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Screening for, and management of, possible arrhythmogenic syndromes (channelopathies/ion channel diseases)
Jesper Hastrup Svendsen
, Peter Geelen, EHRA Scientific Initiative Commitee
9
Citations (Scopus)
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Dive into the research topics of 'Screening for, and management of, possible arrhythmogenic syndromes (channelopathies/ion channel diseases)'. Together they form a unique fingerprint.
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Keyphrases
Family Members
100%
Channelopathy
100%
Brugada Syndrome
100%
Ion Channel Diseases
100%
Catecholaminergic Polymorphic Ventricular Tachycardia
66%
Long QT Syndrome
66%
First-degree Relatives
33%
European Centre
33%
Genetic Testing
33%
New Patients
33%
Index Patient
33%
Electrophysiologist
33%
Management Strategy
33%
Short QT Syndrome
33%
Non-invasive Test
33%
Current Management
33%
Biochemistry, Genetics and Molecular Biology
Channelopathy
100%
Brugada Syndrome
100%
Catecholaminergic Polymorphic Ventricular Tachycardia
66%
Long QT Syndrome
66%
Genetic Screening
33%
Short QT Syndrome
33%