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Volumn 8, Issue 4, 2003, Pages 352-355

Bundle branch reentrant ventricular tachycardia in a patient with the Brugada electrocardiographic pattern

Author keywords

Brugada syndrome; Bundle branch reentrant ventricular tachycardia; Conduction system disease

Indexed keywords

PROCAINAMIDE;

EID: 1542471864     PISSN: 1082720X     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1542-474X.2003.08414.x     Document Type: Article
Times cited : (11)

References (9)
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  • 2
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  • 3
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    • Cellular basis for the Brugada syndrome and other mechanisms of arrhythmogenesis associated with ST-segment elevation
    • Yan G-X, Antzelevitch C. Cellular basis for the Brugada syndrome and other mechanisms of arrhythmogenesis associated with ST-segment elevation. Circulation 1999;100:1660-1666.
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    • Yan, G.-X.1    Antzelevitch, C.2
  • 4
    • 0029775107 scopus 로고    scopus 로고
    • Sustained monomorphic ventricular tachycardia in a patient with Brugada syndrome
    • Shimada M, Miyazaki T, Miyoshi S, et al. Sustained monomorphic ventricular tachycardia in a patient with Brugada syndrome. Jpn Circ J 1996;60:364-370.
    • (1996) Jpn Circ J , vol.60 , pp. 364-370
    • Shimada, M.1    Miyazaki, T.2    Miyoshi, S.3
  • 5
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    • Brugada Syndrome: A case report of monomorphic ventricular tachycardia
    • Boersma LVA, Jaarsma W, Jessurun ER, et al. Brugada Syndrome: A case report of monomorphic ventricular tachycardia. PACE 2001;24:112-115.
    • (2001) PACE , vol.24 , pp. 112-115
    • Boersma, L.V.A.1    Jaarsma, W.2    Jessurun, E.R.3
  • 6
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    • Bundle branch reentry ventricular tachycardia
    • Tchou P, Mehdirad AA. Bundle branch reentry ventricular tachycardia. PACE 1995;18:1427-1437.
    • (1995) PACE , vol.18 , pp. 1427-1437
    • Tchou, P.1    Mehdirad, A.A.2
  • 7
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    • Genetic basis and molecular mechanism for idiopathic ventricular fibrillation
    • Chen Q, Kirsch GE, Zhang D, et al. Genetic basis and molecular mechanism for idiopathic ventricular fibrillation. Nature 1998;392:293-296
    • (1998) Nature , vol.392 , pp. 293-296
    • Chen, Q.1    Kirsch, G.E.2    Zhang, D.3
  • 8
    • 0003096674 scopus 로고    scopus 로고
    • Cardiac conduction defects associate with mutations in SCN5A
    • Schott JJ, Alshinawi C, Kyndt F, et al. Cardiac conduction defects associate with mutations in SCN5A. Nat Genet 1999;23:20.
    • (1999) Nat Genet , vol.23 , pp. 20
    • Schott, J.J.1    Alshinawi, C.2    Kyndt, F.3
  • 9
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    • Novel SCN5A mutation leading either to isolated cardiac conduction defect or Brugada syndrome in a large French family
    • Kyndt F, Probst V, Potet F, et al. Novel SCN5A mutation leading either to isolated cardiac conduction defect or Brugada syndrome in a large French family. Circulation 2001;104:3081-3086.
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    • Kyndt, F.1    Probst, V.2    Potet, F.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.