Persones / Equip Humà

Sergio César Diaz

Buscador de publicacions

Publicacions

  • Ibáñez-Cabellos JS, Baviera-Muñoz R, Alemany-Perna B, Sivera R, Bataller L, César-Díaz S, González-Cabo P, García-Giménez JL, Pallardó FV and Seco-Cervera M.

    Validation of circulating miR-323a-3p and miR-625-3p to classify hypertrophic cardiomyopathy in Friedreich's ataxia

    Scientific Reports . 16(1): .

    [doi:10.1038/s41598-026-50975-4]

  • Gómez-Domínguez D, Epifano C, Hernández I, Vilaplana-Martí B, Martín A, Amarilla-Quintana S, César-Díaz S, de Molina-Iracheta A, Sena-Esteves M, Sarquella-Brugada G and Pérez de Castro I.

    CRISPR-mediated targeting of the LMNA c.745C>T mutation enhances survival and cardiac function in congenital muscular dystrophy.

    molecular therapy. advances . 34(1): 201653-201653.

    [doi:10.1016/j.omta.2025.201653]

  • Nogué L, Mar Bennasar Sans, Guirado L, Zölner F, Reitz J, Axt-Fliedner R, Escobar MC, Martínez JM, Gratacós E, Crispi F and Gómez del Rincón O.

    Prognostic value of fetal growth and prenatal functional echocardiography in tetralogy of FALLOT.

    ACTA OBSTETRICIA ET GYNECOLOGICA SCANDINAVICA . 105(3): 479-491.

    [doi:10.1111/aogs.70137]

  • 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]

  • Norrish G, Hall K, Field E, Cervi E, Boleti O, Ziólkowska L, Olivotto I, Passantino S, Khraiche D, Limongelli G, Weintraub RG, Anastasakis A, Biagini E, Ragni L, Sarquella-Brugada G, César-Díaz S, Prendiville T, McLeod K, Ilina M, Baban A, Ojala TH, Spentzou G, Bhole V, Gran F, Brown E, Delle Donne G, Khodaghalian B, Fernandez A, Daubeney PEF, Linter K, Kubus P, Uzun O, Bökenkamp R, Raimondi F, Marrone C, Medrano C, Gonzalez-Lopez E, Siles A, Luczak-Wozniak K, Bharucha T, Adwani S, Klaassen S, Castro FJ, Guereta L, Yamazawa H, Sinagra G, Popoiu A, Perin F, Chana B, De Wilde H, Rasmussen TB, Mogensen J, Mathur S, Centeno F, Reinhardt Z, Barriales-Villa R, Kubo T, Felice T, Radulescu C, Schouvey S, Chaker M and Kaski JP.

    Sex Differences in Children and Adolescents With Hypertrophic Cardiomyopathy

    JACC-Advances . 4(8): 101907-101907. Nº de cites: 4

    [doi:10.1016/j.jacadv.2025.101907]

  • 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: 4

    [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]