Speaker illustration

Doctor Seiko Ohno

National Cerebral & Cardiovascular Center, Suita (Japan)

Member of:

European Society of Cardiology

Arrhythmogenic right ventricular cardiomyopathy

Event: EHRA 2021

Topic: Treatment

Session: Inherited cardiomyopathies – What´s new?

Thumbnail

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

Thumbnail

Long QT syndrome

Event: EHRA 2018

Topic: Miscellaneous

Session: Diagnosis and management of inherited arrhythmia syndromes

Thumbnail

High frequency of CACNA1C mutations among genotyped LQTS patients

Event: ESC CONGRESS 2017

Topic: Genetic aspects of arrhythmias

Session: Genetic basis

Thumbnail

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

Thumbnail

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

Thumbnail

This platform is supported by

logo Novo Nordisk