Research

Cardiovascular Diseases and Child Development

Search publications

Publications

  • 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. Number of citations: 60

    [doi:10.1016/j.jacc.2020.05.029]

  • Antonelli, R, Jiménez, C, Riley, M, Servidei, T, Riccardi, R, Soriano, A, Roma, J, Martínez-Saez, E, Martini, M, Ruggiero, A, Moreno, L, Sanchez deToledo J, Gallego, S, Bové, J, Hooker, JM and Segura, MF.

    CN133, a Novel Brain-Penetrating Histone Deacetylase Inhibitor, Hampers Tumor Growth in Patient-Derived Pediatric Posterior Fossa Ependymoma Models

    Cancers . 12(7): . Number of citations: 9

    [doi:10.3390/cancers12071922]

  • Walter CC, Bartrons J, Gómez O, Caffarena-Calvar JM and Carretero JM.

    Idiopathic dilatation of the right atrium: a not so benign entity

    CARDIOLOGY IN THE YOUNG . 30(7): 919-922. Number of citations: 5

    [doi:10.1017/S1047951120001353]

  • 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. Number of citations: 32

    [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. Number of citations: 3

    [doi:10.1016/j.gene.2020.144658]

  • Brugada-Terradellas J, Katritsis, DG, Arbelo, E, Arribas, F, Bax, JJ, Blomstrom-Lundqvist, C, Calkins, H, Corrado, D, Deftereos, SG, Diller, GP, Gomez-Doblas, JJ, Gorenek, B, Grace, A, Ho, SY, Kaski, JC, Karl-Heinz, K, Lambiase, PD, Sacher, F, Sarquella-Brugada G, Suwalski, P and Zaza, A.

    2019 ESC Guidelines on the Treatment of Patients With Supraventricular Tachycardia

    REVISTA ESPANOLA DE CARDIOLOGIA . 73(6): .

    [doi:10.1016/j.recesp.2019.12.029]

  • 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): . Number of citations: 6

    [doi:10.3390/jcm9061866]

  • Mazzanti A, Guz D, Trancuccio A, Pagan E, Kukavica D, Chargeishvili T, Olivetti N, Biernacka EK, Sacilotto L, Sarquella-Brugada G, Campuzano O, Nof E, Anastasakis A, Sansone VA, Jimenez-Jaimez J, Cruz F, Sánchez-Quiñones J, Hernandez-Afonso J, Fuentes ME, Sredniawa B, Garoufi A, Andršová I, Izquierdo M, Marinov R, Danon A, Expósito-García V, Garcia-Fernandez A, Muñoz-Esparza C, Ortíz M, Zienciuk-Krajka A, Tavazzani E, Monteforte N, Bloise R, Marino M, Memmi M, Napolitano C, Zorio E, Monserrat L, Bagnardi V and Priori SG.

    Natural History and Risk Stratification in Andersen-Tawil Syndrome Type 1

    JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY . 75(15): 1772-1784. Number of citations: 46

    [doi:10.1016/j.jacc.2020.02.033]

  • 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. Number of citations: 64

    [doi:10.1016/j.ebiom.2020.102732]

  • Walter CC, Soveral I, Bartrons J, Escobar MC, Carretero JM, Quirado L, Gómez O and Sanchez deToledo J.

    Comprehensive Functional Echocardiographic Assessment of Transposition of the Great Arteries: From Fetus to Newborn

    PEDIATRIC CARDIOLOGY . 41(4): 687-694. Number of citations: 10

    [doi:10.1007/s00246-019-02279-w]