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Volumn 10, Issue 6, 2003, Pages 524-526

Catecholaminergic polymorphic ventricular tachycardia in a child: An often unrecognized diagnosis;La tachycardie ventriculaire catécholergique du jeune enfant: Un diagnostic souvent méconnu

Author keywords

Arrhythmia; Child; Sudden death; Syncope; Torsade de pointe; Ventricular tachycardia

Indexed keywords

BETA ADRENERGIC RECEPTOR BLOCKING AGENT;

EID: 0041667809     PISSN: 0929693X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0929-693X(03)00150-7     Document Type: Article
Times cited : (6)

References (9)
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  • 2
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  • 3
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    • Shaw, T.R.1
  • 4
    • 0021915988 scopus 로고
    • Cardiac arrhythmias misdiagnosed as epilepsy
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    • Rutter, N.1    Southall, D.P.2
  • 5
    • 0020053499 scopus 로고
    • Tachyarrythmic syncopes in children with structurally normal hearts with and without QT-prolongation in the electrocardiogram
    • Von Bernuth G, Bernsau U, Guntheil H, Hoffmann W, Huschke U, Jungst BK, et al. Tachyarrythmic syncopes in children with structurally normal hearts with and without QT-prolongation in the electrocardiogram. Eur J Pediatr 1982;138:206-10.
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  • 6
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    • Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardia
    • Priori SG, Napolitano C, Tiso N, Memmi M, Vignati G, Bloise R, et al. Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardia. Circulation 2001;103:196-200.
    • (2001) Circulation , vol.103 , pp. 196-200
    • Priori, S.G.1    Napolitano, C.2    Tiso, N.3    Memmi, M.4    Vignati, G.5    Bloise, R.6
  • 7
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    • Mutations of the cardiac ryanodine receptor (RyR2) gene in familial polymorphic ventricular tachycardia
    • Laitinen PJ, Brown KM, Piippo K, Swan H, Devaney JM, Brahmbhatt B, et al. Mutations of the cardiac ryanodine receptor (RyR2) gene in familial polymorphic ventricular tachycardia. Circulation 2001;103:485-90.
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  • 8
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    • 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, Levy-Nissenbaum E, Bahan T, Friedman E, Khoury A, et al. Autosomal recessive catecholamine or exercise-induced polymorphic ventricular tachycardia: clinical features and assignment of the disease gene to chromosome 1p13-21. Circulation 2001;103:2822-7.
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  • 9
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    • Clinical and molecular characterization of patients with catecholaminergic polymorphic ventricular tachycardia
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    • Priori, S.G.1    Napolitano, C.2    Memmi, M.3    Colombi, B.4    Drago, F.5    Gasparini, M.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.