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Journal Abstract Search

145 related items for PubMed ID: 31875585

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  • 2. Exon 3 deletion of RYR2 encoding cardiac ryanodine receptor is associated with left ventricular non-compaction.
    Ohno S, Omura M, Kawamura M, Kimura H, Itoh H, Makiyama T, Ushinohama H, Makita N, Horie M.
    Europace; 2014 Nov; 16(11):1646-54. PubMed ID: 24394973
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  • 7. Arrhythmia characterization and long-term outcomes in catecholaminergic polymorphic ventricular tachycardia.
    Sy RW, Gollob MH, Klein GJ, Yee R, Skanes AC, Gula LJ, Leong-Sit P, Gow RM, Green MS, Birnie DH, Krahn AD.
    Heart Rhythm; 2011 Jun; 8(6):864-71. PubMed ID: 21315846
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  • 8. Postpacing abnormal repolarization in catecholaminergic polymorphic ventricular tachycardia associated with a mutation in the cardiac ryanodine receptor gene.
    Nof E, Belhassen B, Arad M, Bhuiyan ZA, Antzelevitch C, Rosso R, Fogelman R, Luria D, El-Ani D, Mannens MM, Viskin S, Eldar M, Wilde AA, Glikson M.
    Heart Rhythm; 2011 Oct; 8(10):1546-52. PubMed ID: 21699856
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  • 10. Exon 3 deletion of ryanodine receptor causes left ventricular noncompaction, worsening catecholaminergic polymorphic ventricular tachycardia, and sudden cardiac arrest.
    Campbell MJ, Czosek RJ, Hinton RB, Miller EM.
    Am J Med Genet A; 2015 Sep; 167A(9):2197-200. PubMed ID: 26018045
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  • 11. Deadly proposal: a case of catecholaminergic polymorphic ventricular tachycardia.
    Heiner JD, Bullard-Berent JH, Inbar S.
    Pediatr Emerg Care; 2011 Nov; 27(11):1065-8. PubMed ID: 22068070
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  • 13. Successful treatment of catecholaminergic polymorphic ventricular tachycardia with flecainide: a case report and review of the current literature.
    Pott C, Dechering DG, Reinke F, Muszynski A, Zellerhoff S, Bittner A, Köbe J, Wasmer K, Schulze-Bahr E, Mönnig G, Kotthoff S, Eckardt L.
    Europace; 2011 Jun; 13(6):897-901. PubMed ID: 21292648
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  • 15. Characterization of a novel mutation in the cardiac ryanodine receptor that results in catecholaminergic polymorphic ventricular tachycardia.
    Jiang D, Jones PP, Davis DR, Gow R, Green MS, Birnie DH, Chen SR, Gollob MH.
    Channels (Austin); 2010 Jun; 4(4):302-10. PubMed ID: 20676041
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  • 16. Sudden death after inappropriate shocks of implantable cardioverter defibrillator in a catecholaminergic polymorphic ventricular tachycardia case with a novel RyR2 mutation.
    Itoh H, Murayama T, Kurebayashi N, Ohno S, Kobayashi T, Fujii Y, Watanabe M, Ogawa H, Anzai T, Horie M.
    J Electrocardiol; 2021 Jun; 69():111-118. PubMed ID: 34656916
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  • 17. Advances in the diagnosis and treatment of catecholaminergic polymorphic ventricular tachycardia.
    Roston TM, Cunningham TC, Sanatani S.
    Cardiol Young; 2017 Jan; 27(S1):S49-S56. PubMed ID: 28084961
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  • 18. Clinical and molecular characterization of patients with catecholaminergic polymorphic ventricular tachycardia.
    Priori SG, Napolitano C, Memmi M, Colombi B, Drago F, Gasparini M, DeSimone L, Coltorti F, Bloise R, Keegan R, Cruz Filho FE, Vignati G, Benatar A, DeLogu A.
    Circulation; 2002 Jul 02; 106(1):69-74. PubMed ID: 12093772
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