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PUBMED FOR HANDHELDS

Journal Abstract Search


184 related items for PubMed ID: 38455755

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  • 6. 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; 69():111-118. PubMed ID: 34656916
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  • 7. Search for cardiac calcium cycling gene mutations in familial ventricular arrhythmias resembling catecholaminergic polymorphic ventricular tachycardia.
    Marjamaa A, Laitinen-Forsblom P, Lahtinen AM, Viitasalo M, Toivonen L, Kontula K, Swan H.
    BMC Med Genet; 2009 Feb 12; 10():12. PubMed ID: 19216760
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  • 11. A novel variant in RyR2 causes familiar catecholaminergic polymorphic ventricular tachycardia.
    Bosch C, Campuzano O, Sarquella-Brugada G, Cesar S, Perez-Serra A, Coll M, Mademont I, Mates J, Del Olmo B, Iglesias A, Brugada J, Petersen V, Brugada R.
    Forensic Sci Int; 2017 Jan 12; 270():173-177. PubMed ID: 27988446
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  • 12. Catecholaminergic Polymorphic Ventricular Tachycardia: The Cardiac Arrest Where Epinephrine Is Contraindicated.
    Bellamy D, Nuthall G, Dalziel S, Skinner JR.
    Pediatr Crit Care Med; 2019 Mar 12; 20(3):262-268. PubMed ID: 30640888
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  • 16. A Recurrent Exertional Syncope and Sudden Cardiac Arrest in a Young Athlete with Known Pathogenic p.Arg420Gln Variant in the RYR2 Gene.
    Stępień-Wojno M, Ponińska J, Biernacka EK, Foss-Nieradko B, Chwyczko T, Syska P, Płoski R, Bilińska ZT.
    Diagnostics (Basel); 2020 Jun 27; 10(7):. PubMed ID: 32605058
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  • 20. 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 27; 4(4):302-10. PubMed ID: 20676041
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