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Journal Abstract Search

470 related items for PubMed ID: 9103904

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  • 2. [Creutzfeldt-Jakob disease and other human transmissible spongiform encephalopathies. Part II].
    Zaborowski A.
    Psychiatr Pol; 2004; 38(2):297-309. PubMed ID: 15307294
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  • 5. [Clinical characteristics and diagnostics of human spongiform encephalopathies: an update].
    Hermann P, Goebel S, Zerr I.
    Nervenarzt; 2024 Apr; 95(4):376-384. PubMed ID: 38503894
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  • 7. The epsilon isoform of 14-3-3 protein is a component of the prion protein amyloid deposits of Gerstmann-Sträussler-Scheinker disease.
    Di Fede G, Giaccone G, Limido L, Mangieri M, Suardi S, Puoti G, Morbin M, Mazzoleni G, Ghetti B, Tagliavini F.
    J Neuropathol Exp Neurol; 2007 Feb; 66(2):124-30. PubMed ID: 17278997
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  • 10. [Prion dementias: nosology and diagnostic difficulties in the spectrum of Creutzfeld-Jakob encephalopathy].
    Kálmán J, Járdánházy T, Cserháti A, Szekeres G, Demeter I, Berek I, Dobranovics I, Csernay L, Janka Z.
    Orv Hetil; 1997 Mar 23; 138(12):731-7. PubMed ID: 9157343
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  • 12. Prion protein and the transmissible spongiform encephalopathies.
    Caughey B, Chesebro B.
    Trends Cell Biol; 1997 Feb 23; 7(2):56-62. PubMed ID: 17708907
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  • 13. [Creutzfeldt-Jakob disease and Gerstmann-Sträussler syndrome with reference to their differential diagnosis].
    Frýdl V, Závodská H.
    Zentralbl Pathol; 1991 Feb 23; 137(2):133-9. PubMed ID: 1911728
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  • 16. [Human transmissible subacute spongiform encephalopathy].
    Dormont D.
    Bull Acad Natl Med; 1994 May 23; 178(5):887-903; discussion 904-5. PubMed ID: 7953896
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  • 17. Creutzfeldt-Jakob disease patients with congophilic kuru plaques have the missense variant prion protein common to Gerstmann-Sträussler syndrome.
    Doh-ura K, Tateishi J, Kitamoto T, Sasaki H, Sakaki Y.
    Ann Neurol; 1990 Feb 23; 27(2):121-6. PubMed ID: 2180366
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  • 19. Human prion diseases: from Kuru to variant Creutzfeldt-Jakob disease.
    Sikorska B, Liberski PP.
    Subcell Biochem; 2012 Feb 23; 65():457-96. PubMed ID: 23225013
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  • 20. [Prion diseases or transmissible spongiform encephalopathies].
    Brandel JP.
    Rev Med Interne; 2022 Feb 23; 43(2):106-115. PubMed ID: 34148672
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