Doctor Seiko Ohno
National Cerebral & Cardiovascular Center, Suita (Japan)
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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