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
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
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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