Publicacións nas que colabora con Catarina Allegue Toscano (15)

2022

  1. Identification of Sodium Transients Through NaV1.5 Channels as Regulators of Differentiation in Immortalized Dorsal Root Ganglia Neurons

    Frontiers in Cellular Neuroscience, Vol. 16

2021

  1. Identification of Novel Regulators of Zalcitabine-Induced Neuropathic Pain

    ACS Chemical Neuroscience, Vol. 12, Núm. 14, pp. 2619-2628

2020

  1. Experimental models to study autism spectrum disorders: Hipscs, rodents and zebrafish

    Genes, Vol. 11, Núm. 11, pp. 1-45

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

2014

  1. Sequenom MassARRAY approach in the arrhythmogenic right ventricular cardiomyopathy post-mortem setting: clinical and forensic implications

    International Journal of Legal Medicine, Vol. 129, Núm. 1

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. Estudio genético de la muerte súbita cardíaca: miocardiopatía hipertrófica familiar y síndrome de QT largo

    Estudio genético de la muerte súbita cardíaca: miocardiopatía hipertrófica familiar y síndrome de QT largo

  3. 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

  4. 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