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11. Differences in sino-atrial and atrio-ventricular function with age and sex attributable to the Scn5a+/- mutation in a murine cardiac model. Jeevaratnam K; Zhang Y; Guzadhur L; Duehmke RM; Lei M; Grace AA; Huang CL Acta Physiol (Oxf); 2010 Sep; 200(1):23-33. PubMed ID: 20331542 [TBL] [Abstract][Full Text] [Related]
12. Analyses of a novel SCN5A mutation (C1850S): conduction vs. repolarization disorder hypotheses in the Brugada syndrome. Petitprez S; Jespersen T; Pruvot E; Keller DI; Corbaz C; Schläpfer J; Abriel H; Kucera JP Cardiovasc Res; 2008 Jun; 78(3):494-504. PubMed ID: 18252757 [TBL] [Abstract][Full Text] [Related]
13. Structural myocardial abnormalities in asymptomatic family members with Brugada syndrome and SCN5A gene mutation. Frustaci A; Russo MA; Chimenti C Eur Heart J; 2009 Jul; 30(14):1763. PubMed ID: 19411664 [No Abstract] [Full Text] [Related]
14. Transcriptional profiling of ion channel genes in Brugada syndrome and other right ventricular arrhythmogenic diseases. Gaborit N; Wichter T; Varro A; Szuts V; Lamirault G; Eckardt L; Paul M; Breithardt G; Schulze-Bahr E; Escande D; Nattel S; Demolombe S Eur Heart J; 2009 Feb; 30(4):487-96. PubMed ID: 19029124 [TBL] [Abstract][Full Text] [Related]
16. SCN5A mutations and the role of genetic background in the pathophysiology of Brugada syndrome. Probst V; Wilde AA; Barc J; Sacher F; Babuty D; Mabo P; Mansourati J; Le Scouarnec S; Kyndt F; Le Caignec C; Guicheney P; Gouas L; Albuisson J; Meregalli PG; Le Marec H; Tan HL; Schott JJ Circ Cardiovasc Genet; 2009 Dec; 2(6):552-7. PubMed ID: 20031634 [TBL] [Abstract][Full Text] [Related]
17. A paradoxical effect of lidocaine for the N406S mutation of SCN5A associated with Brugada syndrome. Itoh H; Tsuji K; Sakaguchi T; Nagaoka I; Oka Y; Nakazawa Y; Yao T; Jo H; Ashihara T; Ito M; Horie M; Imoto K Int J Cardiol; 2007 Oct; 121(3):239-48. PubMed ID: 17445919 [TBL] [Abstract][Full Text] [Related]
18. The SCN5A gene in Brugada syndrome: mutations, variants, missense and nonsense. What's a clinician to do? Skinner JR; Love DR Heart Rhythm; 2010 Jan; 7(1):50-1. PubMed ID: 20129285 [No Abstract] [Full Text] [Related]
19. A novel SCN5A deletion mutation in a child with ventricular tachycardia, recurrent aborted sudden death, and Brugada electrocardiographic pattern. Márquez MF; Cruz-Robles D; Inés-Real S; Gallardo GJ; Gonzlez-Hermosillo A; Cárdenas M; Vargas-Alarcón G Arch Cardiol Mex; 2007; 77(4):284-7. PubMed ID: 18361072 [TBL] [Abstract][Full Text] [Related]
20. The occurrence of Brugada syndrome and isolated cardiac conductive disease in the same family could be due to a single SCN5A mutation or to the accidental association of both diseases. Six I; Hermida JS; Huang H; Gouas L; Fressart V; Benammar N; Hainque B; Denjoy I; Chahine M; Guicheney P Europace; 2008 Jan; 10(1):79-85. PubMed ID: 18156160 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]