154 related articles for article (PubMed ID: 34204499)
1. Functional Characterization of Two Novel Mutations in
Balla C; Conte E; Selvatici R; Marsano RM; Gerbino A; Farnè M; Blunck R; Vitali F; Armaroli A; Brieda A; Liantonio A; De Luca A; Ferlini A; Rapezzi C; Bertini M; Gualandi F; Imbrici P
Int J Mol Sci; 2021 Jun; 22(12):. PubMed ID: 34204499
[TBL] [Abstract][Full Text] [Related]
2. Genotype-Phenotype Correlation of
Milman A; Behr ER; Gray B; Johnson DC; Andorin A; Hochstadt A; Gourraud JB; Maeda S; Takahashi Y; Jm Juang J; Kim SH; Kamakura T; Aiba T; Postema PG; Mizusawa Y; Denjoy I; Giustetto C; Conte G; Huang Z; Sarquella-Brugada G; Mazzanti A; Jespersen CH; Arbelo E; Brugada R; Calo L; Corrado D; Casado-Arroyo R; Allocca G; Takagi M; Delise P; Brugada J; Tfelt-Hansen J; Priori SG; Veltmann C; Yan GX; Brugada P; Gaita F; Leenhardt A; Wilde AAM; Kusano KF; Nam GB; Hirao K; Probst V; Belhassen B
Circ Genom Precis Med; 2021 Oct; 14(5):e003222. PubMed ID: 34461752
[TBL] [Abstract][Full Text] [Related]
3. De Novo Mutation in the SCN5A Gene Associated with Brugada Syndrome.
Wang L; Meng X; Yuchi Z; Zhao Z; Xu D; Fedida D; Wang Z; Huang C
Cell Physiol Biochem; 2015; 36(6):2250-62. PubMed ID: 26279430
[TBL] [Abstract][Full Text] [Related]
4. GPD1L-A306del modifies sodium current in a family carrying the dysfunctional SCN5A-G1661R mutation associated with Brugada syndrome.
Semino F; Darche FF; Bruehl C; Koenen M; Skladny H; Katus HA; Frey N; Draguhn A; Schweizer PA
Pflugers Arch; 2024 Feb; 476(2):229-242. PubMed ID: 38036776
[TBL] [Abstract][Full Text] [Related]
5. SCN5A-L256del and L1621F exhibit loss-of-function properties related to autosomal recessive congenital cardiac disorders presenting as sick sinus syndrome, dilated cardiomyopathy, and sudden cardiac death.
Shi J; Pan X; Wang Z; Yi M; Xie S; Zhang X; Tao D; Yang Y; Liu Y
Gene; 2024 Mar; 898():148093. PubMed ID: 38123004
[TBL] [Abstract][Full Text] [Related]
6. SCN5A mutation is associated with a higher Shanghai Score in patients with type 1 Brugada ECG pattern.
Tonelli L; Balla C; Farnè M; Margutti A; Maniscalchi ET; De Feo G; Di Domenico A; De Raffele M; Percesepe A; Uliana V; Barili V; Serra W; Sassone B; Virzì S; De Maria E; Parmeggiani G; Assenza GE; Biagini E; Parisi V; Biffi M; Carinci V; Perugini E; Imbrici P; Ferlini A; Bertini M; Selvatici R; Gualandi F
J Cardiovasc Med (Hagerstown); 2023 Dec; 24(12):864-870. PubMed ID: 37942788
[TBL] [Abstract][Full Text] [Related]
7. Unravelling Novel
Frosio A; Micaglio E; Polsinelli I; Calamaio S; Melgari D; Prevostini R; Ghiroldi A; Binda A; Carrera P; Villa M; Mastrocinque F; Presi S; Salerno R; Boccellino A; Anastasia L; Ciconte G; Ricagno S; Pappone C; Rivolta I
Int J Mol Sci; 2023 Oct; 24(20):. PubMed ID: 37894777
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Role of common and rare variants in SCN10A: results from the Brugada syndrome QRS locus gene discovery collaborative study.
Behr ER; Savio-Galimberti E; Barc J; Holst AG; Petropoulou E; Prins BP; Jabbari J; Torchio M; Berthet M; Mizusawa Y; Yang T; Nannenberg EA; Dagradi F; Weeke P; Bastiaenan R; Ackerman MJ; Haunso S; Leenhardt A; Kääb S; Probst V; Redon R; Sharma S; Wilde A; Tfelt-Hansen J; Schwartz P; Roden DM; Bezzina CR; Olesen M; Darbar D; Guicheney P; Crotti L; ; Jamshidi Y
Cardiovasc Res; 2015 Jun; 106(3):520-9. PubMed ID: 25691538
[TBL] [Abstract][Full Text] [Related]
10. A novel NaV1.5 voltage sensor mutation associated with severe atrial and ventricular arrhythmias.
Wang HG; Zhu W; Kanter RJ; Silva JR; Honeywell C; Gow RM; Pitt GS
J Mol Cell Cardiol; 2016 Mar; 92():52-62. PubMed ID: 26801742
[TBL] [Abstract][Full Text] [Related]
11. Loss of sodium current caused by a Brugada syndrome-associated variant is determined by patient-specific genetic background.
Martínez-Moreno R; Carreras D; Sarquella-Brugada G; Pérez GJ; Selga E; Scornik FS; Brugada R
Heart Rhythm; 2024 Mar; 21(3):331-339. PubMed ID: 38008367
[TBL] [Abstract][Full Text] [Related]
12. H558R, a common SCN5A polymorphism, modifies the clinical phenotype of Brugada syndrome by modulating DNA methylation of SCN5A promoters.
Matsumura H; Nakano Y; Ochi H; Onohara Y; Sairaku A; Tokuyama T; Tomomori S; Motoda C; Amioka M; Hironobe N; Toshishige M; Takahashi S; Imai K; Sueda T; Chayama K; Kihara Y
J Biomed Sci; 2017 Dec; 24(1):91. PubMed ID: 29202755
[TBL] [Abstract][Full Text] [Related]
13. Spectrum and prevalence of mutations involving BrS1- through BrS12-susceptibility genes in a cohort of unrelated patients referred for Brugada syndrome genetic testing: implications for genetic testing.
Crotti L; Marcou CA; Tester DJ; Castelletti S; Giudicessi JR; Torchio M; Medeiros-Domingo A; Simone S; Will ML; Dagradi F; Schwartz PJ; Ackerman MJ
J Am Coll Cardiol; 2012 Oct; 60(15):1410-8. PubMed ID: 22840528
[TBL] [Abstract][Full Text] [Related]
14. Challenges in Brugada Syndrome Stratification: Investigating
Tarantino A; Ciconte G; Ghiroldi A; Mastrocinque F; Micaglio E; Boccellino A; Negro G; Piccoli M; Cirillo F; Vicedomini G; Santinelli V; Anastasia L; Pappone C
Int J Mol Sci; 2023 Nov; 24(23):. PubMed ID: 38068978
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Mannitol and hyponatremia regulate cardiac ventricular conduction in the context of sodium channel loss of function.
Blair GA; Wu X; Bain C; Warren M; Hoeker GS; Poelzing S
Am J Physiol Heart Circ Physiol; 2024 Mar; 326(3):H724-H734. PubMed ID: 38214908
[TBL] [Abstract][Full Text] [Related]
17. Genetic Testing in Brugada Syndrome: A 30-Year Experience.
Pannone L; Bisignani A; Osei R; Gauthey A; Sorgente A; Monaco C; Della Rocca DG; Del Monte A; Strazdas A; Mojica J; Al Housari M; Miraglia V; Mouram S; Vetta G; Paparella G; Ramak R; Overeinder I; Bala G; Almorad A; Ströker E; Pappaert G; Sieira J; de Ravel T; La Meir M; Sarkozy A; Brugada P; Chierchia GB; Van Dooren S; de Asmundis C
Circ Arrhythm Electrophysiol; 2024 Apr; 17(4):e012374. PubMed ID: 38426305
[TBL] [Abstract][Full Text] [Related]
18. Sodium channel current loss of function in induced pluripotent stem cell-derived cardiomyocytes from a Brugada syndrome patient.
Selga E; Sendfeld F; Martinez-Moreno R; Medine CN; Tura-Ceide O; Wilmut SI; Pérez GJ; Scornik FS; Brugada R; Mills NL
J Mol Cell Cardiol; 2018 Jan; 114():10-19. PubMed ID: 29024690
[TBL] [Abstract][Full Text] [Related]
19. Clinical characteristics and electrophysiologic properties of SCN5A variants in fever-induced Brugada syndrome.
Chen GX; Barajas-Martínez H; Ciconte G; Wu CI; Monasky MM; Xia H; Li B; Capra JA; Guo K; Zhang ZH; Chen X; Yang B; Jiang H; Tse G; Mak CM; Aizawa Y; Gollob MH; Antzelevitch C; Wilde AAM; Pappone C; Hu D
EBioMedicine; 2023 Jan; 87():104388. PubMed ID: 36516610
[TBL] [Abstract][Full Text] [Related]
20. Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death.
Bezzina CR; Barc J; Mizusawa Y; Remme CA; Gourraud JB; Simonet F; Verkerk AO; Schwartz PJ; Crotti L; Dagradi F; Guicheney P; Fressart V; Leenhardt A; Antzelevitch C; Bartkowiak S; Borggrefe M; Schimpf R; Schulze-Bahr E; Zumhagen S; Behr ER; Bastiaenen R; Tfelt-Hansen J; Olesen MS; Kääb S; Beckmann BM; Weeke P; Watanabe H; Endo N; Minamino T; Horie M; Ohno S; Hasegawa K; Makita N; Nogami A; Shimizu W; Aiba T; Froguel P; Balkau B; Lantieri O; Torchio M; Wiese C; Weber D; Wolswinkel R; Coronel R; Boukens BJ; Bézieau S; Charpentier E; Chatel S; Despres A; Gros F; Kyndt F; Lecointe S; Lindenbaum P; Portero V; Violleau J; Gessler M; Tan HL; Roden DM; Christoffels VM; Le Marec H; Wilde AA; Probst V; Schott JJ; Dina C; Redon R
Nat Genet; 2013 Sep; 45(9):1044-9. PubMed ID: 23872634
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
