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Structure: Internal structure identifier : 351120
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Phenotype/Genotype Relationship in Left Ventricular Noncompaction: Ion Channel Gene Mutations Are Associated With Preserved Left Ventricular Systolic Function and Biventricular Noncompaction

Marie Cambon-Viala , Hilla Gerard , Karine Nguyen , Pascale Richard , Flavie Ader , et al.
Journal of Cardiac Failure, 2021, 27 (6), pp.677-681. ⟨10.1016/j.cardfail.2021.01.007⟩
Journal articles hal-04073195v1
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Position paper concerning the competence, performance and environment required for the practice of ablation in children and in congenital heart disease

Philippe Maury , Jean Benoit Thambo , Alice Maltret , Nicolas Combes , Sébastien Hascoet , et al.
Archives of cardiovascular diseases, 2020, 113 (8-9), pp.492-502. ⟨10.1016/j.acvd.2020.02.002⟩
Journal articles hal-04073540v1

Inherited Cardiomyopathies Revealed by Clinically Suspected Myocarditis

Flavie Ader , Elodie Surget , Philippe Charron , Alban Redheuil , Amir Zouaghi , et al.
Circulation: Genomic and Precision Medicine, 2020, 13 (4), pp.e002744. ⟨10.1161/CIRCGEN.119.002744⟩
Journal articles inserm-03996719v1
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Genotype-phenotype correlations of pathogenic variants in the FLNC gene

Flavie Ader , Eric Villard , Céline Ledeuil , Philippe Charron , Pascale Richard
Médecine/Sciences, 2018, 34, pp.39-41. ⟨10.1051/medsci/201834s211⟩
Journal articles inserm-03996754v1
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Absence of triadin, a protein of the calcium release complex, is responsible for cardiac arrhythmia with sudden death in human.

Nathalie Roux-Buisson , Marine Cacheux , Anne Fourest-Lieuvin , J. Fauconnier , Julie Brocard , et al.
Human Molecular Genetics, 2012, 21 (12), pp.2759-67. ⟨10.1093/hmg/dds104⟩
Journal articles inserm-00763211v1