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Spontaneous Brugada electrocardiogram patterns are rare in the German general population: results from the KORA study

Europace (London, England), 2009-10, Vol.11 (10), p.1338-1344

2009

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Electrophysiologic investigation in Brugada syndrome. Yield of programmed ventricular stimulation at two ventricular sites with up to three premature beats

European heart journal, 2002-09, Vol.23 (17), p.1394-1401

2002

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Role of programmed ventricular stimulation in patients with Brugada syndrome: a meta-analysis of worldwide published data

European heart journal, 2007-09, Vol.28 (17), p.2126-2133

2007

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Making sense in a nonsense reading frame: suppression of cardiac sodium channel dysfunction

Cardiovascular research, 2009-08, Vol.83 (3), p.423-424

Schulze-Bahr, Eric

2009

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Susceptibility genes and modifiers for cardiac arrhythmias

Cardiovascular research, 2005-08, Vol.67 (3), p.397-413

2005

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New risk predictor of arrhythmias in patients with congenital Long-QT Syndrome

European heart journal, 2023-11, Vol.44 (Supplement_2)

2023

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Role of implantable cardioverter defibrillator therapy in patients with acquired long QT syndrome: A long-term follow-up

Europace (London, England), 2012-03, Vol.14 (3), p.396-401

2012

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Successful treatment of catecholaminergic polymorphic ventricular tachycardia with flecainide: a case report and review of the current literature

Europace (London, England), 2011-06, Vol.13 (6), p.897-901

2011

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THerapy Efficacy in Short or long-coupled idiopathic ventricular fibrillation: an International Survey (THESIS)

Europace (London, England), 2024-05, Vol.26 (Supplement_1)

2024

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Role of sequence variations in the human ether -a -go -go -related gene (HERG, KCNH2) in the brugada syndrome

Cardiovascular research, 2005-12, Vol.68 (3), p.441-453

2005

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Clinical aspects of ventricular arrhythmias associated with QT prolongation

European heart journal supplements, 2001-09, Vol.3 (suppl-K), p.K81-K88

2001

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P4850Variability in the diagnosis of Brugada syndrome

European heart journal, 2018-08, Vol.39 (suppl_1)

2018

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Corrigendum to: 'HRS/EHRA Expert Consensus Statement on the State of Genetic Testing for the Channelopathies and Cardiomyopathies' [Europace 2011;13:1077-109, doi: 10.1093/europace/eur245]

Europace (London, England), 2012-02, Vol.14 (2), p.277-277

2012

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Genetic aspects in acquired long QT syndrome — a piece in the puzzle

European heart journal supplements, 2001-09, Vol.3 (suppl-K), p.K48-K52

2001

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Prediction of variant pathogenicity in congenital LQT syndrome: Performance analyses of 7 programs using 354 validated variants

European heart journal, 2013-08, Vol.34 (suppl 1), p.P2302-P2302

2013

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Whole exome sequencing (WES) in a patient with a cardiac conduction defect and ventricular arrhythmias

European heart journal, 2013-08, Vol.34 (suppl 1), p.P2296-P2296

2013

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Substitution of a conserved alanine in the domain IIIS4-S5 linker of the cardiac sodium channel causes long QT syndrome

Cardiovascular research, 2005-08, Vol.67 (3), p.459-466

2005

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Body surface potential mapping in patients with Brugada syndrome: right precordial ST segment variations and reverse changes in left precordial leads

Cardiovascular research, 2002-04, Vol.54 (1), p.58-66

2002

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793 Electrocardiographic risk stratification in genotyped patients with congenital long QT-syndrome

Europace (London, England), 2005-06, Vol.7 (Supplement_1), p.181-182

2005

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2023 ESC Guidelines for the management of cardiomyopathies

European heart journal, 2023-10, Vol.44 (37), p.3503-3626

2023

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Estradiol regulates human QT-interval: acceleration of cardiac repolarization by enhanced KCNH2 membrane trafficking

European heart journal, 2016-02, Vol.37 (7), p.640-650

2016

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HRS/EHRA Expert Consensus Statement on the State of Genetic Testing for the Channelopathies and Cardiomyopathies

Europace (London, England), 2011-08, Vol.13 (8), p.1077-1109

2011

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Investigation on Sudden Unexpected Death in the Young (SUDY) in Europe: results of the European Heart Rhythm Association Survey

Europace (London, England), 2022-02, Vol.24 (2), p.331-339

2022

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Cardiac sodium channels: Dysregulation meets myocardial failure

Cardiovascular research, 2007-08, Vol.75 (3), p.455-456

SCHULZEBAHR, E

2007

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Spontaneous Brugada electrocardiogram patterns are rare in the German general population: results from the KORA study

Electrophysiologic investigation in Brugada syndrome. Yield of programmed ventricular stimulation at two ventricular sites with up to three premature beats

Role of programmed ventricular stimulation in patients with Brugada syndrome: a meta-analysis of worldwide published data

Making sense in a nonsense reading frame: suppression of cardiac sodium channel dysfunction

Susceptibility genes and modifiers for cardiac arrhythmias

New risk predictor of arrhythmias in patients with congenital Long-QT Syndrome

Role of implantable cardioverter defibrillator therapy in patients with acquired long QT syndrome: A long-term follow-up

Successful treatment of catecholaminergic polymorphic ventricular tachycardia with flecainide: a case report and review of the current literature

THerapy Efficacy in Short or long-coupled idiopathic ventricular fibrillation: an International Survey (THESIS)

Role of sequence variations in the human ether -a -go -go -related gene (HERG, KCNH2) in the brugada syndrome

Clinical aspects of ventricular arrhythmias associated with QT prolongation

P4850Variability in the diagnosis of Brugada syndrome

Corrigendum to: 'HRS/EHRA Expert Consensus Statement on the State of Genetic Testing for the Channelopathies and Cardiomyopathies' [Europace 2011;13:1077-109, doi: 10.1093/europace/eur245]

Genetic aspects in acquired long QT syndrome — a piece in the puzzle

HRS/EHRA expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies: this document was developed as a partnership between the Heart Rhythm Society (HRS) and the European Heart Rhythm Association (EHRA)

Prediction of variant pathogenicity in congenital LQT syndrome: Performance analyses of 7 programs using 354 validated variants

Whole exome sequencing (WES) in a patient with a cardiac conduction defect and ventricular arrhythmias

Substitution of a conserved alanine in the domain IIIS4-S5 linker of the cardiac sodium channel causes long QT syndrome

Body surface potential mapping in patients with Brugada syndrome: right precordial ST segment variations and reverse changes in left precordial leads

793 Electrocardiographic risk stratification in genotyped patients with congenital long QT-syndrome

2023 ESC Guidelines for the management of cardiomyopathies

Estradiol regulates human QT-interval: acceleration of cardiac repolarization by enhanced KCNH2 membrane trafficking

HRS/EHRA Expert Consensus Statement on the State of Genetic Testing for the Channelopathies and Cardiomyopathies

Investigation on Sudden Unexpected Death in the Young (SUDY) in Europe: results of the European Heart Rhythm Association Survey

Cardiac sodium channels: Dysregulation meets myocardial failure

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