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Journal Abstract Search

139 related items for PubMed ID: 16138883

  • 1. Electrophysiological basis and genetics of Brugada syndrome.
    Grant AO.
    J Cardiovasc Electrophysiol; 2005 Sep; 16 Suppl 1():S3-7. PubMed ID: 16138883
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  • 2. [Doubts of the cardiologist regarding an electrocardiogram presenting QRS V1-V2 complexes with positive terminal wave and ST segment elevation. Consensus Conference promoted by the Italian Cardiology Society].
    Oreto G, Corrado D, Delise P, Fedele F, Gaita F, Gentile F, Giustetto C, Michelucci A, Padeletti L, Priori S.
    G Ital Cardiol (Rome); 2010 Nov; 11(11 Suppl 2):3S-22S. PubMed ID: 21361048
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  • 3. The syndrome of right bundle branch block ST segment elevation in V1 to V3 and sudden death--the Brugada syndrome.
    Brugada J, Brugada P, Brugada R.
    Europace; 1999 Jul; 1(3):156-66. PubMed ID: 11225790
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  • 4. Pathophysiological mechanisms of Brugada syndrome: depolarization disorder, repolarization disorder, or more?
    Meregalli PG, Wilde AA, Tan HL.
    Cardiovasc Res; 2005 Aug 15; 67(3):367-78. PubMed ID: 15913579
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  • 5. Sudden cardiac death and inherited arrhythmia syndromes.
    Sarkozy A, Brugada P.
    J Cardiovasc Electrophysiol; 2005 Sep 15; 16 Suppl 1():S8-20. PubMed ID: 16138889
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  • 6. Acquired forms of the Brugada syndrome.
    Shimizu W.
    J Electrocardiol; 2005 Oct 15; 38(4 Suppl):22-5. PubMed ID: 16226070
    [Abstract] [Full Text] [Related]

  • 7. ST-segment elevation in the early repolarization syndrome, idiopathic ventricular fibrillation, and the Brugada syndrome: cellular and clinical linkage.
    Shu J, Zhu T, Yang L, Cui C, Yan GX.
    J Electrocardiol; 2005 Oct 15; 38(4 Suppl):26-32. PubMed ID: 16226071
    [Abstract] [Full Text] [Related]

  • 8. Brugada syndrome--an under-recognized electrical disease in patients with sudden cardiac death.
    Juang JM, Huang SK.
    Cardiology; 2004 Oct 15; 101(4):157-69. PubMed ID: 14967959
    [Abstract] [Full Text] [Related]

  • 9. [Brugada syndrome].
    Matsuo K, Yano K.
    Nihon Rinsho; 2002 Jul 15; 60(7):1408-14. PubMed ID: 12136622
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  • 10. A novel missense mutation in the SCN5A gene associated with Brugada syndrome bidirectionally affecting blocking actions of antiarrhythmic drugs.
    Itoh H, Shimizu M, Takata S, Mabuchi H, Imoto K.
    J Cardiovasc Electrophysiol; 2005 May 15; 16(5):486-93. PubMed ID: 15877619
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  • 12. Phenotypic characterization of a large European family with Brugada syndrome displaying a sudden unexpected death syndrome mutation in SCN5A:
    Hong K, Berruezo-Sanchez A, Poungvarin N, Oliva A, Vatta M, Brugada J, Brugada P, Towbin JA, Dumaine R, Piñero-Galvez C, Antzelevitch C, Brugada R.
    J Cardiovasc Electrophysiol; 2004 Jan 15; 15(1):64-9. PubMed ID: 15028074
    [Abstract] [Full Text] [Related]

  • 13. Electrocardiographic characteristics and SCN5A mutations in idiopathic ventricular fibrillation associated with early repolarization.
    Watanabe H, Nogami A, Ohkubo K, Kawata H, Hayashi Y, Ishikawa T, Makiyama T, Nagao S, Yagihara N, Takehara N, Kawamura Y, Sato A, Okamura K, Hosaka Y, Sato M, Fukae S, Chinushi M, Oda H, Okabe M, Kimura A, Maemura K, Watanabe I, Kamakura S, Horie M, Aizawa Y, Shimizu W, Makita N.
    Circ Arrhythm Electrophysiol; 2011 Dec 15; 4(6):874-81. PubMed ID: 22028457
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  • 15. Letter regarding article by Coronel et al, "right ventricular fibrosis and conduction delay in a patient with clinical signs of Brugada syndrome: a combined electrophysiological, genetic, histopathologic, and computational study".
    Priori SG, Napolitano C, Gasparini M.
    Circulation; 2006 Apr 25; 113(16):e726; author reply 726-7. PubMed ID: 16636182
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  • 20. Human SCN5A gene mutations alter cardiac sodium channel kinetics and are associated with the Brugada syndrome.
    Rook MB, Bezzina Alshinawi C, Groenewegen WA, van Gelder IC, van Ginneken AC, Jongsma HJ, Mannens MM, Wilde AA.
    Cardiovasc Res; 1999 Dec 25; 44(3):507-17. PubMed ID: 10690282
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