335 related articles for article (PubMed ID: 22277643)
1. Criteria to predict carriers of a novel SCN5A mutation in a large Portuguese family affected by the Brugada syndrome.
Santos LF; Rodrigues B; Moreira D; Correia E; Nunes L; Costa A; Elvas L; Pereira T; Machado JC; Castedo S; Henriques C; Matos A; Santos JO
Europace; 2012 Jun; 14(6):882-8. PubMed ID: 22277643
[TBL] [Abstract][Full Text] [Related]
2. [Diagnostic criteria for the Brugada syndrome: can they be improved?].
Santos LF; Pereira T; Rodrigues B; Correia E; Moreira D; Nunes L; Costa A; Elvas L; Machado JC; Castedo S; Henriques C; Matos A; Santos O
Rev Port Cardiol; 2012 May; 31(5):355-62. PubMed ID: 22475738
[TBL] [Abstract][Full Text] [Related]
3. [Doubts of the cardiologist regarding an electrocardiogram presenting QRS V1-V2 complexes with positive terminal wave and ST segment elevation. Consensus Conference promoted by the Italian Cardiology Society].
Oreto G; Corrado D; Delise P; Fedele F; Gaita F; Gentile F; Giustetto C; Michelucci A; Padeletti L; Priori S
G Ital Cardiol (Rome); 2010 Nov; 11(11 Suppl 2):3S-22S. PubMed ID: 21361048
[TBL] [Abstract][Full Text] [Related]
4. Progressive cardiac conduction defect is the prevailing phenotype in carriers of a Brugada syndrome SCN5A mutation.
Probst V; Allouis M; Sacher F; Pattier S; Babuty D; Mabo P; Mansourati J; Victor J; Nguyen JM; Schott JJ; Boisseau P; Escande D; Le Marec H
J Cardiovasc Electrophysiol; 2006 Mar; 17(3):270-5. PubMed ID: 16643399
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. [Novel SCN5A gene mutations associated with Brugada syndrome: V95I, A1649V and delF1617].
Liang P; Liu WL; Hu DY; Li CL; Tao WH; Li L
Zhonghua Xin Xue Guan Bing Za Zhi; 2006 Jul; 34(7):616-9. PubMed ID: 17081365
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. Prospective evaluation of the familial prevalence of the brugada syndrome.
Hermida JS; Dassonvalle E; Six I; Amant C; Coviaux F; Clerc J; Herent D; Hermida A; Rochette J; Jarry G
Am J Cardiol; 2010 Dec; 106(12):1758-62. PubMed ID: 21126620
[TBL] [Abstract][Full Text] [Related]
10. What can be done when asymptomatic patients discover they have Brugada syndrome? A case report of Brugada syndrome.
Doetzer AD; Sotomaior VS; Bubna MH; Raskin S
Int J Cardiol; 2011 Aug; 150(3):e96-7. PubMed ID: 20381179
[TBL] [Abstract][Full Text] [Related]
11. Diagnostic value of flecainide testing in unmasking SCN5A-related Brugada syndrome.
Meregalli PG; Ruijter JM; Hofman N; Bezzina CR; Wilde AA; Tan HL
J Cardiovasc Electrophysiol; 2006 Aug; 17(8):857-64. PubMed ID: 16764707
[TBL] [Abstract][Full Text] [Related]
12. Brugada syndrome.
Napolitano C; Priori SG
Orphanet J Rare Dis; 2006 Sep; 1():35. PubMed ID: 16972995
[TBL] [Abstract][Full Text] [Related]
13. Number of electrocardiogram leads displaying the diagnostic coved-type pattern in Brugada syndrome: a diagnostic consensus criterion to be revised.
Richter S; Sarkozy A; Paparella G; Henkens S; Boussy T; Chierchia GB; Brugada R; Brugada J; Brugada P
Eur Heart J; 2010 Jun; 31(11):1357-64. PubMed ID: 20233789
[TBL] [Abstract][Full Text] [Related]
14. Differences in 12-lead electrocardiogram between symptomatic and asymptomatic Brugada syndrome patients.
Junttila MJ; Brugada P; Hong K; Lizotte E; DE Zutter M; Sarkozy A; Brugada J; Benito B; Perkiomaki JS; Mäkikallio TH; Huikuri HV; Brugada R
J Cardiovasc Electrophysiol; 2008 Apr; 19(4):380-3. PubMed ID: 18081770
[TBL] [Abstract][Full Text] [Related]
15. Facilitatory and inhibitory effects of SCN5A mutations on atrial fibrillation in Brugada syndrome.
Amin AS; Boink GJ; Atrafi F; Spanjaart AM; Asghari-Roodsari A; Molenaar RJ; Ruijter JM; Wilde AA; Tan HL
Europace; 2011 Jul; 13(7):968-75. PubMed ID: 21273195
[TBL] [Abstract][Full Text] [Related]
16. Are women with severely symptomatic brugada syndrome different from men?
Sacher F; Meregalli P; Veltmann C; Field ME; Solnon A; Bru P; Abbey S; Jaïs P; Tan HL; Wolpert C; Lande G; Bertault V; Derval N; Babuty D; Lacroix D; Boveda S; Maury P; Hocini M; Clémenty J; Mabo P; Lemarec H; Mansourati J; Borggrefe M; Wilde A; Haïssaguerre M; Probst V
J Cardiovasc Electrophysiol; 2008 Nov; 19(11):1181-5. PubMed ID: 18554195
[TBL] [Abstract][Full Text] [Related]
17. Comparison of long-term follow-up of electrocardiographic features in Brugada syndrome between the SCN5A-positive probands and the SCN5A-negative probands.
Yokokawa M; Noda T; Okamura H; Satomi K; Suyama K; Kurita T; Aihara N; Kamakura S; Shimizu W
Am J Cardiol; 2007 Aug; 100(4):649-55. PubMed ID: 17697823
[TBL] [Abstract][Full Text] [Related]
18. Sodium channelopathies: do we really understand what's going on?
Postema PG; Mosterd A; Hofman N; Alders M; Wilde AA
J Cardiovasc Electrophysiol; 2011 May; 22(5):590-3. PubMed ID: 20812931
[TBL] [Abstract][Full Text] [Related]
19. Novel sodium channel SCN5A mutations in Brugada syndrome patients from Greece.
Kotta CM; Anastasakis A; Gatzoulis K; Manolis AS; Stefanadis C
Int J Cardiol; 2010 Nov; 145(1):45-8. PubMed ID: 19406494
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]