Lista de obras -

A novel mutation in lamin a/c causing familial dilated cardiomyopathy associated with sudden cardiac death

artículo científico publicado en 2014

Analysis of mRNA from human heart tissue and putative applications in forensic molecular pathology.

artículo científico publicado en 2010

Analysis of the arrhythmogenic substrate in human heart failure

artículo científico publicado en 2012

Brugada syndrome and p.E61X_RANGRF.

artículo científico publicado en 2013

Clinical and molecular characterization of a cardiac ryanodine receptor founder mutation causing catecholaminergic polymorphic ventricular tachycardia

artículo científico publicado en 2015

Comprehensive Genetic Characterization of a Spanish Brugada Syndrome Cohort

artículo científico publicado en 2015

Conduction abnormalities in the right ventricular outflow tract in Brugada syndrome detected body surface potential mapping

scientific article published on 01 January 2010

Gender differences in clinical manifestations of Brugada syndrome.

artículo científico publicado en 2008

Genetic analysis, in silico prediction, and family segregation in long QT syndrome

artículo científico publicado en 2014

Genetics of arrhythmogenic right ventricular cardiomyopathy.

artículo científico

Integration of "Omics" Strategies for Biomarkers Discovery and for the Elucidation of Molecular Mechanisms Underlying Brugada Syndrome

scientific article published on 20 July 2018

Patients With Brugada Syndrome and Implanted Cardioverter-Defibrillators: Long-Term Follow-Up.

artículo científico publicado en 2017

Role of novel DSP_p.Q986X genetic variation in arrhythmogenic right ventricular cardiomyopathy

artículo científico publicado en 2013

Sinus rhythm detection of conducting channels and ventricular tachycardia isthmus in arrhythmogenic right ventricular cardiomyopathy

artículo científico publicado en 2014

Spatiotemporal Characteristics of QRS Complexes Enable the Diagnosis of Brugada Syndrome Regardless of the Appearance of a Type 1 ECG.

artículo científico publicado en 2016

Stop-gain mutations in PKP2 are associated with a later age of onset of arrhythmogenic right ventricular cardiomyopathy

artículo científico publicado en 2014

Lista de obras de

A novel mutation in lamin a/c causing familial dilated cardiomyopathy associated with sudden cardiac death

Analysis of mRNA from human heart tissue and putative applications in forensic molecular pathology.

Analysis of the arrhythmogenic substrate in human heart failure

Brugada syndrome and p.E61X_RANGRF.

Clinical and molecular characterization of a cardiac ryanodine receptor founder mutation causing catecholaminergic polymorphic ventricular tachycardia

Comprehensive Genetic Characterization of a Spanish Brugada Syndrome Cohort

Conduction abnormalities in the right ventricular outflow tract in Brugada syndrome detected body surface potential mapping

Gender differences in clinical manifestations of Brugada syndrome.

Genetic analysis, in silico prediction, and family segregation in long QT syndrome

Genetics of arrhythmogenic right ventricular cardiomyopathy.

Integration of "Omics" Strategies for Biomarkers Discovery and for the Elucidation of Molecular Mechanisms Underlying Brugada Syndrome

Patients With Brugada Syndrome and Implanted Cardioverter-Defibrillators: Long-Term Follow-Up.

Role of novel DSP_p.Q986X genetic variation in arrhythmogenic right ventricular cardiomyopathy

Sinus rhythm detection of conducting channels and ventricular tachycardia isthmus in arrhythmogenic right ventricular cardiomyopathy

Spatiotemporal Characteristics of QRS Complexes Enable the Diagnosis of Brugada Syndrome Regardless of the Appearance of a Type 1 ECG.

Stop-gain mutations in PKP2 are associated with a later age of onset of arrhythmogenic right ventricular cardiomyopathy