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Journal Abstract Search

203 related items for PubMed ID: 19100032

  • 1. [Detection of gene mutations of SCN5A in 7 patients with Brugada syndrome].
    Yuan BB, Shan QJ, Yang B, Chen ML, Zou JG, Chen C, Xu DJ, Cao KJ.
    Zhonghua Xin Xue Guan Bing Za Zhi; 2008 May; 36(5):404-7. PubMed ID: 19100032
    [Abstract] [Full Text] [Related]

  • 2. [Novel SCN5A gene mutations associated with Brugada syndrome: V95I, A1649V and delF1617].
    Liang P, Liu WL, Hu DY, Li CL, Tao WH, Li L.
    Zhonghua Xin Xue Guan Bing Za Zhi; 2006 Jul; 34(7):616-9. PubMed ID: 17081365
    [Abstract] [Full Text] [Related]

  • 3. 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
    [Abstract] [Full Text] [Related]

  • 4. Non-SCN5A related Brugada syndromes: verification of normal splicing and trafficking of SCN5A without exonic mutations.
    Nakano Y, Tashiro S, Kinoshita E, Kinoshita-Kikuta E, Takenaka S, Miyoshi M, Ogi H, Sakoda E, Oda N, Suenari K, Tonouchi Y, Okimoto T, Hirai Y, Miura F, Yamaoka K, Koike T, Chayama K.
    Ann Hum Genet; 2007 Jan 30; 71(Pt 1):8-17. PubMed ID: 17227473
    [Abstract] [Full Text] [Related]

  • 5. 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
    [Abstract] [Full Text] [Related]

  • 6. A paradoxical effect of lidocaine for the N406S mutation of SCN5A associated with Brugada syndrome.
    Itoh H, Tsuji K, Sakaguchi T, Nagaoka I, Oka Y, Nakazawa Y, Yao T, Jo H, Ashihara T, Ito M, Horie M, Imoto K.
    Int J Cardiol; 2007 Oct 18; 121(3):239-48. PubMed ID: 17445919
    [Abstract] [Full Text] [Related]

  • 7. SCN5A mutations and the role of genetic background in the pathophysiology of Brugada syndrome.
    Probst V, Wilde AA, Barc J, Sacher F, Babuty D, Mabo P, Mansourati J, Le Scouarnec S, Kyndt F, Le Caignec C, Guicheney P, Gouas L, Albuisson J, Meregalli PG, Le Marec H, Tan HL, Schott JJ.
    Circ Cardiovasc Genet; 2009 Dec 18; 2(6):552-7. PubMed ID: 20031634
    [Abstract] [Full Text] [Related]

  • 8. Novel human pathological mutations. Gene symbol: SCN5A. Disease: Brugada Syndrome.
    Crotti L, Pedrazzini M, Insolia R, Cuoretti A, Ghidoni A, Dagradi F, Taravelli E, Chieffo E, Vicentini A, Schwartz PJ.
    Hum Genet; 2009 Aug 18; 126(2):339. PubMed ID: 19694019
    [No Abstract] [Full Text] [Related]

  • 9. Genetic modulation of brugada syndrome by a common polymorphism.
    Lizotte E, Junttila MJ, Dube MP, Hong K, Benito B, DE Zutter M, Henkens S, Sarkozy A, Huikuri HV, Towbin J, Vatta M, Brugada P, Brugada J, Brugada R.
    J Cardiovasc Electrophysiol; 2009 Oct 18; 20(10):1137-41. PubMed ID: 19549036
    [Abstract] [Full Text] [Related]

  • 10. The occurrence of Brugada syndrome and isolated cardiac conductive disease in the same family could be due to a single SCN5A mutation or to the accidental association of both diseases.
    Six I, Hermida JS, Huang H, Gouas L, Fressart V, Benammar N, Hainque B, Denjoy I, Chahine M, Guicheney P.
    Europace; 2008 Jan 18; 10(1):79-85. PubMed ID: 18156160
    [Abstract] [Full Text] [Related]

  • 11. 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
    [Abstract] [Full Text] [Related]

  • 12. Efficacy of low-dose bepridil for prevention of ventricular fibrillation in patients with Brugada syndrome with and without SCN5A mutation.
    Murakami M, Nakamura K, Kusano KF, Morita H, Nakagawa K, Tanaka M, Tada T, Toh N, Nishii N, Nagase S, Hata Y, Kohno K, Miura D, Ohe T, Ito H.
    J Cardiovasc Pharmacol; 2010 Oct 01; 56(4):389-95. PubMed ID: 20625312
    [Abstract] [Full Text] [Related]

  • 13. Structural myocardial abnormalities in asymptomatic family members with Brugada syndrome and SCN5A gene mutation.
    Frustaci A, Russo MA, Chimenti C.
    Eur Heart J; 2009 Jul 01; 30(14):1763. PubMed ID: 19411664
    [No Abstract] [Full Text] [Related]

  • 14. Novel sodium channel SCN5A mutations in Brugada syndrome patients from Greece.
    Kotta CM, Anastasakis A, Gatzoulis K, Manolis AS, Stefanadis C.
    Int J Cardiol; 2010 Nov 05; 145(1):45-8. PubMed ID: 19406494
    [Abstract] [Full Text] [Related]

  • 15. A novel SCN5A deletion mutation in a child with ventricular tachycardia, recurrent aborted sudden death, and Brugada electrocardiographic pattern.
    Márquez MF, Cruz-Robles D, Inés-Real S, Gallardo GJ, Gonzlez-Hermosillo A, Cárdenas M, Vargas-Alarcón G.
    Arch Cardiol Mex; 2007 Nov 05; 77(4):284-7. PubMed ID: 18361072
    [Abstract] [Full Text] [Related]

  • 16. Gene symbol: SCN5A. Disease: Brugada syndrome.
    Crotti L, Pedrazzini M, Insolia R, Ferrandi C, Ghidoni A, Sanzo A, Dagradi F, De Ferrari GM, Swartz PJ.
    Hum Genet; 2008 Jun 05; 123(5):542. PubMed ID: 20960618
    [No Abstract] [Full Text] [Related]

  • 17. Gene symbol: SCN5A. Disease: Brugada syndrome.
    Crotti L, Ferrandi C, Pedrazzini M, Insolia R, Cuoretti A, Sanzo A, Dagradi F, De Ferrari GM, Schwartz PJ.
    Hum Genet; 2008 Jun 05; 123(5):542. PubMed ID: 20960617
    [No Abstract] [Full Text] [Related]

  • 18. SCN5A channelopathies--an update on mutations and mechanisms.
    Zimmer T, Surber R.
    Prog Biophys Mol Biol; 2008 Jun 05; 98(2-3):120-36. PubMed ID: 19027780
    [Abstract] [Full Text] [Related]

  • 19. Comparison of long-term follow-up of electrocardiographic features in Brugada syndrome between the SCN5A-positive probands and the SCN5A-negative probands.
    Yokokawa M, Noda T, Okamura H, Satomi K, Suyama K, Kurita T, Aihara N, Kamakura S, Shimizu W.
    Am J Cardiol; 2007 Aug 15; 100(4):649-55. PubMed ID: 17697823
    [Abstract] [Full Text] [Related]

  • 20. Characterization of a novel SCN5A mutation associated with Brugada syndrome reveals involvement of DIIIS4-S5 linker in slow inactivation.
    Casini S, Tan HL, Bhuiyan ZA, Bezzina CR, Barnett P, Cerbai E, Mugelli A, Wilde AA, Veldkamp MW.
    Cardiovasc Res; 2007 Dec 01; 76(3):418-29. PubMed ID: 17854786
    [Abstract] [Full Text] [Related]

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