ESC Premium Access

Role of implantable cardioverter defibrillator device therapy in patients with progressive Fabry disease

Topic: Genetic aspects of arrhythmias

Congress Presentation

About the speaker

Doctor Daniel Oder

University Hospital Würzburg, Würzburg (Germany)
0 follower

9 more presentations in this session

Whole exome sequencing of families with atrial fibrillation - a Danish nationwide study.

Speaker: Doctor L. Refsgaard (Copenhagen, DK)

Thumbnail

Age and gender related differences in corrected QT interval in children and adolescents with LQT1 and LQT2

Speaker: Doctor S. Vink (Amsterdam, NL)

Thumbnail

Genetic determinants of arrhythmia in dilated cardiomyopathy

Speaker: Doctor U. Tayal (London, GB)

Thumbnail

Location of SCN5A mutation determines severity of phenotype and response to sodium channel blockage

Speaker: Mr Y. Reckman (Amsterdam, NL)

Thumbnail

Cardiac phenotype and prognosis of patients with mutations in NKX2.5 gene

Speaker: Doctor P. Maury (Toulouse, FR)

Thumbnail

Access the full session

Gene and arrhythmias

Speakers: Doctor D. Oder, Doctor L. Refsgaard, Doctor S. Vink, Doctor U. Tayal, Mr Y. Reckman...
Thumbnail

About the event

Image

ESC Congress 2016

27 August - 31 August 2016

Sessions Presentations

ESC 365 is supported by

logo Novo Nordisk
logo Bristol Myers Squibb