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 *

172 related articles for article (PubMed ID: 10408557)

  • 1. An inherited prion disease with a PrP P105L mutation: clinicopathologic and PrP heterogeneity.
    Yamada M; Itoh Y; Inaba A; Wada Y; Takashima M; Satoh S; Kamata T; Okeda R; Kayano T; Suematsu N; Kitamoto T; Otomo E; Matsushita M; Mizusawa H
    Neurology; 1999 Jul; 53(1):181-8. PubMed ID: 10408557
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. A novel PRNP-P105S mutation associated with atypical prion disease and a rare PrPSc conformation.
    Tunnell E; Wollman R; Mallik S; Cortes CJ; Dearmond SJ; Mastrianni JA
    Neurology; 2008 Oct; 71(18):1431-8. PubMed ID: 18955686
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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; 70(8):698-702. PubMed ID: 21760536
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A new inherited prion disease (PrP-P105L mutation) showing spastic paraparesis.
    Kitamoto T; Amano N; Terao Y; Nakazato Y; Isshiki T; Mizutani T; Tateishi J
    Ann Neurol; 1993 Dec; 34(6):808-13. PubMed ID: 8250529
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Inherited prion disease with an alanine to valine mutation at codon 117 in the prion protein gene.
    Mallucci GR; Campbell TA; Dickinson A; Beck J; Holt M; Plant G; de Pauw KW; Hakin RN; Clarke CE; Howell S; Davies-Jones GA; Lawden M; Smith CM; Ince P; Ironside JW; Bridges LR; Dean A; Weeks I; Collinge J
    Brain; 1999 Oct; 122 ( Pt 10)():1823-37. PubMed ID: 10506086
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Novel missense variants of prion protein in Creutzfeldt-Jakob disease or Gerstmann-Sträussler syndrome.
    Kitamoto T; Ohta M; Doh-ura K; Hitoshi S; Terao Y; Tateishi J
    Biochem Biophys Res Commun; 1993 Mar; 191(2):709-14. PubMed ID: 8461023
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Prion protein amyloidosis.
    Ghetti B; Piccardo P; Frangione B; Bugiani O; Giaccone G; Young K; Prelli F; Farlow MR; Dlouhy SR; Tagliavini F
    Brain Pathol; 1996 Apr; 6(2):127-45. PubMed ID: 8737929
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Prion disease (PrP-A117V) presenting with ataxia instead of dementia.
    Mastrianni JA; Curtis MT; Oberholtzer JC; Da Costa MM; DeArmond S; Prusiner SB; Garbern JY
    Neurology; 1995 Nov; 45(11):2042-50. PubMed ID: 7501157
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A variant of Gerstmann-Sträussler-Scheinker disease carrying codon 105 mutation with codon 129 polymorphism of the prion protein gene: a clinicopathological study.
    Itoh Y; Yamada M; Hayakawa M; Shozawa T; Tanaka J; Matsushita M; Kitamoto T; Tateishi J; Otomo E
    J Neurol Sci; 1994 Dec; 127(1):77-86. PubMed ID: 7699395
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Unusual clinical and molecular-pathological profile of gerstmann-Sträussler-Scheinker disease associated with a novel PRNP mutation (V176G).
    Simpson M; Johanssen V; Boyd A; Klug G; Masters CL; Li QX; Pamphlett R; McLean C; Lewis V; Collins SJ
    JAMA Neurol; 2013 Sep; 70(9):1180-5. PubMed ID: 23857164
    [TBL] [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; 63(2):240-6. PubMed ID: 9285466
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Neuropathologic variants of sporadic Creutzfeldt-Jakob disease and codon 129 of PrP gene.
    Hauw JJ; Sazdovitch V; Laplanche JL; Peoc'h K; Kopp N; Kemeny J; Privat N; Delasnerie-Lauprêtre N; Brandel JP; Deslys JP; Dormont D; Alpérovitch A
    Neurology; 2000 Apr; 54(8):1641-6. PubMed ID: 10762506
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Homozygous R136S mutation in PRNP gene causes inherited early onset prion disease.
    Ximelis T; Marín-Moreno A; Espinosa JC; Eraña H; Charco JM; Hernández I; Riveira C; Alcolea D; González-Roca E; Aldecoa I; Molina-Porcel L; Parchi P; Rossi M; Castilla J; Ruiz-García R; Gelpi E; Torres JM; Sánchez-Valle R
    Alzheimers Res Ther; 2021 Oct; 13(1):176. PubMed ID: 34663460
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. 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]  

  • 18. Gerstmann-Straeussler-Scheinker disease with P102L prion protein gene mutation presenting with rapidly progressive clinical course.
    Iwasaki Y; Mori K; Ito M; Nokura K; Tatsumi S; Mimuro M; Kitamoto T; Yoshida M
    Clin Neuropathol; 2014; 33(5):344-53. PubMed ID: 24986180
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Inherited prion disease with A117V mutation of the prion protein gene: a novel Hungarian family.
    Kovács GG; Ertsey C; Majtényi C; Jelencsik I; László L; Flicker H; Strain L; Szirmai I; Budka H
    J Neurol Neurosurg Psychiatry; 2001 Jun; 70(6):802-5. PubMed ID: 11385020
    [TBL] [Abstract][Full Text] [Related]  

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

    [Next]    [New Search]
    of 9.