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Frontiers in Cardiovascular Medicine|May 19, 2022
Prognosis of Adults With Isolated Left Ventricular Non-Compaction: Results of a Prospective Multicentric StudyHilla Gerard, Nicolas Iline, Hélène Martel, et al.Journal of Neuromuscular Diseases|July 9, 2026
2025 update of the National French consensus on gene lists for the diagnosis of muscle diseases using high-throughput sequencingEmmanuelle Pion, Mireille Cossée, Valérie Biancalana, et al.Circulation. Arrhythmia and Electrophysiology|August 11, 2016
Multicenter Experience With Catheter Ablation for Ventricular Tachycardia in Lamin A/C CardiomyopathySaurabh Kumar, Alexander F A Androulakis, Jean-Marc Sellal, et al.JAMA Cardiology|July 2, 2025
Location of LMNA Variants and Clinical Outcomes in CardiomyopathyAshwin Bhaskaran, Rabah Ben Yaou, Adam S Helms, et al.Orphanet Journal of Rare Diseases|June 10, 2025
Comparison of two genetic strategies for diagnostic work-up of hypertrophic cardiomyopathy: impact on the diagnosis of Fabry disease or transthyretin amyloidosisAurélien Palmyre, Fairouz Koraichi, Flavie Ader, et al.Journal of the American College of Cardiology|November 26, 2016
Long-Term Arrhythmic and Nonarrhythmic Outcomes of Lamin A/C Mutation CarriersSaurabh Kumar, Samuel H Baldinger, Estelle Gandjbakhch, et al.Journal of Neuropathology and Experimental Neurology|August 23, 2013
Skeletal muscle biopsy analysis in reducing body myopathy and other FHL1-related disordersEdoardo Malfatti, Montse Olivé, Ana Lía Taratuto, et al.International Journal of Cardiology|November 16, 2024
Clinical impact of genetic testing in a large cohort of pediatric cardiomyopathiesFlavie Ader, Neil Derridj, Anne Claire Brehin, et al.Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|April 22, 2017
High prevalence of arrhythmic and myocardial complications in patients with cardiac glycogenosis due to PRKAG2 mutationsJulien Thevenon, Gabriel Laurent, Flavie Ader, et al.Annals of Neurology|June 14, 2008
De novo LMNA mutations cause a new form of congenital muscular dystrophySusana Quijano-Roy, Blaise Mbieleu, Carsten G Bönnemann, et al.Pageof 16