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Journal Abstract Search

114 related items for PubMed ID: 7912945

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  • 2. [Familial Creutzfeldt-Jakob disease with the heterozygous point mutation at codon 200 of the prion protein gene (Glu-->Lys)--report of CJD200 brothers of Yamanashi Prefecture origin].
    Kawauchi Y, Okada M, Kuroiwa Y, Ishihara O, Akai J.
    No To Shinkei; 1997 May; 49(5):460-4. PubMed ID: 9163760
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  • 4. [An autopsy-verified case of Creutzfeldt-Jakob disease with codon 129 polymorphism and codon 180 point mutation].
    Matsumura T, Kojima S, Kuroiwa Y, Takagi A, Unakami M, Kitamoto T.
    Rinsho Shinkeigaku; 1995 Mar; 35(3):282-5. PubMed ID: 7614752
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  • 5. [A case of probable Creutzfeldt-Jakob disease with a point mutation of prion protein gene codon 180 and atypical MRI findings].
    Kobayashi S, Ohuchi T, Maki T.
    Rinsho Shinkeigaku; 1997 Aug; 37(8):671-4. PubMed ID: 9404141
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  • 9. [A case of Creutzfeldt-Jakob disease with a point mutation of prion protein at codon 180].
    Tanaka T, Kinoshita I, Saitoh Y, Satoh K, Nishiura Y, Shirabe S, Kitamoto T.
    No To Shinkei; 2004 Dec; 56(12):1025-8. PubMed ID: 15729879
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  • 13. Diffusion-weighted MRI in familial Creutzfeldt-Jakob disease with the codon 200 mutation in the prion protein gene.
    Tsuboi Y, Baba Y, Doh-ura K, Imamura A, Fujioka S, Yamada T.
    J Neurol Sci; 2005 May 15; 232(1-2):45-9. PubMed ID: 15850581
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  • 15. [Psychiatric manifestations of a new variant of Creutzfeldt-Jakob disease. Apropos of a case].
    Dervaux A, Vicart S, Lopes F, Le Borgne MH.
    Encephale; 2001 May 15; 27(2):194-7. PubMed ID: 11407273
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  • 16. An autopsied case of panencephalopathic-type Creutzfeldt-Jakob disease with mutation in the prion protein gene at codon 232 and type 1 prion protein.
    Hama T, Iwasaki Y, Niwa H, Yoshida M, Hashizume Y, Kitamoto T, Murakami N, Sobue G.
    Neuropathology; 2009 Dec 15; 29(6):727-34. PubMed ID: 19422533
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  • 17. 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 15; 45(6):812-6. PubMed ID: 10360778
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  • 20. Novel prion protein gene mutation at codon 196 (E196A) in a septuagenarian with Creutzfeldt-Jakob disease.
    Zhang H, Wang M, Wu L, Zhang H, Jin T, Wu J, Sun L.
    J Clin Neurosci; 2014 Jan 15; 21(1):175-8. PubMed ID: 23787189
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