Personas / Equipo Humano

Georgia Sarquella Brugada

Buscador de publicaciones

Publicaciones

  • Martínez-Barrios E, Greco A, Cruzalegui JC, César-Díaz S, Nuria Díez Escuté, Patricia Cerralbo Martín, Chipa F, Zschaeck-Luzardo I, Slanovic L, Mangas A, Toro R, Brugada-Terradellas J, Sarquella-Brugada G and Campuzano O.

    Interpreting the actionable clinical role of rare variants associated with short QT syndrome

    HUMAN GENETICS . : .

    [doi:10.1007/s00439-024-02713-x]

  • de Frutos F, Ochoa JP, Webster G, Jansen M, Remior P, Rasmussen TB, Sabater-Molina M, Barriales-Villa R, Girolami F, César-Díaz S, Fuentes-Cañamero ME, Alvarez García-Rovés R, Wahbi K, Limeres J, Kubanek M, Slieker MG, Sarquella-Brugada G, Abrams DJ, Dooijes D, Domínguez F and Garcia-Pavia P.

    Clinical Features and Outcomes of Pediatric MYH7-Related Dilated Cardiomyopathy

    JOURNAL OF THE AMERICAN HEART ASSOCIATION . 13(21): .

    [doi:10.1161/JAHA.124.036208]

  • Martínez-Barrios E, Campuzano O, Greco A, Cruzalegui JC and Sarquella-Brugada G.

    Cardiac channelopathies in pediatrics: a genetic update.

    EUROPEAN JOURNAL OF PEDIATRICS . 183(11): 4635-4640.

    [doi:10.1007/s00431-024-05757-3]

  • Lamba A, Roston TM, Peltenburg PJ, Kallas D, Franciosi S, Lieve KVV, Kannankeril PJ, Horie M, Ohno S, Brugada R, Aiba T, Fischbach P, Knight L, Till J, Kwok SY, Probst V, Backhoff D, LaPage MJ, Batra AS, Drago F, Haugaa K, Krahn AD, Robyns T, Swan H, Tavacova T, Atallah J, Borggrefe M, Rudic B, Sarquella-Brugada G, Chorin E, Hill A, Kammeraad J, Kamp A, Law I, Perry J, Roberts JD, Tisma-Dupanovic S, Semsarian C, Skinner JR, Tfelt-Hansen J, Denjoy I, Leenhardt A, Schwartz PJ, Ackerman MJ, Wilde AAM, van der Werf C and Sanatani S.

    An international multicenter cohort study on implantable cardioverter-defibrillators for the treatment of symptomatic children with catecholaminergic polymorphic ventricular tachycardia.

    Heart Rhythm . 21(10): 1767-1776. Nº de citas: 3

    [doi:10.1016/j.hrthm.2024.04.006]

  • Bergonti M, Ciconte G, Cruzalegui JC, Crotti L, Arbelo E, Casella M, Saenen J, Rossi A, Pannone L, Martínez-Barrios E, Compagnucci P, Russo V, Berne P, Van Leuven O, Boccellino A, Marcon L, Dagradi F, Landra F, Özkartal T, Comune A, Conti S, Ribatti V, Campuzano O, Brugada P, de Asmundis C, Brugada J, Pappone C, Tondo C, Schwartz PJ, Auricchio A, Sarquella-Brugada G and Conte G.

    Continuous Rhythm Monitoring With Implanted Loop Recorders in Children and Adolescents With Brugada Syndrome

    JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY . 84(10): 921-933. Nº de citas: 1

    [doi:10.1016/j.jacc.2024.04.070]

  • Camiña-Conforto G, Ivars M, Sarquella-Brugada G, Carlos Valera Dávila, Salvador-Hernandez H, Rovira-Zurriaga C and Baselga E.

    Phacomatosis pigmentokeratotica: Exploring extracutaneous comorbidities and topical therapy.

    PEDIATRIC DERMATOLOGY . 41(5): 904-907.

    [doi:10.1111/pde.15632]

  • Bonet, F, Campuzano, O, Cordoba-Caballero, J, Alcalde, M, Sarquella-Brugada G, Braza-Boils, A, Brugada, R, Hernandez-Torres, F, Quezada-Feijoo, M, Ramos, M, Mangas, A, Ranea, JAG and Toro, R.

    Role of miRNA-mRNA Interactome in Pathophysiology of Arrhythmogenic Cardiomyopathy

    Biomedicines . 12(8): .

    [doi:10.3390/biomedicines12081807]

  • Sarquella-Brugada G, Martínez-Barrios E, César-Díaz S, Toro R, Cruzalegui JC, Greco A, Nuria Díez Escuté, Patricia Cerralbo Martín, Chipa F, Arbelo E, Diez-López C, Grazioli G, Balderrábano N and Campuzano O.

    A narrative review of inherited arrhythmogenic syndromes in young population: role of genetic diagnosis in exercise recommendations.

    BMJ OPEN SPORT & EXERCISE MEDICINE . 10(3): .

    [doi:10.1136/bmjsem-2023-001852]

  • Olorón, PM, Alegría, I, César-Díaz S, del Olmo, B, Martínez-Barrios E, Carrera-García L, Natera-de Benito D, Nascimento-Osorio A, Campuzano, O and Sarquella-Brugada G.

    Congenital LMNA-Related Muscular Dystrophy in Paediatrics: Cardiac Management in Monozygotic Twins.

    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES . 25(11): .

    [doi:10.3390/ijms25115836]

  • Fogaça-da-Mata M, Martínez-Barrios E, Jiménez-Montañés L, Cruzalegui JC, Chipa-Ccasani F, Greco A, César-Díaz S, Nuria Díez Escuté, Patricia Cerralbo Martín, Zschaeck-Luzardo I, Clavero Adell M, Ayerza-Casas A, Palanca-Arias D, López M, Campuzano O, Brugada-Terradellas J and Sarquella-Brugada G.

    Brugada Syndrome and Pulmonary Atresia with Intact Interventricular Septum: Fortuitous Finding or New Genetic Connection?

    GENES . 15(5): .

    [doi:10.3390/genes15050638]