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Journal Abstract Search

369 related items for PubMed ID: 12200619

  • 1. 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; 104(4):342-50. PubMed ID: 12200619
    [Abstract] [Full Text] [Related]

  • 2. 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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  • 3. An autopsy report of three kindred in a Gerstmann-Sträussler-Scheinker disease P105L family with a special reference to prion protein, tau, and beta-amyloid.
    Ishizawa K, Mitsufuji T, Shioda K, Kobayashi A, Komori T, Nakazato Y, Kitamoto T, Araki N, Yamamoto T, Sasaki A.
    Brain Behav; 2018 Oct; 8(10):e01117. PubMed ID: 30240140
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  • 4. Immunohistochemical localization of 14.3.3 zeta protein in amyloid plaques in human spongiform encephalopathies.
    Richard M, Biacabe AG, Streichenberger N, Ironside JW, Mohr M, Kopp N, Perret-Liaudet A.
    Acta Neuropathol; 2003 Mar; 105(3):296-302. PubMed ID: 12557018
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  • 5. Gerstmann-Sträussler-Scheinker: a new phenotype with 'curly' PrP deposits.
    Colucci M, Moleres FJ, Xie ZL, Ray-Chaudhury A, Gutti S, Butefisch CM, Cervenakova L, Wang W, Goldfarb LG, Kong Q, Ghetti B, Chen SG, Gambetti P.
    J Neuropathol Exp Neurol; 2006 Jul; 65(7):642-51. PubMed ID: 16825951
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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. Toluidine blue-O staining of prion protein deposits.
    Sánchez A, Guzmán A, Ortiz A, Rembao D, Espinosa B, Zenteno E, Guevara J.
    Histochem Cell Biol; 2001 Dec; 116(6):519-24. PubMed ID: 11810193
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  • 8. Amyloid precursor protein cytoplasmic domain with phospho-Thr668 accumulates in Alzheimer's disease and its transgenic models: a role to mediate interaction of Abeta and tau.
    Shin RW, Ogino K, Shimabuku A, Taki T, Nakashima H, Ishihara T, Kitamoto T.
    Acta Neuropathol; 2007 Jun; 113(6):627-36. PubMed ID: 17431643
    [Abstract] [Full Text] [Related]

  • 9. The epsilon isoform of 14-3-3 protein is a component of the prion protein amyloid deposits of Gerstmann-Sträussler-Scheinker disease.
    Di Fede G, Giaccone G, Limido L, Mangieri M, Suardi S, Puoti G, Morbin M, Mazzoleni G, Ghetti B, Tagliavini F.
    J Neuropathol Exp Neurol; 2007 Feb; 66(2):124-30. PubMed ID: 17278997
    [Abstract] [Full Text] [Related]

  • 10. 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
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  • 11. Cerebral amyloid angiopathy with co-localization of prion protein and beta-amyloid in an 85-year-old patient with sporadic Creutzfeldt-Jakob disease.
    Paquet C, Privat N, Kaci R, Polivka M, Dupont O, Haïk S, Laplanche JL, Hauw JJ, Gray F.
    Acta Neuropathol; 2008 Nov 30; 116(5):567-73. PubMed ID: 18551298
    [Abstract] [Full Text] [Related]

  • 12. Neurofibrillary tangles in Gerstmann-Sträussler-Scheinker syndrome with the A117V prion gene mutation.
    Tranchant C, Sergeant N, Wattez A, Mohr M, Warter JM, Delacourte A.
    J Neurol Neurosurg Psychiatry; 1997 Aug 30; 63(2):240-6. PubMed ID: 9285466
    [Abstract] [Full Text] [Related]

  • 13. Alzheimer's amyloid precursor protein-positive degenerative neurites exist even within kuru plaques not specific to Alzheimer's disease.
    Ohgami T, Kitamoto T, Weidmann A, Beyreuther K, Tateishi J.
    Am J Pathol; 1991 Dec 30; 139(6):1245-50. PubMed ID: 1684265
    [Abstract] [Full Text] [Related]

  • 14. Transgenic mice overexpressing amyloid beta protein are an incomplete model of Alzheimer disease.
    Schwab C, Hosokawa M, McGeer PL.
    Exp Neurol; 2004 Jul 30; 188(1):52-64. PubMed ID: 15191802
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  • 16. Gerstmann-Sträussler-Scheinker disease and the French-Alsatian A117V variant.
    Mohr M, Tranchant C, Steinmetz G, Floquet J, Grignon Y, Warter JM.
    Clin Exp Pathol; 1999 Jul 30; 47(3-4):161-75. PubMed ID: 10472736
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