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Volumn 18, Issue 11, 2007, Pages 1157-1160

In vivo effects of mutant HERG K+ channel inhibition by disopyramide in patients with a short QT-1 Syndrome: A pilot study

Author keywords

[No Author keywords available]

Indexed keywords

DISOPYRAMIDE; POTASSIUM CHANNEL HERG; QUINIDINE;

EID: 35348967333     PISSN: 10453873     EISSN: 15408167     Source Type: Journal    
DOI: 10.1111/j.1540-8167.2007.00925.x     Document Type: Article
Times cited : (42)

References (17)
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  • 5
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    • Congenital short QT syndrome and implantable cardioverter defibrillator treatment: Inherent risk for inappropriate shock delivery
    • Schimpf R, Wolpert C, Bianchi F, Giustetto C, Gaita F, Bauersfeld U, Borggrefe M : Congenital short QT syndrome and implantable cardioverter defibrillator treatment: Inherent risk for inappropriate shock delivery. J Cardiovasc Electrophysiol 2003 14 : 1273 1277.
    • (2003) J Cardiovasc Electrophysiol , vol.14 , pp. 1273-1277
    • Schimpf, R.1    Wolpert, C.2    Bianchi, F.3    Giustetto, C.4    Gaita, F.5    Bauersfeld, U.6    Borggrefe, M.7
  • 9
    • 33748430102 scopus 로고    scopus 로고
    • Disopyramide is an effective inhibitor of mutant HERG K+ channels involved in variant 1 short QT syndrome
    • McPate MJ, Duncan RS, Witchel HJ, Hancox JC : Disopyramide is an effective inhibitor of mutant HERG K+ channels involved in variant 1 short QT syndrome. J Mol Cell Cardiol 2006 41 : 563 566.
    • (2006) J Mol Cell Cardiol , vol.41 , pp. 563-566
    • McPate, M.J.1    Duncan, R.S.2    Witchel, H.J.3    Hancox, J.C.4
  • 10
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    • Disopyramide: Although potentially life-threatening in the setting of long QT, could it be life-saving in short QT syndrome?
    • Dumaine R, Antzelevitch C : Disopyramide: Although potentially life-threatening in the setting of long QT, could it be life-saving in short QT syndrome? J Mol Cell Cardiol 2006 41 : 421 423.
    • (2006) J Mol Cell Cardiol , vol.41 , pp. 421-423
    • Dumaine, R.1    Antzelevitch, C.2
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    • An improved method for adjusting the QT interval for heart rate (the Framingham Heart Study)
    • Sagie A, Larson MG, Goldberg RJ, Bengtson JR, Levy D : An improved method for adjusting the QT interval for heart rate (the Framingham Heart Study). Am J Cardiol 1992 70 : 797 801.
    • (1992) Am J Cardiol , vol.70 , pp. 797-801
    • Sagie, A.1    Larson, M.G.2    Goldberg, R.J.3    Bengtson, J.R.4    Levy, D.5
  • 13
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    • Modulation of transmural repolarization
    • Antzelevitch C : Modulation of transmural repolarization. Ann NY Acad Sci 2005 1047 : 314 323.
    • (2005) Ann NY Acad Sci , vol.1047 , pp. 314-323
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  • 16
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    • Modulation of I(Kr) inactivation by mutation N588K in KCNH2: A link to arrhythmogenesis in short QT syndrome
    • Cordeiro JM, Brugada R, Wu YS, Hong K, Dumaine R : Modulation of I(Kr) inactivation by mutation N588K in KCNH2: A link to arrhythmogenesis in short QT syndrome. Cardiovasc Res 2005 67 : 498 509.
    • (2005) Cardiovasc Res , vol.67 , pp. 498-509
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    • Comparison of the effect of class IA antiarrhythmic drugs on transmembrane potassium currents in rabbit ventricular myocytes
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.