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166 related items for PubMed ID: 34674339

  • 1. Pregnancy in women with Brugada syndrome: Is there an increased arrhythmia risk? A case-series report.
    van der Crabben SN, Kowsoleea AIE, Clur SB, Wilde AAM.
    J Cardiovasc Electrophysiol; 2022 Jan; 33(1):123-127. PubMed ID: 34674339
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  • 2. Variants in the SCN5A Promoter Associated With Various Arrhythmia Phenotypes.
    Yagihara N, Watanabe H, Barnett P, Duboscq-Bidot L, Thomas AC, Yang P, Ohno S, Hasegawa K, Kuwano R, Chatel S, Redon R, Schott JJ, Probst V, Koopmann TT, Bezzina CR, Wilde AA, Nakano Y, Aiba T, Miyamoto Y, Kamakura S, Darbar D, Donahue BS, Shigemizu D, Tanaka T, Tsunoda T, Suda M, Sato A, Minamino T, Endo N, Shimizu W, Horie M, Roden DM, Makita N.
    J Am Heart Assoc; 2016 Sep 13; 5(9):. PubMed ID: 27625342
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  • 3. Elevated oxidative stress is associated with ventricular fibrillation episodes in patients with Brugada-type electrocardiogram without SCN5A mutation.
    Tanaka M, Nakamura K, Kusano KF, Morita H, Ohta-Ogo K, Miura D, Miura A, Nakagawa K, Tada T, Murakami M, Nishii N, Nagase S, Hata Y, Kohno K, Ouchida M, Shimizu K, Yutani C, Ohe T, Ito H.
    Cardiovasc Pathol; 2011 Sep 13; 20(1):e37-42. PubMed ID: 20219395
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  • 6. Reentry in cardiac ventricular epicardial tissue due to SCN5A L812Q gene mutation: a computational study.
    Satish H, Reddy MR.
    Biomed Phys Eng Express; 2022 Apr 14; 8(3):. PubMed ID: 35320795
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  • 7. Update on Genetic Basis of Brugada Syndrome: Monogenic, Polygenic or Oligogenic?
    Campuzano O, Sarquella-Brugada G, Cesar S, Arbelo E, Brugada J, Brugada R.
    Int J Mol Sci; 2020 Sep 28; 21(19):. PubMed ID: 32998306
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  • 8. Myotonic dystrophy type 1 mimics and exacerbates Brugada phenotype induced by Nav1.5 sodium channel loss-of-function mutation.
    Pambrun T, Mercier A, Chatelier A, Patri S, Schott JJ, Le Scouarnec S, Chahine M, Degand B, Bois P.
    Heart Rhythm; 2014 Aug 28; 11(8):1393-400. PubMed ID: 24768612
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  • 10. Brugada syndrome: clinical presentation and genotype-correlation with magnetic resonance imaging parameters.
    Rudic B, Schimpf R, Veltmann C, Doesch C, Tülümen E, Schoenberg SO, Borggrefe M, Papavassiliu T.
    Europace; 2016 Sep 28; 18(9):1411-9. PubMed ID: 26511399
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  • 11. Differential effects of cardiac sodium channel mutations on initiation of ventricular arrhythmias in patients with Brugada syndrome.
    Morita H, Nagase S, Miura D, Miura A, Hiramatsu S, Tada T, Murakami M, Nishii N, Nakamura K, Morita ST, Oka T, Kusano KF, Ohe T.
    Heart Rhythm; 2009 Apr 28; 6(4):487-92. PubMed ID: 19324308
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  • 12. Risk factors for cardiac events in patients with Brugada syndrome: A PRISMA-compliant meta-analysis and systematic review.
    Wu W, Tian L, Ke J, Sun Y, Wu R, Zhu J, Ke Q.
    Medicine (Baltimore); 2016 Jul 28; 95(30):e4214. PubMed ID: 27472692
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  • 13. Brugada syndrome and abnormal splicing of SCN5A in myotonic dystrophy type 1.
    Wahbi K, Algalarrondo V, Bécane HM, Fressart V, Beldjord C, Azibi K, Lazarus A, Berber N, Radvanyi-Hoffman H, Stojkovic T, Béhin A, Laforêt P, Eymard B, Hatem S, Duboc D.
    Arch Cardiovasc Dis; 2013 Dec 28; 106(12):635-43. PubMed ID: 24140416
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  • 14. Brugada syndrome with a novel missense mutation in SCN5A gene: a case report from Bangladesh.
    Sayeed MZ, Salam MA, Haque MZ, Islam AK.
    Indian Heart J; 2014 Dec 28; 66(1):104-7. PubMed ID: 24581105
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  • 15. Impact of clinical and genetic findings on the management of young patients with Brugada syndrome.
    Andorin A, Behr ER, Denjoy I, Crotti L, Dagradi F, Jesel L, Sacher F, Petit B, Mabo P, Maltret A, Wong LC, Degand B, Bertaux G, Maury P, Dulac Y, Delasalle B, Gourraud JB, Babuty D, Blom NA, Schwartz PJ, Wilde AA, Probst V.
    Heart Rhythm; 2016 Jun 28; 13(6):1274-82. PubMed ID: 26921764
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  • 17. Dual phenotypic transmission in Brugada syndrome.
    Hermida JS, Arnalsteen-Dassonvalle E, Kubala M, Mathiron A, Traulle S, Anbazhagan K, Hermida A, Rochette J.
    Arch Cardiovasc Dis; 2013 Jun 28; 106(6-7):366-72. PubMed ID: 23810369
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  • 18. Idiopathic ventricular fibrillation and the V1764fsX1786 frameshift mutation of the SCN5A gene in a myotonic dystrophy type 1 patient.
    Shimoyama T, Hayashi H, Suzuki F, Nishiyama Y, Miyamoto Y, Aiba T, Shimizu W, Kimura K.
    J Clin Neurosci; 2020 Apr 28; 74():242-244. PubMed ID: 32063450
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  • 19. Brugada syndrome.
    Brugada R, Campuzano O, Sarquella-Brugada G, Brugada J, Brugada P.
    Methodist Debakey Cardiovasc J; 2014 Apr 28; 10(1):25-8. PubMed ID: 24932359
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  • 20. Testing the burden of rare variation in arrhythmia-susceptibility genes provides new insights into molecular diagnosis for Brugada syndrome.
    Le Scouarnec S, Karakachoff M, Gourraud JB, Lindenbaum P, Bonnaud S, Portero V, Duboscq-Bidot L, Daumy X, Simonet F, Teusan R, Baron E, Violleau J, Persyn E, Bellanger L, Barc J, Chatel S, Martins R, Mabo P, Sacher F, Haïssaguerre M, Kyndt F, Schmitt S, Bézieau S, Le Marec H, Dina C, Schott JJ, Probst V, Redon R.
    Hum Mol Genet; 2015 May 15; 24(10):2757-63. PubMed ID: 25650408
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