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Page 1
Additional value of screening for minor genes and copy number variants in hypertrophic cardiomyopathy.
Mademont-Soler I, Mates J, Yotti R, Espinosa MA, Pérez-Serra A, Fernandez-Avila AI, Coll M, Méndez I, Iglesias A, Del Olmo B, Riuró H, Cuenca S, Allegue C, Campuzano O, Picó F, Ferrer-Costa C, Álvarez P, Castillo S, Garcia-Pavia P, Gonzalez-Lopez E, Padron-Barthe L, Díaz de Bustamante A, Darnaude MT, González-Hevia JI, Brugada J, Fernandez-Aviles F, Brugada R. Mademont-Soler I, et al. Among authors: riuro h. PLoS One. 2017 Aug 3;12(8):e0181465. doi: 10.1371/journal.pone.0181465. eCollection 2017. PLoS One. 2017. PMID: 28771489 Free PMC article.
Large Genomic Imbalances in Brugada Syndrome.
Mademont-Soler I, Pinsach-Abuin ML, Riuró H, Mates J, Pérez-Serra A, Coll M, Porres JM, Del Olmo B, Iglesias A, Selga E, Picó F, Pagans S, Ferrer-Costa C, Sarquella-Brugada G, Arbelo E, Cesar S, Brugada J, Campuzano Ó, Brugada R. Mademont-Soler I, et al. Among authors: riuro h. PLoS One. 2016 Sep 29;11(9):e0163514. doi: 10.1371/journal.pone.0163514. eCollection 2016. PLoS One. 2016. PMID: 27684715 Free PMC article.
Comprehensive Genetic Characterization of a Spanish Brugada Syndrome Cohort.
Selga E, Campuzano O, Pinsach-Abuin ML, Pérez-Serra A, Mademont-Soler I, Riuró H, Picó F, Coll M, Iglesias A, Pagans S, Sarquella-Brugada G, Berne P, Benito B, Brugada J, Porres JM, López Zea M, Castro-Urda V, Fernández-Lozano I, Brugada R. Selga E, et al. Among authors: riuro h. PLoS One. 2015 Jul 14;10(7):e0132888. doi: 10.1371/journal.pone.0132888. eCollection 2015. PLoS One. 2015. PMID: 26173111 Free PMC article.
Contribution of Cardiac Sodium Channel β-Subunit Variants to Brugada Syndrome.
Peeters U, Scornik F, Riuró H, Pérez G, Komurcu-Bayrak E, Van Malderen S, Pappaert G, Tarradas A, Pagans S, Daneels D, Breckpot K, Brugada P, Bonduelle M, Brugada R, Van Dooren S. Peeters U, et al. Among authors: riuro h. Circ J. 2015;79(10):2118-29. doi: 10.1253/circj.CJ-15-0164. Epub 2015 Jul 15. Circ J. 2015. PMID: 26179811 Free article. Clinical Trial.
Analysis of the arrhythmogenic substrate in human heart failure.
Partemi S, Batlle M, Berne P, Berruezo A, Campos B, Mont L, Riuró H, Roig E, Pérez-Villa F, Ortiz J, Pascali VL, Oliva A, Brugada R, Brugada J. Partemi S, et al. Among authors: riuro h. Cardiovasc Pathol. 2013 Mar-Apr;22(2):133-40. doi: 10.1016/j.carpath.2012.07.003. Epub 2012 Oct 1. Cardiovasc Pathol. 2013. PMID: 23036686
Rare Titin (TTN) Variants in Diseases Associated with Sudden Cardiac Death.
Campuzano O, Sanchez-Molero O, Mademont-Soler I, Riuró H, Allegue C, Coll M, Pérez-Serra A, Mates J, Picó F, Iglesias A, Brugada R. Campuzano O, et al. Among authors: riuro h. Int J Mol Sci. 2015 Oct 27;16(10):25773-87. doi: 10.3390/ijms161025773. Int J Mol Sci. 2015. PMID: 26516846 Free PMC article.
Genetic analysis, in silico prediction, and family segregation in long QT syndrome.
Riuró H, Campuzano O, Berne P, Arbelo E, Iglesias A, Pérez-Serra A, Coll-Vidal M, Partemi S, Mademont-Soler I, Picó F, Allegue C, Oliva A, Gerstenfeld E, Sarquella-Brugada G, Castro-Urda V, Fernández-Lozano I, Mont L, Brugada J, Scornik FS, Brugada R. Riuró H, et al. Eur J Hum Genet. 2015 Jan;23(1):79-85. doi: 10.1038/ejhg.2014.54. Epub 2014 Mar 26. Eur J Hum Genet. 2015. PMID: 24667783 Free PMC article.
An SCN1B Variant Affects Both Cardiac-Type (NaV1.5) and Brain-Type (NaV1.1) Sodium Currents and Contributes to Complex Concomitant Brain and Cardiac Disorders.
Martinez-Moreno R, Selga E, Riuró H, Carreras D, Parnes M, Srinivasan C, Wangler MF, Pérez GJ, Scornik FS, Brugada R. Martinez-Moreno R, et al. Among authors: riuro h. Front Cell Dev Biol. 2020 Sep 29;8:528742. doi: 10.3389/fcell.2020.528742. eCollection 2020. Front Cell Dev Biol. 2020. PMID: 33134290 Free PMC article.
14 results