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  • Greco A, César-Díaz S, Martínez-Barrios E, Cruzalegui JC, Chipa F, Carretero JM, Merchán F, Nuria Díez Escuté, Patricia Cerralbo Martín, Luján AL, Zschaeck-Luzardo I, Díez-López C, de Frutos F, Arbelo E, García-Álvarez A, Toro R, Maria Estella Pie Raventos, Campuzano Ó and Sarquella-Brugada G.

    Clinical usefulness of genetic diagnosis in early-onset cardiomyopathies.

    Revista espanola de cardiologia (English ed.) . : .

    [doi:10.1016/j.rec.2026.01.004]

  • Martínez-Barrios E, Cruzalegui JC, Hidalgo-Sanuy M, Greco A, César-Díaz S, Chipa F, Nuria Díez Escuté, Patricia Cerralbo Martín, Zschaeck-Luzardo I, Merchán F, Balsells S, Brugada-Terradellas J, Campuzano O and Sarquella-Brugada G.

    Clinical Spectrum of Arrhythmogenic Entities in Spanish Children Carrying Deleterious SCN5A Variants

    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES . 27(2): .

    [doi:10.3390/ijms27020880]

  • Campuzano O, Tirón C, Martínez-Barrios E, Greco A, Cruzalegui JC, Chipa F, César-Díaz S, Merchan EF, Coll M, Fernández-Falgueras A, Brugada R, Ortega M, Molina N, Barberia E, Toro R, Oliva A, Grassi S and Sarquella-Brugada G.

    The Role of Molecular Autopsy in Concealed Cardiomyopathies

    Genes . 16(11): .

    [doi:10.3390/genes16111273]

  • Greco A, Chipa, Fredy, Cruzalegui JC, Tolosana, Jose Maria, Moscoso BA and Sarquella-Brugada G.

    Implantation of new VR leadless pacemaker in a 4-year-old, 16-kg patient with complete atrioventricular block.

    HeartRhythm Case Reports . 11(10): 1007-1013.

    [doi:10.1016/j.hrcr.2025.07.007]

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

    Appropriate time interval to update ambiguous genetic diagnosis in inherited arrhythmogenic syndromes

    iScience . 28(5): 112300-112300. Nº de cites: 2

    [doi:10.1016/j.isci.2025.112300]

  • Greco A, Martínez-Barrios E, Cruzalegui JC, César-Díaz S, Chipa, F, Nuria Díez Escuté, Patricia Cerralbo Martín, Zschaeck-Luzardo I, Loredo, P, Sarquella-Brugada G and Campuzano, O.

    Brugada Syndrome and GPD1L: Definite Genotype-Phenotype Association?

    Cardiogenetics . 15(1): .

    [doi:10.3390/cardiogenetics15010009]

  • 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 . 143(12): 1499-1508. Nº de cites: 1

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

  • Martínez-Barrios E, Greco A, Cruzalegui JC, César-Díaz S, Nuria Díez Escuté, Patricia Cerralbo Martín, Chipa F, Zschaeck-Luzardo I, Fogaça-da-Mata M, Díez-López C, Arbelo E, Grassi S, Oliva A, Toro R, Sarquella-Brugada G and Campuzano O.

    Actionable Variants of Unknown Significance in Inherited Arrhythmogenic Syndromes: A Further Step Forward in Genetic Diagnosis

    Biomedicines . 12(11): . Nº de cites: 1

    [doi:10.3390/biomedicines12112553]

  • 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. Nº de cites: 1

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

  • 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

    JACC-JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY . 84(10): 921-933. Nº de cites: 12

    [doi:10.1016/j.jacc.2024.04.070]