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Journal Abstract Search

864 related items for PubMed ID: 18549912

  • 21. [New perspectives in long QT syndrome].
    Medeiros-Domingo A, Iturralde-Torres P, Canizales-Quinteros S, Hernández-Cruz A, Tusié-Luna MT.
    Rev Invest Clin; 2007; 59(1):57-72. PubMed ID: 17569301
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  • 22. [Molecular genetics of the long QT syndrome. Genes causing syncope and sudden death].
    Fosdal I, Wettrell G, Christiansen M, Kanters JK, Larsen LA.
    Lakartidningen; 2001 Feb 21; 98(8):810-5. PubMed ID: 11265565
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  • 24. [Long QT syndrome and Brugada syndrome. Drugs, ablation or ICD?].
    Haverkamp W, Rolf S, Eckardt L, Mönnig G.
    Herz; 2005 Mar 21; 30(2):111-8. PubMed ID: 15875099
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  • 25. Risk of aborted cardiac arrest or sudden cardiac death during adolescence in the long-QT syndrome.
    Hobbs JB, Peterson DR, Moss AJ, McNitt S, Zareba W, Goldenberg I, Qi M, Robinson JL, Sauer AJ, Ackerman MJ, Benhorin J, Kaufman ES, Locati EH, Napolitano C, Priori SG, Towbin JA, Vincent GM, Zhang L.
    JAMA; 2006 Sep 13; 296(10):1249-54. PubMed ID: 16968849
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  • 26. Clinical features of the idiopathic long QT syndrome.
    Moss AJ, Robinson J.
    Circulation; 1992 Jan 13; 85(1 Suppl):I140-4. PubMed ID: 1345816
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  • 27. [Value of genetic testing in the management of the congenital long QT syndrome].
    Lupoglazoff JM, Denjoy I, Guicheney P.
    Arch Mal Coeur Vaiss; 2003 May 13; 96(5):539-47. PubMed ID: 12838849
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  • 30. Who are the long-QT syndrome patients who receive an implantable cardioverter-defibrillator and what happens to them?: data from the European Long-QT Syndrome Implantable Cardioverter-Defibrillator (LQTS ICD) Registry.
    Schwartz PJ, Spazzolini C, Priori SG, Crotti L, Vicentini A, Landolina M, Gasparini M, Wilde AA, Knops RE, Denjoy I, Toivonen L, Mönnig G, Al-Fayyadh M, Jordaens L, Borggrefe M, Holmgren C, Brugada P, De Roy L, Hohnloser SH, Brink PA.
    Circulation; 2010 Sep 28; 122(13):1272-82. PubMed ID: 20837891
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  • 31. Left cardiac sympathetic denervation for the management of life-threatening ventricular tachyarrhythmias in young patients with catecholaminergic polymorphic ventricular tachycardia and long QT syndrome.
    Schneider HE, Steinmetz M, Krause U, Kriebel T, Ruschewski W, Paul T.
    Clin Res Cardiol; 2013 Jan 28; 102(1):33-42. PubMed ID: 22821214
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  • 33. [Long QT syndrome--genes, mechanisms and risks. Indication for genetic family screening?].
    Bundgaard H, Havndrup O, Christiansen M, Andersen PS, Jensen HK, Svendsen JH, Kjeldsen KP.
    Ugeskr Laeger; 2006 Jun 26; 168(26-32):2537-42. PubMed ID: 16824406
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  • 34. Incidence and risk factors of arrhythmic events in catecholaminergic polymorphic ventricular tachycardia.
    Hayashi M, Denjoy I, Extramiana F, Maltret A, Buisson NR, Lupoglazoff JM, Klug D, Hayashi M, Takatsuki S, Villain E, Kamblock J, Messali A, Guicheney P, Lunardi J, Leenhardt A.
    Circulation; 2009 May 12; 119(18):2426-34. PubMed ID: 19398665
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  • 36. Clinical and molecular genetics of the short QT syndrome.
    Schimpf R, Borggrefe M, Wolpert C.
    Curr Opin Cardiol; 2008 May 12; 23(3):192-8. PubMed ID: 18382206
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  • 37. Age- and genotype-specific triggers for life-threatening arrhythmia in the genotyped long QT syndrome.
    Sakaguchi T, Shimizu W, Itoh H, Noda T, Miyamoto Y, Nagaoka I, Oka Y, Ashihara T, Ito M, Tsuji K, Ohno S, Makiyama T, Kamakura S, Horie M.
    J Cardiovasc Electrophysiol; 2008 Aug 12; 19(8):794-9. PubMed ID: 18373596
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  • 39. Successful parental use of an automated external defibrillator for an infant with long-QT syndrome.
    Divekar A, Soni R.
    Pediatrics; 2006 Aug 12; 118(2):e526-9. PubMed ID: 16816007
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  • 40. Mechanisms and clinical management of inherited channelopathies: long QT syndrome, Brugada syndrome, catecholaminergic polymorphic ventricular tachycardia, and short QT syndrome.
    Kaufman ES.
    Heart Rhythm; 2009 Aug 12; 6(8 Suppl):S51-5. PubMed ID: 19631908
    [Abstract] [Full Text] [Related]

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