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Mutations in SCN10A Are Responsible for a Large Fraction of Cases of Brugada Syndrome

Journal of the American College of Cardiology, 2014-07, Vol.64 (1), p.66-79

2014

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Long-Term Follow-Up of Patients With Short QT Syndrome

Journal of the American College of Cardiology, 2011-08, Vol.58 (6), p.587-595

2011

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Genetik bei Vorhofflimmern und malignen Arrhythmiesyndromen

Herzschrittmachertherapie & Elektrophysiologie, 2024-03, Vol.35 (1), p.1-2

2024

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Genetics in atrial fibrillation and malignant arrhythmia syndromes

Herzschrittmachertherapie & Elektrophysiologie, 2024-03, Vol.35 (1), p.1-2

2024

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Loss-of-function mutations in the cardiac calcium channel underlie a new clinical entity characterized by ST-segment elevation, short QT intervals, and sudden cardiac death

Circulation (New York, N.Y.), 2007-01, Vol.115 (4), p.442-449

2007

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24-jähriger Patient mit erfolgreicher Wiederbelebung bei Kammerflimmern unklarer Genese

Herzschrittmachertherapie & Elektrophysiologie, 2021-12, Vol.32 (4), p.479-483

2021

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Subcutaneous implantable cardioverter-defibrillator: First single-center experience with other cardiac implantable electronic devices

Heart rhythm, 2015-11, Vol.12 (11), p.2230-2238

2015

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Autonome Innervation des Herzens

Herzschrittmachertherapie & Elektrophysiologie, 2021-09, Vol.32 (3), p.293-294

2021

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24-year-old man with successful resuscitation due to ventricular fibrillation without evident cause

Herzschrittmachertherapie & Elektrophysiologie, 2021-12, Vol.32 (4), p.479-483

2021

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Early repolarization pattern is associated with ventricular fibrillation in patients with acute myocardial infarction

Heart rhythm, 2012-08, Vol.9 (8), p.1295-1300

2012

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Long-Term Follow-Up of Patients With Short QT Syndrome: Clinical Profile and Outcome

Journal of the American Heart Association, 2018-12, Vol.7 (23), p.e010073-e010073

2018

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Impact of Antiarrhythmic Drugs on the Outcome of Short QT Syndrome

Frontiers in pharmacology, 2019-08, Vol.10, p.771-771

2019

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Autonomic innervation of the heart

Herzschrittmachertherapie & Elektrophysiologie, 2021-09, Vol.32 (3), p.293-294

2021

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Further Insights in the Most Common SCN5A Mutation Causing Overlapping Phenotype of Long QT Syndrome, Brugada Syndrome, and Conduction Defect

Journal of the American Heart Association, 2016-07, Vol.5 (7), p.n/a

2016

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A novel rare variant in SCN1Bb linked to Brugada syndrome and SIDS by combined modulation of Na(v)1.5 and K(v)4.3 channel currents

Heart rhythm, 2012-05, Vol.9 (5), p.760-769

2012

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Differences in Short QT Syndrome Subtypes: A Systematic Literature Review and Pooled Analysis

Frontiers in genetics, 2020-01, Vol.10, p.1312

2020

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Short QT Syndrome - Review of Diagnosis and Treatment

Arrhythmia & electrophysiology review, 2014-08, Vol.3 (2), p.76-79

2014

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Clinical and molecular genetics of the short QT syndrome

Current opinion in cardiology, 2008-05, Vol.23 (3), p.192-198

2008

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Usefulness of Short-Term Variability of QT Intervals as a Predictor for Electrical Remodeling and Proarrhythmia in Patients With Nonischemic Heart Failure

The American journal of cardiology, 2010-07, Vol.106 (2), p.216-220

2010

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Reduction of Dispersion of Repolarization and Prolongation of Postrepolarization Refractoriness Explain the Antiarrhythmic Effects of Quinidine in a Model of Short QT Syndrome

Journal of cardiovascular electrophysiology, 2007-06, Vol.18 (6), p.658-664

2007

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Drug-induced QT-interval shortening following antiepileptic treatment with oral rufinamide

Heart rhythm, 2012-05, Vol.9 (5), p.776-781

2012

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Fatal Inappropriate ICD Shock

Journal of cardiovascular electrophysiology, 2007-03, Vol.18 (3), p.326-328

2007

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PQ segment depression in patients with short QT syndrome: A novel marker for diagnosing short QT syndrome?

Heart rhythm, 2014-06, Vol.11 (6), p.1024-1030

2014

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Mutations in SCN10A Are Responsible for a Large Fraction of Cases of Brugada Syndrome

Long-Term Follow-Up of Patients With Short QT Syndrome

Genetik bei Vorhofflimmern und malignen Arrhythmiesyndromen

Genetics in atrial fibrillation and malignant arrhythmia syndromes

Loss-of-function mutations in the cardiac calcium channel underlie a new clinical entity characterized by ST-segment elevation, short QT intervals, and sudden cardiac death

Mutations in the cardiac L-type calcium channel associated with inherited J-wave syndromes and sudden cardiac death

24-jähriger Patient mit erfolgreicher Wiederbelebung bei Kammerflimmern unklarer Genese

Subcutaneous implantable cardioverter-defibrillator: First single-center experience with other cardiac implantable electronic devices

Autonome Innervation des Herzens

Molecular genetic and functional association of Brugada and early repolarization syndromes with S422L missense mutation in KCNJ8

24-year-old man with successful resuscitation due to ventricular fibrillation without evident cause

Early repolarization pattern is associated with ventricular fibrillation in patients with acute myocardial infarction

Long-Term Follow-Up of Patients With Short QT Syndrome: Clinical Profile and Outcome

Impact of Antiarrhythmic Drugs on the Outcome of Short QT Syndrome

Autonomic innervation of the heart

Further Insights in the Most Common SCN5A Mutation Causing Overlapping Phenotype of Long QT Syndrome, Brugada Syndrome, and Conduction Defect

A novel rare variant in SCN1Bb linked to Brugada syndrome and SIDS by combined modulation of Na(v)1.5 and K(v)4.3 channel currents

Differences in Short QT Syndrome Subtypes: A Systematic Literature Review and Pooled Analysis

Short QT Syndrome - Review of Diagnosis and Treatment

Clinical and molecular genetics of the short QT syndrome

Usefulness of Short-Term Variability of QT Intervals as a Predictor for Electrical Remodeling and Proarrhythmia in Patients With Nonischemic Heart Failure

Reduction of Dispersion of Repolarization and Prolongation of Postrepolarization Refractoriness Explain the Antiarrhythmic Effects of Quinidine in a Model of Short QT Syndrome

Drug-induced QT-interval shortening following antiepileptic treatment with oral rufinamide

Fatal Inappropriate ICD Shock

PQ segment depression in patients with short QT syndrome: A novel marker for diagnosing short QT syndrome?

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