Buscador de publicaciones

Publicaciones

  • Mates J, Mademont-Soler I, Fernandez-Falgueras A, Sarquella-Brugada G, César-Díaz S, Arbelo E, García-Álvarez A, Jordà P, Toro R, Coll M, Fiol JV, Iglesias A, Perez-Serra A, Olmo BD, Alcalde M, Puigmulé M, Pico F, Lopez L, Ferrer C, Tiron C, Grassi S, Oliva A, Brugada-Terradellas J, Brugada R and Campuzano O.

    Sudden Cardiac Death and Copy Number Variants: What Do We Know after 10 Years of Genetic Analysis?

    FORENSIC SCIENCE INTERNATIONAL-GENETICS . 47: 102281-102281. Nº de citas: 20

    [doi:10.1016/j.fsigen.2020.102281]

  • Salazar-Mendiguchía J, Díez-López C, Claver E, César-Díaz S, Campuzano O, Sarquella-Brugada G and Monserrat L.

    Familial evaluation reveals a distinct genetic cause in a large Spanish family with neurofibromatosis 1 and hypertrophic cardiomyopathy

    Gene . 746: 144658-144658. Nº de citas: 2

    [doi:10.1016/j.gene.2020.144658]

  • Brugada-Terradellas J, Katritsis, DG, Arbelo, E, Arribas, F, Bax, JJ, Blomstrom-Lundqvist, C, Calkins, H, Corrado, D, Deftereos, SG, Diller, GP, Gomez-Doblas, JJ, Gorenek, B, Grace, A, Ho, SY, Kaski, JC, Karl-Heinz, K, Lambiase, PD, Sacher, F, Sarquella-Brugada G, Suwalski, P and Zaza, A.

    2019 ESC Guidelines on the Treatment of Patients With Supraventricular Tachycardia

    REVISTA ESPANOLA DE CARDIOLOGIA . 73(6): .

    [doi:10.1016/j.recesp.2019.12.029]

  • Campuzano O, Sarquella-Brugada G, Arbelo E, César-Díaz S, Jordà P, Pérez-Serra A, Toro R, Brugada-Terradellas J and Brugada R.

    Genetic Variants as Sudden-Death Risk Markers in Inherited Arrhythmogenic Syndromes: Personalized Genetic Interpretation

    Journal of Clinical Medicine . 9(6): . Nº de citas: 5

    [doi:10.3390/jcm9061866]

  • Mazzanti A, Guz D, Trancuccio A, Pagan E, Kukavica D, Chargeishvili T, Olivetti N, Biernacka EK, Sacilotto L, Sarquella-Brugada G, Campuzano O, Nof E, Anastasakis A, Sansone VA, Jimenez-Jaimez J, Cruz F, Sánchez-Quiñones J, Hernandez-Afonso J, Fuentes ME, Sredniawa B, Garoufi A, Andršová I, Izquierdo M, Marinov R, Danon A, Expósito-García V, Garcia-Fernandez A, Muñoz-Esparza C, Ortíz M, Zienciuk-Krajka A, Tavazzani E, Monteforte N, Bloise R, Marino M, Memmi M, Napolitano C, Zorio E, Monserrat L, Bagnardi V and Priori SG.

    Natural History and Risk Stratification in Andersen-Tawil Syndrome Type 1

    JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY . 75(15): 1772-1784. Nº de citas: 33

    [doi:10.1016/j.jacc.2020.02.033]

  • Campuzano O, Sarquella-Brugada G, Fernandez-Falgueras A, Coll M, Iglesias A, Ferrer-Costa C, César-Díaz S, Arbelo E, García-Álvarez A, Jordà P, Toro R, Tiron de Llano C, Grassi S, Oliva A, Brugada J and Brugada R.

    Reanalysis and reclassification of rare genetic variants associated with inherited arrhythmogenic syndromes

    EBioMedicine . 54: 102732-102732. Nº de citas: 41

    [doi:10.1016/j.ebiom.2020.102732]

  • Mingirulli N, Pyle A, Hathazi D, Alston CL, Kohlschmidt N, O'Grady G, Leigh W, Evesson F, Cooper SBT, Turner C, Duff J, Topf A, Yubero-Siles D, Jou-Munoz C, Nascimento-Osorio A, Ortez-Gonzalez CI, Garcia-Cazorla A, Gross C, O'Callaghan-Gordo M, Santra S, Preece MA, Champion M, Korenev S, Chronopoulou E, Anirban M, Pierre G, McArthur D, Thompson K, Navas P, Ribes A, Tort F, Schlüter A, Pujol A, Montero-Sanchez R, Sarquella-Brugada G, Lochmüller H, Jimenez-Mallebrera C, Taylor RW, Artuch-Iriberri R, Kirschner J, Grünert SC, Roos A and Horvath R.

    Clinical presentation and proteomic signature of patients with TANGO2 mutations

    JOURNAL OF INHERITED METABOLIC DISEASE . 43(2): 297-308. Nº de citas: 32

    [doi:10.1002/jimd.12156]

  • Brugada-Terradellas J, Katritsis, DG, Arbelo, E, Arribas, F, Bax, JJ, Blomstrom-Lundqvist, C, Calkins, H, Corrado, D, Deftereos, SG, Diller, GP, Gomez-Doblas, JJ, Gorenek, B, Grace, A, Ho, SY, Kaski, JC, Kuck, KH, Lambiase, PD, Sacher, F, Sarquella-Brugada G, Suwalski, P and Zaza, A.

    2019 ESC Guidelines for the management of patients with supraventricular tachycardia The Task Force for the management of patients with supraventricular tachycardia of the European Society of Cardiology (ESC): Developed in collaboration with the Association for European Paediatric and Congenital Cardiology (AEPC)

    EUROPEAN HEART JOURNAL . 41(5): 655-720. Nº de citas: 520

    [doi:10.1093/eurheartj/ehz467]

  • Hernandez-Ojeda J, Arbelo E, Jorda P, Borras R, Campuzano O, Sarquella-Brugada G, Iglesias A, Mont L, Brugada R and Brugada-Terradellas J.

    The role of clinical assessment and electrophysiology study in Brugada syndrome patients with syncope

    AMERICAN HEART JOURNAL . 220: 213-223. Nº de citas: 9

    [doi:10.1016/j.ahj.2019.10.016]

  • Pérez-Lescure Picarzo J, Centeno Malfaz F, Collell Hernández R, Crespo Marcos D, Fernández Soria T, Manso García B, Rojo Sombrero H, Sabaté Rotés A and Sarquella-Brugada G.

    Recommendations of the Spanish Society of Paediatric Cardiology and Congenital Heart Disease as regards the use of drugs in attention deficit hyperactivity disorder in children and adolescents with a known heart disease, as well as in the general paediatric population: Position statement by the Spanish Paediatric Association

    ANALES DE PEDIATRIA . 92(2): . Nº de citas: 2

    [doi:10.1016/j.anpedi.2019.09.002]