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Ventricular tachycardia after in vivo DC shock ablation in dogs : electrophysiologic and histologic correlation

Circulation (New York, N.Y.), 1991-07, Vol.84 (1), p.267-278

1991

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Permanent Leadless Cardiac Pacing: Results of the LEADLESS Trial

Circulation (New York, N.Y.), 2014-04, Vol.129 (14), p.1466-1471

2014

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Long-Term Prognosis of Patients Diagnosed With Brugada Syndrome: Results From the FINGER Brugada Syndrome Registry

Circulation (New York, N.Y.), 2010-02, Vol.121 (5), p.635-643

2010

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Quinidine, A Life-Saving Medication for Brugada Syndrome, Is Inaccessible in Many Countries

Journal of the American College of Cardiology, 2013-06, Vol.61 (23), p.2383-2387

2013

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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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The Response of the QT Interval to the Brief Tachycardia Provoked by Standing: A Bedside Test for Diagnosing Long QT Syndrome

Journal of the American College of Cardiology, 2010-05, Vol.55 (18), p.1955-1961

2010

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Expanding spectrum of human RYR2-related disease : New electrocardiographic, structural, and genetic features

Circulation (New York, N.Y.), 2007-10, Vol.116 (14), p.1569-1576

2007

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The Entirely Subcutaneous Implantable Cardioverter-Defibrillator: Initial Clinical Experience in a Large Dutch Cohort

Journal of the American College of Cardiology, 2012-11, Vol.60 (19), p.1933-1939

2012

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Familial Evaluation in Catecholaminergic Polymorphic Ventricular Tachycardia: Disease Penetrance and Expression in Cardiac Ryanodine Receptor Mutation–Carrying Relatives

Circulation. Arrhythmia and electrophysiology, 2012-08, Vol.5 (4), p.748-756

2012

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Right ventricular fibrosis and conduction delay in a patient with clinical signs of brugada syndrome : A combined electrophysiological, genetic, histopathologic, and computational study

Circulation (New York, N.Y.), 2005-11, Vol.112 (18), p.2769-2777

2005

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Distinguishing Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia–Associated Mutations From Background Genetic Noise

Journal of the American College of Cardiology, 2011-06, Vol.57 (23), p.2317-2327

2011

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Genotype-phenotype relationship in Brugada syndrome: electrocardiographic features differentiate SCN5A-related patients from non–SCN5A-related patients

Journal of the American College of Cardiology, 2002-07, Vol.40 (2), p.350-356

2002

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Familial sudden death is an important risk factor for primary ventricular fibrillation : A case-control study in acute myocardial infarction patients

Circulation (New York, N.Y.), 2006-09, Vol.114 (11), p.1140-1145

2006

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A Gain-of-Function TBX5 Mutation Is Associated With Atypical Holt–Oram Syndrome and Paroxysmal Atrial Fibrillation

Circulation research, 2008-06, Vol.102 (11), p.1433-1442

2008

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Navigating the mini-maze: Systematic review of the first results and progress of minimally-invasive surgery in the treatment of atrial fibrillation

International journal of cardiology, 2013-06, Vol.166 (1), p.132-140

2013

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Long-term prognosis of individuals with right precordial ST-segment-elevation Brugada syndrome

Circulation (New York, N.Y.), 2005-01, Vol.111 (3), p.257-263

2005

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The Brugada ECG Pattern: A Marker of Channelopathy, Structural Heart Disease, or Neither? Toward a Unifying Mechanism of the Brugada Syndrome

Circulation. Arrhythmia and electrophysiology, 2010-06, Vol.3 (3), p.283-290

2010

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Thoracoscopic Video-Assisted Pulmonary Vein Antrum Isolation, Ganglionated Plexus Ablation, and Periprocedural Confirmation of Ablation Lesions: First Results of a Hybrid Surgical-Electrophysiological Approach for Atrial Fibrillation

Circulation. Arrhythmia and electrophysiology, 2011-06, Vol.4 (3), p.262-270

2011

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Delay in right ventricular activation contributes to Brugada syndrome

Circulation (New York, N.Y.), 2004-03, Vol.109 (10), p.1272-1277

2004

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Somatic mosaicism contributes to phenotypic variation in Timothy syndrome

American journal of medical genetics. Part A, 2011-10, Vol.155 (10), p.2578-2583

2011

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A Single Na+ Channel Mutation Causing Both Long-QT and Brugada Syndromes

Circulation research, 1999-12, Vol.85 (12), p.1206-1206

1999

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A sodium-channel mutation causes isolated cardiac conduction disease

Nature (London), 2001-02, Vol.409 (6823), p.1043-1047

2001

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Exercise-Induced ECG Changes in Brugada Syndrome

Circulation. Arrhythmia and electrophysiology, 2009-10, Vol.2 (5), p.531-539

2009

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Ventricular tachycardia after in vivo DC shock ablation in dogs : electrophysiologic and histologic correlation

Permanent Leadless Cardiac Pacing: Results of the LEADLESS Trial

Long-Term Prognosis of Patients Diagnosed With Brugada Syndrome: Results From the FINGER Brugada Syndrome Registry

Quinidine, A Life-Saving Medication for Brugada Syndrome, Is Inaccessible in Many Countries

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

The Response of the QT Interval to the Brief Tachycardia Provoked by Standing: A Bedside Test for Diagnosing Long QT Syndrome

Expanding spectrum of human RYR2-related disease : New electrocardiographic, structural, and genetic features

The Entirely Subcutaneous Implantable Cardioverter-Defibrillator: Initial Clinical Experience in a Large Dutch Cohort

Who Are the Long-QT Syndrome Patients Who Receive an Implantable Cardioverter-Defibrillator and What Happens to Them?: Data From the European Long-QT Syndrome Implantable Cardioverter-Defibrillator (LQTS ICD) Registry

Familial Evaluation in Catecholaminergic Polymorphic Ventricular Tachycardia: Disease Penetrance and Expression in Cardiac Ryanodine Receptor Mutation–Carrying Relatives

Right ventricular fibrosis and conduction delay in a patient with clinical signs of brugada syndrome : A combined electrophysiological, genetic, histopathologic, and computational study

Distinguishing Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia–Associated Mutations From Background Genetic Noise

Genotype-phenotype relationship in Brugada syndrome: electrocardiographic features differentiate SCN5A-related patients from non–SCN5A-related patients

Familial sudden death is an important risk factor for primary ventricular fibrillation : A case-control study in acute myocardial infarction patients

A Gain-of-Function TBX5 Mutation Is Associated With Atypical Holt–Oram Syndrome and Paroxysmal Atrial Fibrillation

Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy: Pathogenic Desmosome Mutations in Index-Patients Predict Outcome of Family Screening: Dutch Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy Genotype-Phenotype Follow-Up Study

Navigating the mini-maze: Systematic review of the first results and progress of minimally-invasive surgery in the treatment of atrial fibrillation

Long-term prognosis of individuals with right precordial ST-segment-elevation Brugada syndrome

The Brugada ECG Pattern: A Marker of Channelopathy, Structural Heart Disease, or Neither? Toward a Unifying Mechanism of the Brugada Syndrome

Thoracoscopic Video-Assisted Pulmonary Vein Antrum Isolation, Ganglionated Plexus Ablation, and Periprocedural Confirmation of Ablation Lesions: First Results of a Hybrid Surgical-Electrophysiological Approach for Atrial Fibrillation

Delay in right ventricular activation contributes to Brugada syndrome

Somatic mosaicism contributes to phenotypic variation in Timothy syndrome

A Single Na+ Channel Mutation Causing Both Long-QT and Brugada Syndromes

A sodium-channel mutation causes isolated cardiac conduction disease

Exercise-Induced ECG Changes in Brugada Syndrome

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