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Journal Abstract Search

316 related items for PubMed ID: 1962178

  • 21. [Creutzfeldt-Jakob disease--a human prion disease].
    Buchwald E, Vorstrup S.
    Nord Med; 1996 Jun; 111(6):180-3. PubMed ID: 8700643
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  • 22. Gerstmann-Sträussler-Scheinker syndrome,fatal familial insomnia, and kuru: a review of these less common human transmissible spongiform encephalopathies.
    Collins S, McLean CA, Masters CL.
    J Clin Neurosci; 2001 Sep; 8(5):387-97. PubMed ID: 11535002
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  • 26. The human prion diseases. A review with special emphasis on new variant CJD and comments on surveillance.
    Keohane C.
    Clin Exp Pathol; 1999 Sep; 47(3-4):125-32. PubMed ID: 10472732
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  • 29. Bovine spongiform encephalopathy, multiple sclerosis, and creutzfeldt-jakob disease are probably autoimmune diseases evoked by Acinetobacter bacteria.
    Ebringer A, Rashid T, Wilson C.
    Ann N Y Acad Sci; 2005 Jun; 1050():417-28. PubMed ID: 16014559
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  • 30. [Prion diseases].
    Warter JM, Steinmetz G, Mohr M, Tranchant C.
    Rev Neurol (Paris); 2002 Oct; 158(10 Pt 1):998-1007. PubMed ID: 12407310
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  • 31. [Prions and transmissible neurodegenerative diseases].
    Domínguez García A, Mata Albert E, Salleras Sanmartí L.
    Med Clin (Barc); 1998 May 30; 110(19):751-7. PubMed ID: 9672870
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  • 34. 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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  • 35. Prion protein and the transmissible spongiform encephalopathies.
    Caughey B, Chesebro B.
    Trends Cell Biol; 1997 Feb 02; 7(2):56-62. PubMed ID: 17708907
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  • 39. Classic slow virus diseases.
    Lennette EH.
    Bull Pan Am Health Organ; 1977 Feb 02; 11(2):157-61. PubMed ID: 143298
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