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Journal Abstract Search

717 related items for PubMed ID: 15174020

  • 1. Prion protein heterogeneity in sporadic but not variant Creutzfeldt-Jakob disease: UK cases 1991-2002.
    Head MW, Bunn TJ, Bishop MT, McLoughlin V, Lowrie S, McKimmie CS, Williams MC, McCardle L, MacKenzie J, Knight R, Will RG, Ironside JW.
    Ann Neurol; 2004 Jun; 55(6):851-9. PubMed ID: 15174020
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  • 8. Prion protein accumulation in eyes of patients with sporadic and variant Creutzfeldt-Jakob disease.
    Head MW, Northcott V, Rennison K, Ritchie D, McCardle L, Bunn TJ, McLennan NF, Ironside JW, Tullo AB, Bonshek RE.
    Invest Ophthalmol Vis Sci; 2003 Jan; 44(1):342-6. PubMed ID: 12506094
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  • 10. Neuropathological and biochemical criteria to identify acquired Creutzfeldt-Jakob disease among presumed sporadic cases.
    Kobayashi A, Parchi P, Yamada M, Mohri S, Kitamoto T.
    Neuropathology; 2016 Jun; 36(3):305-10. PubMed ID: 26669818
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  • 11. 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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  • 12. Neuropathology and molecular biology of variant Creutzfeldt-Jakob disease.
    Ironside JW, Head MW.
    Curr Top Microbiol Immunol; 2004 Mar 02; 284():133-59. PubMed ID: 15148991
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  • 13. Defining sporadic Creutzfeldt-Jakob disease strains and their transmission properties.
    Bishop MT, Will RG, Manson JC.
    Proc Natl Acad Sci U S A; 2010 Jun 29; 107(26):12005-10. PubMed ID: 20547859
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  • 16. Detection of type 1 prion protein in variant Creutzfeldt-Jakob disease.
    Yull HM, Ritchie DL, Langeveld JP, van Zijderveld FG, Bruce ME, Ironside JW, Head MW.
    Am J Pathol; 2006 Jan 29; 168(1):151-7. PubMed ID: 16400018
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