135 related articles for article (PubMed ID: 25051102)
1. SCN5A mutations and polymorphisms in patients with ventricular fibrillation during acute myocardial infarction.
Boehringer T; Bugert P; Borggrefe M; Elmas E
Mol Med Rep; 2014 Oct; 10(4):2039-44. PubMed ID: 25051102
[TBL] [Abstract][Full Text] [Related]
2. Genetic Variants on SCN5A, KCNQ1, and KCNH2 in Patients with Ventricular Arrhythmias during Acute Myocardial Infarction in a Chinese Population.
Wang F; Liu Y; Liao H; Xue Y; Zhan X; Fang X; Liang Y; Wei W; Rao F; Zhang Q; Deng H; Lin Y; Liu F; Lin W; Zhang B; Wu S
Cardiology; 2020; 145(1):38-45. PubMed ID: 31751991
[TBL] [Abstract][Full Text] [Related]
3. Novel mutation in the SCN5A gene associated with arrhythmic storm development during acute myocardial infarction.
Hu D; Viskin S; Oliva A; Carrier T; Cordeiro JM; Barajas-Martinez H; Wu Y; Burashnikov E; Sicouri S; Brugada R; Rosso R; Guerchicoff A; Pollevick GD; Antzelevitch C
Heart Rhythm; 2007 Aug; 4(8):1072-80. PubMed ID: 17675083
[TBL] [Abstract][Full Text] [Related]
4. A Common Variant in SCN5A and the Risk of Ventricular Fibrillation Caused by First ST-Segment Elevation Myocardial Infarction.
Jabbari R; Glinge C; Jabbari J; Risgaard B; Winkel BG; Terkelsen CJ; Tilsted HH; Jensen LO; Hougaard M; Haunsø S; Engstrøm T; Albert CM; Tfelt-Hansen J
PLoS One; 2017; 12(1):e0170193. PubMed ID: 28085969
[TBL] [Abstract][Full Text] [Related]
5. Genetic predisposition and cellular basis for ischemia-induced ST-segment changes and arrhythmias.
Hu D; Viskin S; Oliva A; Cordeiro JM; Guerchicoff A; Pollevick GD; Antzelevitch C
J Electrocardiol; 2007; 40(6 Suppl):S26-9. PubMed ID: 17993325
[TBL] [Abstract][Full Text] [Related]
6. SCN5A mutation associated with acute myocardial infarction.
Oliva A; Hu D; Viskin S; Carrier T; Cordeiro JM; Barajas-Martinez H; Wu Y; Burashnikov E; Brugada R; Rosso R; Guerchicoff A; Pollevick G; Pascali VL; Antzelevitch C
Leg Med (Tokyo); 2009 Apr; 11 Suppl 1(Suppl 1):S206-9. PubMed ID: 19345130
[TBL] [Abstract][Full Text] [Related]
7. [SCN5A mutation in patients with Brugada electrocardiographic pattern induced by fever].
Yu JH; Hu JZ; Zhou H; Liu X; Cao Q; Shen Y; Ma JY; Zhou SZ; Liu XX; Li JX; Chen Q; Cheng XS; Hong K
Zhonghua Xin Xue Guan Bing Za Zhi; 2013 Dec; 41(12):1010-4. PubMed ID: 24524602
[TBL] [Abstract][Full Text] [Related]
8. Role of SCN5A coding and non-coding sequences in Brugada syndrome onset: What's behind the scenes?
Daimi H; Khelil AH; Neji A; Ben Hamda K; Maaoui S; Aranega A; Be Chibani J; Franco D
Biomed J; 2019 Aug; 42(4):252-260. PubMed ID: 31627867
[TBL] [Abstract][Full Text] [Related]
9. Mutation analysis ion channel genes ventricular fibrillation survivors with coronary artery disease.
Novotny T; Kadlecova J; Raudenska M; Bittnerova A; Andrsova I; Florianova A; Vasku A; Neugebauer P; Kozak M; Sepsi M; Krivan L; Gaillyova R; Spinar J
Pacing Clin Electrophysiol; 2011 Jun; 34(6):742-9. PubMed ID: 21410720
[TBL] [Abstract][Full Text] [Related]
10. Elevated oxidative stress is associated with ventricular fibrillation episodes in patients with Brugada-type electrocardiogram without SCN5A mutation.
Tanaka M; Nakamura K; Kusano KF; Morita H; Ohta-Ogo K; Miura D; Miura A; Nakagawa K; Tada T; Murakami M; Nishii N; Nagase S; Hata Y; Kohno K; Ouchida M; Shimizu K; Yutani C; Ohe T; Ito H
Cardiovasc Pathol; 2011; 20(1):e37-42. PubMed ID: 20219395
[TBL] [Abstract][Full Text] [Related]
11. 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]
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. A study of the SCN5A gene in a cohort of 76 patients with Brugada syndrome.
García-Molina E; Lacunza J; Ruiz-Espejo F; Sabater M; García-Alberola A; Gimeno JR; Cañizares F; García A; Martínez P; Valdés M; Tovar I
Clin Genet; 2013 Jun; 83(6):530-8. PubMed ID: 22984773
[TBL] [Abstract][Full Text] [Related]
14. [Single nucleotide polymorphism in SCN5A and the distribution in Chinese Han ethnic group].
Xie XD; Wang XX; Chen JZ; Tao M; Shang YP; Guo XG; Zheng LR
Sheng Li Xue Bao; 2004 Feb; 56(1):36-40. PubMed ID: 14985827
[TBL] [Abstract][Full Text] [Related]
15. SCN5A mutation in Chinese patients with arrhythmogenic right ventricular dysplasia.
Yu J; Hu J; Dai X; Cao Q; Xiong Q; Liu X; Liu X; Shen Y; Chen Q; Hua W; Hong K
Herz; 2014 Mar; 39(2):271-5. PubMed ID: 24317018
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. KCNJ11 polymorphisms and sudden cardiac death in patients with acute myocardial infarction.
Jeron A; Hengstenberg C; Holmer S; Wollnik B; Riegger GA; Schunkert H; Erdmann J
J Mol Cell Cardiol; 2004 Feb; 36(2):287-93. PubMed ID: 14871556
[TBL] [Abstract][Full Text] [Related]
18. Reentry in cardiac ventricular epicardial tissue due to SCN5A L812Q gene mutation: a computational study.
Satish H; Reddy MR
Biomed Phys Eng Express; 2022 Apr; 8(3):. PubMed ID: 35320795
[TBL] [Abstract][Full Text] [Related]
19. Spectrum and prevalence of cardiac sodium channel variants among black, white, Asian, and Hispanic individuals: implications for arrhythmogenic susceptibility and Brugada/long QT syndrome genetic testing.
Ackerman MJ; Splawski I; Makielski JC; Tester DJ; Will ML; Timothy KW; Keating MT; Jones G; Chadha M; Burrow CR; Stephens JC; Xu C; Judson R; Curran ME
Heart Rhythm; 2004 Nov; 1(5):600-7. PubMed ID: 15851227
[TBL] [Abstract][Full Text] [Related]
20. Association of human SCN5A polymorphisms with idiopathic ventricular arrhythmia in a Chinese Han cohort.
Fang DH; Wu LQ; Lu L; Lou S; Gu G; Chen QJ; Pu LJ; Shen WF
Circ J; 2008 Apr; 72(4):592-7. PubMed ID: 18362431
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
