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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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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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A Cardiac Sodium Channel Mutation Cosegregates With a Rare Connexin40 Genotype in Familial Atrial Standstill

Circulation research, 2003-01, Vol.92 (1), p.14-22

2003

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Electrocardiographic evidence of ventricular repolarization remodelling during atrial fibrillation

Europace (London, England), 2008-01, Vol.10 (1), p.99-104

2008

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Contemporary use of devices in chronic heart failure in the Netherlands

ESC Heart Failure, 2020-08, Vol.7 (4), p.1771-1780

2020

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De novo mutation in the SCN5A gene associated with early onset of sudden infant death

Circulation (New York, N.Y.), 2001-09, Vol.104 (10), p.1158-1164

2001

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Serum potassium level and mineralocorticoid receptor antagonist dose in a large cohort of chronic heart failure patients

ESC Heart Failure, 2023-04, Vol.10 (2), p.1481-1487

2023

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A mutation in the human cardiac sodium channel (E161K) contributes to sick sinus syndrome, conduction disease and Brugada syndrome in two families

Journal of molecular and cellular cardiology, 2005-06, Vol.38 (6), p.969-981

2005

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Genetic control of sodium channel function

Cardiovascular research, 2003-03, Vol.57 (4), p.961-973

2003

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Conduction slowing by the gap junctional uncoupler carbenoxolone

Cardiovascular research, 2003-11, Vol.60 (2), p.288-297

2003

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Mechanisms of inherited cardiac conduction disease

Europace (London, England), 2005-03, Vol.7 (2), p.122-137

2005

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Cardiac sodium channels and inherited electrophysiologic disorders: a pharmacogenetic overview

Expert opinion on pharmacotherapy, 2008-03, Vol.9 (4), p.537-549

2008

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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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Genotype–Phenotype Relationship in the Brugada Syndrome

The Brugada Syndrome: From Bench to Bedside, 2005, p.140-148

2005

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

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

A Cardiac Sodium Channel Mutation Cosegregates With a Rare Connexin40 Genotype in Familial Atrial Standstill

Electrocardiographic evidence of ventricular repolarization remodelling during atrial fibrillation

Contemporary use of devices in chronic heart failure in the Netherlands

De novo mutation in the SCN5A gene associated with early onset of sudden infant death

Serum potassium level and mineralocorticoid receptor antagonist dose in a large cohort of chronic heart failure patients

A mutation in the human cardiac sodium channel (E161K) contributes to sick sinus syndrome, conduction disease and Brugada syndrome in two families

Genetic control of sodium channel function

Conduction slowing by the gap junctional uncoupler carbenoxolone

Mechanisms of inherited cardiac conduction disease

Cardiac sodium channels and inherited electrophysiologic disorders: a pharmacogenetic overview

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

Genotype–Phenotype Relationship in the Brugada Syndrome

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