메뉴 건너뛰기




Volumn 93, Issue 2, 2004, Pages 231-234

A novel form of familial bidirectional ventricular tachycardia

Author keywords

[No Author keywords available]

Indexed keywords

CALCIUM;

EID: 0348223717     PISSN: 00029149     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.amjcard.2003.09.049     Document Type: Article
Times cited : (11)

References (17)
  • 6
    • 0035895322 scopus 로고    scopus 로고
    • Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardia
    • Priori S., Napolitano C., Tiso N., Memmi M., Viganti G., Bloise R., Sorrentino V., Danieli E. Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardia. Circulation. 103:2001;196-200.
    • (2001) Circulation , vol.103 , pp. 196-200
    • Priori, S.1    Napolitano, C.2    Tiso, N.3    Memmi, M.4    Viganti, G.5    Bloise, R.6    Sorrentino, V.7    Danieli, E.8
  • 9
    • 0035253502 scopus 로고    scopus 로고
    • Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy 2 (ARVD2)
    • Tiso N., Stephan D.A., Nava A., Bagattin A., Devaney J.M., Stanchi F., Larderet G., Brahmbhatt B., Brown K., Bauce B., et al. Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy 2 (ARVD2). Hum Mol Gent. 10:2001;189-194.
    • (2001) Hum Mol Gent , vol.10 , pp. 189-194
    • Tiso, N.1    Stephan, D.A.2    Nava, A.3    Bagattin, A.4    Devaney, J.M.5    Stanchi, F.6    Larderet, G.7    Brahmbhatt, B.8    Brown, K.9    Bauce, B.10
  • 10
    • 0001127258 scopus 로고
    • An analysis of the time relation of electrocardiograms
    • Bazzet HC. An analysis of the time relation of electrocardiograms. Heart 1920:353-370.
    • (1920) Heart , pp. 353-370
    • Bazzet, H.C.1
  • 11
    • 85030915704 scopus 로고    scopus 로고
    • Primer 3. Availabe at: http://www-genome.wi.mit.edu/cgi-bin/primer/ primer 3_www.cgi.
    • Primer 3
  • 12
    • 85030928366 scopus 로고    scopus 로고
    • GDB. Available at: http://www.gdb.org/.
  • 13
    • 0030770826 scopus 로고    scopus 로고
    • Complex formation between junctin, triadin, calsequestrin, and the ryanodine receptor. Proteins of the cardiac junctional sarcoplasmic reticulum membrane
    • Zhang L., Kelly J., Schmeisser G., Kobayashi Y.M., Jones L.R. Complex formation between junctin, triadin, calsequestrin, and the ryanodine receptor. Proteins of the cardiac junctional sarcoplasmic reticulum membrane. J Biol Chem. 272:1997;23389-23397.
    • (1997) J Biol Chem , vol.272 , pp. 23389-23397
    • Zhang, L.1    Kelly, J.2    Schmeisser, G.3    Kobayashi, Y.M.4    Jones, L.R.5
  • 14
    • 0036645576 scopus 로고    scopus 로고
    • Clinical implications of cardiac ryanodine receptor/calcium release channel mutations linked to sudden cardiac death
    • Marks A. Clinical implications of cardiac ryanodine receptor/calcium release channel mutations linked to sudden cardiac death. Circulation. 106:2002;8-10.
    • (2002) Circulation , vol.106 , pp. 8-10
    • Marks, A.1
  • 15
    • 0035849570 scopus 로고    scopus 로고
    • Autosomal recessive catecholamine- or exercise-induced polymorphic ventricular tachycardia: Clinical features and assignment of the disease gene to chromosome 1p13-21
    • Lahat H., Eldar M., Nissenbaum E., Bahan T., Freidman E., Khoury A., Lorber A., Kastner D., Goldman B., Pras E. Autosomal recessive catecholamine- or exercise-induced polymorphic ventricular tachycardia clinical features and assignment of the disease gene to chromosome 1p13-21 . Circulation. 103:2001;2822-2827.
    • (2001) Circulation , vol.103 , pp. 2822-2827
    • Lahat, H.1    Eldar, M.2    Nissenbaum, E.3    Bahan, T.4    Freidman, E.5    Khoury, A.6    Lorber, A.7    Kastner, D.8    Goldman, B.9    Pras, E.10
  • 16
    • 0035205336 scopus 로고    scopus 로고
    • A missense mutation in a highly conserved region of CASQ2 is associated with autosomal recessive catecholamine-induced polymorphic ventricular tachycardia in Bedouin families from Israel
    • Lahat H., Pras E., Olender T., Avidan N., Ben-Asher E., Man O., Levy-Nissenbaum E., Khoury A., Lorber A., Goldman B., Lancet D., Eldar M. A missense mutation in a highly conserved region of CASQ2 is associated with autosomal recessive catecholamine-induced polymorphic ventricular tachycardia in Bedouin families from Israel. Am J Genet. 69:2001;1378-1384.
    • (2001) Am J Genet , vol.69 , pp. 1378-1384
    • Lahat, H.1    Pras, E.2    Olender, T.3    Avidan, N.4    Ben-Asher, E.5    Man, O.6    Levy-Nissenbaum, E.7    Khoury, A.8    Lorber, A.9    Goldman, B.10    Lancet, D.11    Eldar, M.12


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.