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Journal Abstract Search

232 related items for PubMed ID: 2063076

  • 1. [Mutation of codon 117 of the prion gene in Gerstmann-Sträussler-Scheinker disease].
    Tranchant C, Doh-Ura K, Steinmetz G, Chevalier Y, Kitamoto T, Tateishi J, Warter JM.
    Rev Neurol (Paris); 1991; 147(4):274-8. PubMed ID: 2063076
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  • 2. Gerstmann-Sträussler-Scheinker disease in an Alsatian family: clinical and genetic studies.
    Tranchant C, Doh-ura K, Warter JM, Steinmetz G, Chevalier Y, Hanauer A, Kitamoto T, Tateishi J.
    J Neurol Neurosurg Psychiatry; 1992 Mar; 55(3):185-7. PubMed ID: 1348783
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  • 3. [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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  • 4. Linkage of the Indiana kindred of Gerstmann-Sträussler-Scheinker disease to the prion protein gene.
    Dlouhy SR, Hsiao K, Farlow MR, Foroud T, Conneally PM, Johnson P, Prusiner SB, Hodes ME, Ghetti B.
    Nat Genet; 1992 Apr; 1(1):64-7. PubMed ID: 1363809
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  • 5. 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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  • 6. 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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  • 7. Gerstmann-Sträussler-Scheinker disease with A117V mutation in a second French-Alsatian family.
    Heldt N, Boellaard JW, Brown P, Cervenákova L, Doerr-Schott J, Thomas C, Scherer C, Rohmer F.
    Clin Neuropathol; 1998 Jul; 17(4):229-34. PubMed ID: 9707339
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  • 11. Familial spongiform encephalopathy associated with a novel prion protein gene mutation.
    Nitrini R, Rosemberg S, Passos-Bueno MR, da Silva LS, Iughetti P, Papadopoulos M, Carrilho PM, Caramelli P, Albrecht S, Zatz M, LeBlanc A.
    Ann Neurol; 1997 Aug; 42(2):138-46. PubMed ID: 9266722
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  • 16. [Gerstmann-Sträussler-Scheinker syndrome with a Pro102Leu mutation in the prion protein gene and atypical MRI findings, hyperthermia, tachycardia, and hyperhidrosis].
    Imaiso Y, Mitsuo K.
    Rinsho Shinkeigaku; 1998 Aug; 38(10-11):920-5. PubMed ID: 10203975
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  • 17. A case of Gerstmann-Sträussler-Scheinker syndrome with the P105L prion protein gene mutation presenting with ataxia and extrapyramidal signs without spastic paraparesis.
    Iwasaki Y, Kizawa M, Hori N, Kitamoto T, Sobue G.
    Clin Neurol Neurosurg; 2009 Sep; 111(7):606-9. PubMed ID: 19443103
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  • 18. [A case of Gerstmann-Sträussler-Scheinker disease with severe muscular atrophy and vertical gaze palsy].
    Oba N, Fujimoto Y, Hirata K, Ando N, Saida K.
    Rinsho Shinkeigaku; 2000 Jul; 40(7):726-31. PubMed ID: 11186913
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