Publicacións nas que colabora con María José Brión Martínez (10)

2015

  1. Genetic analysis of arrhythmogenic diseases in the era of NGS: The complexity of clinical decision-making in Brugada Syndrome

    PLoS ONE, Vol. 10, Núm. 7

2012

  1. Sarcomeric gene mutations in sudden infant death syndrome (SIDS)

    Forensic Science International, Vol. 219, Núm. 1-3, pp. 278-281

2011

  1. Prevalence of HCM and long QT syndrome mutations in young sudden cardiac death-related cases

    International Journal of Legal Medicine, Vol. 125, Núm. 4, pp. 565-572

2010

  1. A new approach to long QT syndrome mutation detection by Sequenom MassARRAY® system

    Electrophoresis, Vol. 31, Núm. 10, pp. 1648-1655

  2. Identification of a novel MYBPC3 gene variant in a patient with hypertrophic cardiomyopathy

    Annals of Clinical and Laboratory Science, Vol. 40, Núm. 3, pp. 285-289

  3. New technologies in the genetic approach to sudden cardiac death in the young

    Forensic Science International, Vol. 203, Núm. 1-3, pp. 15-24

2009

  1. Involvement of hypertrophic cardiomyopathy genes in sudden infant death syndrome (SIDS)

    Forensic Science International: Genetics Supplement Series, Vol. 2, Núm. 1, pp. 495-496

  2. Sequenom MassArray™ application in the long QT syndrome mutation detection

    Forensic Science International: Genetics Supplement Series, Vol. 2, Núm. 1, pp. 497-498

2008

  1. Large scale analysis of HCM mutations in sudden cardiac death

    Forensic Science International: Genetics Supplement Series, Vol. 1, Núm. 1, pp. 549-550

  2. Molecular genetics of sudden cardiac death

    Forensic Science International, Vol. 182, Núm. 1-3, pp. 1-12