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Genetic analysis and electrocardiographic patterns in Brugada syndrome

29 August 2025 (07:00 - 18:00)
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Congress Presentation Part of: Molecular and genetic mechanisms of arrhythmias: from calcium dysregulation to syndromic signatures Genetics, Epigenetics, ncRNA ESC Professional Premium Access ESC Congress 2025 European Society of Cardiology

About the speaker

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Miss Martina Modena

Sant'Anna School of Advanced Studies, Pisa (Italy)

6 More presentations in this session

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Synapsin 2 deficiency impairs NCX1 transport and increases susceptibility to ventricular arrhythmias and heart failure mortality
Doctor A. Ottesen (Nordbyhagen, NO)
Abstract Slides Video
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Identification of a small SN derivative that inhibits CaMKII activity
Miss I. Rugolo (Oslo, NO)
Abstract Slides Video
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PDE1 inhibition potentiates arrhythmogenic disturbances in calcium homeostasis and electrical activity induced by pathological adenosine levels in mouse ventricular myocytes
Miss C. Aceituno (Barcelona, ES)
Abstract Slides Video
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Digging into the pathophysiological complexity of CPVT5
Mr K. Hernandez Lopez (Madrid, ES)
Abstract Slides Video
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Peptide array-derived optimized secretoneurin variants enhance CaMKII inhibition and reduce pathological cardiomyocyte Ca2+ handling
Miss I. Rugolo (Oslo, NO)
Abstract Slides Video

Access the full session

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Molecular and genetic mechanisms of arrhythmias: from calcium dysregulation to syndromic signatures

The Event

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ESC Congress 2025

29 August - 1 September 2025
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ESC 365 is supported by

novartis Explore sponsored resources

ESC 365 is supported by

novartis Explore sponsored resources