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Journal Abstract Search

253 related items for PubMed ID: 25109669

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  • 28. Functional compensation by other voltage-gated Ca2+ channels in mouse basal forebrain neurons with Ca(V)2.1 mutations.
    Etheredge JA, Murchison D, Abbott LC, Griffith WH.
    Brain Res; 2007 Apr 06; 1140():105-19. PubMed ID: 16364258
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  • 29. Purkinje cell-specific ablation of Cav2.1 channels is sufficient to cause cerebellar ataxia in mice.
    Todorov B, Kros L, Shyti R, Plak P, Haasdijk ED, Raike RS, Frants RR, Hess EJ, Hoebeek FE, De Zeeuw CI, van den Maagdenberg AM.
    Cerebellum; 2012 Mar 06; 11(1):246-58. PubMed ID: 21870131
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  • 30. Early onset, non fluctuating spinocerebellar ataxia and a novel missense mutation in CACNA1A gene.
    Tonelli A, D'Angelo MG, Salati R, Villa L, Germinasi C, Frattini T, Meola G, Turconi AC, Bresolin N, Bassi MT.
    J Neurol Sci; 2006 Feb 15; 241(1-2):13-7. PubMed ID: 16325861
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  • 31. Episodic ataxia type 2: phenotype characteristics of a novel CACNA1A mutation and review of the literature.
    Nachbauer W, Nocker M, Karner E, Stankovic I, Unterberger I, Eigentler A, Schneider R, Poewe W, Delazer M, Boesch S.
    J Neurol; 2014 May 15; 261(5):983-91. PubMed ID: 24658662
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  • 34. CaV2.1 channelopathies.
    Pietrobon D.
    Pflugers Arch; 2010 Jul 15; 460(2):375-93. PubMed ID: 20204399
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  • 38. Mutation Spectrum in the CACNA1A Gene in 49 Patients with Episodic Ataxia.
    Sintas C, Carreño O, Fernàndez-Castillo N, Corominas R, Vila-Pueyo M, Toma C, Cuenca-León E, Barroeta I, Roig C, Volpini V, Macaya A, Cormand B.
    Sci Rep; 2017 May 31; 7(1):2514. PubMed ID: 28566750
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  • 39. A Single Amino Acid Deletion (ΔF1502) in the S6 Segment of CaV2.1 Domain III Associated with Congenital Ataxia Increases Channel Activity and Promotes Ca2+ Influx.
    Bahamonde MI, Serra SA, Drechsel O, Rahman R, Marcé-Grau A, Prieto M, Ossowski S, Macaya A, Fernández-Fernández JM.
    PLoS One; 2015 May 31; 10(12):e0146035. PubMed ID: 26716990
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