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 *

155 related articles for article (PubMed ID: 9932941)

  • 1. Involvement of the spinal posterior horn in Gerstmann-Sträussler-Scheinker disease (PrP P102L).
    Yamada M; Tomimitsu H; Yokota T; Tomi H; Sunohara N; Mukoyama M; Itoh Y; Suematsu N; Otomo E; Okeda R; Matsushita M; Mizusawa H
    Neurology; 1999 Jan; 52(2):260-5. PubMed ID: 9932941
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Involvement of the peripheral nervous system in human prion diseases including dural graft associated Creutzfeldt-Jakob disease.
    Ishida C; Okino S; Kitamoto T; Yamada M
    J Neurol Neurosurg Psychiatry; 2005 Mar; 76(3):325-9. PubMed ID: 15716520
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Different patterns of truncated prion protein fragments correlate with distinct phenotypes in P102L Gerstmann-Sträussler-Scheinker disease.
    Parchi P; Chen SG; Brown P; Zou W; Capellari S; Budka H; Hainfellner J; Reyes PF; Golden GT; Hauw JJ; Gajdusek DC; Gambetti P
    Proc Natl Acad Sci U S A; 1998 Jul; 95(14):8322-7. PubMed ID: 9653185
    [TBL] [Abstract][Full Text] [Related]  

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

  • 6. 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]  

  • 7. 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]  

  • 8. 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; 302(1-2):85-8. PubMed ID: 21167505
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Early neurophysiological biomarkers and spinal cord pathology in inherited prion disease.
    Rudge P; Jaunmuktane Z; Hyare H; Ellis M; Koltzenburg M; Collinge J; Brandner S; Mead S
    Brain; 2019 Mar; 142(3):760-770. PubMed ID: 30698738
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Early clinical signs and imaging findings in Gerstmann-Sträussler-Scheinker syndrome (Pro102Leu).
    Arata H; Takashima H; Hirano R; Tomimitsu H; Machigashira K; Izumi K; Kikuno M; Ng AR; Umehara F; Arisato T; Ohkubo R; Nakabeppu Y; Nakajo M; Osame M; Arimura K
    Neurology; 2006 Jun; 66(11):1672-8. PubMed ID: 16769939
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Gerstmann-Sträussler-Scheinker disease (PRNP P102L): amyloid deposits are best recognized by antibodies directed to epitopes in PrP region 90-165.
    Piccardo P; Ghetti B; Dickson DW; Vinters HV; Giaccone G; Bugiani O; Tagliavini F; Young K; Dlouhy SR; Seiler C
    J Neuropathol Exp Neurol; 1995 Nov; 54(6):790-801. PubMed ID: 7595652
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Gerstmann-Sträussler-Scheinker disease. I. Human diseases.
    Liberski PP; Budka H
    Folia Neuropathol; 2004; 42 Suppl B():120-40. PubMed ID: 16903147
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [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
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Atypical frontotemporal dementia as a new clinical phenotype of Gerstmann-Straussler-Scheinker disease with the PrP-P102L mutation. Description of a previously unreported Italian family.
    Giovagnoli AR; Di Fede G; Aresi A; Reati F; Rossi G; Tagliavini F
    Neurol Sci; 2008 Dec; 29(6):405-10. PubMed ID: 19030774
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A Japanese family with a variant of Gerstmann-Sträussler-Scheinker disease.
    Tanaka Y; Minematsu K; Moriyasu H; Yamaguchi T; Yutani C; Kitamoto T; Furukawa H
    J Neurol Neurosurg Psychiatry; 1997 May; 62(5):454-7. PubMed ID: 9153600
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Gerstmann-Sträussler-Scheinker disease.
    Liberski PP
    Adv Exp Med Biol; 2012; 724():128-37. PubMed ID: 22411239
    [TBL] [Abstract][Full Text] [Related]  

  • 19. NGS study in a sicilian case series with a genetic diagnosis for Gerstmann-Sträussler-Scheinker syndrome (PRNP, p.P102L).
    Salemi M; Mandarà LGM; Salluzzo MG; Schillaci FA; Castiglione R; Cordella A; Iorio R; Perrotta CS; Ferri R; Romano C
    Mol Biol Rep; 2023 Nov; 50(11):9715-9720. PubMed ID: 37812352
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Polymorphism at codon 129 or codon 219 of PRNP and clinical heterogeneity in a previously unreported family with Gerstmann-Sträussler-Scheinker disease (PrP-P102L mutation).
    Barbanti P; Fabbrini G; Salvatore M; Petraroli R; Cardone F; Maras B; Equestre M; Macchi G; Lenzi GL; Pocchiari M
    Neurology; 1996 Sep; 47(3):734-41. PubMed ID: 8797472
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.