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Cardiovascular Pathology : the Official Journal of the Society for Cardiovascular Pathology|November 1, 2011
Molecular changes in the heart of a severe case of arrhythmogenic right ventricular cardiomyopathy caused by a desmoglein-2 null alleleKatja Gehmlich, Petros Syrris, Mareike Reimann, et al.
The Journal of Heart Valve Disease|March 26, 2015
'Paradoxical' low-flow, low-gradient severe aortic valve stenosis: an entity with limited improvement following transcatheter aortic valve implantationMarkus Reinthaler, Anna Schwabe, Ulf Landmesser, et al.
European Journal of Heart Failure|November 18, 2017
Long-term outcomes for different surgical strategies to treat left ventricular outflow tract obstruction in hypertrophic cardiomyopathyRichard Collis, Oliver Watkinson, Constantinos O'Mahony, 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|January 15, 2021
Arrhythmogenic potential of myocardial disarray in hypertrophic cardiomyopathy: genetic basis, functional consequences and relation to sudden cardiac deathGherardo Finocchiaro, Nabeel Sheikh, Ornella Leone, et al.
International Journal of Cardiology|May 22, 2017
Desmoplakin missense and non-missense mutations in arrhythmogenic right ventricular cardiomyopathy: Genotype-phenotype correlationSilvia Castelletti, Annina S Vischer, Petros Syrris, et al.
The International Journal of Cardiovascular Imaging|November 27, 2015
Epicardial myocardial strain abnormalities may identify the earliest stages of arrhythmogenic cardiomyopathyPatricia Réant, Arnaud D Hauer, Silvia Castelletti, et al.
Heart (British Cardiac Society)|November 1, 2016
Relationship between aetiology and left ventricular systolic dysfunction in hypertrophic cardiomyopathyStefania Rosmini, Elena Biagini, Costantinos O'Mahony, et al.
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