ESC 365 - Doctor Seiko Ohno

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Doctor Seiko Ohno

National Cerebral & Cardiovascular Center, Suita (Japan)

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Desmoglein 2 mutant mice reproduce arrhythmogenic right ventricular cardiomyopathy patients' phenotype

Event: ESC Congress 2022

Topic: Arrhythmias

Session: Pathophysiological mechanisms in cardiomyopathies and hypertrophic remodeling

Arrhythmogenic right ventricular cardiomyopathy

Event: EHRA 2021

Topic: Treatment

Session: Inherited cardiomyopathies – What´s new?

Mutation specific clinical characteristics in long QT syndrome type 8; severe phenotype in Timothy syndrome patients

Event: ESC Congress 2019

Topic: Genetic Aspects of Arrhythmias

Session: Basic science atrial fibrillation

Long QT syndrome

Event: EHRA 2018

Topic: Miscellaneous

Session: Diagnosis and management of inherited arrhythmia syndromes

High frequency of CACNA1C mutations among genotyped LQTS patients

Event: ESC Congress 2017

Topic: Genetic aspects of arrhythmias

Session: Genetic basis

Specific phenotypes caused by RYR2 mutations relate with bradycardia but not with mutation locations in RYR2

Event: ESC Congress 2016

Topic: Genetic aspects of arrhythmias

Session: Genetic aspects of arrhythmias

Triple mutations in three major genes for long QT syndrome are very rare and cause complicated phenotypes with ventricular arrhythmia

Event: ESC Congress 2016

Topic: Genetic aspects of arrhythmias

Session: Miscellaneous in arrhythmia

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