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6. SCN5A gene variants and arrhythmic risk in Brugada syndrome: An updated systematic review and meta-analysis. Doundoulakis I; Pannone L; Chiotis S; Della Rocca DG; Sorgente A; Tsioufis P; Del Monte A; Vetta G; Piperis C; Overeinder I; Bala G; Almorad A; Ströker E; Sieira J; La Meir M; Brugada P; Tsiachris D; Sarkozy A; Chierchia GB; de Asmundis C Heart Rhythm; 2024 Oct; 21(10):1987-1997. PubMed ID: 38614189 [TBL] [Abstract][Full Text] [Related]
7. Comparable clinical characteristics in Brugada syndrome patients harboring SCN5A or novel SCN10A variants. Monasky MM; Micaglio E; Vicedomini G; Locati ET; Ciconte G; Giannelli L; Giordano F; Crisà S; Vecchi M; Borrelli V; Ghiroldi A; D'Imperio S; Di Resta C; Benedetti S; Ferrari M; Santinelli V; Anastasia L; Pappone C Europace; 2019 Oct; 21(10):1550-1558. PubMed ID: 31292628 [TBL] [Abstract][Full Text] [Related]
8. Brugada syndrome: clinical presentation and genotype-correlation with magnetic resonance imaging parameters. Rudic B; Schimpf R; Veltmann C; Doesch C; Tülümen E; Schoenberg SO; Borggrefe M; Papavassiliu T Europace; 2016 Sep; 18(9):1411-9. PubMed ID: 26511399 [TBL] [Abstract][Full Text] [Related]
9. Unique clinical characteristics and SCN5A mutations in patients with Brugada syndrome in Taiwan. Juang JM; Tsai CT; Lin LY; Liu YB; Yu CC; Hwang JJ; Chen JJ; Chiu FC; Chen WJ; Tseng CD; Chiang FT; Yeh HM; Sherri Yeh SF; Lai LP; Lin JL J Formos Med Assoc; 2015 Jul; 114(7):620-6. PubMed ID: 26154754 [TBL] [Abstract][Full Text] [Related]
10. GSTM3 variant is a novel genetic modifier in Brugada syndrome, a disease with risk of sudden cardiac death. Juang JJ; Binda A; Lee SJ; Hwang JJ; Chen WJ; Liu YB; Lin LY; Yu CC; Ho LT; Huang HC; Chen CJ; Lu TP; Lai LC; Yeh SS; Lai LP; Chuang EY; Rivolta I; Antzelevitch C EBioMedicine; 2020 Jul; 57():102843. PubMed ID: 32645615 [TBL] [Abstract][Full Text] [Related]
11. Functionally validated SCN5A variants allow interpretation of pathogenicity and prediction of lethal events in Brugada syndrome. Ishikawa T; Kimoto H; Mishima H; Yamagata K; Ogata S; Aizawa Y; Hayashi K; Morita H; Nakajima T; Nakano Y; Nagase S; Murakoshi N; Kowase S; Ohkubo K; Aiba T; Morimoto S; Ohno S; Kamakura S; Nogami A; Takagi M; Karakachoff M; Dina C; Schott JJ; Yoshiura KI; Horie M; Shimizu W; Nishimura K; Kusano K; Makita N Eur Heart J; 2021 Jul; 42(29):2854-2863. PubMed ID: 34219138 [TBL] [Abstract][Full Text] [Related]
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14. Impact of clinical and genetic findings on the management of young patients with Brugada syndrome. Andorin A; Behr ER; Denjoy I; Crotti L; Dagradi F; Jesel L; Sacher F; Petit B; Mabo P; Maltret A; Wong LC; Degand B; Bertaux G; Maury P; Dulac Y; Delasalle B; Gourraud JB; Babuty D; Blom NA; Schwartz PJ; Wilde AA; Probst V Heart Rhythm; 2016 Jun; 13(6):1274-82. PubMed ID: 26921764 [TBL] [Abstract][Full Text] [Related]
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16. Genetic interpretation and clinical translation of minor genes related to Brugada syndrome. Campuzano O; Sarquella-Brugada G; Fernandez-Falgueras A; Cesar S; Coll M; Mates J; Arbelo E; Perez-Serra A; Del Olmo B; Jordá P; Fiol V; Iglesias A; Puigmulé M; Lopez L; Pico F; Brugada J; Brugada R Hum Mutat; 2019 Jun; 40(6):749-764. PubMed ID: 30821013 [TBL] [Abstract][Full Text] [Related]
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19. Multisite Validation of a Functional Assay to Adjudicate Ma JG; O'Neill MJ; Richardson E; Thomson KL; Ingles J; Muhammad A; Solus JF; Davogustto G; Anderson KC; Shoemaker MB; Stergachis AB; Floyd BJ; Dunn K; Parikh VN; Chubb H; Perrin MJ; Roden DM; Vandenberg JI; Ng CA; Glazer AM Circ Genom Precis Med; 2024 Aug; 17(4):e004569. PubMed ID: 38953211 [TBL] [Abstract][Full Text] [Related]
20. Brugada Syndrome: From Molecular Mechanisms and Genetics to Risk Stratification. Popa IP; Șerban DN; Mărănducă MA; Șerban IL; Tamba BI; Tudorancea I Int J Mol Sci; 2023 Feb; 24(4):. PubMed ID: 36834739 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]