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The failing heart

Nature (London), 2002-01, Vol.415 (6868), p.227-233

2002

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Ionic Mechanisms Responsible for the Electrocardiographic Phenotype of the Brugada Syndrome Are Temperature Dependent

Circulation research, 1999-10, Vol.85 (9), p.803-809

1999

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Spectrum of mutations in long-QT syndrome genes : KVLQT1, HERG, SCN5A, KCNE1, and KCNE2

Circulation (New York, N.Y.), 2000-09, Vol.102 (10), p.1178-1185

2000

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Sodium channel blockers identify risk for sudden death in patients with ST-segment elevation and right bundle branch block but structurally normal hearts

Circulation (New York, N.Y.), 2000-02, Vol.101 (5), p.510-515

2000

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20p12.3 microdeletion predisposes to Wolff–Parkinson–White syndrome with variable neurocognitive deficits

Journal of medical genetics, 2009-03, Vol.46 (3), p.168-175

2009

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The Brugada syndrome: clinical, electrophysiologic and genetic aspects

Journal of the American College of Cardiology, 1999-01, Vol.33 (1), p.5-15

1999

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Effectiveness and limitations of β-blocker therapy in congenital long-QT syndrome

Circulation (New York, N.Y.), 2000-02, Vol.101 (6), p.616-623

2000

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Altered regional cardiac wall mechanics are associated with differential cardiomyocyte calcium handling due to nebulette mutations in preclinical inherited dilated cardiomyopathy

Journal of molecular and cellular cardiology, 2013-07, Vol.60, p.151-160

2013

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Genetic basis and molecular mechanism for idiopathic ventricular fibrillation

Nature (London), 1998-03, Vol.392 (6673), p.293-296

1998

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Echocardiographic predictors of adverse clinical events in children with dilated cardiomyopathy: a prospective clinical study

Heart (British Cardiac Society), 2004-08, Vol.90 (8), p.908-915

2004

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Spectrum of ST-T-wave patterns and repolarization parameters in congenital long-QT syndrome : ECG findings identify genotypes

Circulation (New York, N.Y.), 2000-12, Vol.102 (23), p.2849-2855

2000

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Gene-specific response of dynamic ventricular repolarization to sympathetic stimulation in LQT1, LQT2 and LQT3 forms of congenital long QT syndrome

European heart journal, 2002-06, Vol.23 (12), p.975-983

2002

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Proposed Diagnostic Criteria for the Brugada Syndrome

European heart journal, 2002-11, Vol.23 (21), p.1648-1654

2002

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Age- and sex-related differences in clinical manifestations in patients with congenital long-QT syndrome : Findings from the international LQTS registry

Circulation (New York, N.Y.), 1998-06, Vol.97 (22), p.2237-2244

1998

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Gastric emptying for liquids of different compositions in children

British journal of anaesthesia : BJA, 2017-11, Vol.119 (5), p.948-955

2017

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Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias

Nature genetics, 1996-01, Vol.12 (1), p.17-23

1996

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Genetic and molecular basis of cardiac arrhythmias : Impact on clinical management parts I and II

Circulation (New York, N.Y.), 1999-02, Vol.99 (4), p.518-528

1999

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Long QT syndrome patients with mutations of the SCN5A and HERG genes have differential responses to Na+ channel blockade and to increases in heart rate : implications for gene-specific therapy

Circulation (New York, N.Y.), 1995-12, Vol.92 (12), p.3381-3386

1995

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Familial hypertrophic cardiomyopathy in Maine coon cats : An animal model of human disease

Circulation (New York, N.Y.), 1999-06, Vol.99 (24), p.3172-3180

1999

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Adenovirus infection in the lung results in graft failure after lung transplantation

The Journal of thoracic and cardiovascular surgery, 1998-10, Vol.116 (4), p.617-623

1998

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Detection of adenoviral genome in the myocardium of adult patients with idiopathic left ventricular dysfunction

Circulation (New York, N.Y.), 1999-03, Vol.99 (10), p.1348-1354

1999

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Human herpes virus 6 in archival cardiac tissues from children with idiopathic dilated cardiomyopathy or congenital heart disease

Journal of clinical pathology, 2009-01, Vol.62 (1), p.80-83

2009

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Comparison of clinical and genetic variables of cardiac events associated with loud noise versus swimming among subjects with the long QT syndrome

The American journal of cardiology, 1999-10, Vol.84 (8), p.876-879

1999

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ECG T-wave patterns in genetically distinct forms of the hereditary long QT syndrome

Circulation (New York, N.Y.), 1995-11, Vol.92 (10), p.2929-2934

1995

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Molecular biology and the prolonged QT syndromes

The American journal of medicine, 2001-04, Vol.110 (5), p.385-398

2001

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The failing heart

Ionic Mechanisms Responsible for the Electrocardiographic Phenotype of the Brugada Syndrome Are Temperature Dependent

Spectrum of mutations in long-QT syndrome genes : KVLQT1, HERG, SCN5A, KCNE1, and KCNE2

Sodium channel blockers identify risk for sudden death in patients with ST-segment elevation and right bundle branch block but structurally normal hearts

20p12.3 microdeletion predisposes to Wolff–Parkinson–White syndrome with variable neurocognitive deficits

The Brugada syndrome: clinical, electrophysiologic and genetic aspects

Effectiveness and limitations of β-blocker therapy in congenital long-QT syndrome

Altered regional cardiac wall mechanics are associated with differential cardiomyocyte calcium handling due to nebulette mutations in preclinical inherited dilated cardiomyopathy

Genetic basis and molecular mechanism for idiopathic ventricular fibrillation

Echocardiographic predictors of adverse clinical events in children with dilated cardiomyopathy: a prospective clinical study

Spectrum of ST-T-wave patterns and repolarization parameters in congenital long-QT syndrome : ECG findings identify genotypes

Gene-specific response of dynamic ventricular repolarization to sympathetic stimulation in LQT1, LQT2 and LQT3 forms of congenital long QT syndrome

Proposed Diagnostic Criteria for the Brugada Syndrome

Age- and sex-related differences in clinical manifestations in patients with congenital long-QT syndrome : Findings from the international LQTS registry

Gastric emptying for liquids of different compositions in children

Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias

Genetic and molecular basis of cardiac arrhythmias : Impact on clinical management parts I and II

Long QT syndrome patients with mutations of the SCN5A and HERG genes have differential responses to Na+ channel blockade and to increases in heart rate : implications for gene-specific therapy

Familial hypertrophic cardiomyopathy in Maine coon cats : An animal model of human disease

Adenovirus infection in the lung results in graft failure after lung transplantation

Detection of adenoviral genome in the myocardium of adult patients with idiopathic left ventricular dysfunction

Human herpes virus 6 in archival cardiac tissues from children with idiopathic dilated cardiomyopathy or congenital heart disease

Comparison of clinical and genetic variables of cardiac events associated with loud noise versus swimming among subjects with the long QT syndrome

ECG T-wave patterns in genetically distinct forms of the hereditary long QT syndrome

Molecular biology and the prolonged QT syndromes

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