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Publicaciones

  • 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: 240

    [doi:10.1001/jamacardio.2019.2861]

  • 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: 32

    [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: 41

    [doi:10.1002/humu.23730]

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

    Personalized Interpretation and Clinical Translation of Genetic Variants Associated With Cardiomyopathies

    Frontiers in Genetics . 10: 450-450. Nº de citas: 8

    [doi:10.3389/fgene.2019.00450]

  • García-Otero L, López M, Guitart-Mampel M, Morén C, Goncé A, Esteve-Matanza C, Salazar L, Gómez O, Martínez JM, Torres B, César-Díaz S, Garrabou G, Crispi F and Gratacós E.

    Cardiac and mitochondrial function in HIV-uninfected fetuses exposed to antiretroviral treatment

    PLoS One . 14(3): . Nº de citas: 25

    [doi:10.1371/journal.pone.0213279]

  • Sarquella-Brugada G, César-Díaz S, Zambrano MD, Fernandez-Falgueras A, Fiol JV, Iglesias A, Torres F, Garcia-Algar O, Arbelo E, Brugada-Terradellas J, Brugada R and Campuzano O.

    Electrocardiographic Assessment and Genetic Analysis in Neonates: a Current Topic of Discussion.

    CURRENT CARDIOLOGY REVIEWS . 15(1): 30-37. Nº de citas: 11

    [doi:10.2174/1573403X14666180913114806]

  • Campuzano O, Beltramo P, Fernandez A, Iglesias A, García L, Allegue C, Sarquella-Brugada G, Coll M, Perez-Serra A, Mademont-Soler I, Mates J, Del Olmo B, Rodríguez Á, Maciel N, Puigmulé M, Pico F, César-Díaz S, Brugada-Terradellas J, Cuesta A, Gutierrez C and Brugada R.

    Molecular autopsy in a cohort of infants died suddenly at rest

    Forensic Science International-Genetics . 37: 54-63. Nº de citas: 25

    [doi:10.1016/j.fsigen.2018.07.023]

  • Campuzano O, Sarquella-Brugada G, César-Díaz S, Arbelo E, Brugada-Terradellas J and Brugada R.

    Recent Advances in Short QT Syndrome

    Frontiers in Cardiovascular Medicine . 5: 149-149. Nº de citas: 66

    [doi:10.3389/fcvm.2018.00149]

  • César-Díaz S.

    Neuromuscular diseases with hypertrophic cardiomyopathy.

    Global cardiology science & practice . 2018(3): 27-27.

    [doi:10.21542/gcsp.2018.27]

  • Mates J, Mademont-Soler I, Del Olmo B, Ferrer-Costa C, Coll M, Pérez-Serra A, Picó F, Allegue C, Fernandez-Falgueras A, Álvarez P, Yotti R, Espinosa MA, Sarquella-Brugada G, César-Díaz S, Carro-Fernandez E, Brugada-Terradellas J, Arbelo E, Garcia-Pavia P, Borregan M, Tizzano E, López-Granados A, Mazuelos F, Díaz de Bustamante A, Darnaude MT, González-Hevia JI, Díaz-Flores F, Trujillo F, Iglesias A, Fernandez-Aviles F, Campuzano O and Brugada R.

    Role of copy number variants in sudden cardiac death and related diseases: genetic analysis and translation into clinical practice

    EUROPEAN JOURNAL OF HUMAN GENETICS . 26(7): 1014-1025. Nº de citas: 35

    [doi:10.1038/s41431-018-0119-1]