메뉴 건너뛰기




Volumn 4, Issue 12, 2007, Pages 1568-1572

Coinheritance of long QT syndrome and Kearns-Sayre syndrome

Author keywords

Complete atrioventricular block; Kearns Sayre syndrome; Long QT syndrome mutation; Mitochondrial disorder; Torsades de pointes

Indexed keywords

LACTIC ACID; MITOCHONDRIAL DNA; NADOLOL; POTASSIUM; POTASSIUM CHANNEL KCNQ1;

EID: 36749011258     PISSN: 15475271     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.hrthm.2007.08.013     Document Type: Article
Times cited : (15)

References (16)
  • 4
    • 0019351926 scopus 로고
    • Myocardial ultrastructure and the development of atrioventricular block in Kearns-Sayre syndrome
    • Charles R., Holt S., Kay J.M., Epstein E.J., and Russell Rees J. Myocardial ultrastructure and the development of atrioventricular block in Kearns-Sayre syndrome. Circulation 63 (1981) 214-219
    • (1981) Circulation , vol.63 , pp. 214-219
    • Charles, R.1    Holt, S.2    Kay, J.M.3    Epstein, E.J.4    Russell Rees, J.5
  • 5
    • 0023794212 scopus 로고
    • Syndrome de Kearns-Sayre: bloc auriculoventriculaire complet, torsade de pointes et fibrillation ventriculaire (abstract)
    • Biard F., Philippe C., Berrut G., Lardy B., and Slama R. Syndrome de Kearns-Sayre: bloc auriculoventriculaire complet, torsade de pointes et fibrillation ventriculaire (abstract). Ann Cardiol Angeiol 37 (1988) 529-534
    • (1988) Ann Cardiol Angeiol , vol.37 , pp. 529-534
    • Biard, F.1    Philippe, C.2    Berrut, G.3    Lardy, B.4    Slama, R.5
  • 6
    • 0036200092 scopus 로고    scopus 로고
    • Kearns-Sayre syndrome: association with long QT syndrome?
    • Rashid A., and Kim M.H. Kearns-Sayre syndrome: association with long QT syndrome?. J Cardiovasc Electrophysiol 13 (2002) 184-185
    • (2002) J Cardiovasc Electrophysiol , vol.13 , pp. 184-185
    • Rashid, A.1    Kim, M.H.2
  • 8
    • 33846308490 scopus 로고    scopus 로고
    • Torsades de pointes in a patient with Kearns-Sayre syndrome: a fortunate finding
    • Subbiah R.N., Kuchar D., and Baron D. Torsades de pointes in a patient with Kearns-Sayre syndrome: a fortunate finding. Pace 30 (2007) 137-139
    • (2007) Pace , vol.30 , pp. 137-139
    • Subbiah, R.N.1    Kuchar, D.2    Baron, D.3
  • 11
    • 17144415220 scopus 로고    scopus 로고
    • Compendium of cardiac channel mutations in 541 consecutive unrelated patients referred for long QT syndrome genetic testing
    • Tester D.J., Will M.L., Haglund C.M., and Ackerman M.J. Compendium of cardiac channel mutations in 541 consecutive unrelated patients referred for long QT syndrome genetic testing. Heart Rhythm 2 (2005) 507-517
    • (2005) Heart Rhythm , vol.2 , pp. 507-517
    • Tester, D.J.1    Will, M.L.2    Haglund, C.M.3    Ackerman, M.J.4
  • 13
    • 0025314193 scopus 로고
    • Renal tubular involvement mimicking Bartter syndrome in a patient with Kearns-Sayre syndrome
    • Goto Y., Itami N., Kajii N., Tochimaru H., Endo M., and Horai S. Renal tubular involvement mimicking Bartter syndrome in a patient with Kearns-Sayre syndrome. J Pediatr 116 (1990) 904-910
    • (1990) J Pediatr , vol.116 , pp. 904-910
    • Goto, Y.1    Itami, N.2    Kajii, N.3    Tochimaru, H.4    Endo, M.5    Horai, S.6
  • 15
    • 0027442575 scopus 로고
    • Identification of a proline residue as a transduction element involved in voltage gating of gap junctions
    • Suchyna T.M., Xu L.X., Gao F., Fourtner C.R., and Nicholsen B.J. Identification of a proline residue as a transduction element involved in voltage gating of gap junctions. Nature 365 (1993) 847-849
    • (1993) Nature , vol.365 , pp. 847-849
    • Suchyna, T.M.1    Xu, L.X.2    Gao, F.3    Fourtner, C.R.4    Nicholsen, B.J.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.