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1,105 results

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Discerning the Ambiguous Role of Missense TTN Variants in Inherited Arrhythmogenic Syndromes.
Martínez-Barrios E, Sarquella-Brugada G, Pérez-Serra A, Fernández-Falgueras A, Cesar S, Coll M, Puigmulé M, Iglesias A, Alcalde M, Vallverdú-Prats M, Ferrer-Costa C, Del Olmo B, Picó F, López L, Fiol V, Cruzalegui J, Hernández C, Arbelo E, Grassi S, Oliva A, Toro R, Brugada J, Brugada R, Campuzano O. Martínez-Barrios E, et al. Among authors: oliva a. J Pers Med. 2022 Feb 8;12(2):241. doi: 10.3390/jpm12020241. J Pers Med. 2022. PMID: 35207729 Free PMC article.
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: oliva a. 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
Genetics of arrhythmogenic right ventricular cardiomyopathy.
Campuzano O, Alcalde M, Allegue C, Iglesias A, García-Pavía P, Partemi S, Oliva A, Pascali VL, Berne P, Sarquella-Brugada G, Brugada J, Brugada P, Brugada R. Campuzano O, et al. Among authors: oliva a. J Med Genet. 2013 May;50(5):280-9. doi: 10.1136/jmedgenet-2013-101523. Epub 2013 Mar 6. J Med Genet. 2013. PMID: 23468208 Review.
Coexistence of epilepsy and Brugada syndrome in a family with SCN5A mutation.
Parisi P, Oliva A, Coll Vidal M, Partemi S, Campuzano O, Iglesias A, Pisani D, Pascali VL, Paolino MC, Villa MP, Zara F, Tassinari CA, Striano P, Brugada R. Parisi P, et al. Among authors: oliva a. Epilepsy Res. 2013 Aug;105(3):415-8. doi: 10.1016/j.eplepsyres.2013.02.024. Epub 2013 Mar 25. Epilepsy Res. 2013. PMID: 23538271
1,105 results