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Journal Abstract Search

167 related items for PubMed ID: 20670590

  • 1. [Catecholaminergic polymorphic ventricular tachycardia is a rare inherited heart disease].
    Holst AG, Tfelt-Hansen J, Olesen MS, Theilade J, Winkel BG, Christensen AH, Bundgaard H, Haunsø S, Svendsen JH.
    Ugeskr Laeger; 2010 Aug 02; 172(31):2140-4. PubMed ID: 20670590
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  • 3. [Catecholaminergic polymorphic ventricular tachycardia].
    Leren IS, Haugaa KH, Edvardsen T, Anfinsen OG, Kongsgård E, Berge KE, Leren TP, Amlie JP.
    Tidsskr Nor Laegeforen; 2010 Jan 28; 130(2):139-42. PubMed ID: 20125202
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  • 4. Deadly proposal: a case of catecholaminergic polymorphic ventricular tachycardia.
    Heiner JD, Bullard-Berent JH, Inbar S.
    Pediatr Emerg Care; 2011 Nov 28; 27(11):1065-8. PubMed ID: 22068070
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  • 5. Catecholaminergic polymorphic ventricular tachycardia.
    Liu N, Colombi B, Raytcheva-Buono EV, Bloise R, Priori SG.
    Herz; 2007 May 28; 32(3):212-7. PubMed ID: 17497254
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  • 9. Calcium channel antagonism reduces exercise-induced ventricular arrhythmias in catecholaminergic polymorphic ventricular tachycardia patients with RyR2 mutations.
    Swan H, Laitinen P, Kontula K, Toivonen L.
    J Cardiovasc Electrophysiol; 2005 Feb 28; 16(2):162-6. PubMed ID: 15720454
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  • 10. 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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  • 11. Unusual clinical presentation in a family with catecholaminergic polymorphic ventricular tachycardia due to a G14876A ryanodine receptor gene mutation.
    Allouis M, Probst V, Jaafar P, Schott JJ, Le Marec H.
    Am J Cardiol; 2005 Mar 01; 95(5):700-2. PubMed ID: 15721128
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  • 13. Catecholaminergic polymorphic ventricular tachycardia: RYR2 mutations, bradycardia, and follow up of the patients.
    Postma AV, Denjoy I, Kamblock J, Alders M, Lupoglazoff JM, Vaksmann G, Dubosq-Bidot L, Sebillon P, Mannens MM, Guicheney P, Wilde AA.
    J Med Genet; 2005 Nov 01; 42(11):863-70. PubMed ID: 16272262
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  • 14. Catecholaminergic polymorphic ventricular tachycardia: a current overview.
    Leite LR, Henz BD, Macedo PG, Santos SN, Barreto JR, Zanatta A, Fenelon G, Cruz Filho FE.
    Future Cardiol; 2009 Mar 01; 5(2):191-9. PubMed ID: 19371192
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  • 16. Catecholaminergic polymorphic ventricular tachycardia caused by a novel mutation in the cardiac ryanodine receptor.
    Hasdemir C, Aydin HH, Sahin S, Wollnik B.
    Anadolu Kardiyol Derg; 2008 Oct 16; 8(5):E35-6. PubMed ID: 18849218
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  • 19. A delayed diagnosis of catecholaminergic polymorphic ventricular tachycardia with a mutant of RYR2 at c.7580T>G for 6 years in a 9-year-old child.
    Duan H, Lu Y, Yan S, Qiao L, Hua Y, Li Y, Zhou K, Wang C.
    Medicine (Baltimore); 2018 Apr 16; 97(16):e0368. PubMed ID: 29668588
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  • 20. Complex atrial arrhythmias as first manifestation of catecholaminergic polymorphic ventricular tachycardia: an unusual course in a patient with a new mutation in ryanodine receptor type 2 gene.
    Lawrenz W, Krogmann ON, Wieczorek M.
    Cardiol Young; 2014 Aug 16; 24(4):741-4. PubMed ID: 23985380
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