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4. SCN5A--a mechanistic link between inherited cardiomyopathies and a predisposition to arrhythmias? Adler E; Fuster V JAMA; 2005 Jan; 293(4):491-3. PubMed ID: 15671436 [No Abstract] [Full Text] [Related]
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6. Divergent biophysical defects caused by mutant sodium channels in dilated cardiomyopathy with arrhythmia. Nguyen TP; Wang DW; Rhodes TH; George AL Circ Res; 2008 Feb; 102(3):364-71. PubMed ID: 18048769 [TBL] [Abstract][Full Text] [Related]
7. Congenital sick sinus syndrome caused by recessive mutations in the cardiac sodium channel gene (SCN5A). Benson DW; Wang DW; Dyment M; Knilans TK; Fish FA; Strieper MJ; Rhodes TH; George AL J Clin Invest; 2003 Oct; 112(7):1019-28. PubMed ID: 14523039 [TBL] [Abstract][Full Text] [Related]
8. Genetic Na+ channelopathies and sinus node dysfunction. Lei M; Huang CL; Zhang Y Prog Biophys Mol Biol; 2008; 98(2-3):171-8. PubMed ID: 19027778 [TBL] [Abstract][Full Text] [Related]
9. Cavotricuspid isthmus ablation and subcutaneous monitoring device implantation in a 2-year-old baby with 2 SCN5A mutations, sinus node dysfunction, atrial flutter recurrences, and drug induced long-QT syndrome: a tricky case of pediatric overlap syndrome? De Filippo P; Ferrari P; Iascone M; Racheli M; Senni M J Cardiovasc Electrophysiol; 2015 Mar; 26(3):346-9. PubMed ID: 25346400 [TBL] [Abstract][Full Text] [Related]
11. SCN5A mutation associated with dilated cardiomyopathy, conduction disorder, and arrhythmia. McNair WP; Ku L; Taylor MR; Fain PR; Dao D; Wolfel E; Mestroni L; Circulation; 2004 Oct; 110(15):2163-7. PubMed ID: 15466643 [TBL] [Abstract][Full Text] [Related]
12. Nav 1.5 mutations linked to dilated cardiomyopathy phenotypes: Is the gating pore current the missing link? Gosselin-Badaroudine P; Moreau A; Chahine M Channels (Austin); 2014; 8(1):90-4. PubMed ID: 24300601 [TBL] [Abstract][Full Text] [Related]
13. Complexities of Genetic Testing in Familial Dilated Cardiomyopathy. Wolf MJ; Noeth D; Rammohan C; Shah SH Circ Cardiovasc Genet; 2016 Feb; 9(1):95-9. PubMed ID: 26884609 [No Abstract] [Full Text] [Related]
14. Novel pore mutation in SCN5A manifests as a spectrum of phenotypes ranging from atrial flutter, conduction disease, and Brugada syndrome to sudden cardiac death. Rossenbacker T; Carroll SJ; Liu H; Kuipéri C; de Ravel TJ; Devriendt K; Carmeliet P; Kass RS; Heidbüchel H Heart Rhythm; 2004 Nov; 1(5):610-5. PubMed ID: 15851228 [TBL] [Abstract][Full Text] [Related]
15. A novel C-terminal truncation SCN5A mutation from a patient with sick sinus syndrome, conduction disorder and ventricular tachycardia. Tan BH; Iturralde-Torres P; Medeiros-Domingo A; Nava S; Tester DJ; Valdivia CR; Tusié-Luna T; Ackerman MJ; Makielski JC Cardiovasc Res; 2007 Dec; 76(3):409-17. PubMed ID: 17897635 [TBL] [Abstract][Full Text] [Related]
16. Sodium channel mutations and susceptibility to heart failure and atrial fibrillation. Olson TM; Michels VV; Ballew JD; Reyna SP; Karst ML; Herron KJ; Horton SC; Rodeheffer RJ; Anderson JL JAMA; 2005 Jan; 293(4):447-54. PubMed ID: 15671429 [TBL] [Abstract][Full Text] [Related]
17. Multiple loss-of-function mechanisms contribute to SCN5A-related familial sick sinus syndrome. Gui J; Wang T; Jones RP; Trump D; Zimmer T; Lei M PLoS One; 2010 Jun; 5(6):e10985. PubMed ID: 20539757 [TBL] [Abstract][Full Text] [Related]
18. Autosomal recessive paediatric sick sinus syndrome associated with novel compound mutations in SCN5A. Kodama T; Serio A; Disertori M; Bronzetti G; Diegoli M; Narula N; Grasso M; Mazzola S; Arbustini E Int J Cardiol; 2013 Sep; 167(6):3078-80. PubMed ID: 23200271 [No Abstract] [Full Text] [Related]
19. Autosomal recessive atrial disease presenting with sick sinus syndrome (SSS), right atrial fibrosis and biatrial dilatation: Clinical impact of genetic diagnosis. De Regibus V; Rordorf R; Giorgianni C; Canclini C; Vicentini A; Taravelli E; Petracci B; Savastano S; De Servi S; Arbustini E Int J Cardiol; 2016 Apr; 208():67-9. PubMed ID: 26828384 [No Abstract] [Full Text] [Related]
20. Mutation-specific effects of polymorphism H558R in SCN5A-related sick sinus syndrome. Gui J; Wang T; Trump D; Zimmer T; Lei M J Cardiovasc Electrophysiol; 2010 May; 21(5):564-73. PubMed ID: 20384651 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]