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Cellular and molecular electrophysiology

Event: ESC CONGRESS 2017
Topic: Ion channels and electrophysiology
Session type: Moderated Posters
Date: 29 August 2017
Time: 15:35 - 16:25


7 presentations in this session

Characterization of a novel genetic variant associated with Brugada syndrome: beta-2-syntrophin mutation impairs interaction with SCN5A and reduces Na+ current in human cardiomyocytes

Speaker: Doctor C. Schmidt (Heidelberg, DE)

A mutation in the gene encoding the tbx5 transcription factor is associated with the Brugada Syndrome

Speaker: Professor R. Caballero (Madrid, ES)

Optogenetic cardioversion terminates atrial fibrillation in wild-type mice after gene transfer

Speaker: Doctor T. Beiert (Bonn, DE)

Local epicardial light pulse terminates ventricular arrhythmias in the adult rat heart upon optogenetic modification: towards biological shockless defibrillation.

Speaker: Mr E. Nyns (Leiden, NL)

Patient-specific iPSC-derived cardiomyocytes reveal a disease-causing role of an ACTN2 mutation in HCM and an unexpected LQT phenotype

Speaker: Doctor M. Lemoine (Hamburg, DE)

Structural and functional plasticity of myocardial slices in response to prolonged mechanical loading and unloading in vitro

Speaker: Mr S. Watson (London, GB)

PP1 activation as novel antiarrhythmic approach in human heart failure

Speaker: Mr J. Eiringhaus (Hannover, DE)

7 speakers from this session

Doctor Constanze Schmidt

University Hospital of Heidelberg, Heidelberg (Germany)
3 presentations
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Professor Ricardo Caballero

Complutense University of Madrid, Madrid (Spain)
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Doctor Thomas Beiert

University Hospital Bonn, Bonn (Germany)
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Mr Emile Nyns

Leiden University Medical Centre, Leiden (Netherlands (The))
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Doctor Marc D Lemoine

University Heart Center Hamburg, Hamburg (Germany)
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Mr Samuel Alexander Watson

Imperial College London, London (United Kingdom of Great Britain & Northern Ireland)
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Mr Joerg Eiringhaus

Hannover Medical School, Hannover (Germany)
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