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Atrial fibrillation in long QT syndrome as a risk indicator of cardiac events

Topic: Genetic aspects of arrhythmias

Congress Session

About the speaker

Professor Pyotr Platonov

Skane University Hospital, Lund (Sweden)
1 presentation
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9 more presentations in this session

Identification of TNFSF13, SPATC1L, SLC22A25, and SALL4 as novel susceptibility loci for atrial fibrillation in Japanese individuals by an exome-wide association study

Speaker: Doctor H. Horibe (Tajimi, JP)

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Genetic background of sudden cardiac death caused by idiopathic myocardial fibrosis.

Speaker: Mr L. Holmstrom (Oulu, FI)

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Gene-based risk stratification for cardiac disorders in LMNA mutation carriers

Speaker: Doctor S. Nishiuchi (Nara, JP)

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Unexpected risk profile in a large paediatric population with Brugada syndrome.

Speaker: Doctor A. Mazzanti (Pavia, IT)

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Desmoglein 2 gene mutation (DSG2-F531C) caused arrhythmogenic right ventricular cardiomyopathy in human and mice is gene dose-dependent

Speaker: Doctor D. Wang (Nanjing, CN)

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Access the full session

Genetics and cardiac arrhythmias

Speakers: Professor P. Platonov, Doctor H. Horibe, Mr L. Holmstrom, Doctor S. Nishiuchi, Doctor A. Mazzanti...
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ESC CONGRESS 2017

26 August - 30 August 2017

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