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 *

224 related articles for article (PubMed ID: 1348851)

  • 1. Prion protein mutation at codon 102 in an Italian family with Gerstmann-Sträussler-Scheinker syndrome.
    Kretzschmar HA; Kufer P; Riethmüller G; DeArmond S; Prusiner SB; Schiffer D
    Neurology; 1992 Apr; 42(4):809-10. PubMed ID: 1348851
    [TBL] [Abstract][Full Text] [Related]  

  • 2. An Israeli family with Gerstmann-Sträussler-Scheinker disease manifesting the codon 102 mutation in the prion protein gene.
    Goldhammer Y; Gabizon R; Meiner Z; Sadeh M
    Neurology; 1993 Dec; 43(12):2718-9. PubMed ID: 7902971
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Gerstmann-Sträussler-Scheinker disease with mutation at codon 102 and methionine at codon 129 of PRNP in previously unreported patients.
    Young K; Jones CK; Piccardo P; Lazzarini A; Golbe LI; Zimmerman TR; Dickson DW; McLachlan DC; St George-Hyslop P; Lennox A
    Neurology; 1995 Jun; 45(6):1127-34. PubMed ID: 7783876
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. A missense mutation at codon 105 with codon 129 polymorphism of the prion protein gene in a new variant of Gerstmann-Sträussler-Scheinker disease.
    Yamada M; Itoh Y; Fujigasaki H; Naruse S; Kaneko K; Kitamoto T; Tateishi J; Otomo E; Hayakawa M; Tanaka J
    Neurology; 1993 Dec; 43(12):2723-4. PubMed ID: 7902972
    [No Abstract]   [Full Text] [Related]  

  • 6. A prion protein variant in a family with the telencephalic form of Gerstmann-Sträussler-Scheinker syndrome.
    Hsiao KK; Cass C; Schellenberg GD; Bird T; Devine-Gage E; Wisniewski H; Prusiner SB
    Neurology; 1991 May; 41(5):681-4. PubMed ID: 1674116
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. New variant prion protein in a Japanese family with Gerstmann-Sträussler syndrome.
    Furukawa H; Kitamoto T; Tanaka Y; Tateishi J
    Brain Res Mol Brain Res; 1995 Jun; 30(2):385-8. PubMed ID: 7637591
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Gerstmann-Sträussler-Scheinker syndrome with variable phenotype in a new kindred with PRNP-P102L mutation.
    Riudavets MA; Sraka MA; Schultz M; Rojas E; Martinetto H; Begué C; Noher de Halac I; Poleggi A; Equestre M; Pocchiari M; Sevlever G; Taratuto AL
    Brain Pathol; 2014 Mar; 24(2):142-7. PubMed ID: 23944754
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [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; 147(4):274-8. PubMed ID: 2063076
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Spontaneous neurodegeneration in transgenic mice with prion protein codon 101 proline----leucine substitution.
    Hsiao K; Scott M; Foster D; DeArmond SJ; Groth D; Serban H; Prusiner SB
    Ann N Y Acad Sci; 1991; 640():166-70. PubMed ID: 1685642
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. A new PRNP mutation (G131V) associated with Gerstmann-Sträussler-Scheinker disease.
    Panegyres PK; Toufexis K; Kakulas BA; Cernevakova L; Brown P; Ghetti B; Piccardo P; Dlouhy SR
    Arch Neurol; 2001 Nov; 58(11):1899-902. PubMed ID: 11709001
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Prion protein mutation in family first reported by Gerstmann, Sträussler, and Scheinker.
    Kretzschmar HA; Honold G; Seitelberger F; Feucht M; Wessely P; Mehraein P; Budka H
    Lancet; 1991 May; 337(8750):1160. PubMed ID: 1674033
    [No Abstract]   [Full Text] [Related]  

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

  • 16. Molecular genetics and transgenic model of Gertsmann-Sträussler-Scheinker disease.
    Hsiao K; Prusiner SB
    Alzheimer Dis Assoc Disord; 1991; 5(3):155-62. PubMed ID: 1685324
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. 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]  

  • 19. 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]  

  • 20. Gerstmann-Sträussler-Scheinker disease with the PRNP P102L mutation and valine at codon 129.
    Young K; Clark HB; Piccardo P; Dlouhy SR; Ghetti B
    Brain Res Mol Brain Res; 1997 Feb; 44(1):147-50. PubMed ID: 9030710
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.