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2020 1
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Page 1
BAG3 Genetic Cardiomyopathy May Overlap Fulminant Myocarditis Clinical Findings.
Jordà P, Martínez D, Farrero M, Marcos MÁ, Sandoval E, Castel MÁ, Pereda D, Quintana E, Arbelo E, Sánchez A, Campuzano Ò, Tirón de Llano C, Brugada R, Brugada J, Castellá M, Pérez-Villa F, García-Álvarez A. Jordà P, et al. Among authors: tiron de llano c. Circ Heart Fail. 2022 Mar;15(3):e008443. doi: 10.1161/CIRCHEARTFAILURE.121.008443. Epub 2021 Dec 6. Circ Heart Fail. 2022. PMID: 35290091 No abstract available.
Rare Variants Associated with Arrhythmogenic Cardiomyopathy: Reclassification Five Years Later.
Vallverdú-Prats M, Alcalde M, Sarquella-Brugada G, Cesar S, Arbelo E, Fernandez-Falgueras A, Coll M, Pérez-Serra A, Puigmulé M, Iglesias A, Fiol V, Ferrer-Costa C, Olmo BD, Picó F, Lopez L, Jordà P, García-Álvarez A, Llano CT, Toro R, Grassi S, Oliva A, Brugada J, Brugada R, Campuzano O. Vallverdú-Prats M, et al. Among authors: llano ct. J Pers Med. 2021 Feb 26;11(3):162. doi: 10.3390/jpm11030162. J Pers Med. 2021. PMID: 33652588 Free PMC article.
Clinical impact of rare variants associated with inherited channelopathies: a 5-year update.
Sarquella-Brugada G, Fernandez-Falgueras A, Cesar S, Arbelo E, Coll M, Perez-Serra A, Puigmulé M, Iglesias A, Alcalde M, Vallverdú-Prats M, Fiol V, Ferrer-Costa C, Del Olmo B, Picó F, Lopez L, García-Alvarez A, Jordà P, Tiron de Llano C, Toro R, Grassi S, Oliva A, Brugada J, Brugada R, Campuzano O. Sarquella-Brugada G, et al. Among authors: tiron de llano c. Hum Genet. 2022 Oct;141(10):1579-1589. doi: 10.1007/s00439-021-02370-4. Epub 2021 Sep 21. Hum Genet. 2022. PMID: 34546463 Free PMC article.
Implementing a New Algorithm for Reinterpretation of Ambiguous Variants in Genetic Dilated Cardiomyopathy.
Pérez-Serra A, Toro R, Martinez-Barrios E, Iglesias A, Fernandez-Falgueras A, Alcalde M, Coll M, Puigmulé M, Del Olmo B, Picó F, Lopez L, Arbelo E, Cesar S, Llano CT, Mangas A, Brugada J, Sarquella-Brugada G, Brugada R, Campuzano O. Pérez-Serra A, et al. Among authors: llano ct. Int J Mol Sci. 2024 Mar 29;25(7):3807. doi: 10.3390/ijms25073807. Int J Mol Sci. 2024. PMID: 38612618 Free PMC article.
Reanalysis and reclassification of rare genetic variants associated with inherited arrhythmogenic syndromes.
Campuzano O, Sarquella-Brugada G, Fernandez-Falgueras A, Coll M, Iglesias A, Ferrer-Costa C, Cesar S, Arbelo E, García-Álvarez A, Jordà P, Toro R, Tiron de Llano C, Grassi S, Oliva A, Brugada J, Brugada R. Campuzano O, et al. Among authors: tiron de llano c. EBioMedicine. 2020 Apr;54:102732. doi: 10.1016/j.ebiom.2020.102732. Epub 2020 Apr 5. EBioMedicine. 2020. PMID: 32268277 Free PMC article.