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List of works by Vincent Probst

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Role of electrophysiological studies in predicting risk of ventricular arrhythmia in early repolarization syndrome

scientific article published in January 2015
Fine-scale human genetic structure in Western France

scientific article published on 3 September 2014
The Brugada Syndrome: A Rare Arrhythmia Disorder with Complex Inheritance

scientific article
Prevalence and significance of rare RYR2 variants in arrhythmogenic right ventricular cardiomyopathy/dysplasia: Results of a systematic screening

article
Monomorphic ventricular tachycardia in patients with Brugada syndrome: A multicenter retrospective study.

scientific article published on 29 October 2015
Incidence and predictors of sudden death, major conduction defects and sustained ventricular tachyarrhythmias in 1388 patients with myotonic dystrophy type 1.

scientific article published in March 2017
Inherited progressive cardiac conduction disorders

scientific article
Biallelic PPA2 Mutations Cause Sudden Unexpected Cardiac Arrest in Infancy

scientific journal article
Monomorphic ventricular tachycardia due to Brugada syndrome successfully treated by hydroquinidine therapy in a 3-year-old child.

scientific article published in January 2006
New Family With Catecholaminergic Polymorphic Ventricular Tachycardia Linked to the Triadin Gene

scientific article
Benign vs. malignant inferolateral early repolarization: Focus on the T wave

scientific article published on 16 November 2015
Characteristics and long-term outcome of non-immune isolated atrioventricular block diagnosed in utero or early childhood: a multicentre study

scientific article published on 14 September 2011
Dysfunction of the Voltage-Gated K+ Channel β2 Subunit in a Familial Case of Brugada Syndrome

scientific article published on 10 June 2016
The psychological impact of implantable cardioverter defibrillator implantation on Brugada syndrome patients

scientific article published on March 21, 2011
Fever-Related Arrhythmic Events in the Multicenter Survey on Arrhythmic Events in Brugada Syndrome (SABRUS).

scientific article published on 9 April 2018
Complex Brugada syndrome inheritance in a family harbouring compound SCN5A and CACNA1C mutations

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

scientific article
Targeted resequencing identifies TRPM4 as a major gene predisposing to progressive familial heart block type I

article
New insights into mitral valve dystrophy: a Filamin-A genotype-phenotype and outcome study

scientific article
The QUIDAM study: Hydroquinidine therapy for the management of Brugada syndrome patients at high arrhythmic risk.

scientific article published on 11 April 2017
Differential calcium sensitivity in NaV 1.5 mixed syndrome mutants

scientific article published on 22 July 2017
Practical Instructions for the 2018 ESC Guidelines for the diagnosis and management of syncope

scientific article published on 01 June 2018
Parental electrocardiographic screening identifies a high degree of inheritance for congenital and childhood nonimmune isolated atrioventricular block

scientific article published on 16 August 2012
Gender differences in patients with Brugada syndrome and arrhythmic events: Data from a survey on arrhythmic events in 678 patients

scientific article published on 13 June 2018
Predictors for short-term progressive heart failure death in New York Heart Association II patients implanted with a cardioverter defibrillator—the EVADEF study

scientific article published on 01 April 2010
Progressive Atrial Conduction Defects Associated With Bone Malformation Caused by a Connexin-45 Mutation.

scientific article published in July 2017
Profile of Brugada Syndrome Patients Presenting with Their First Documented Arrhythmic Event. Data from the Survey on Arrhythmic Events in BRUgada Syndrome (SABRUS).

scientific article published on 8 January 2018
Ventricular fibrillation in loop recorder memories in a patient with early repolarization syndrome.

scientific article published on 15 August 2011
T-wave oversensing in patients with Brugada syndrome: true bipolar versus integrated bipolar implantable cardioverter defibrillator leads: multicenter retrospective study.

scientific article published on 3 June 2015
Cardiac Phenotype and Long-Term Follow-Up of Patients With Mutations in NKX2-5 Gene

scientific article published on 01 November 2016
Variants in the SCN5A Promoter Associated With Various Arrhythmia Phenotypes

scientific article published on 13 September 2016
Safety, feasibility, and outcome results of cardiac resynchronization with triple-site ventricular stimulation compared to conventional cardiac resynchronization.

scientific article
Circulating PCSK9 levels in acute coronary syndrome: Results from the PC-SCA-9 prospective study

scientific article published on 31 August 2017
Sodium-channel blocker challenge in the familial screening of Brugada syndrome: Safety and predictors of positivity.

scientific article
Electropharmacological characterization of cardiac repolarization in German shepherd dogs with an inherited syndrome of sudden death: abnormal response to potassium channel blockers

scientific article published on 01 September 2000
Lack of genotype-phenotype correlation in Brugada Syndrome and Sudden Arrhythmic Death Syndrome families with reported pathogenic SCN1B variants

scientific article published on 11 May 2018
Value of the sodium-channel blocker challenge in Brugada syndrome

scientific article published on 04 August 2017
Sodium channel blocker tests allow a clear distinction of electrophysiological characteristics and prognosis in patients with a type 2 or 3 Brugada electrocardiogram pattern.

scientific article published on 31 August 2008
Development and Validation of a New Scoring System to Predict Survival in Patients With Myotonic Dystrophy Type 1.

scientific article published on 5 February 2018
Quinidine therapy in children affected by Brugada syndrome: are we far from a safe alternative?

scientific article published on 9 September 2009
Risk of ventricular arrhythmia in patients with myocardial infarction and non-obstructive coronary arteries and normal ejection fraction

scientific article published on March 2017
Age of First Arrhythmic Event in Brugada Syndrome: Data From the SABRUS (Survey on Arrhythmic Events in Brugada Syndrome) in 678 Patients

scientific article published on 18 December 2017
Identification of a strong genetic background for progressive cardiac conduction defect by epidemiological approach

scientific article published on 19 June 2012
An African loss-of-function CACNA1C variant p.T1787M associated with a risk of ventricular fibrillation

scientific article published in Scientific Reports
Erratum: KLHL3 mutations cause familial hyperkalemic hypertension by impairing ion transport in the distal nephron

article
Heart rate variability and repolarization characteristics in symptomatic and asymptomatic Brugada syndrome.

scientific article published on 13 October 2016
Ethnic differences in patients with Brugada syndrome and arrhythmic events: New insights from Survey on Arrhythmic Events in Brugada Syndrome

scientific article published on 05 July 2019
Incomplete Timothy syndrome secondary to a mosaic mutation of the CACNA1C gene diagnosed using next-generation sequencing

article
Characterization and Management of Arrhythmic Events in Young Patients With Brugada Syndrome

scientific article published on 01 April 2019
Early Repolarization Disease

scientific article

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