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Journal Abstract Search

167 related items for PubMed ID: 8100355

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  • 2. Immunohistochemical localization of 14.3.3 zeta protein in amyloid plaques in human spongiform encephalopathies.
    Richard M, Biacabe AG, Streichenberger N, Ironside JW, Mohr M, Kopp N, Perret-Liaudet A.
    Acta Neuropathol; 2003 Mar; 105(3):296-302. PubMed ID: 12557018
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  • 4. A special report I. Prion protein (PrP)--amyloid plaques in the transmissible spongiform encephalopathies, or prion diseases revisited.
    Liberski PP, Bratosiewicz J, Waliś A, Kordek R, Jeffrey M, Brown P.
    Folia Neuropathol; 2001 Mar; 39(4):217-35. PubMed ID: 11928893
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  • 12. Immunohistochemical investigations of the prion protein accumulation in human spongiform encephalopathies. Special report II.
    Zaborowski A, Kordek R, Botts GT, Liberski PP.
    Pol J Pathol; 2003 Mar; 54(1):39-47. PubMed ID: 12817879
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  • 14. Localization of A11-reactive oligomeric species in prion diseases.
    Aidt FH, Hasholt LF, Christiansen M, Laursen H.
    Histopathology; 2013 Jun; 62(7):994-1001. PubMed ID: 23570304
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  • 17. Toluidine blue-O staining of prion protein deposits.
    Sánchez A, Guzmán A, Ortiz A, Rembao D, Espinosa B, Zenteno E, Guevara J.
    Histochem Cell Biol; 2001 Dec; 116(6):519-24. PubMed ID: 11810193
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  • 19. Dystrophic neurites around amyloid plaques of human patients with Gerstmann-Sträussler-Scheinker disease contain ubiquitinated inclusions.
    Migheli A, Attanasio A, Vigliani MC, Schiffer D.
    Neurosci Lett; 1991 Jan 02; 121(1-2):55-8. PubMed ID: 1708486
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  • 20. Cerebral amyloid in human prion disease.
    Watanabe R, Duchen LW.
    Neuropathol Appl Neurobiol; 1993 Jun 02; 19(3):253-60. PubMed ID: 8355811
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