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Volumn 90, Issue SPEC. ISS. 3, 1997, Pages 25-35

Congenital Long QT syndromes;Syndromes du QT long congenital

Author keywords

Genetique; Phenotype; Syndromes du QT long

Indexed keywords

CHROMOSOME 11; CHROMOSOME 3; CHROMOSOME 4; CHROMOSOME 7; CONFERENCE PAPER; DOMINANT INHERITANCE; ELECTROCARDIOGRAM; GENE LOCATION; HUMAN; LONG QT SYNDROME; MOLECULAR GENETICS; RECESSIVE INHERITANCE; ACTION POTENTIAL; ARTICLE; CHROMOSOME MAP; GENETICS; GENOTYPE; MORTALITY; PATHOPHYSIOLOGY; PHENOTYPE;

EID: 0030795928     PISSN: 00039683     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Conference Paper
Times cited : (4)

References (28)
  • 1
    • 8544241271 scopus 로고
    • Taubstummheit und taubstummtbildung
    • Meisner FL. Taubstummheit und taubstummtbildung. Leipzig und Heidelberg, 1856 ; 119-20.
    • (1856) Leipzig und Heidelberg , pp. 119-120
    • Meisner, F.L.1
  • 2
    • 0011941477 scopus 로고
    • Familial myoclonus epilepsy associated with deaf mutism in a family showing other psychological abnormalities
    • Latham AD, Munro TA. Familial myoclonus epilepsy associated with deaf mutism in a family showing other psychological abnormalities. Ann Eugen Lond 1937 ; 8 : 166-75.
    • (1937) Ann Eugen Lond , vol.8 , pp. 166-175
    • Latham, A.D.1    Munro, T.A.2
  • 4
    • 49749174698 scopus 로고
    • Congenital deaf mutism, functional heart disease with prolongation of the QT interval and sudden death
    • Jervell A, Lange-Nielsen F. Congenital deaf mutism, functional heart disease with prolongation of the QT interval and sudden death. Am Heart J 1957 ; 54 : 59.
    • (1957) Am Heart J , vol.54 , pp. 59
    • Jervell, A.1    Lange-Nielsen, F.2
  • 5
    • 0000819933 scopus 로고
    • Aritmie cardiache rare dell'eta pediatrica
    • Romano C, Gemme G, Pongiglione R. Aritmie cardiache rare dell'eta pediatrica. Clin Pediatr 1963 ; 45 : 658-83.
    • (1963) Clin Pediatr , vol.45 , pp. 658-683
    • Romano, C.1    Gemme, G.2    Pongiglione, R.3
  • 6
    • 0000387603 scopus 로고
    • New familial cardiac syndrome in children
    • Ward OC. New familial cardiac syndrome in children. J Irish Med Assoc 1964; 54 : 103-6.
    • (1964) J Irish Med Assoc , vol.54 , pp. 103-106
    • Ward, O.C.1
  • 7
    • 0026759352 scopus 로고
    • The spectrum of symptoms and QT intervals in carriers of the gene for the long QT syndrome
    • Vincent GM, Timothy KW, Leppert M, Keating M. The spectrum of symptoms and QT intervals in carriers of the gene for the long QT syndrome. N Engl J Med 1992 ; 327 : 846-52.
    • (1992) N Engl J Med , vol.327 , pp. 846-852
    • Vincent, G.M.1    Timothy, K.W.2    Leppert, M.3    Keating, M.4
  • 8
    • 0025935591 scopus 로고
    • The long QT syndrome : Prospective longitudinal study of 328 families
    • Moss AJ, Schwarte PJ, Crampton RS et al. The long QT syndrome : prospective longitudinal study of 328 families. Circulation 1991 ; 84 : 1136-44.
    • (1991) Circulation , vol.84 , pp. 1136-1144
    • Moss, A.J.1    Schwarte, P.J.2    Crampton, R.S.3
  • 9
    • 0025847714 scopus 로고
    • Linkage of a cardiac arrhythmia, the long QT syndrome, and the Harvey ras-1 gene
    • Keating M, Atkinson d, Dunn C, Timothy K, Leppert M, Vincent GM. Linkage of a cardiac arrhythmia, the long QT syndrome, and the Harvey ras-1 gene. Science 1991 ; 252 : 704-6.
    • (1991) Science , vol.252 , pp. 704-706
    • Keating, M.1    Atkinson, D.2    Dunn, C.3    Timothy, K.4    Leppert, M.5    Vincent, G.M.6
  • 10
    • 0028101967 scopus 로고
    • Two long QT syndrome loci map to chromosomes 3 and 7 with evidence for further heterogeneity
    • Jian C, Atkinson D et al. Two long QT syndrome loci map to chromosomes 3 and 7 with evidence for further heterogeneity. Nature Genet 1994 ; 8 : 141-7.
    • (1994) Nature Genet , vol.8 , pp. 141-147
    • Jian, C.1    Atkinson, D.2
  • 11
    • 0028819671 scopus 로고
    • Mapping of a gene for long QT syndrome to chromosome 4q25-27
    • Schott JJ, Charpentier F, Peltier S et al. Mapping of a gene for long QT syndrome to chromosome 4q25-27. Am J Hum Genet 1995 ; 57 : 1114-22.
    • (1995) Am J Hum Genet , vol.57 , pp. 1114-1122
    • Schott, J.J.1    Charpentier, F.2    Peltier, S.3
  • 12
    • 0028082351 scopus 로고
    • Clinical relevance of cardiac arrhythmias generated by afterdepolarizations. Role of M cells in the generation of U waves, triggered activity and torsade de pointe
    • Antzelevitch C, Sicouri S. Clinical relevance of cardiac arrhythmias generated by afterdepolarizations. Role of M cells in the generation of U waves, triggered activity and torsade de pointe. J Am Coll Cardiol 1994 ; 23 : 259-77.
    • (1994) J Am Coll Cardiol , vol.23 , pp. 259-277
    • Antzelevitch, C.1    Sicouri, S.2
  • 13
    • 0027394358 scopus 로고
    • Early after depolarizations and triggered activity : Mechanisms and autonomic regulation
    • Charpentier F, Drouin E, Gauthier C, Le Marec H. Early after depolarizations and triggered activity : mechanisms and autonomic regulation. Fund Clin Pharmacol, 1993 ; 7 : 39-49.
    • (1993) Fund Clin Pharmacol , vol.7 , pp. 39-49
    • Charpentier, F.1    Drouin, E.2    Gauthier, C.3    Le Marec, H.4
  • 15
    • 0028292927 scopus 로고
    • A family of potassium channel genes related to eag in drosophila and mammals
    • Warmke JW, Ganetzky B. A family of potassium channel genes related to eag in drosophila and mammals. Proc Natl Acad Sci USA 1994 ; 91 : 3438-42.
    • (1994) Proc Natl Acad Sci USA , vol.91 , pp. 3438-3442
    • Warmke, J.W.1    Ganetzky, B.2
  • 18
    • 0028905566 scopus 로고
    • SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome
    • Wang Q, She J, Splawski I et al. SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome. Cell 1995 ; 80 : 805-11.
    • (1995) Cell , vol.80 , pp. 805-811
    • Wang, Q.1    She, J.2    Splawski, I.3
  • 20
    • 0029097799 scopus 로고
    • Molecular mechanism for an inherited cardiac arrhythmia
    • Bennett PB, Yazawa K, Makita N, George AJ. Molecular mechanism for an inherited cardiac arrhythmia. Nature 1995 ; 376 : 683-5.
    • (1995) Nature , vol.376 , pp. 683-685
    • Bennett, P.B.1    Yazawa, K.2    Makita, N.3    George, A.J.4
  • 21
    • 0018349527 scopus 로고
    • Steady-state TTX-sensitive (window) current in cardiac Purkinje fibre
    • Attwell D, Cohen I, Eisner D, Ohba M, Ojeda C. Steady-state TTX-sensitive (window) current in cardiac Purkinje fibre. Pflügers Arch 1979 ; 379 : 1137-49.
    • (1979) Pflügers Arch , vol.379 , pp. 1137-1149
    • Attwell, D.1    Cohen, I.2    Eisner, D.3    Ohba, M.4    Ojeda, C.5
  • 22
    • 0029002969 scopus 로고
    • A mechanistic link between an inherited et an acquired cardiac arrhythmia : HERG encodes the IKr potassium channel
    • Sanguinetti MC, Jiang C, Curran ME, Keating MT. A mechanistic link between an inherited et an acquired cardiac arrhythmia : HERG encodes the IKr potassium channel. Cell 1995 ; 81 : 299-307.
    • (1995) Cell , vol.81 , pp. 299-307
    • Sanguinetti, M.C.1    Jiang, C.2    Curran, M.E.3    Keating, M.T.4
  • 26
    • 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
  • 27
    • 0026666322 scopus 로고
    • Clinical aspects of the idiopathic long QT syndrome
    • Moss AJ, Robinson JL. Clinical aspects of the idiopathic long QT syndrome. Ann NY Acad Sci USA 1992 ; 103-11.
    • (1992) Ann NY Acad Sci USA , pp. 103-111
    • Moss, A.J.1    Robinson, J.L.2
  • 28
    • 0028874658 scopus 로고
    • + channel blockade and to increase in heart rate. Implications for gene-specific therapy
    • + channel blockade and to increase in heart rate. Implications for gene-specific therapy. Circulation 1995 ; 92 : 3381-6.
    • (1995) Circulation , vol.92 , pp. 3381-3386
    • Schwartz, P.J.1    Prior, S.G.2    Locati, E.H.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.