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Journal Abstract Search

190 related items for PubMed ID: 9669705

  • 21. Panencephalopathic Creutzfeldt-Jakob disease with distinct pattern of prion protein deposition in a patient with D178N mutation and homozygosity for valine at codon 129 of the prion protein Gene.
    Marcon G, Indaco A, Di Fede G, Suardi S, Finato N, Moretti V, Micoli S, Fociani P, Zerbi P, Pincherle A, Redaelli V, Tagliavini F, Giaccone G.
    Brain Pathol; 2014 Mar; 24(2):148-51. PubMed ID: 24118545
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  • 25. Prion protein gene analysis in three kindreds with fatal familial insomnia (FFI): codon 178 mutation and codon 129 polymorphism.
    Medori R, Tritschler HJ.
    Am J Hum Genet; 1993 Oct; 53(4):822-7. PubMed ID: 8105681
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  • 26. Identification in Israel of 2 Jewish Creutzfeld-Jakob disease patients with a 178 mutation at their PrP gene.
    Rosenmann H, Vardi J, Finkelstein Y, Chapman J, Gabizon R.
    Acta Neurol Scand; 1998 Mar; 97(3):184-7. PubMed ID: 9531435
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  • 28. D178N, 129Val and N171S, 129Val genotype in a family with Creutzfeldt-Jakob disease.
    Appleby BS, Appleby KK, Hall RC, Wallin MT.
    Dement Geriatr Cogn Disord; 2010 Mar; 30(5):424-31. PubMed ID: 21071944
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  • 29. Absence of spontaneous disease and comparative prion susceptibility of transgenic mice expressing mutant human prion proteins.
    Asante EA, Gowland I, Grimshaw A, Linehan JM, Smidak M, Houghton R, Osiguwa O, Tomlinson A, Joiner S, Brandner S, Wadsworth JDF, Collinge J.
    J Gen Virol; 2009 Mar; 90(Pt 3):546-558. PubMed ID: 19218199
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  • 30. Familial fatal insomnia with atypical clinical features in a patient with D178N mutation and homozygosity for Met at codon 129 of the prion protein gene.
    Sun L, Li X, Lin X, Yan F, Chen K, Xiao S.
    Prion; 2015 Mar; 9(3):228-35. PubMed ID: 26074146
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  • 36. A novel phenotype in familial Creutzfeldt-Jakob disease: prion protein gene E200K mutation coupled with valine at codon 129 and type 2 protease-resistant prion protein.
    Hainfellner JA, Parchi P, Kitamoto T, Jarius C, Gambetti P, Budka H.
    Ann Neurol; 1999 Jun; 45(6):812-6. PubMed ID: 10360778
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  • 38. First experimental transmission of fatal familial insomnia.
    Tateishi J, Brown P, Kitamoto T, Hoque ZM, Roos R, Wollman R, Cervenáková L, Gajdusek DC.
    Nature; 1995 Aug 03; 376(6539):434-5. PubMed ID: 7630420
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  • 39. The prion diseases.
    Brown K, Mastrianni JA.
    J Geriatr Psychiatry Neurol; 2010 Dec 03; 23(4):277-98. PubMed ID: 20938044
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