List of works - Vincent Probst

SCN5A mutations in 442 neonates and children: genotype-phenotype correlation and identification of higher-risk subgroups

scientific article published in August 2018

Reply to the Editor-Brugada syndrome is not an ECG.

scientific article

Cosegregation of the Marfan syndrome and the long QT syndrome in the same family leads to a severe cardiac phenotype

scientific article published on 01 March 2003

From gene-discovery to gene-tailored clinical management: 25 years of research in channelopathies and cardiomyopathies

Insufficiency of electrocardiogram alone in predicting infrahisian abnormalities in patients with type 1 myotonic dystrophy

scientific article published on 11 February 2014

Idiopathic Ventricular Fibrillation: Role of Purkinje System and Microstructural Myocardial Abnormalities

scientific article published on 01 June 2020

Cadherin 2-Related Arrhythmogenic Cardiomyopathy

Sodium channel blocker challenge in Brugada syndrome: Role in risk stratification

scientific article published on 01 August 2018

Reply to the Editor--PQ-segment depression in short QT syndrome patients: a novel marker for diagnosing short QT syndrome?

scientific article

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

scientific article published on 7 September 2020

Cardiac remote monitoring in France.

scientific article published on 04 April 2014

aTrial arrhythmias in inhEriTed aRrhythmIa Syndromes: results from the TETRIS study

Brugada syndrome: Keep an eye on the electrocardiogram

scientific article published on 07 July 2018

A consistent arrhythmogenic trait in Brugada syndrome cellular phenotype

scientific article published on 07 June 2021

Characteristics of Patients with Spontaneous Versus Drug-Induced Brugada Electrocardiogram: Sub-Analysis From the SABRUS

scientific article published in January 2023

Correlation of intracardiac electrogram with surface electrocardiogram in Brugada syndrome patients

scientific article published on 25 September 2013

Brugada syndrome: where are you?

scientific article published in October 2009

SCN1Bb, atrial fibrillation, and Brugada syndrome: just another brick in the wall …

scientific article published on 30 December 2011

Age at diagnosis of Brugada syndrome: Influence on clinical characteristics and risk of arrhythmia

scientific article published on 29 November 2019

Ajmaline challenge: to stop or not to stop...

scientific article published on 11 March 2009

Familial Catecholamine-Induced QT Prolongation in Unexplained Sudden Cardiac Death.

scientific article

Time-to-first appropriate shock in patients implanted prophylactically with an implantable cardioverter-defibrillator: data from the Survey on Arrhythmic Events in BRUgada Syndrome (SABRUS)

scientific article published on 01 May 2019

163 Genetic Modifiers in Carriers of the SCN5A E1784K Mutation with Variable Phenotypic Expression - Long QT3 / Brugada Syndrome Overlap Disease

scientific article published on 31 May 2014

Response to the Letter by Kattygnarath et al

SCN5A Mutation Type and a Genetic Risk Score Associate Variably with Brugada Syndrome Phenotype in SCN5A Families

scientific article published on 09 November 2020

List of works by Vincent Probst

SCN5A mutations in 442 neonates and children: genotype-phenotype correlation and identification of higher-risk subgroups

Reply to the Editor-Brugada syndrome is not an ECG.

Cosegregation of the Marfan syndrome and the long QT syndrome in the same family leads to a severe cardiac phenotype

From gene-discovery to gene-tailored clinical management: 25 years of research in channelopathies and cardiomyopathies

Insufficiency of electrocardiogram alone in predicting infrahisian abnormalities in patients with type 1 myotonic dystrophy

Idiopathic Ventricular Fibrillation: Role of Purkinje System and Microstructural Myocardial Abnormalities

Cadherin 2-Related Arrhythmogenic Cardiomyopathy

Sodium channel blocker challenge in Brugada syndrome: Role in risk stratification

Reply to the Editor--PQ-segment depression in short QT syndrome patients: a novel marker for diagnosing short QT syndrome?

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

Cardiac remote monitoring in France.

aTrial arrhythmias in inhEriTed aRrhythmIa Syndromes: results from the TETRIS study

Brugada syndrome: Keep an eye on the electrocardiogram

A consistent arrhythmogenic trait in Brugada syndrome cellular phenotype

Characteristics of Patients with Spontaneous Versus Drug-Induced Brugada Electrocardiogram: Sub-Analysis From the SABRUS

Correlation of intracardiac electrogram with surface electrocardiogram in Brugada syndrome patients

Brugada syndrome: where are you?

SCN1Bb, atrial fibrillation, and Brugada syndrome: just another brick in the wall …

Age at diagnosis of Brugada syndrome: Influence on clinical characteristics and risk of arrhythmia

Ajmaline challenge: to stop or not to stop...

Familial Catecholamine-Induced QT Prolongation in Unexplained Sudden Cardiac Death.

Time-to-first appropriate shock in patients implanted prophylactically with an implantable cardioverter-defibrillator: data from the Survey on Arrhythmic Events in BRUgada Syndrome (SABRUS)

163 Genetic Modifiers in Carriers of the SCN5A E1784K Mutation with Variable Phenotypic Expression - Long QT3 / Brugada Syndrome Overlap Disease

Response to the Letter by Kattygnarath et al

SCN5A Mutation Type and a Genetic Risk Score Associate Variably with Brugada Syndrome Phenotype in SCN5A Families