Gudrun Pappaert

In vivo mapping of human polymorphic ventricular tachycardia.

Journal: Journal of interventional cardiac electrophysiology : an international journal of arrhythmias and pacing

Published: June 09, 2025

Genetic variants associated with ventricular arrhythmias during ajmaline test in Brugada syndrome.

Journal: Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology

Published: March 03, 2025

In Vivo Mapping of Human Ventricular Fibrillation in Brugada Syndrome: The Role of Repolarization Heterogeneity.

Journal: Circulation. Arrhythmia and electrophysiology

Published: December 03, 2024

Implantable Cardioverter-Defibrillator Therapy in Brugada Syndrome: A 30-Year Single-Center Experience.

Journal: JACC. Clinical electrophysiology

Published: October 22, 2024

Assessment of activation delay in the right ventricular outflow tract as a potential complementary diagnostic tool for Brugada Syndrome.

Journal: Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology

Published: October 09, 2024

Predicting and Recognizing Drug-Induced Type I Brugada Pattern Using ECG-Based Deep Learning.

Journal: Journal of the American Heart Association

Published: May 10, 2024

Genetic Testing in Brugada Syndrome: A 30-Year Experience.

Journal: Circulation. Arrhythmia and electrophysiology

Published: March 01, 2024

Correlations of ventricular fibrillation and monomorphic ventricular tachycardia with SCN5A mutations and other clinical variables in Brugada syndrome.

Journal: Heart rhythm

Published: February 17, 2024

In vivo mapping of human polymorphic ventricular tachycardia.

In vivo mapping of human polymorphic ventricular tachycardia.

Genetic variants associated with ventricular arrhythmias during ajmaline test in Brugada syndrome.

Genetic variants associated with ventricular arrhythmias during ajmaline test in Brugada syndrome.

In Vivo Mapping of Human Ventricular Fibrillation in Brugada Syndrome: The Role of Repolarization Heterogeneity.

In Vivo Mapping of Human Ventricular Fibrillation in Brugada Syndrome: The Role of Repolarization Heterogeneity.

Implantable Cardioverter-Defibrillator Therapy in Brugada Syndrome: A 30-Year Single-Center Experience.

Implantable Cardioverter-Defibrillator Therapy in Brugada Syndrome: A 30-Year Single-Center Experience.

Assessment of activation delay in the right ventricular outflow tract as a potential complementary diagnostic tool for Brugada Syndrome.

Assessment of activation delay in the right ventricular outflow tract as a potential complementary diagnostic tool for Brugada Syndrome.

Predicting and Recognizing Drug-Induced Type I Brugada Pattern Using ECG-Based Deep Learning.

Predicting and Recognizing Drug-Induced Type I Brugada Pattern Using ECG-Based Deep Learning.

Genetic Testing in Brugada Syndrome: A 30-Year Experience.

Genetic Testing in Brugada Syndrome: A 30-Year Experience.

Correlations of ventricular fibrillation and monomorphic ventricular tachycardia with SCN5A mutations and other clinical variables in Brugada syndrome.

Correlations of ventricular fibrillation and monomorphic ventricular tachycardia with SCN5A mutations and other clinical variables in Brugada syndrome.

Patient-reported outcome measures on mental health and psychosocial factors in patients with Brugada syndrome.

Patient-reported outcome measures on mental health and psychosocial factors in patients with Brugada syndrome.

Atrial Abnormalities in Brugada Syndrome: Evaluation With ECG Imaging.

Atrial Abnormalities in Brugada Syndrome: Evaluation With ECG Imaging.

Genetic testing in children with Brugada syndrome: results from a large prospective registry.

Genetic testing in children with Brugada syndrome: results from a large prospective registry.

Case report: Coexistence of myotonia congenita and Brugada syndrome in one family.

Case report: Coexistence of myotonia congenita and Brugada syndrome in one family.