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Journal Abstract Search

407 related items for PubMed ID: 22028457

  • 1. 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; 4(6):874-81. PubMed ID: 22028457
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  • 2. Clinical and electrophysiological characteristics of Brugada syndrome caused by a missense mutation in the S5-pore site of SCN5A.
    Itoh H, Shimizu M, Mabuchi H, Imoto K.
    J Cardiovasc Electrophysiol; 2005 Apr; 16(4):378-83. PubMed ID: 15828879
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  • 3. Analyses of a novel SCN5A mutation (C1850S): conduction vs. repolarization disorder hypotheses in the Brugada syndrome.
    Petitprez S, Jespersen T, Pruvot E, Keller DI, Corbaz C, Schläpfer J, Abriel H, Kucera JP.
    Cardiovasc Res; 2008 Jun 01; 78(3):494-504. PubMed ID: 18252757
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  • 8. Sudden cardiac arrest associated with early repolarization.
    Haïssaguerre M, Derval N, Sacher F, Jesel L, Deisenhofer I, de Roy L, Pasquié JL, Nogami A, Babuty D, Yli-Mayry S, De Chillou C, Scanu P, Mabo P, Matsuo S, Probst V, Le Scouarnec S, Defaye P, Schlaepfer J, Rostock T, Lacroix D, Lamaison D, Lavergne T, Aizawa Y, Englund A, Anselme F, O'Neill M, Hocini M, Lim KT, Knecht S, Veenhuyzen GD, Bordachar P, Chauvin M, Jais P, Coureau G, Chene G, Klein GJ, Clémenty J.
    N Engl J Med; 2008 May 08; 358(19):2016-23. PubMed ID: 18463377
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  • 9. A novel SCN5A mutation, F1344S, identified in a patient with Brugada syndrome and fever-induced ventricular fibrillation.
    Keller DI, Huang H, Zhao J, Frank R, Suarez V, Delacrétaz E, Brink M, Osswald S, Schwick N, Chahine M.
    Cardiovasc Res; 2006 Jun 01; 70(3):521-9. PubMed ID: 16616735
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  • 10. Progressive cardiac conduction defect is the prevailing phenotype in carriers of a Brugada syndrome SCN5A mutation.
    Probst V, Allouis M, Sacher F, Pattier S, Babuty D, Mabo P, Mansourati J, Victor J, Nguyen JM, Schott JJ, Boisseau P, Escande D, Le Marec H.
    J Cardiovasc Electrophysiol; 2006 Mar 01; 17(3):270-5. PubMed ID: 16643399
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  • 15. [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 01; 11(11 Suppl 2):3S-22S. PubMed ID: 21361048
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  • 16. Significance of non-type 1 anterior early repolarization in patients with inferolateral early repolarization syndrome.
    Kamakura T, Kawata H, Nakajima I, Yamada Y, Miyamoto K, Okamura H, Noda T, Satomi K, Aiba T, Takaki H, Aihara N, Kamakura S, Kimura T, Shimizu W.
    J Am Coll Cardiol; 2013 Oct 22; 62(17):1610-8. PubMed ID: 23850930
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  • 17. Electrophysiological basis and genetics of Brugada syndrome.
    Grant AO.
    J Cardiovasc Electrophysiol; 2005 Sep 22; 16 Suppl 1():S3-7. PubMed ID: 16138883
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  • 18. A novel mutation in the SCN5A gene is associated with Brugada syndrome.
    Shin DJ, Kim E, Park SB, Jang WC, Bae Y, Han J, Jang Y, Joung B, Lee MH, Kim SS, Huang H, Chahine M, Yoon SK.
    Life Sci; 2007 Jan 30; 80(8):716-24. PubMed ID: 17141278
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  • 19. 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 30; 16(5):486-93. PubMed ID: 15877619
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