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  • Alvarez-Mora MI, Agusti I, Wijngaard R, Martínez-Barrios E, Barcos T, Borras A, Peralta S, Guimera M, Goday A, Manau D and Rodriguez-Revenga L.

    Evaluation of FMR4, FMR5 and FMR6 Expression Levels as Non-Invasive Biomarkers for the Diagnosis of Fragile X-Associated Primary Ovarian Insufficiency (FXPOI).

    Journal of Clinical Medicine . 11(8): .

    [doi:10.3390/jcm11082186]

  • Martínez-Barrios E, Arbelo E, Cesar S, Cruzalegui JC, Fiol JV, Díez-Escuté N, Hernández-Cera C, Brugada R, Brugada-Terradellas J, Campuzano O and Sarquella-Brugada G.

    Brugada Syndrome in Women: What Do We Know After 30 Years?

    frontiers in cardiovascular medicine . 9: 874992-874992.

    [doi:10.3389/fcvm.2022.874992]

  • Martínez-Barrios E, Sarquella-Brugada G, Pérez-Serra A, Fernández-Falgueras A, Cesar S, Coll M, Puigmulé M, Iglesias A, Alcalde M, Vallverdú-Prats M, Ferrer-Costa C, Del Olmo B, Picó F, López L, Fiol JV, Cruzalegui JC, Hernández-Cera C, Arbelo E, Grassi S, Oliva A, Toro R, Brugada-Terradellas J, Brugada R and Campuzano O.

    Discerning the Ambiguous Role of Missense TTN Variants in Inherited Arrhythmogenic Syndromes

    Journal of Personalized Medicine . 12(2): .

    [doi:10.3390/jpm12020241]

  • Martínez-Barrios E, Cesar S, Cruzalegui JC, Hernández-Cera C, Arbelo E, Fiol JV, Brugada-Terradellas J, Brugada R, Campuzano O and Sarquella-Brugada G.

    Clinical Genetics of Inherited Arrhythmogenic Disease in the Pediatric Population.

    Biomedicines . 10(1): .

    [doi:10.3390/biomedicines10010106]

  • Martins da Silva V, Martínez-Barrios E, Tell-Martí G, Dabad M, Carrera C, Aguilera P, Daniel Antoni Brualla Palazón, Esteve-Codina A, Vicente-Villa MA, Puig S, Puig-Butillé JA and Malvehy J.

    Genetic Abnormalities in Large to Giant Congenital Nevi: Beyond NRAS Mutations.

    JOURNAL OF INVESTIGATIVE DERMATOLOGY . 139(4): 900-908.

    [doi:10.1016/j.jid.2018.07.045]