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Mutational spectrum in the cardiac transcription factor gene NKX2.5 (CSX) associated with congenital heart disease

Clinical genetics, 2010-12, Vol.78 (6), p.533-540

2010

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

Europace (London, England), 2009-10, Vol.11 (10), p.1338-1344

2009

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Diagnosis and treatment of cardiac amyloidosis: position statement of the German Cardiac Society (DGK)

Clinical research in cardiology, 2021-04, Vol.110 (4), p.479-506

2021

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Long-Term Prognosis of Patients Diagnosed With Brugada Syndrome: Results From the FINGER Brugada Syndrome Registry

Circulation (New York, N.Y.), 2010-02, Vol.121 (5), p.635-643

2010

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Pharmacological targeting in inherited arrhythmia syndromes

Current medicinal chemistry, 2014, Vol.21 (11), p.1308-1319

2014

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Biventricular myocardial strain analysis using cardiac magnetic resonance feature tracking (CMR-FT) in patients with distinct types of right ventricular diseases comparing arrhythmogenic right ventricular cardiomyopathy (ARVC), right ventricular outflow-tract tachycardia (RVOT-VT), and Brugada syndrome (BrS)

Clinical research in cardiology, 2019-10, Vol.108 (10), p.1147-1162

2019

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Brugada-like cardiac disease in myotonic dystrophy type 2: report of two unrelated patients

European journal of neurology, 2011-01, Vol.18 (1), p.191-194

2011

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Sudden unexpected cardiac death and postmortem identification of a novel RYR2 gene mutation

International journal of legal medicine, 2019-11, Vol.133 (6), p.1835-1838

2019

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Amiodarone and acetazolamide for the treatment of genetically confirmed severe Andersen syndrome

Neurology, 2002-08, Vol.59 (3), p.466-466

2002

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Polymorphisms in the cardiac sodium channel promoter displaying variant in vitro expression activity

European journal of human genetics : EJHG, 2008-03, Vol.16 (3), p.350-357

2008

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Molecular genetic diagnostics for ventricular arrhythmias and sudden cardiac death syndromes

Herz, 2017-08, Vol.42 (5), p.476-484

2017

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Long QT syndrome and life threatening arrhythmia in a newborn: molecular diagnosis and treatment response

British heart journal, 2004-01, Vol.90 (1), p.13-16

2004

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Komplett subkutaner Kardioverter-Defibrillator (S-ICD®): Aktuelle Erfahrungen und Ausblick

Herz, 2011-10, Vol.36 (7), p.586-591

2011

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Kardiogenetik in Deutschland – ein (Rück‑)Blick

Herzschrittmachertherapie & Elektrophysiologie, 2024-03, Vol.35 (Suppl 1), p.127-137

Schulze-Bahr, E.

2024

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QT interval prolongation and risk for cardiac events in genotyped LQTS-index children

European journal of pediatrics, 2009-09, Vol.168 (9), p.1107-1115

2009

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Brugada syndrome. Report of the second consensus conference. Endorsed by the Heart Rhythm Society and the European Heart Rhythm Association

Circulation (New York, N.Y.), 2005-02, Vol.111 (5), p.659-670

2005

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Electrophysiologic investigation in Brugada syndrome. Yield of programmed ventricular stimulation at two ventricular sites with up to three premature beats

European heart journal, 2002-09, Vol.23 (17), p.1394-1401

2002

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Arrhythmogenic right ventricular cardiomyopathy: An update on pathophysiology, genetics, diagnosis, and risk stratification

Herzschrittmachertherapie & Elektrophysiologie, 2012-09, Vol.23 (3), p.186-195

2012

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Genome-Wide Association Analysis Identifies 3 Common Variants Predisposing to Brugada Syndrome, a Rare Disease with High Risk of Sudden Cardiac Death

Heart rhythm, 2013-11, Vol.10 (11), p.1743-1744

2013

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Totally subcutaneous cardioverter-defibrillator (S-ICD®) : recent experience and future perspectives

Herz, 2011-10, Vol.36 (7), p.586-591

2011

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Effective long-term control of cardiac events with β-blockers in a family with a common LQT1 mutation

Clinical genetics, 2004-03, Vol.65 (3), p.233-241

2004

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Mutations in the desmosomal protein plakophilin-2 are common in arrhythmogenic right ventricular cardiomyopathy

Nature genetics, 2004-11, Vol.36 (11), p.1162-1164

2004

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The Jervell and Lange-Nielsen syndrome: natural history, molecular basis, and clinical outcome

Circulation (New York, N.Y.), 2006-02, Vol.113 (6), p.783-790

2006

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Cardiogenetics in Germany- a view and review

Herzschrittmachertherapie & Elektrophysiologie, 2024-03, Vol.35 (Suppl 1), p.127-137

Schulze-Bahr, E

2024

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Pacemaker channel dysfunction in a patient with sinus node disease

The Journal of clinical investigation, 2003-05, Vol.111 (10), p.1537-1545

2003

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Mutational spectrum in the cardiac transcription factor gene NKX2.5 (CSX) associated with congenital heart disease

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

Diagnosis and treatment of cardiac amyloidosis: position statement of the German Cardiac Society (DGK)

Long-Term Prognosis of Patients Diagnosed With Brugada Syndrome: Results From the FINGER Brugada Syndrome Registry

Pharmacological targeting in inherited arrhythmia syndromes

Brugada-like cardiac disease in myotonic dystrophy type 2: report of two unrelated patients

Sudden unexpected cardiac death and postmortem identification of a novel RYR2 gene mutation

Amiodarone and acetazolamide for the treatment of genetically confirmed severe Andersen syndrome

Polymorphisms in the cardiac sodium channel promoter displaying variant in vitro expression activity

Molecular genetic diagnostics for ventricular arrhythmias and sudden cardiac death syndromes

Long QT syndrome and life threatening arrhythmia in a newborn: molecular diagnosis and treatment response

Komplett subkutaner Kardioverter-Defibrillator (S-ICD®): Aktuelle Erfahrungen und Ausblick

Kardiogenetik in Deutschland – ein (Rück‑)Blick

QT interval prolongation and risk for cardiac events in genotyped LQTS-index children

Brugada syndrome. Report of the second consensus conference. Endorsed by the Heart Rhythm Society and the European Heart Rhythm Association

Electrophysiologic investigation in Brugada syndrome. Yield of programmed ventricular stimulation at two ventricular sites with up to three premature beats

Arrhythmogenic right ventricular cardiomyopathy: An update on pathophysiology, genetics, diagnosis, and risk stratification

Genome-Wide Association Analysis Identifies 3 Common Variants Predisposing to Brugada Syndrome, a Rare Disease with High Risk of Sudden Cardiac Death

Totally subcutaneous cardioverter-defibrillator (S-ICD®) : recent experience and future perspectives

Effective long-term control of cardiac events with β-blockers in a family with a common LQT1 mutation

Mutations in the desmosomal protein plakophilin-2 are common in arrhythmogenic right ventricular cardiomyopathy

The Jervell and Lange-Nielsen syndrome: natural history, molecular basis, and clinical outcome

Cardiogenetics in Germany- a view and review

Pacemaker channel dysfunction in a patient with sinus node disease

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