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Presentations

Retrograde approach for a slow pathway modification in a Fontan patient.

Event: EHRA 2025

Topic: Clinical

Session: Congenital heart disease

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Enhancing mutant IKS channel activity by increasing endogenous PIP2 levels and its interaction with PKA signalling pathway

Event: EHRA 2021

Topic: Arrhythmias

Session: WGCCE

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The novel long QT syndrome type 1 mutation KCNQ1-p.Thr247dup causes severe channel dysfunction but retains preserved adrenergic regulation

Event: EHRA 2018

Topic: Ventricular Arrhythmias and SCD - Pathophysiology and Mechanisms

Session: Young EP Poster Session - Young meets Experienced

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