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Doctor Olga Svecova

Masaryk University, Brno (Czechia)

Clinical, genetic and functional analysis of R562S-Kv7.1 mutation associated with long QT syndrome type 1

Event: EHRA 2021

Topic: Basic Science

Session: Ion channel (dys)function

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Mutation R591C associated with long QT syndrome type 1: clinical, genetic, and functional analysis

Event: EHRA 2019

Topic: Ion Channels, Electrophysiology

Session: Poster Session 1 - 43rd EWGCCE Meeting

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New method for determination of tubular membrane capacity in intact cardiomyocytes

Event: EHRA EUROPACE - CARDIOSTIM 2017

Topic: Cellular Electrophysiology

Session: Poster Session 2 - 41st EWGCCE Meeting

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