Lista de obras -

Clinical and ECG variables to predict the outcome of genetic testing in hypertrophic cardiomyopathy

artículo científico publicado en 2019

Clinical characterization of the first Belgian SCN5A founder mutation cohort

artículo científico publicado en 2020

Combining noninvasive risk stratification parameters improves the prediction of mortality and appropriate ICD shocks

scientific article published on 28 September 2018

Evaluation of Index of Cardio-Electrophysiological Balance (iCEB) as a New Biomarker for the Identification of Patients at Increased Arrhythmic Risk.

artículo científico publicado en 2015

Genotype-phenotype relationship and risk stratification in loss-of-function SCN5A mutation carriers

scientific article published on 30 April 2018

Heart Rate Recovery After Exercise Is Associated With Arrhythmic Events in Patients With Catecholaminergic Polymorphic Ventricular Tachycardia

artículo científico publicado en 2020

Implantable cardioverter-defibrillators in previously undiagnosed patients with catecholaminergic polymorphic ventricular tachycardia resuscitated from sudden cardiac arrest

scientific article published on 1 September 2019

Improving long QT syndrome diagnosis by a polynomial-based T-wave morphology characterization

artículo científico publicado en 2020

Individualized corrected QT interval is superior to QT interval corrected using the Bazett formula in predicting mutation carriage in families with long QT syndrome.

artículo científico publicado en 2017

Inferior and anterior QRS fragmentation have different prognostic value in patients who received an implantable defibrillator in primary prevention of sudden cardiac death.

artículo científico publicado en 2017

Inter- and intra-observer variability of visual fragmented QRS scoring in ischemic and non-ischemic cardiomyopathy

artículo científico publicado en 2017

Prognostic value of electrocardiographic time intervals and QT rate dependence in hypertrophic cardiomyopathy

scientific article published on 12 September 2018

QT correction across the heart rate spectrum, in atrial fibrillation and ventricular conduction defects

scientific article published on 12 July 2018

Reduced Penetrance and Variable Expression of SCN5A Mutations and the Importance of Co-inherited Genetic Variants: Case Report and Review of the Literature.

artículo científico publicado en 2014

Repeat genetic testing with targeted capture sequencing in primary arrhythmia syndrome and cardiomyopathy

artículo científico publicado en 2017

Response of Robyns to the Tse's letter to editor.

artículo científico publicado en 2017

Targeted capture sequencing in a large LQTS family reveals a new pathogenic mutation c.2038delG in KCNH2 initially missed due to allelic dropout.

artículo científico publicado en 2015

The impact of changes in LVEF and renal function on the prognosis of ICD patients after elective device replacement

artículo científico

Which QT Correction Formulae to Use for QT Monitoring?

artículo científico publicado en 2016

Whole exome sequencing in a large pedigree with DCM identifies a novel mutation in RBM20

scientific article published on 04 October 2019

Lista de obras de

Clinical and ECG variables to predict the outcome of genetic testing in hypertrophic cardiomyopathy

Clinical characterization of the first Belgian SCN5A founder mutation cohort

Combining noninvasive risk stratification parameters improves the prediction of mortality and appropriate ICD shocks

Evaluation of Index of Cardio-Electrophysiological Balance (iCEB) as a New Biomarker for the Identification of Patients at Increased Arrhythmic Risk.

Genotype-phenotype relationship and risk stratification in loss-of-function SCN5A mutation carriers

Heart Rate Recovery After Exercise Is Associated With Arrhythmic Events in Patients With Catecholaminergic Polymorphic Ventricular Tachycardia

Implantable cardioverter-defibrillators in previously undiagnosed patients with catecholaminergic polymorphic ventricular tachycardia resuscitated from sudden cardiac arrest

Improving long QT syndrome diagnosis by a polynomial-based T-wave morphology characterization

Individualized corrected QT interval is superior to QT interval corrected using the Bazett formula in predicting mutation carriage in families with long QT syndrome.

Inferior and anterior QRS fragmentation have different prognostic value in patients who received an implantable defibrillator in primary prevention of sudden cardiac death.

Inter- and intra-observer variability of visual fragmented QRS scoring in ischemic and non-ischemic cardiomyopathy

Prognostic value of electrocardiographic time intervals and QT rate dependence in hypertrophic cardiomyopathy

QT correction across the heart rate spectrum, in atrial fibrillation and ventricular conduction defects

Reduced Penetrance and Variable Expression of SCN5A Mutations and the Importance of Co-inherited Genetic Variants: Case Report and Review of the Literature.

Repeat genetic testing with targeted capture sequencing in primary arrhythmia syndrome and cardiomyopathy

Response of Robyns to the Tse's letter to editor.

Targeted capture sequencing in a large LQTS family reveals a new pathogenic mutation c.2038delG in KCNH2 initially missed due to allelic dropout.

The impact of changes in LVEF and renal function on the prognosis of ICD patients after elective device replacement

Which QT Correction Formulae to Use for QT Monitoring?

Whole exome sequencing in a large pedigree with DCM identifies a novel mutation in RBM20