These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

223 related articles for article (PubMed ID: 8337941)

  • 1. Microglia is a component of the prion protein amyloid plaque in the Gerstmann-Sträussler-Scheinker syndrome.
    Barcikowska M; Liberski PP; Boellaard JW; Brown P; Gajdusek DC; Budka H
    Acta Neuropathol; 1993; 85(6):623-7. PubMed ID: 8337941
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Relationship of microglia and scrapie amyloid-immunoreactive plaques in kuru, Creutzfeldt-Jakob disease and Gerstmann-Sträussler syndrome.
    Guiroy DC; Wakayama I; Liberski PP; Gajdusek DC
    Acta Neuropathol; 1994; 87(5):526-30. PubMed ID: 8059606
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Ultrastructural study of florid plaques in variant Creutzfeldt-Jakob disease: a comparison with amyloid plaques in kuru, sporadic Creutzfeldt-Jakob disease and Gerstmann-Sträussler-Scheinker disease.
    Sikorska B; Liberski PP; Sobów T; Budka H; Ironside JW
    Neuropathol Appl Neurobiol; 2009 Feb; 35(1):46-59. PubMed ID: 18513219
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Colocalization of prion protein and beta protein in the same amyloid plaques in patients with Gerstmann-Sträussler syndrome.
    Miyazono M; Kitamoto T; Iwaki T; Tateishi J
    Acta Neuropathol; 1992; 83(4):333-9. PubMed ID: 1349451
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A special report I. Prion protein (PrP)--amyloid plaques in the transmissible spongiform encephalopathies, or prion diseases revisited.
    Liberski PP; Bratosiewicz J; Waliś A; Kordek R; Jeffrey M; Brown P
    Folia Neuropathol; 2001; 39(4):217-35. PubMed ID: 11928893
    [TBL] [Abstract][Full Text] [Related]  

  • 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
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Gerstmann-Sträussler-Scheinker disease showing beta-protein type cerebellar and cerebral amyloid angiopathy.
    Ikeda SI; Yanagisawa N; Allsop D; Glenner GG
    Acta Neuropathol; 1994; 88(3):262-6. PubMed ID: 7810298
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Gerstmann-Sträussler-Scheinker disease and "anchorless prion protein" mice share prion conformational properties diverging from sporadic Creutzfeldt-Jakob disease.
    Zanusso G; Fiorini M; Ferrari S; Meade-White K; Barbieri I; Brocchi E; Ghetti B; Monaco S
    J Biol Chem; 2014 Feb; 289(8):4870-81. PubMed ID: 24398683
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Immunoreactivity of cerebral amyloidosis is enhanced by protein denaturation treatments.
    Doi-Yi R; Kitamoto T; Tateishi J
    Acta Neuropathol; 1991; 82(4):260-5. PubMed ID: 1684688
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Specific amyloid-β42 deposition in the brain of a Gerstmann-Sträussler-Scheinker disease patient with a P105L mutation on the prion protein gene.
    Furukawa F; Sanjo N; Kobayashi A; Hamaguchi T; Yamada M; Kitamoto T; Mizusawa H; Yokota T
    Prion; 2018; 12(5-6):315-319. PubMed ID: 30394185
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Gerstmann-Sträussler-Scheinker Disease with F198S Mutation Induces Independent Tau and Prion Protein Pathologies in Bank Voles.
    Bruno R; Pirisinu L; Riccardi G; D'Agostino C; De Cecco E; Legname G; Cardone F; Gambetti P; Nonno R; Agrimi U; Di Bari MA
    Biomolecules; 2022 Oct; 12(10):. PubMed ID: 36291746
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A comparative immunohistochemical study of Kuru and senile plaques with a special reference to glial reactions at various stages of amyloid plaque formation.
    Miyazono M; Iwaki T; Kitamoto T; Kaneko Y; Doh-ura K; Tateishi J
    Am J Pathol; 1991 Sep; 139(3):589-98. PubMed ID: 1679596
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Miniplaques and shapeless cerebral amyloid deposits in a case of Gerstmann-Sträussler-Scheinker's syndrome.
    Boellaard JW; Doerr-Schott J; Schlote W
    Acta Neuropathol; 1993; 86(5):532-5. PubMed ID: 8310806
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Neuropathology of Gerstmann-Sträussler-Scheinker disease.
    Bugiani O; Giaccone G; Piccardo P; Morbin M; Tagliavini F; Ghetti B
    Microsc Res Tech; 2000 Jul; 50(1):10-5. PubMed ID: 10871543
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Dominantly inherited prion protein cerebral amyloidoses - a modern view of Gerstmann-Sträussler-Scheinker.
    Ghetti B; Piccardo P; Zanusso G
    Handb Clin Neurol; 2018; 153():243-269. PubMed ID: 29887140
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Proteinase-K-resistant prion protein isoforms in Gerstmann-Sträussler-Scheinker disease (Indiana kindred).
    Piccardo P; Seiler C; Dlouhy SR; Young K; Farlow MR; Prelli F; Frangione B; Bugiani O; Tagliavini F; Ghetti B
    J Neuropathol Exp Neurol; 1996 Nov; 55(11):1157-63. PubMed ID: 8939199
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Hereditary prion protein amyloidoses.
    Ghetti B; Tagliavini F; Takao M; Bugiani O; Piccardo P
    Clin Lab Med; 2003 Mar; 23(1):65-85, viii. PubMed ID: 12733425
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.