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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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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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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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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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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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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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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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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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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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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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Variants in the 3' untranslated region of the KCNQ1-encoded Kv7.1 potassium channel modify disease severity in patients with type 1 long QT syndrome in an allele-specific manner

European heart journal, 2012-03, Vol.33 (6), p.714-723

2012

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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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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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Exercise-Induced ECG Changes in Brugada Syndrome

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

2009

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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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Genotype-phenotype correlation in the long-QT syndrome: Gene-specific triggers for life-threatening arrhythmias

Circulation (New York, N.Y.), 2001-01, Vol.103 (1), p.89-95

2001

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The yield of risk stratification for sudden cardiac death in hypertrophic cardiomyopathy myosin-binding protein C gene mutation carriers: focus on predictive screening

European heart journal, 2010-04, Vol.31 (7), p.842-848

2010

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Lamin A/C mutation is independently associated with an increased risk of arterial and venous thromboembolic complications

International journal of cardiology, 2013-09, Vol.168 (1), p.472-477

2013

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The site of origin of torsade de pointes

Heart (British Cardiac Society), 2011-10, Vol.97 (20), p.1650-1654

2011

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Auditory stimuli as a trigger for arrhythmic events differentiate HERG-related (LQTS2) patients from KVLQT1-related patients (LQTS1)

Journal of the American College of Cardiology, 1999-02, Vol.33 (2), p.327-332

1999

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Less invasive determination of cardiac output from the arterial pressure by aortic diameter-calibrated pulse contour

British journal of anaesthesia : BJA, 2005-09, Vol.95 (3), p.326-331

2005

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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

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

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

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

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

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

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

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

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

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

Variants in the 3' untranslated region of the KCNQ1-encoded Kv7.1 potassium channel modify disease severity in patients with type 1 long QT syndrome in an allele-specific manner

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

Somatic mosaicism contributes to phenotypic variation in Timothy syndrome

Exercise-Induced ECG Changes in Brugada Syndrome

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

A sodium-channel mutation causes isolated cardiac conduction disease

Genotype-phenotype correlation in the long-QT syndrome: Gene-specific triggers for life-threatening arrhythmias

The yield of risk stratification for sudden cardiac death in hypertrophic cardiomyopathy myosin-binding protein C gene mutation carriers: focus on predictive screening

Lamin A/C mutation is independently associated with an increased risk of arterial and venous thromboembolic complications

The site of origin of torsade de pointes

Coxsackie and Adenovirus Receptor Is a Modifier of Cardiac Conduction and Arrhythmia Vulnerability in the Setting of Myocardial Ischemia

Auditory stimuli as a trigger for arrhythmic events differentiate HERG-related (LQTS2) patients from KVLQT1-related patients (LQTS1)

Less invasive determination of cardiac output from the arterial pressure by aortic diameter-calibrated pulse contour

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