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296 related items for PubMed ID: 1346338

  • 21. Codon 129 polymorphism and the E200K mutation do not affect the cellular prion protein isoform composition in the cerebrospinal fluid from patients with Creutzfeldt-Jakob disease.
    Schmitz M, Schlomm M, Hasan B, Beekes M, Mitrova E, Korth C, Breil A, Carimalo J, Gawinecka J, Varges D, Zerr I.
    Eur J Neurosci; 2010 Jun; 31(11):2024-31. PubMed ID: 20529115
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  • 22. Allelic origin of the abnormal prion protein isoform in familial prion diseases.
    Chen SG, Parchi P, Brown P, Capellari S, Zou W, Cochran EJ, Vnencak-Jones CL, Julien J, Vital C, Mikol J, Lugaresi E, Autilio-Gambetti L, Gambetti P.
    Nat Med; 1997 Sep; 3(9):1009-15. PubMed ID: 9288728
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  • 24. Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease.
    Parchi P, Castellani R, Capellari S, Ghetti B, Young K, Chen SG, Farlow M, Dickson DW, Sima AA, Trojanowski JQ, Petersen RB, Gambetti P.
    Ann Neurol; 1996 Jun; 39(6):767-78. PubMed ID: 8651649
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  • 29. Towards authentic transgenic mouse models of heritable PrP prion diseases.
    Watts JC, Giles K, Bourkas ME, Patel S, Oehler A, Gavidia M, Bhardwaj S, Lee J, Prusiner SB.
    Acta Neuropathol; 2016 Oct; 132(4):593-610. PubMed ID: 27350609
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  • 30. Genetic Creutzfeldt-Jakob disease and fatal familial insomnia: insights into phenotypic variability and disease pathogenesis.
    Capellari S, Strammiello R, Saverioni D, Kretzschmar H, Parchi P.
    Acta Neuropathol; 2011 Jan; 121(1):21-37. PubMed ID: 20978903
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  • 31. [Genetic background of human prion diseases].
    Kovács GG.
    Ideggyogy Sz; 2007 Nov 30; 60(11-12):438-46. PubMed ID: 18198790
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  • 32. Thalamic form of Creutzfeldt-Jakob disease or fatal insomnia? Report of a sporadic case with normal prion protein genotype.
    Kawasaki K, Wakabayashi K, Kawakami A, Higuchi M, Kitamoto T, Tsuji S, Takahashi H.
    Acta Neuropathol; 1997 Mar 30; 93(3):317-22. PubMed ID: 9083566
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  • 36. Profoundly different prion diseases in knock-in mice carrying single PrP codon substitutions associated with human diseases.
    Jackson WS, Borkowski AW, Watson NE, King OD, Faas H, Jasanoff A, Lindquist S.
    Proc Natl Acad Sci U S A; 2013 Sep 03; 110(36):14759-64. PubMed ID: 23959875
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  • 37. Sporadic and familial CJD: classification and characterisation.
    Gambetti P, Kong Q, Zou W, Parchi P, Chen SG.
    Br Med Bull; 2003 Sep 03; 66():213-39. PubMed ID: 14522861
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  • 38. Fatal familial insomnia: a new Austrian family.
    Almer G, Hainfellner JA, Brücke T, Jellinger K, Kleinert R, Bayer G, Windl O, Kretzschmar HA, Hill A, Sidle K, Collinge J, Budka H.
    Brain; 1999 Jan 03; 122 ( Pt 1)():5-16. PubMed ID: 10050890
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  • 40. Mutation of the prion protein gene at codon 208 in familial Creutzfeldt-Jakob disease.
    Mastrianni JA, Iannicola C, Myers RM, DeArmond S, Prusiner SB.
    Neurology; 1996 Nov 03; 47(5):1305-12. PubMed ID: 8909447
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