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Volumn 38, Issue 4 SUPPL., 2005, Pages 60-63

Depolarization/repolarization, electrocardiographic abnormalities, and arrhythmias in cardiac channelopathies

Author keywords

Brugada syndrome; Cardiac channelopathies; Catecholaminergic polymorphic ventricular tachycardia; Long QT syndrome; Progressive cardiac conduction defect; Short QT syndrome

Indexed keywords

BRUGADA SYNDROME; CONFERENCE PAPER; ELECTROCARDIOGRAPHY; GENE FUNCTION; HEART ARRHYTHMIA; HEART DEPOLARIZATION; HEART REPOLARIZATION; HEART VENTRICLE ARRHYTHMIA; HUMAN; ION TRANSPORT; JAPAN; MEMBRANE TRANSPORT; MOLECULAR RECOGNITION; PATHOGENESIS; PRIORITY JOURNAL; QT INTERVAL; SOUTHEAST ASIA;

EID: 26444571257     PISSN: 00220736     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jelectrocard.2005.06.007     Document Type: Conference Paper
Times cited : (5)

References (19)
  • 1
    • 3042800339 scopus 로고    scopus 로고
    • Genetics of cardiac arrhythmias and sudden cardiac death
    • S. Priori, and C. Napolitano Genetics of cardiac arrhythmias and sudden cardiac death Ann N Y Acad Sci 1015 2004 96
    • (2004) Ann N Y Acad Sci , vol.1015 , pp. 96
    • Priori, S.1    Napolitano, C.2
  • 2
    • 0034487308 scopus 로고    scopus 로고
    • Idiopathic short QT interval: A new clinical syndrome?
    • I. Gussak, P. Brugada, and J. Brugada Idiopathic short QT interval: a new clinical syndrome? Cardiology 94 2000 99
    • (2000) Cardiology , vol.94 , pp. 99
    • Gussak, I.1    Brugada, P.2    Brugada, J.3
  • 3
    • 13444300924 scopus 로고    scopus 로고
    • Brugada syndrome. Report of the second consensus conference
    • C. Anztelevitch, P. Brugada, and M. Borggrefe Brugada syndrome. Report of the second consensus conference Circulation 111 2005 659
    • (2005) Circulation , vol.111 , pp. 659
    • Anztelevitch, C.1    Brugada, P.2    Borggrefe, M.3
  • 4
    • 2442698830 scopus 로고    scopus 로고
    • Cellular basis and mechanism underlying normal and abnormal myocardial repolarization and arrhythmogenesis
    • C. Antzelevitch Cellular basis and mechanism underlying normal and abnormal myocardial repolarization and arrhythmogenesis Ann Med 36 Suppl 1 2004 5
    • (2004) Ann Med , vol.36 , Issue.1 SUPPL. , pp. 5
    • Antzelevitch, C.1
  • 5
    • 2442712549 scopus 로고    scopus 로고
    • Genes, exercise and sudden death: Molecular basis of familial catecholaminergic polymorphic ventricular tachycardia
    • P.J. Laitinen, H. Swan, and K. Piippo Genes, exercise and sudden death: molecular basis of familial catecholaminergic polymorphic ventricular tachycardia Ann Med 36 Suppl. 1 2004 81
    • (2004) Ann Med , vol.36 , Issue.1 SUPPL. , pp. 81
    • Laitinen, P.J.1    Swan, H.2    Piippo, K.3
  • 6
    • 20044374511 scopus 로고    scopus 로고
    • Double SCN5A mutation underlying asymptomatic Brugada syndrome
    • H. Yokoi, N. Makita, and K. Sasaki Double SCN5A mutation underlying asymptomatic Brugada syndrome Heart Rhythm 2 2005 285
    • (2005) Heart Rhythm , vol.2 , pp. 285
    • Yokoi, H.1    Makita, N.2    Sasaki, K.3
  • 7
    • 0037027484 scopus 로고    scopus 로고
    • Ambulatory electrocardiographic evidence of transmural dispersion of repolarization in patients with long-QT syndrome type 1 and 2
    • M. Viitasalo, L. Oikarinen, and H. Swan Ambulatory electrocardiographic evidence of transmural dispersion of repolarization in patients with long-QT syndrome type 1 and 2 Circulation 106 2002 2473
    • (2002) Circulation , vol.106 , pp. 2473
    • Viitasalo, M.1    Oikarinen, L.2    Swan, H.3
  • 8
    • 0035909898 scopus 로고    scopus 로고
    • Novel SCN5A mutation leading either to isolated cardiac conduction defect or Brugada syndrome in a large French family
    • F. Kyndt, V. Probst, and F. Potet Novel SCN5A mutation leading either to isolated cardiac conduction defect or Brugada syndrome in a large French family Circulation 104 2001 3081
    • (2001) Circulation , vol.104 , pp. 3081
    • Kyndt, F.1    Probst, V.2    Potet, F.3
  • 9
    • 0037428218 scopus 로고    scopus 로고
    • KCNQ1 gain-of-function mutation in familial atrial fibrillation
    • Y.H. Chen, S.J. Xu, and S. Bendahhou KCNQ1 gain-of-function mutation in familial atrial fibrillation Science 299 2003 251
    • (2003) Science , vol.299 , pp. 251
    • Chen, Y.H.1    Xu, S.J.2    Bendahhou, S.3
  • 10
    • 0346727397 scopus 로고    scopus 로고
    • Sudden death associated with short-QT syndrome linked to mutations in HERG
    • R. Brugada, K. Hong, and R. Dumaine Sudden death associated with short-QT syndrome linked to mutations in HERG Circulation 109 2004 30
    • (2004) Circulation , vol.109 , pp. 30
    • Brugada, R.1    Hong, K.2    Dumaine, R.3
  • 11
    • 19944433739 scopus 로고    scopus 로고
    • Further insights into the effect of quinidine in short QT syndrome caused by a mutation in HERG
    • C. Wolpert, R. Schimpf, and C. Giustetto Further insights into the effect of quinidine in short QT syndrome caused by a mutation in HERG J Cardiovasc Electrophysiol 16 2005 54
    • (2005) J Cardiovasc Electrophysiol , vol.16 , pp. 54
    • Wolpert, C.1    Schimpf, R.2    Giustetto, C.3
  • 12
    • 14744273673 scopus 로고    scopus 로고
    • Calcium channel antagonism reduces exercise-induced ventricular arrhythmias in catecholaminergic polymorphic ventricular tachycardia patients with RYR2 mutations
    • H. Swan, P. Laitinen, K. Kontula, and L. Toivonen Calcium channel antagonism reduces exercise-induced ventricular arrhythmias in catecholaminergic polymorphic ventricular tachycardia patients with RYR2 mutations J Cardiovasc Electrophysiol 16 2005 162
    • (2005) J Cardiovasc Electrophysiol , vol.16 , pp. 162
    • Swan, H.1    Laitinen, P.2    Kontula, K.3    Toivonen, L.4
  • 13
    • 0037454049 scopus 로고    scopus 로고
    • Haploinsufficiency in combination with aging causes SCN5A-linked hereditary Lenègre disease
    • V. Probst, F. Kyndt, and F. Potet Haploinsufficiency in combination with aging causes SCN5A-linked hereditary Lenègre disease J Am Coll Cardiol 41 2003 643
    • (2003) J Am Coll Cardiol , vol.41 , pp. 643
    • Probst, V.1    Kyndt, F.2    Potet, F.3
  • 14
    • 0036324229 scopus 로고    scopus 로고
    • Functional and clinical characterization of KCNJ2 mutations associated with LQT7 (Andersen syndrome)
    • M. Tristani-Firouzi, J.L. Jensen, and M.R. Donaldson Functional and clinical characterization of KCNJ2 mutations associated with LQT7 (Andersen syndrome) J Clin Invest 110 2002 381
    • (2002) J Clin Invest , vol.110 , pp. 381
    • Tristani-Firouzi, M.1    Jensen, J.L.2    Donaldson, M.R.3
  • 15
  • 16
    • 0242713010 scopus 로고    scopus 로고
    • A new oral therapy for long QT syndrome. Long-term oral potassium improves repolarization in patients with HERG mutations
    • S.P. Etheridge, S.J. Compton, M. Tristani-Firouzi, and J.W. Mason A new oral therapy for long QT syndrome. Long-term oral potassium improves repolarization in patients with HERG mutations J Am Coll Cardiol 42 2003 1777
    • (2003) J Am Coll Cardiol , vol.42 , pp. 1777
    • Etheridge, S.P.1    Compton, S.J.2    Tristani-Firouzi, M.3    Mason, J.W.4
  • 17
    • 2442662544 scopus 로고    scopus 로고
    • Novel therapeutics for treatment of long-QT syndrome and torsade de pointes
    • I.A. Khan, and R.M. Gowda Novel therapeutics for treatment of long-QT syndrome and torsade de pointes Int J Cardiol 95 2004 1
    • (2004) Int J Cardiol , vol.95 , pp. 1
    • Khan, I.A.1    Gowda, R.M.2
  • 19
    • 20044368228 scopus 로고    scopus 로고
    • Intravenous drug challenge using flecainide and ajmaline in patients with Brugada syndrome
    • C. Wolpert, C. Echternach, and C. Veltmann Intravenous drug challenge using flecainide and ajmaline in patients with Brugada syndrome Heart Rhythm 2 2005 254
    • (2005) Heart Rhythm , vol.2 , pp. 254
    • Wolpert, C.1    Echternach, C.2    Veltmann, C.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.