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 *

219 related articles for article (PubMed ID: 8797472)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. Divergent clinical and neuropathological phenotype in a Gerstmann-Sträussler-Scheinker P102L family.
    Popova SN; Tarvainen I; Capellari S; Parchi P; Hannikainen P; Pirinen E; Haapasalo H; Alafuzoff I
    Acta Neurol Scand; 2012 Nov; 126(5):315-23. PubMed ID: 22211828
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. Variable phenotype in a P102L Gerstmann-Sträussler-Scheinker Italian family.
    De Michele G; Pocchiari M; Petraroli R; Manfredi M; Caneve G; Coppola G; Casali C; Saccà F; Piccardo P; Salvatore E; Berardelli A; Orio M; Barbieri F; Ghetti B; Filla A
    Can J Neurol Sci; 2003 Aug; 30(3):233-6. PubMed ID: 12945948
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Gerstmann-Sträussler-Scheinker disease with P102L-V129 mutation: a case with psychiatric manifestations at onset.
    Bianca M; Bianca S; Vecchio I; Raffaele R; Ingegnosi C; Nicoletti F
    Ann Genet; 2003; 46(4):467-9. PubMed ID: 14659783
    [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. 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]  

  • 12. 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]  

  • 13. 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]  

  • 14. 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]  

  • 15. 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]  

  • 16. 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]  

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

  • 18. High phenotypic variability in Gerstmann-Sträussler-Scheinker disease.
    Smid J; Studart A; Landemberger MC; Machado CF; Nóbrega PR; Canedo NHS; Schultz RR; Naslavsky MS; Rosemberg S; Kok F; Chimelli L; Martins VR; Nitrini R
    Arq Neuropsiquiatr; 2017 Jun; 75(6):331-338. PubMed ID: 28658400
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. A novel seven-octapeptide repeat insertion in the prion protein gene (PRNP) in a Dutch pedigree with Gerstmann-Sträussler-Scheinker disease phenotype: comparison with similar cases from the literature.
    Jansen C; Voet W; Head MW; Parchi P; Yull H; Verrips A; Wesseling P; Meulstee J; Baas F; van Gool WA; Ironside JW; Rozemuller AJ
    Acta Neuropathol; 2011 Jan; 121(1):59-68. PubMed ID: 20198483
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.