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Journal Abstract Search

795 related items for PubMed ID: 23225013

  • 1. Human prion diseases: from Kuru to variant Creutzfeldt-Jakob disease.
    Sikorska B, Liberski PP.
    Subcell Biochem; 2012; 65():457-96. PubMed ID: 23225013
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  • 5. [Prion diseases or transmissible spongiform encephalopathies].
    Brandel JP.
    Rev Med Interne; 2022 Feb; 43(2):106-115. PubMed ID: 34148672
    [Abstract] [Full Text] [Related]

  • 6. An overview of human prion diseases.
    Imran M, Mahmood S.
    Virol J; 2011 Dec 24; 8():559. PubMed ID: 22196171
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  • 7. The many faces of human prion diseases in Belgium and the world.
    Van Everbroeck B, Pals P, Quoilin S, Martin JJ, Cras P.
    Acta Neurol Belg; 2001 Jun 24; 101(2):81-7. PubMed ID: 11486562
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  • 8. Human transmissible spongiform encephalopathies: historic view.
    Asher DM, Gregori L.
    Handb Clin Neurol; 2018 Jun 24; 153():1-17. PubMed ID: 29887130
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  • 9. Prion protein and the transmissible spongiform encephalopathies.
    Caughey B, Chesebro B.
    Trends Cell Biol; 1997 Feb 24; 7(2):56-62. PubMed ID: 17708907
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  • 10. [Creutzfeldt-Jakob disease and other human transmissible spongiform encephalopathies. Part I].
    Zaborowski A.
    Psychiatr Pol; 2004 Feb 24; 38(2):283-96. PubMed ID: 15307293
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  • 11. The human prion diseases. A review with special emphasis on new variant CJD and comments on surveillance.
    Keohane C.
    Clin Exp Pathol; 1999 Feb 24; 47(3-4):125-32. PubMed ID: 10472732
    [Abstract] [Full Text] [Related]

  • 12. Identification of a second bovine amyloidotic spongiform encephalopathy: molecular similarities with sporadic Creutzfeldt-Jakob disease.
    Casalone C, Zanusso G, Acutis P, Ferrari S, Capucci L, Tagliavini F, Monaco S, Caramelli M.
    Proc Natl Acad Sci U S A; 2004 Mar 02; 101(9):3065-70. PubMed ID: 14970340
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  • 13. [A trend of molecular genetics on prion diseases and prion protein].
    Muramatsu Y, Shinagawa M.
    Nihon Rinsho; 1993 Sep 02; 51(9):2494-502. PubMed ID: 8411733
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  • 14. [Human transmissible subacute spongiform encephalopathy].
    Dormont D.
    Bull Acad Natl Med; 1994 May 02; 178(5):887-903; discussion 904-5. PubMed ID: 7953896
    [Abstract] [Full Text] [Related]

  • 15. Kuru: its ramifications after fifty years.
    Liberski PP, Brown P.
    Exp Gerontol; 2009 May 02; 44(1-2):63-9. PubMed ID: 18606515
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  • 16. The prion diseases.
    Brown K, Mastrianni JA.
    J Geriatr Psychiatry Neurol; 2010 Dec 02; 23(4):277-98. PubMed ID: 20938044
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  • 17. [Prion diseases and a new variant of Creutzfeldt-Jakob disease].
    Doh-ura K, Kitamoto T.
    Rinsho Shinkeigaku; 1996 Dec 02; 36(12):1370-2. PubMed ID: 9128415
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  • 18. Neuropathology of human prion diseases (spongiform encephalopathies).
    Kretzschmar HA.
    Dev Biol Stand; 1993 Dec 02; 80():71-90. PubMed ID: 8270118
    [Abstract] [Full Text] [Related]

  • 19. [Creutzfeldt-Jakob disease(CJD) and Gerstmann-Sträussler-Scheinker syndrome(GSS)].
    Udaka F, Fujisawa M, Kameyama M.
    Nihon Rinsho; 1997 Apr 02; 55(4):972-7. PubMed ID: 9103904
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  • 20. Transmissible spongiform encephalopathies in humans.
    Belay ED.
    Annu Rev Microbiol; 1999 Apr 02; 53():283-314. PubMed ID: 10547693
    [Abstract] [Full Text] [Related]

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