Persones / Equip Humà

Sergio César Diaz

Buscador de publicacions

Publicacions

  • 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]

  • Sarquella-Brugada G, Fernandez-Falgueras A, César-Díaz S, Arbelo E, Jordà P, García-Álvarez A, Cruzalegui JC, Merchan EF, Fiol JV, Brugada-Terradellas J, Brugada R and Campuzano O.

    Pediatric Malignant Arrhythmias Caused by Rare Homozygous Genetic Variants in TRDN: A Comprehensive Interpretation

    Frontiers in pediatrics . 8: 601708-601708. Nº de cites: 3

    [doi:10.3389/fped.2020.601708]

  • Jordà P, Toro R, Diez C, Salazar-Mendiguchía J, Fernandez-Falgueras A, Perez-Serra A, Coll M, Puigmulé M, Arbelo E, García-Álvarez A, Sarquella-Brugada G, César-Díaz S, Tiron C, Iglesias A, Brugada J, Brugada R and Campuzano O.

    Malignant Arrhythmogenic Role Associated with RBM20: A Comprehensive Interpretation Focused on a Personalized Approach

    Journal of Personalized Medicine . 11(2): 130. Nº de cites: 4

    [doi:10.3390/jpm11020130]

  • Natera-de Benito D, Ortez-Gonzalez CI, Jou-Munoz C, Jimenez-Mallebrera C, Codina-Bergadà A, Carrera-García L, Exposito-Escudero JM, César-Díaz S, Martorell-Sampol L, Gallano P, Gonzalez-Quereda L, Cuadras-Palleja D, Colomer J, Yubero-Siles D, Palau F and Nascimento-Osorio A.

    The Phenotype and Genotype of Congenital Myopathies Based on a Large Pediatric Cohort

    PEDIATRIC NEUROLOGY . 115: 50-65. Nº de cites: 7

    [doi:10.1016/j.pediatrneurol.2020.11.002]

  • García-Otero L, LÓpez M, GoncÉ A, Fortuny-Guasch C, Salazar L, Valenzuela-Alcaraz BI, Guirado L, César-Díaz S, Gratacós E and Fàtima Crispi Brillas.

    Cardiac Remodeling and Hypertension in HIV-Uninfected Infants Exposed in utero to Antiretroviral Therapy

    CLINICAL INFECTIOUS DISEASES . 73(4): 586-593. Nº de cites: 9

    [doi:10.1093/cid/ciab030]

  • Clark BC, Sanchez deToledo J, Bautista Rodríguez C, Choueiter N, Lara D, Kang H, Mohsin S, Fraisse A, César-Díaz S, Sattar Shaikh A, Escobar-Diaz MC, Hsu DT, Randanne PC, Aslam N, Kleinmahon J, Lamour JM, Johnson JN, Sarquella-Brugada G and Chowdhury D.

    Cardiac Abnormalities Seen in Pediatric Patients During the SARS-CoV2 Pandemic: An International Experience

    JOURNAL OF THE AMERICAN HEART ASSOCIATION . 9(21): . Nº de cites: 35

    [doi:10.1161/JAHA.120.018007]

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

    Update on Genetic Basis of Brugada Syndrome: Monogenic, Polygenic or Oligogenic?

    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES . 21(19): . Nº de cites: 27

    [doi:10.3390/ijms21197155]

  • Lopez-Sainz A, Dominguez F, Lopes LR, Ochoa JP, Barriales-Villa R, Climent V, Linschoten M, Tiron C, Chiriatti C, Marques N, Rasmussen TB, Espinosa MÁ, Beinart R, Quarta G, César-Díaz S, Field E, Garcia-Pinilla JM, Bilinska Z, Muir AR, Roberts AM, Santas E, Zorio E, Peña-Peña ML, Navarro-Aguirre M, Fernandez A, Palomino-Doza J, Azevedo O, Lorenzini M, García-Álvarez MI, Bento D, Jensen MK, Méndez I, Pezzoli L, Sarquella-Brugada G, Campuzano O, Gonzalez-Lopez E, Mogensen J, Kaski JP, Arad M, Brugada-Terradellas J, Asselbergs FW, Monserrat L, Olivotto I, Elliott PM, Garcia-Pavia P and European Genetic Cardiomyopathies Initiative Investigators.

    Clinical Features and Natural History of PRKAG2 Variant Cardiac Glycogenosis

    JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY . 76(2): 186-197. Nº de cites: 40

    [doi:10.1016/j.jacc.2020.05.029]