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Volumn 12, Issue 5, 2010, Pages 741-742

Screening for, and management of, possible arrhythmogenic syndromes (channelopathies/ion channel diseases)

Author keywords

Brugada syndrome; Cardiac arrhythmia; Catecholaminergic polymorphic ventricular tachycardia; Channelopathies; Long QT syndrome; Short QT syndrome

Indexed keywords

ARRHYTHMOGENESIS; BRUGADA SYNDROME; CATECHOLAMINERGIC POLYMORPHIC VENTRICULAR TACHYCARDIA; CHANNELOPATHY; ELECTROCARDIOGRAPHY; EUROPE; GENETIC ANALYSIS; HEALTH SURVEY; HEART ELECTROPHYSIOLOGY; HUMAN; LONG QT SYNDROME; NON INVASIVE PROCEDURE; PRIORITY JOURNAL; RELATIVE; SCREENING TEST; SHORT QT SYNDROME; SHORT SURVEY; ARRHYTHMIAS, CARDIAC; CHANNELOPATHIES; CLINICAL TRIAL; HEART FUNCTION TEST; INFORMATION PROCESSING; MASS SCREENING; MULTICENTER STUDY; PATHOPHYSIOLOGY; PHYSIOLOGIC MONITORING; TACHYCARDIA, VENTRICULAR; TRENDS;

EID: 77951967643     PISSN: 10995129     EISSN: 15322092     Source Type: Journal    
DOI: 10.1093/europace/euq126     Document Type: Short Survey
Times cited : (9)

References (6)
  • 1
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    • Inherited arrhythmias: A national heart, lung, and blood institute and office of rare diseases workshop consensus report about the diagnosis, phenotyping, molecular mechanisms, and therapeutic approaches for primary cardiomyopathies of gene mutations affecting ion channel function
    • Lehnart SE, Ackerman MJ, Benson DW Jr, Brugada R, Clancy CE, Donahue JK et al. Inherited arrhythmias: a National Heart, Lung, and Blood Institute and Office of Rare Diseases workshop consensus report about the diagnosis, phenotyping, molecular mechanisms, and therapeutic approaches for primary cardiomyopathies of gene mutations affecting ion channel function. Circulation 2007;116, 2325-45.
    • (2007) Circulation , vol.116 , pp. 2325-2345
    • Lehnart, S.E.1    Ackerman, M.J.2    Benson Jr., D.W.3    Brugada, R.4    Clancy, C.E.5    Donahue, J.K.6
  • 3
    • 67651089884 scopus 로고    scopus 로고
    • Mechanisms and clinical management of inherited channelopathies: Long QT syndrome, Brugada syndrome, catecholaminergic polymorphic ventricular tachycardia, and short QT syndrome
    • Kaufman ES. Mechanisms and clinical management of inherited channelopathies: long QT syndrome, Brugada syndrome, catecholaminergic polymorphic ventricular tachycardia, and short QT syndrome. Heart Rhythm 2009;6 (Suppl. 8) : S51-5.
    • (2009) Heart Rhythm , vol.6 , Issue.8 SUPPL.
    • Kaufman, E.S.1
  • 4
    • 38449113610 scopus 로고    scopus 로고
    • Channelopathies in children and adults
    • Wilde AA. Channelopathies in children and adults. Pacing Clin Electrophysiol 2008;31 (Suppl. 1) : S41-5.
    • (2008) Pacing Clin. Electrophysiol. , vol.31 , Issue.1 SUPPL.
    • Wilde, A.A.1
  • 6
    • 50149112857 scopus 로고    scopus 로고
    • The QT syndromes: Long and short
    • Morita H, Wu J, Zipes DP. The QT syndromes: long and short. Lancet 2008;372:750-63.
    • (2008) Lancet , vol.372 , pp. 750-763
    • Morita, H.1    Wu, J.2    Zipes, D.P.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.