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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

202 related items for PubMed ID: 1490317

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  • 5. [A case of Gerstmann-Sträussler-Scheinker syndrome (P102L) accompanied by optic atrophy].
    Sugai F, Nakamori M, Nakatsuji Y, Abe K, Sakoda S.
    Rinsho Shinkeigaku; 2000 Sep; 40(9):926-8. PubMed ID: 11257791
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  • 6. [A case of variant Gerstmann-Sträussler-Scheinker disease with the mutation of codon P105L].
    Kubo M, Nishimura T, Shikata E, Kokubun Y, Takasu T.
    Rinsho Shinkeigaku; 1995 Aug; 35(8):873-7. PubMed ID: 8665729
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  • 9. Mutant prion proteins in Gerstmann-Sträussler-Scheinker disease with neurofibrillary tangles.
    Hsiao K, Dlouhy SR, Farlow MR, Cass C, Da Costa M, Conneally PM, Hodes ME, Ghetti B, Prusiner SB.
    Nat Genet; 1992 Apr; 1(1):68-71. PubMed ID: 1363810
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  • 11. [Familial prion disease (GSS, familial CJD, FFI)].
    Arata H, Takashima H.
    Nihon Rinsho; 2007 Aug; 65(8):1433-7. PubMed ID: 17695280
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  • 12. [Case of Gerstmann-Sträussler-Scheinker syndrome (GSS-P102L) mimicking variant Creurtzfeldt-Jakob disease in clinical manifestation and MRI findings].
    Kanata A, Saigoh K, Mitsui Y, Kitamoto T, Kusunoki S.
    Rinsho Shinkeigaku; 2008 Mar; 48(3):179-83. PubMed ID: 18409537
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  • 16. Neuropathological features of a case with schizophrenia and prion protein gene P102L mutation before onset of Gerstmann-Sträussler-Scheinker disease.
    Sasaki K, Doh-ura K, Furuta A, Nakashima S, Morisada Y, Tateishi J, Iwaki T.
    Acta Neuropathol; 2003 Jul; 106(1):92-6. PubMed ID: 12682740
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  • 20. [Gerstmann-Straüssler-Scheinker syndrome].
    Tranchant C, Warter JM.
    Rev Neurol (Paris); 1998 Feb; 154(2):152-7. PubMed ID: 9773036
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