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Journal Abstract Search

146 related items for PubMed ID: 27668923

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  • 26. Involvement of the cardiac ryanodine receptor/calcium release channel in catecholaminergic polymorphic ventricular tachycardia.
    Marks AR, Priori S, Memmi M, Kontula K, Laitinen PJ.
    J Cell Physiol; 2002 Jan; 190(1):1-6. PubMed ID: 11807805
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  • 28. 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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  • 29. Juvenile sudden death in a family with polymorphic ventricular arrhythmias caused by a novel RyR2 gene mutation: evidence of specific morphological substrates.
    d'Amati G, Bagattin A, Bauce B, Rampazzo A, Autore C, Basso C, King K, Romeo MD, Gallo P, Thiene G, Danieli GA, Nava A.
    Hum Pathol; 2005 Jul 01; 36(7):761-7. PubMed ID: 16084945
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  • 32. Catecholaminergic polymorphic ventricular tachycardia.
    Liu N, Colombi B, Raytcheva-Buono EV, Bloise R, Priori SG.
    Herz; 2007 May 01; 32(3):212-7. PubMed ID: 17497254
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  • 38. A novel variant of RyR2 gene in a family misdiagnosed as congenital long QT syndrome: The importance of genetic testing.
    Letsas KP, Prappa E, Bazoukis G, Lioni L, Pantou MP, Gourzi P, Degiannis D, Sideris A.
    J Electrocardiol; 2020 May 01; 60():8-11. PubMed ID: 32179276
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  • 39. A novel heterozygous mutation in cardiac calsequestrin causes autosomal dominant catecholaminergic polymorphic ventricular tachycardia.
    Gray B, Bagnall RD, Lam L, Ingles J, Turner C, Haan E, Davis A, Yang PC, Clancy CE, Sy RW, Semsarian C.
    Heart Rhythm; 2016 Aug 01; 13(8):1652-60. PubMed ID: 27157848
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  • 40. Catecholaminergic Polymorphic Ventricular Tachycardia with QT Prolongation.
    Tanaka Y, Kawabata M, Scheinman MM, Hirao K.
    Pacing Clin Electrophysiol; 2015 Dec 01; 38(12):1499-502. PubMed ID: 26256814
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