Personas / Equipo Humano

Georgia Sarquella Brugada

Buscador de publicaciones

Publicaciones

  • Sarquella-Brugada G, Campuzano O, Iglesias A, Grueso J, Bradley DJ, Kerst G, Shmorhun D, Brugada-Terradellas J and Brugada R.

    Short QT and atrial fibrillation: A KCNQ1 mutation-specific disease. Late follow-up in three unrelated children

    Heart Rhythm . 1(4): 193-197.

  • Alcalde M, Campuzano O, Sarquella-Brugada G, Arbelo E, Allegue C, Partemi S, Iglesias A, Oliva A, Brugada-Terradellas J and Brugada R.

    Clinical interpretation of genetic variants in arrhythmogenic right ventricular cardiomyopathy

    CLINICAL RESEARCH IN CARDIOLOGY . 104(4): 288-303. Nº de citas: 15

    [doi:10.1007/s00392-014-0794-z]

  • Pérez-Serra A, Toro R, Campuzano O, Sarquella-Brugada G, Berne P, Iglesias A, Mangas A, Brugada-Terradellas J and Brugada R.

    A Novel Mutation in Lamin A/C Causing Familial Dilated Cardiomyopathy Associated With Sudden Cardiac Death

    JOURNAL OF CARDIAC FAILURE . 21(3): 217-225. Nº de citas: 19

    [doi:10.1016/j.cardfail.2014.12.003]

  • Sarquella-Brugada G, Rodríguez-Fanjul J, Camprubí-Camprubí M, Arango Posada CA, Moreno-Hernando J and Prada F.

    Aortic thrombosis successfully treated with local recombinant tissue plasminogen activator in a newborn

    JOURNAL OF THROMBOSIS AND THROMBOLYSIS . 39(2): 251-253. Nº de citas: 2

    [doi:10.1007/s11239-014-1106-1]

  • Riuró H, Campuzano O, Berne P, Arbelo E, Iglesias A, Pérez-Serra A, Coll-Vidal M, Partemi S, Mademont-Soler I, Picó F, Allegue C, Oliva A, Gerstenfeld E, Sarquella-Brugada G, Castro-Urda V, Fernández-Lozano I, Mont L, Brugada-Terradellas J, Scornik FS and Brugada R.

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

    EUROPEAN JOURNAL OF HUMAN GENETICS . 23(1): 79-85. Nº de citas: 13

    [doi:10.1038/ejhg.2014.54]

  • Campuzano O, Sarquella-Brugada G, Brugada R and Brugada-Terradellas J.

    Genetics of channelopathies associated with sudden cardiac death.

    Global cardiology science & practice . 2015(3): 39-39. Nº de citas: 24

    [doi:10.5339/gcsp.2015.39]

  • Campuzano O, Sarquella-Brugada G, Mademont-Soler I, Allegue C, César-Díaz S, Ferrer-Costa C, Coll M, Mates J, Iglesias A, Brugada-Terradellas J and Brugada R.

    Identification of Genetic Alterations, as Causative Genetic Defects in Long QT Syndrome, Using Next Generation Sequencing Technology

    PLoS One . 9(12): . Nº de citas: 30

    [doi:10.1371/journal.pone.0114894]

  • Campuzano O, Sanchez-Molero O, Allegue C, Coll M, Mademont-Soler I, Selga E, Ferrer-Costa C, Mates J, Iglesias A, Sarquella-Brugada G, César-Díaz S, Brugada-Terradellas J, Castellà J, Medallo J and Brugada R.

    Post-mortem genetic analysis in juvenile cases of sudden cardiac death

    FORENSIC SCIENCE INTERNATIONAL . 245: 30-37. Nº de citas: 41

    [doi:10.1016/j.forsciint.2014.10.004]

  • Altit G, Sarquella-Brugada G, Dahdah N, Dallaire F, Carceller AM, Abadir S and Fournier A.

    Effect of Dual-Chamber Pacemaker Implantation on Aortic Dilatation in Patients With Congenital Heart Block

    AMERICAN JOURNAL OF CARDIOLOGY . 114(10): 1573-1577. Nº de citas: 5

    [doi:10.1016/j.amjcard.2014.08.022]

  • Campuzano O, Allegue C, Sarquella-Brugada G, Coll M, Mates J, Alcalde M, Ferrer-Costa C, Iglesias A, Brugada-Terradellas J and Brugada R.

    The role of clinical, genetic and segregation evaluation in sudden infant death

    FORENSIC SCIENCE INTERNATIONAL . 242: 9-15. Nº de citas: 20

    [doi:10.1016/j.forsciint.2014.06.007]