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Journal Abstract Search

98 related items for PubMed ID: 7783864

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  • 2. Fatal familial insomnia, a prion disease with a mutation at codon 178 of the prion protein gene.
    Medori R, Tritschler HJ, LeBlanc A, Villare F, Manetto V, Chen HY, Xue R, Leal S, Montagna P, Cortelli P.
    N Engl J Med; 1992 Feb 13; 326(7):444-9. PubMed ID: 1346338
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  • 3. Creutzfeldt-Jakob disease with a novel four extra-repeat insertional mutation in the PrP gene.
    Rossi G, Giaccone G, Giampaolo L, Iussich S, Puoti G, Frigo M, Cavaletti G, Frattola L, Bugiani O, Tagliavini F.
    Neurology; 2000 Aug 08; 55(3):405-10. PubMed ID: 10932276
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  • 4. Sporadic Creutzfeldt-Jakob disease with MM1-type prion protein and plaques.
    Ishida C, Kakishima A, Okino S, Furukawa Y, Kano M, Oda Y, Nakanishi I, Makifuchi T, Kitamoto T, Yamada M.
    Neurology; 2003 Feb 11; 60(3):514-7. PubMed ID: 12578942
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  • 5. A case of progressive subcortical gliosis associated with deposition of abnormal prion protein (PrP).
    Revesz T, Daniel SE, Lees AJ, Will RG.
    J Neurol Neurosurg Psychiatry; 1995 Jun 11; 58(6):759-60. PubMed ID: 7608689
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  • 9. Molecular biology of prions causing infectious and genetic encephalopathies of humans as well as scrapie of sheep and BSE of cattle.
    Prusiner SB.
    Dev Biol Stand; 1991 Jun 11; 75():55-74. PubMed ID: 1686599
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  • 14. Involvement of the peripheral nervous system in human prion diseases including dural graft associated Creutzfeldt-Jakob disease.
    Ishida C, Okino S, Kitamoto T, Yamada M.
    J Neurol Neurosurg Psychiatry; 2005 Mar 11; 76(3):325-9. PubMed ID: 15716520
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  • 16. Prion disease with a 144 base pair insertion: unusual cerebellar prion protein immunoreactivity.
    Gelpi E, Kovacs GG, Ströbel T, Koperek O, Voigtländer T, Liberski PP, Budka H.
    Acta Neuropathol; 2005 Nov 11; 110(5):513-9. PubMed ID: 16155763
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