BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

126 related articles for article (PubMed ID: 21167505)

  • 1. 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]  

  • 2. 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]  

  • 3. [Gerstmann-Sträussler-Scheinker syndrome with a Pro102Leu mutation in the prion protein gene and atypical MRI findings, hyperthermia, tachycardia, and hyperhidrosis].
    Imaiso Y; Mitsuo K
    Rinsho Shinkeigaku; 1998; 38(10-11):920-5. PubMed ID: 10203975
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [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]  

  • 5. [Familial prion disease (GSS, familial CJD, FFI)].
    Arata H; Takashima H
    Nihon Rinsho; 2007 Aug; 65(8):1433-7. PubMed ID: 17695280
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Gerstmann-Straüssler-Scheinker syndrome].
    Tranchant C; Warter JM
    Rev Neurol (Paris); 1998 Feb; 154(2):152-7. PubMed ID: 9773036
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A case of Gerstmann-Sträussler-Scheinker syndrome with the P105L prion protein gene mutation presenting with ataxia and extrapyramidal signs without spastic paraparesis.
    Iwasaki Y; Kizawa M; Hori N; Kitamoto T; Sobue G
    Clin Neurol Neurosurg; 2009 Sep; 111(7):606-9. PubMed ID: 19443103
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Gerstmann-Sträussler-Scheinker disease with heterozygous codon change at prion protein codon 129].
    Terao Y; Hitoshi S; Shimizu J; Sakuta M; Kitamoto T
    Rinsho Shinkeigaku; 1992 Aug; 32(8):880-3. PubMed ID: 1490317
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [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]  

  • 10. Gerstmann-Sträussler-Scheinker syndrome with the P102L pathogenic mutation presenting as familial Creutzfeldt-Jakob disease: a case report and review of the literature.
    Rusina R; Fiala J; Holada K; Matějčková M; Nováková J; Ampapa R; Koukolík F; Matěj R
    Neurocase; 2013; 19(1):41-53. PubMed ID: 22494260
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Gerstmann-Sträussler-Scheinker disease with A117V mutation in a second French-Alsatian family.
    Heldt N; Boellaard JW; Brown P; Cervenákova L; Doerr-Schott J; Thomas C; Scherer C; Rohmer F
    Clin Neuropathol; 1998; 17(4):229-34. PubMed ID: 9707339
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. [Patient with Gerstmann-Striussler-Scheinker syndrome (GSS P102L) presenting high intensity lesions in the cerebral cortex on diffusion weighted MRI].
    Misumi M; Nishida Y; Araki S
    Rinsho Shinkeigaku; 2006 Apr; 46(4):291-3. PubMed ID: 16768100
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Gerstmann-Sträussler-Scheinker disease with the Q217R mutation mimicking frontotemporal dementia.
    Woulfe J; Kertesz A; Frohn I; Bauer S; George-Hyslop PS; Bergeron C
    Acta Neuropathol; 2005 Sep; 110(3):317-9. PubMed ID: 16025285
    [No Abstract]   [Full Text] [Related]  

  • 16. [A case of Gerstmann-Sträussler-Scheinker disease with severe muscular atrophy and vertical gaze palsy].
    Oba N; Fujimoto Y; Hirata K; Ando N; Saida K
    Rinsho Shinkeigaku; 2000 Jul; 40(7):726-31. PubMed ID: 11186913
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. A distinct phenotype of leg hyperreflexia in a Japanese family with Gerstmann-Sträussler-Scheinker syndrome (P102L).
    Takazawa T; Ikeda K; Ito H; Aoyagi J; Nakamura Y; Miura K; Iwamoto K; Kano O; Kawabe K; Iwasaki Y
    Intern Med; 2010; 49(4):339-42. PubMed ID: 20154442
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 7.