Lista de obras -

A large candidate gene survey identifies the KCNE1 D85N polymorphism as a possible modulator of drug-induced torsades de pointes

artículo científico publicado en 2011

An International Multicenter Evaluation of Type 5 Long QT Syndrome: A Low Penetrant Primary Arrhythmic Condition

scientific article published on 16 January 2020

An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing

artículo científico publicado en 2009

Analysis for Genetic Modifiers of Disease Severity in Patients With Long-QT Syndrome Type 2

artículo científico publicado en 2015

Atrial Arrhythmias in long-QT syndrome under daily life conditions: a nested case control study

artículo científico publicado en 2008

Brugada Syndrome: Overview

Brugada syndrome: report of the second consensus conference.

artículo científico publicado en 2005

Brugada syndrome: report of the second consensus conference: endorsed by the Heart Rhythm Society and the European Heart Rhythm Association.

artículo científico publicado en 2005

Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death

artículo científico publicado en 2013

Early repolarization pattern: a marker of increased risk in patients with catecholaminergic polymorphic ventricular tachycardia

artículo científico publicado en 2015

Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls

artículo científico publicado en 2020

First report on an inotropic peptide activating tetrodotoxin-sensitive, "neuronal" sodium currents in the heart

artículo científico publicado en 2014

Genetic basis and molecular mechanism for idiopathic ventricular fibrillation

artículo científico publicado en 1998

Genome wide analysis of drug-induced torsades de pointes: lack of common variants with large effect sizes

artículo científico publicado en 2013

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).

artículo científico

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).

artículo científico publicado en 2011

Ivabradine in patients with inappropriate sinus tachycardia

artículo científico publicado en 2010

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

artículo científico publicado en 2005

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

scientific article published on 04 August 2009

Lista de obras de

A large candidate gene survey identifies the KCNE1 D85N polymorphism as a possible modulator of drug-induced torsades de pointes

An International Multicenter Evaluation of Type 5 Long QT Syndrome: A Low Penetrant Primary Arrhythmic Condition

An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing

Analysis for Genetic Modifiers of Disease Severity in Patients With Long-QT Syndrome Type 2

Atrial Arrhythmias in long-QT syndrome under daily life conditions: a nested case control study

Brugada Syndrome: Overview

Brugada syndrome: report of the second consensus conference.

Brugada syndrome: report of the second consensus conference: endorsed by the Heart Rhythm Society and the European Heart Rhythm Association.

Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death

Early repolarization pattern: a marker of increased risk in patients with catecholaminergic polymorphic ventricular tachycardia

Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls

First report on an inotropic peptide activating tetrodotoxin-sensitive, "neuronal" sodium currents in the heart

Genetic basis and molecular mechanism for idiopathic ventricular fibrillation

Genome wide analysis of drug-induced torsades de pointes: lack of common variants with large effect sizes

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).

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).

Ivabradine in patients with inappropriate sinus tachycardia

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

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