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Genetic analysis and electrocardiographic patterns in Brugada syndrome

Session: Molecular and genetic mechanisms of arrhythmias: from calcium dysregulation to syndromic signatures
Topic: Genetics, Epigenetics, ncRNA
Speaker: Miss M. Modena (Pisa, IT)
Event: ESC Congress 2025

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Miss Martina Modena

Sant'Anna School of Advanced Studies, Pisa (Italy)
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6 more presentations in this session

Synapsin 2 deficiency impairs NCX1 transport and increases susceptibility to ventricular arrhythmias and heart failure mortality

Speaker: Doctor A. Ottesen (Nordbyhagen, NO)

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Identification of a small SN derivative that inhibits CaMKII activity

Speaker: Miss I. Rugolo (Oslo, NO)

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PDE1 inhibition potentiates arrhythmogenic disturbances in calcium homeostasis and electrical activity induced by pathological adenosine levels in mouse ventricular myocytes

Speaker: Miss C. Aceituno (Barcelona, ES)

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Digging into the pathophysiological complexity of CPVT5

Speaker: Mr K. Hernandez Lopez (Madrid, ES)

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Peptide array-derived optimized secretoneurin variants enhance CaMKII inhibition and reduce pathological cardiomyocyte Ca2+ handling

Speaker: Miss I. Rugolo (Oslo, NO)

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Access the full session

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

Speakers: Miss M. Modena, Doctor A. Ottesen, Miss I. Rugolo, Miss C. Aceituno, Mr K. Hernandez Lopez...
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About the event

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ESC Congress 2025

29 August - 1 September 2025

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