Persones / Equip Humà

Sergio César Diaz

Buscador de publicacions

Publicacions

  • Martínez-Barrios E, Arbelo E, César-Díaz 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. Nº de cites: 4

    [doi:10.3389/fcvm.2022.874992]

  • Cruzalegui JC, César-Díaz S, Campuzano O, Fiol JV, Brugada-Terradellas J and Sarquella-Brugada G.

    Pediatric Left Posteroseptal Accessory Pathway Ablation from Giant Coronary Sinus with Persistent Left Superior Cava

    Journal of Cardiovascular Development and Disease . 9(4): .

    [doi:10.3390/jcdd9040109]

  • Martínez-Barrios E, Sarquella-Brugada G, Pérez-Serra A, Fernández-Falgueras A, César-Díaz 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): . Nº de cites: 2

    [doi:10.3390/jpm12020241]

  • Sarquella-Brugada G, Fernandez-Falgueras A, César-Díaz S, Arbelo E, Coll M, Perez-Serra A, Puigmulé M, Iglesias A, Alcalde M, Vallverdú-Prats M, Fiol JV, Ferrer-Costa C, Del Olmo B, Picó F, Lopez L, García-Alvarez A, Jordà P, Tiron de Llano C, Toro R, Grassi S, Oliva A, Brugada-Terradellas J, Brugada R and Campuzano O.

    Clinical impact of rare variants associated with inherited channelopathies: a 5-year update

    HUMAN GENETICS . 141(10): 1579-1589. Nº de cites: 7

    [doi:10.1007/s00439-021-02370-4]

  • Martínez-Barrios E, César-Díaz 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): . Nº de cites: 7

    [doi:10.3390/biomedicines10010106]

  • Norrish G, Topriceanu C, Qu C, Field E, Walsh H, Ziólkowska L, Olivotto I, Passantino S, Favilli S, Anastasakis A, Vlagkouli V, Weintraub R, King I, Biagini E, Ragni L, Prendiville T, Duignan S, McLeod K, Ilina M, Fernández A, Bökenkamp R, Baban A, Drago F, Kubuš P, Daubeney PEF, Chivers S, Sarquella-Brugada G, César-Díaz S, Marrone C, Medrano C, Alvarez Garcia-Roves R, Uzun O, Gran F, Castro FJ, Gimeno JR, Barriales-Villa R, Rueda F, Adwani S, Searle J, Bharucha T, Siles A, Usano A, Rasmussen TB, Jones CB, Kubo T, Mogensen J, Reinhardt Z, Cervi E, Elliott PM, Omar RZ and Kaski JP.

    The role of the electrocardiographic phenotype in risk stratification for sudden cardiac death in childhood hypertrophic cardiomyopathy

    EUROPEAN JOURNAL OF PREVENTIVE CARDIOLOGY . 29(4): 645-653. Nº de cites: 20

    [doi:10.1093/eurjpc/zwab046]

  • Paredes-Fuentes AJ, César-Díaz S, Montero-Sanchez R, Latre C, Genovés-Escarré J, Martorell-Sampol L, Cuadras-Palleja D, Colom H, Pineda M, O'Callaghan-Gordo M, Sarquella-Brugada G, Darling A and Artuch-Iriberri R.

    Plasma idebenone monitoring in Friedreich's ataxia patients during a long-term follow-up

    BIOMEDICINE & PHARMACOTHERAPY . 143: 112143-112143. Nº de cites: 5

    [doi:10.1016/j.biopha.2021.112143]

  • Sarquella-Brugada G, Algarrada L, Zambrano MD, Fernández-Falgueres A, Sailer S, César-Díaz S, Sebastiani G, Martí-Almor J, Aurensanz E, Cruzalegui JC, Merchan EF, Coll M, Pérez-Serra A, Del Olmo B, Fiol JV, Iglesias A, Ferrer-Costa C, Puigmulé M, Lopez L, Pico F, Arbelo E, Jordà P, Brugada-Terradellas J, Brugada R and Campuzano O.

    Early Identification of Prolonged QT Interval for Prevention of Sudden Infant Death

    Frontiers in pediatrics . 9: 704580-704580. Nº de cites: 2

    [doi:10.3389/fped.2021.704580]

  • Diz OM, Toro R, César-Díaz S, Gomez O, Sarquella-Brugada G and Campuzano O.

    Personalized Genetic Diagnosis of Congenital Heart Defects in Newborns

    Journal of Personalized Medicine . 11(6): 562. Nº de cites: 3

    [doi:10.3390/jpm11060562]

  • Vallverdú-Prats M, Alcalde M, Sarquella-Brugada G, César-Díaz S, Arbelo E, Fernandez-Falgueras A, Coll M, Pérez-Serra A, Puigmulé M, Iglesias A, Fiol JV, Ferrer-Costa C, Olmo BD, Picó F, Lopez L, Jordà P, García-Álvarez A, Llano CT, Toro R, Grassi S, Oliva A, Brugada-Terradellas J, Brugada R and Campuzano O.

    Rare Variants Associated with Arrhythmogenic Cardiomyopathy: Reclassification Five Years Later

    Journal of Personalized Medicine . 11(3): 162. Nº de cites: 13

    [doi:10.3390/jpm11030162]