Persones / Equip Humà

Andrea Greco

Buscador de publicacions

Publicacions

  • Campuzano O, Grassi S, Martínez-Barrios E, Greco A, Arena V, Sarquella-Brugada G and Oliva A.

    Brugada syndrome in the forensic field: what do we know to date?

    frontiers in cardiovascular medicine . 12: 1618762-1618762.

    [doi:10.3389/fcvm.2025.1618762]

  • 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: 1

    [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.

    [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.

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

  • 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): . Nº de cites: 1

    [doi:10.1136/bmjsem-2023-001852]

  • 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]

  • Coccia, E, Valeri, L, Zuntini, R, Caraffi, SG, Peluso, F, Pagliai, L, Vezzani, A, Pietrangiolillo, Z, Leo, F, Melli, N, Fiorini, V, Greco A, Lepri, FR, Pisaneschi, E, Marozza, A, Carli, D, Mussa, A, Radio, FC, Conti, B, Iascone, M, Gargano, G, Novelli, A, Tartaglia, M, Zuffardi, O, Bedeschi, MF and Garavelli, L.

    Prenatal Clinical Findings in RASA1-Related Capillary Malformation-Arteriovenous Malformation Syndrome

    GENES . 14(3): . Nº de cites: 9

    [doi:10.3390/genes14030549]