메뉴 건너뛰기




Volumn , Issue SPEC. ISS., 2002, Pages 11-12

Congenital long QT syndrome;Le syndrome du QT long congénital

(1)  Denjoy, Isabelle a  

a NONE

Author keywords

[No Author keywords available]

Indexed keywords

SODIUM CHANNEL;

EID: 0036743934     PISSN: 1261694X     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Conference Paper
Times cited : (1)

References (10)
  • 1
    • 0031054075 scopus 로고    scopus 로고
    • A novel mutation in the potassium gene channel KvLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome
    • Neyroud N, Tesson F, Denjoy I et al. A novel mutation in the potassium gene channel KvLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome. Nature Genet 1997; 15: 186-7.
    • (1997) Nature Genet , vol.15 , pp. 186-187
    • Neyroud, N.1    Tesson, F.2    Denjoy, I.3
  • 3
    • 0030981050 scopus 로고    scopus 로고
    • Molecular genetics of long QT syndrome from gene to patients
    • Wang Q, Chen Q, Li H et al. Molecular genetics of long QT syndrome from gene to patients. Curr Opin Cardiol 1997; 12: 310-20.
    • (1997) Curr Opin Cardiol , vol.12 , pp. 310-320
    • Wang, Q.1    Chen, Q.2    Li, H.3
  • 4
    • 0029847602 scopus 로고    scopus 로고
    • Multiple mecanisms in the long QT syndrome. Current knoledge, gaps and future directions
    • Roden JM, Lazzara R, Rosen M et al. Multiple mecanisms in the long QT syndrome. Current knoledge, gaps and future directions. Circulation 1996; 94:1996-2012.
    • (1996) Circulation , vol.94 , pp. 1996-2012
    • Roden, J.M.1    Lazzara, R.2    Rosen, M.3
  • 5
    • 0028861892 scopus 로고
    • ECG T-wave patterns in genetically distinct forms of the hereditary long QT syndrome
    • Moss AJ, Zareba W, Benhorin J et al. ECG T-wave patterns in genetically distinct forms of the hereditary long QT syndrome. Circulation 1995; 92: 2929-34.
    • (1995) Circulation , vol.92 , pp. 2929-2934
    • Moss, A.J.1    Zareba, W.2    Benhorin, J.3
  • 6
    • 0035957045 scopus 로고    scopus 로고
    • Notched T waves on Holter recordings enhance detection of patients with LQt2 (HERG) mutations
    • Lupoglazoff JM, Denjoy I, Berthet M et al. Notched T waves on Holter recordings enhance detection of patients with LQt2 (HERG) mutations. Circulation 2001; 103: 1095-101.
    • (2001) Circulation , vol.103 , pp. 1095-1101
    • Lupoglazoff, J.M.1    Denjoy, I.2    Berthet, M.3
  • 7
    • 0035830365 scopus 로고    scopus 로고
    • Genotype-phenotype correlation in the long QT syndrome - Gene-specific triggers for life threatening arrhythmias
    • Schwartz PJ, Priori SG, Spazzolini C et al. Genotype-phenotype correlation in the long QT syndrome - gene-specific triggers for life threatening arrhythmias. Circulation 2001; 103: 89-95.
    • (2001) Circulation , vol.103 , pp. 89-95
    • Schwartz, P.J.1    Priori, S.G.2    Spazzolini, C.3
  • 8
    • 0032189139 scopus 로고    scopus 로고
    • Influence of genotype on the clinical course of the long QT syndrome
    • Zareba W, Moss AJ, Schwartz PJ et al. Influence of genotype on the clinical course of the long QT syndrome. N Engl J Med 1998; 339: 960-5.
    • (1998) N Engl J Med , vol.339 , pp. 960-965
    • Zareba, W.1    Moss, A.J.2    Schwartz, P.J.3
  • 9
    • 0032499656 scopus 로고    scopus 로고
    • Age and gender-related differences in cardiac event in patients with congenital long QT syndrome: Findings from the international LQTS Registry
    • Locati EH, Zareba W, Moss AJ et al. Age and gender-related differences in cardiac event in patients with congenital long QT syndrome: findings from the international LQTS Registry. Circulation 1998; 97: 2237-44.
    • (1998) Circulation , vol.97 , pp. 2237-2244
    • Locati, E.H.1    Zareba, W.2    Moss, A.J.3
  • 10
    • 6844260553 scopus 로고    scopus 로고
    • Intervalle QT et médicaments: Recommandations pour la prescription des médicaments chez les patients atteints de SQTL congénital
    • Le Heuzey JY, Davy JM, Weissenburger J et al. Intervalle QT et médicaments: recommandations pour la prescription des médicaments chez les patients atteints de SQTL congénital Arch Mal Cœur 1998; 91: 59-66.
    • (1998) Arch Mal Cœur , vol.91 , pp. 59-66
    • Le Heuzey, J.Y.1    Davy, J.M.2    Weissenburger, J.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.