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Presentations Articles

New phenotypic association for SMAD6 gene: its role in the development of cardiac conduction disorders and pulmonary arterial hypertension/hereditary haemorrhagic telangiectasia.

Event: ESC Congress 2025

Topic: Genetic Aspects of Arrhythmias

Session: Mechanisms of arrhythmias

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The role of TBX20 truncating variants in dilated and left ventricular non-compaction cardiomyopathy

Event: ESC Congress 2023

Topic: Dilated Cardiomyopathy

Session: Dilated cardiomyopathy and 'non-compaction': genetics and prognostic outcomes

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Prevalence of genetically confirmed familial hypercholesterolemia in patients with acute coronary syndrome

Event: ESC Congress 2017

Topic: CAD and comorbidities

Session: Impact of concomitant disease on coronary artery disease

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