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Journal Abstract Search

162 related items for PubMed ID: 11771163

  • 1. [A case of Gerstmann-Sträussler-Scheinker syndrome (GSS) with late onset--a haplotype analysis of Glu219Lys polymorphism in PrP gene].
    Takase K, Furuya H, Murai H, Yamada T, Oh-yagi Y, Doh-ura K, Iwaki T, Tobimatsu S, Kira J.
    Rinsho Shinkeigaku; 2001 Jun; 41(6):318-21. PubMed ID: 11771163
    [Abstract] [Full Text] [Related]

  • 2. Lower limb areflexia without central and peripheral conduction abnormalities is highly suggestive of Gerstmann-Sträussler-Scheinker disease Pro102Leu.
    Salsano E, Fancellu R, Di Fede G, Ciano C, Scaioli V, Nanetti L, Politi LS, Tagliavini F, Mariotti C, Pareyson D.
    J Neurol Sci; 2011 Mar 15; 302(1-2):85-8. PubMed ID: 21167505
    [Abstract] [Full Text] [Related]

  • 3. 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 15; 1(1):68-71. PubMed ID: 1363810
    [Abstract] [Full Text] [Related]

  • 4. [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 15; 40(9):926-8. PubMed ID: 11257791
    [Abstract] [Full Text] [Related]

  • 5. [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 Sep 15; 38(10-11):920-5. PubMed ID: 10203975
    [Abstract] [Full Text] [Related]

  • 6. [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 Sep 15; 147(4):274-8. PubMed ID: 2063076
    [Abstract] [Full Text] [Related]

  • 7. [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 15; 40(7):726-31. PubMed ID: 11186913
    [Abstract] [Full Text] [Related]

  • 8. [Patient with Gerstmann-Striussler-Scheinker syndrome (GSS P102L) presenting high intensity lesions in the cerebral cortex on diffusion weighted MRI].
    Misumi M, Nishida Y, Araki S.
    Rinsho Shinkeigaku; 2006 Apr 15; 46(4):291-3. PubMed ID: 16768100
    [Abstract] [Full Text] [Related]

  • 9. 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 15; 111(7):606-9. PubMed ID: 19443103
    [Abstract] [Full Text] [Related]

  • 10. [Gerstmann-Sträussler-Scheinker disease with heterozygous codon change at prion protein codon 129].
    Terao Y, Hitoshi S, Shimizu J, Sakuta M, Kitamoto T.
    Rinsho Shinkeigaku; 1992 Aug 15; 32(8):880-3. PubMed ID: 1490317
    [Abstract] [Full Text] [Related]

  • 11. 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 15; 1(1):64-7. PubMed ID: 1363809
    [Abstract] [Full Text] [Related]

  • 12. Hyperphosphorylated tau deposition parallels prion protein burden in a case of Gerstmann-Sträussler-Scheinker syndrome P102L mutation complicated with dementia.
    Ishizawa K, Komori T, Shimazu T, Yamamoto T, Kitamoto T, Shimazu K, Hirose T.
    Acta Neuropathol; 2002 Oct 15; 104(4):342-50. PubMed ID: 12200619
    [Abstract] [Full Text] [Related]

  • 13. A second case of Gerstmann-Sträussler-Scheinker disease linked to the G131V mutation in the prion protein gene in a Dutch patient.
    Jansen C, Parchi P, Capellari S, Strammiello R, Dopper EG, van Swieten JC, Kamphorst W, Rozemuller AJ.
    J Neuropathol Exp Neurol; 2011 Aug 15; 70(8):698-702. PubMed ID: 21760536
    [Abstract] [Full Text] [Related]

  • 14. [Gerstmann-Straüssler-Scheinker syndrome].
    Tranchant C, Warter JM.
    Rev Neurol (Paris); 1998 Feb 15; 154(2):152-7. PubMed ID: 9773036
    [Abstract] [Full Text] [Related]

  • 15. Aggregation/fibrillogenesis of recombinant human prion protein and Gerstmann-Sträussler-Scheinker disease peptides in the presence of metal ions.
    Ricchelli F, Buggio R, Drago D, Salmona M, Forloni G, Negro A, Tognon G, Zatta P.
    Biochemistry; 2006 May 30; 45(21):6724-32. PubMed ID: 16716083
    [Abstract] [Full Text] [Related]

  • 16. An amber mutation of prion protein in Gerstmann-Sträussler syndrome with mutant PrP plaques.
    Kitamoto T, Iizuka R, Tateishi J.
    Biochem Biophys Res Commun; 1993 Apr 30; 192(2):525-31. PubMed ID: 8097911
    [Abstract] [Full Text] [Related]

  • 17. Detecting prion protein gene mutations by denaturing gradient gel electrophoresis.
    Fink JK, Peacock ML, Warren JT, Roses AD, Prusiner SB.
    Hum Mutat; 1994 Apr 30; 4(1):42-50. PubMed ID: 7951257
    [Abstract] [Full Text] [Related]

  • 18. Anesthetic management of a patient with Gerstmann-Sträussler-Scheinker syndrome (mutation of prion protein).
    Nakamura M, Ogata M, Matsuo Y, Sata T.
    Anesth Analg; 2006 Apr 30; 102(4):1285-6. PubMed ID: 16551938
    [Abstract] [Full Text] [Related]

  • 19. [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 30; 35(8):873-7. PubMed ID: 8665729
    [Abstract] [Full Text] [Related]

  • 20. Familial Prion Disease: First Indian Kindred with Gerstmann-Sträussler-Scheinker Syndrome.
    Bhatia S, Bijarnia-Mahay S, Dubey S, Gourie-Devi M.
    Neurol India; 2020 Aug 30; 68(6):1431-1434. PubMed ID: 33342883
    [Abstract] [Full Text] [Related]

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