Personas / Equipo Humano

Sergio César Diaz

Buscador de publicaciones

Publicaciones

  • Mates J, Mademont-Soler I, Fernandez-Falgueras A, Sarquella-Brugada G, César-Díaz S, Arbelo E, García-Álvarez A, Jordà P, Toro R, Coll M, Fiol JV, Iglesias A, Perez-Serra A, Olmo BD, Alcalde M, Puigmulé M, Pico F, Lopez L, Ferrer C, Tiron C, Grassi S, Oliva A, Brugada-Terradellas J, Brugada R and Campuzano O.

    Sudden Cardiac Death and Copy Number Variants: What Do We Know after 10 Years of Genetic Analysis?

    FORENSIC SCIENCE INTERNATIONAL-GENETICS . 47: 102281-102281. Nº de citas: 20

    [doi:10.1016/j.fsigen.2020.102281]

  • Salazar-Mendiguchía J, Díez-López C, Claver E, César-Díaz S, Campuzano O, Sarquella-Brugada G and Monserrat L.

    Familial evaluation reveals a distinct genetic cause in a large Spanish family with neurofibromatosis 1 and hypertrophic cardiomyopathy

    Gene . 746: 144658-144658. Nº de citas: 2

    [doi:10.1016/j.gene.2020.144658]

  • Campuzano O, Sarquella-Brugada G, Arbelo E, César-Díaz S, Jordà P, Pérez-Serra A, Toro R, Brugada-Terradellas J and Brugada R.

    Genetic Variants as Sudden-Death Risk Markers in Inherited Arrhythmogenic Syndromes: Personalized Genetic Interpretation

    Journal of Clinical Medicine . 9(6): . Nº de citas: 5

    [doi:10.3390/jcm9061866]

  • Campuzano O, Sarquella-Brugada G, Fernandez-Falgueras A, Coll M, Iglesias A, Ferrer-Costa C, César-Díaz S, Arbelo E, García-Álvarez A, Jordà P, Toro R, Tiron de Llano C, Grassi S, Oliva A, Brugada J and Brugada R.

    Reanalysis and reclassification of rare genetic variants associated with inherited arrhythmogenic syndromes

    EBioMedicine . 54: 102732-102732. Nº de citas: 41

    [doi:10.1016/j.ebiom.2020.102732]

  • Calderon-Dominguez M, Belmonte T, Quezada-Feijoo M, Ramos-Sánchez M, Fernández-Armenta J, Pérez-Navarro A, César-Díaz S, Peña LP, Vea À, Llorente-Cortés V, Mangas A, de Gonzalo-Calvo D and Toro R.

    Emerging role of microRNAs in dilated cardiomyopathy: evidence regarding etiology.

    TRANSLATIONAL RESEARCH . 215: 86-101. Nº de citas: 23

    [doi:10.1016/j.trsl.2019.08.007]

  • London, KS, Hartwell, C, César-Díaz S, Sarquella-Brugada G and White, JL.

    CAN SUDDEN CARDIAC DEATH RISK IN THE YOUNG BE IDENTIFIED IN THE EMERGENCY DEPARTMENT?

    JOURNAL OF EMERGENCY NURSING . 46(1): 105-110. Nº de citas: 2

    [doi:10.1016/j.jen.2019.09.009]

  • Norrish G, Ding T, Field E, Ziólkowska L, Olivotto I, Limongelli G, Anastasakis A, Weintraub R, Biagini E, Ragni L, Prendiville T, Duignan S, McLeod K, Ilina M, Fernández A, Bökenkamp R, Baban A, Kubuš P, Daubeney PEF, Sarquella-Brugada G, César-Díaz S, Marrone C, Bhole V, Medrano C, Uzun O, Brown E, Gran F, Castro FJ, Stuart G, Vignati G, Barriales-Villa R, Guereta LG, Adwani S, Linter K, Bharucha T, Garcia-Pavia P, Rasmussen TB, Calcagnino MM, Jones CB, De Wilde H, Toru-Kubo J, Felice T, Mogensen J, Mathur S, Reinhardt Z, O'Mahony C, Elliott PM, Omar RZ and Kaski JP.

    Development of a Novel Risk Prediction Model for Sudden Cardiac Death in Childhood Hypertrophic Cardiomyopathy (HCM Risk-Kids)

    JAMA Cardiology . 4(9): 918-927. Nº de citas: 136

    [doi:10.1001/jamacardio.2019.2861]

  • Herranz Barbero A, César-Díaz S, Martinez-Osorio J, Margarit A, Moreno-Hernando J, Campuzano O, Iglesias-Platas I, Brugada-Terradellas J and Sarquella-Brugada G.

    Long-term outcome of neonates and infants with permanent junctional reciprocating tachycardia. When cardiac ablation changes natural history

    JOURNAL OF ELECTROCARDIOLOGY . 56: 85-89. Nº de citas: 6

    [doi:10.1016/j.jelectrocard.2019.05.006]

  • Campuzano O, Fernandez-Falgueras A, Lemus X, Sarquella-Brugada G, César-Díaz S, Coll M, Mates J, Arbelo E, Jordà P, Perez-Serra A, Del Olmo B, Ferrer-Costa C, Iglesias A, Fiol JV, Puigmulé M, Lopez L, Pico F, Brugada-Terradellas J and Brugada R.

    Short QT Syndrome: A Comprehensive Genetic Interpretation and Clinical Translation of Rare Variants

    Journal of Clinical Medicine . 8(7): . Nº de citas: 20

    [doi:10.3390/jcm8071035]

  • Campuzano O, Sarquella-Brugada G, Fernandez-Falgueras A, César-Díaz S, Coll M, Mates J, Arbelo E, Perez-Serra A, Del Olmo B, Jordá P, Fiol JV, Iglesias A, Puigmulé M, Lopez L, Pico F, Brugada-Terradellas J and Brugada R.

    Genetic interpretation and clinical translation of minor genes related to Brugada syndrome

    HUMAN MUTATION . 40(6): 749-764. Nº de citas: 29

    [doi:10.1002/humu.23730]