406 related articles for article (PubMed ID: 32998306)
1. Update on Genetic Basis of Brugada Syndrome: Monogenic, Polygenic or Oligogenic?
Campuzano O; Sarquella-Brugada G; Cesar S; Arbelo E; Brugada J; Brugada R
Int J Mol Sci; 2020 Sep; 21(19):. PubMed ID: 32998306
[TBL] [Abstract][Full Text] [Related]
2. Dual phenotypic transmission in Brugada syndrome.
Hermida JS; Arnalsteen-Dassonvalle E; Kubala M; Mathiron A; Traulle S; Anbazhagan K; Hermida A; Rochette J
Arch Cardiovasc Dis; 2013; 106(6-7):366-72. PubMed ID: 23810369
[TBL] [Abstract][Full Text] [Related]
3. A balanced translocation disrupting SCN5A in a family with Brugada syndrome and sudden cardiac death.
Yeates L; Ingles J; Gray B; Singarayar S; Sy RW; Semsarian C; Bagnall RD
Heart Rhythm; 2019 Feb; 16(2):231-238. PubMed ID: 30170230
[TBL] [Abstract][Full Text] [Related]
4. [Genetic and molecular basis for sodium channel-mediated Brugada syndrome].
Barajas-Martínez H; Hu D; Antzelevitch C
Arch Cardiol Mex; 2013; 83(4):295-302. PubMed ID: 24269159
[TBL] [Abstract][Full Text] [Related]
5. Genetic Analysis of Arrhythmogenic Diseases in the Era of NGS: The Complexity of Clinical Decision-Making in Brugada Syndrome.
Allegue C; Coll M; Mates J; Campuzano O; Iglesias A; Sobrino B; Brion M; Amigo J; Carracedo A; Brugada P; Brugada J; Brugada R
PLoS One; 2015; 10(7):e0133037. PubMed ID: 26230511
[TBL] [Abstract][Full Text] [Related]
6. Variants in the SCN5A Promoter Associated With Various Arrhythmia Phenotypes.
Yagihara N; Watanabe H; Barnett P; Duboscq-Bidot L; Thomas AC; Yang P; Ohno S; Hasegawa K; Kuwano R; Chatel S; Redon R; Schott JJ; Probst V; Koopmann TT; Bezzina CR; Wilde AA; Nakano Y; Aiba T; Miyamoto Y; Kamakura S; Darbar D; Donahue BS; Shigemizu D; Tanaka T; Tsunoda T; Suda M; Sato A; Minamino T; Endo N; Shimizu W; Horie M; Roden DM; Makita N
J Am Heart Assoc; 2016 Sep; 5(9):. PubMed ID: 27625342
[TBL] [Abstract][Full Text] [Related]
7. Pilsicainide Administration Unmasks a Phenotype of Brugada Syndrome in a Patient with Overlap Syndrome due to the E1784K SCN5A Mutation.
Hasebe H; Yokoya T; Murakoshi N; Kurebayashi N
Intern Med; 2020 Jan; 59(1):83-87. PubMed ID: 31484910
[TBL] [Abstract][Full Text] [Related]
8. The Genetics of Brugada Syndrome.
Cerrone M; Costa S; Delmar M
Annu Rev Genomics Hum Genet; 2022 Aug; 23():255-274. PubMed ID: 35567276
[TBL] [Abstract][Full Text] [Related]
9. Brugada syndrome.
Brugada R; Campuzano O; Sarquella-Brugada G; Brugada J; Brugada P
Methodist Debakey Cardiovasc J; 2014; 10(1):25-8. PubMed ID: 24932359
[TBL] [Abstract][Full Text] [Related]
10. Lack of genotype-phenotype correlation in Brugada Syndrome and Sudden Arrhythmic Death Syndrome families with reported pathogenic SCN1B variants.
Gray B; Hasdemir C; Ingles J; Aiba T; Makita N; Probst V; Wilde AAM; Newbury-Ecob R; Sheppard MN; Semsarian C; Sy RW; Behr ER
Heart Rhythm; 2018 Jul; 15(7):1051-1057. PubMed ID: 29758173
[TBL] [Abstract][Full Text] [Related]
11. Identification of a SCN5A founder mutation causing sudden death, Brugada syndrome, and conduction blocks in Southern Italy.
Curcio A; Malovini A; Mazzanti A; Memmi M; Gambelli P; La Rosa F; Bloise R; Indolfi C; Bellazzi R; Napolitano C
Heart Rhythm; 2021 Oct; 18(10):1698-1706. PubMed ID: 34245912
[TBL] [Abstract][Full Text] [Related]
12. Brugada syndrome and abnormal splicing of SCN5A in myotonic dystrophy type 1.
Wahbi K; Algalarrondo V; Bécane HM; Fressart V; Beldjord C; Azibi K; Lazarus A; Berber N; Radvanyi-Hoffman H; Stojkovic T; Béhin A; Laforêt P; Eymard B; Hatem S; Duboc D
Arch Cardiovasc Dis; 2013 Dec; 106(12):635-43. PubMed ID: 24140416
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Reappraisal of Reported Genes for Sudden Arrhythmic Death: Evidence-Based Evaluation of Gene Validity for Brugada Syndrome.
Hosseini SM; Kim R; Udupa S; Costain G; Jobling R; Liston E; Jamal SM; Szybowska M; Morel CF; Bowdin S; Garcia J; Care M; Sturm AC; Novelli V; Ackerman MJ; Ware JS; Hershberger RE; Wilde AAM; Gollob MH;
Circulation; 2018 Sep; 138(12):1195-1205. PubMed ID: 29959160
[TBL] [Abstract][Full Text] [Related]
15. Novel
Monasky MM; Micaglio E; Ciconte G; Rivolta I; Borrelli V; Ghiroldi A; D'Imperio S; Binda A; Melgari D; Benedetti S; Mitrovic P; Anastasia L; Mecarocci V; Ćalović Ž; Casari G; Pappone C
Int J Mol Sci; 2021 Apr; 22(9):. PubMed ID: 33946750
[TBL] [Abstract][Full Text] [Related]
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]
17. Myotonic dystrophy type 1 mimics and exacerbates Brugada phenotype induced by Nav1.5 sodium channel loss-of-function mutation.
Pambrun T; Mercier A; Chatelier A; Patri S; Schott JJ; Le Scouarnec S; Chahine M; Degand B; Bois P
Heart Rhythm; 2014 Aug; 11(8):1393-400. PubMed ID: 24768612
[TBL] [Abstract][Full Text] [Related]
18. In silico validation revealed the role of SCN5A mutations and their genotype-phenotype correlations in Brugada syndrome.
Pham HM; Nguyen DP; Ta TD; Le TP; Phan PH; Trinh HA; Tran TV; Luong TLA; Nguyen HM; Bui TH; Tran TH; Ta TV; Tran VK
Mol Genet Genomic Med; 2023 Dec; 11(12):e2263. PubMed ID: 37547970
[TBL] [Abstract][Full Text] [Related]
19. Enhanced Classification of Brugada Syndrome-Associated and Long-QT Syndrome-Associated Genetic Variants in the SCN5A-Encoded Na(v)1.5 Cardiac Sodium Channel.
Kapplinger JD; Giudicessi JR; Ye D; Tester DJ; Callis TE; Valdivia CR; Makielski JC; Wilde AA; Ackerman MJ
Circ Cardiovasc Genet; 2015 Aug; 8(4):582-95. PubMed ID: 25904541
[TBL] [Abstract][Full Text] [Related]
20. Risk factors for cardiac events in patients with Brugada syndrome: A PRISMA-compliant meta-analysis and systematic review.
Wu W; Tian L; Ke J; Sun Y; Wu R; Zhu J; Ke Q
Medicine (Baltimore); 2016 Jul; 95(30):e4214. PubMed ID: 27472692
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
