of the American College of Cardiology|July 7, 2012
Multifocal ectopic Purkinje-related premature contractions: a new SCN5A-related cardiac channelopathyGabriel Laurent, Samuel Saal, Mohamed Yassine Amarouch, et al.
Health and Quality of Life Outcomes|July 29, 2021
Health-related quality of life and physical activity in children with inherited cardiac arrhythmia or inherited cardiomyopathy: the prospective multicentre controlled QUALIMYORYTHM study rationale, design and methodsPascal Amedro, Oscar Werner, Hamouda Abassi, et al.
Orphanet Journal of Rare Diseases|October 30, 2024
Improving genetic testing pathways for transthyretin amyloidosis in France: challenges and strategiesBérénice Hebrard, Marie-Lise Babonneau, Philippe Charron, et al.
European Heart Journal. Quality of Care & Clinical Outcomes|July 11, 2025
Current Management of Transition and Multidisciplinary Care of Patients with Inherited and Rare Cardiomyopathies in Europe: Results of the European Reference Network for Rare and Low Prevalence Complex Diseases of the Heart (ERN GUARD-HEART)Emanuele Monda, Elena Biagini, Nico Blom, et al.
European Heart Journal. Cardiovascular Imaging|May 17, 2017
Multimodality Imaging in Restrictive Cardiomyopathies: An EACVI expert consensus document In collaboration with the "Working Group on myocardial and pericardial diseases" of the European Society of Cardiology Endorsed by The Indian Academy of EchocardiographyGilbert Habib, Chiara Bucciarelli-Ducci, Alida L P Caforio, et al.
European Heart Journal|March 20, 2026
Genetic counselling implementation in dilated cardiomyopathyJob A J Verdonschot, Karin Y van Spaendonck-Zwarts, Debby M E I Hellebrekers, et al.
International Journal of Cardiology|July 10, 2021
A novel risk model for predicting potentially life-threatening arrhythmias in non-ischemic dilated cardiomyopathy (DCM-SVA risk)Elham Kayvanpour, Arjan Sammani, Farbod Sedaghat-Hamedani, et al.
Genome Biology|September 15, 2017
Natural genetic variation of the cardiac transcriptome in non-diseased donors and patients with dilated cardiomyopathyMatthias Heinig, Michiel E Adriaens, Sebastian Schafer, et al.
Pageof 17

Showing results (131-140 of 167) with videos related to

Sort By:
Pageof 17
European Journal of Heart Failure|November 28, 2012
Gender-specific differences in major cardiac events and mortality in lamin A/C mutation carriersIngrid A W van Rijsingen, Eline A Nannenberg, Eloisa Arbustini, et al.
Open Heart|June 28, 2019
Heritability in genetic heart disease: the role of genetic backgroundJoeri A Jansweijer, Karin Y van Spaendonck-Zwarts, Michael W T Tanck, et al.
Journal of the American College of Cardiology|July 7, 2012
Multifocal ectopic Purkinje-related premature contractions: a new SCN5A-related cardiac channelopathyGabriel Laurent, Samuel Saal, Mohamed Yassine Amarouch, et al.
Health and Quality of Life Outcomes|July 29, 2021
Health-related quality of life and physical activity in children with inherited cardiac arrhythmia or inherited cardiomyopathy: the prospective multicentre controlled QUALIMYORYTHM study rationale, design and methodsPascal Amedro, Oscar Werner, Hamouda Abassi, et al.
Orphanet Journal of Rare Diseases|October 30, 2024
Improving genetic testing pathways for transthyretin amyloidosis in France: challenges and strategiesBérénice Hebrard, Marie-Lise Babonneau, Philippe Charron, et al.
European Heart Journal. Quality of Care & Clinical Outcomes|July 11, 2025
Current Management of Transition and Multidisciplinary Care of Patients with Inherited and Rare Cardiomyopathies in Europe: Results of the European Reference Network for Rare and Low Prevalence Complex Diseases of the Heart (ERN GUARD-HEART)Emanuele Monda, Elena Biagini, Nico Blom, et al.
European Heart Journal. Cardiovascular Imaging|May 17, 2017
Multimodality Imaging in Restrictive Cardiomyopathies: An EACVI expert consensus document In collaboration with the "Working Group on myocardial and pericardial diseases" of the European Society of Cardiology Endorsed by The Indian Academy of EchocardiographyGilbert Habib, Chiara Bucciarelli-Ducci, Alida L P Caforio, et al.
European Heart Journal|March 20, 2026
Genetic counselling implementation in dilated cardiomyopathyJob A J Verdonschot, Karin Y van Spaendonck-Zwarts, Debby M E I Hellebrekers, et al.
International Journal of Cardiology|July 10, 2021
A novel risk model for predicting potentially life-threatening arrhythmias in non-ischemic dilated cardiomyopathy (DCM-SVA risk)Elham Kayvanpour, Arjan Sammani, Farbod Sedaghat-Hamedani, et al.
Genome Biology|September 15, 2017
Natural genetic variation of the cardiac transcriptome in non-diseased donors and patients with dilated cardiomyopathyMatthias Heinig, Michiel E Adriaens, Sebastian Schafer, et al.
Pageof 17