BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

305 related articles for article (PubMed ID: 17695280)

  • 1. [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]  

  • 2. [Inherited Creutzfeldt-Jakob disease].
    Toda H; Kishida H; Kuroiwa Y
    Nihon Rinsho; 2004 Jan; 62 Suppl():261-5. PubMed ID: 15011362
    [No Abstract]   [Full Text] [Related]  

  • 3. 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]  

  • 4. [Creutzfeldt-Jakob disease(CJD) and Gerstmann-Sträussler-Scheinker syndrome(GSS)].
    Udaka F; Fujisawa M; Kameyama M
    Nihon Rinsho; 1997 Apr; 55(4):972-7. PubMed ID: 9103904
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [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]  

  • 6. [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]  

  • 7. [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]  

  • 8. Prion diseases.
    Knight RS; Will RG
    J Neurol Neurosurg Psychiatry; 2004 Mar; 75 Suppl 1(Suppl 1):i36-42. PubMed ID: 14978149
    [No Abstract]   [Full Text] [Related]  

  • 9. [Gerstmann-Sträussler-Scheinker disease, fatal familial insomnia and less common human prion diseases].
    Kawashima T
    Nihon Rinsho; 2003 Mar; 61 Suppl 3():17-21. PubMed ID: 12717941
    [No Abstract]   [Full Text] [Related]  

  • 10. Gerstmann-Sträussler-Scheinker syndrome,fatal familial insomnia, and kuru: a review of these less common human transmissible spongiform encephalopathies.
    Collins S; McLean CA; Masters CL
    J Clin Neurosci; 2001 Sep; 8(5):387-97. PubMed ID: 11535002
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Detecting prion protein gene mutations by denaturing gradient gel electrophoresis.
    Fink JK; Peacock ML; Warren JT; Roses AD; Prusiner SB
    Hum Mutat; 1994; 4(1):42-50. PubMed ID: 7951257
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Creutzfeldt-Jakob disease and other human transmissible spongiform encephalopathies. Part I].
    Zaborowski A
    Psychiatr Pol; 2004; 38(2):283-96. PubMed ID: 15307293
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. [A trend of molecular genetics on prion diseases and prion protein].
    Muramatsu Y; Shinagawa M
    Nihon Rinsho; 1993 Sep; 51(9):2494-502. PubMed ID: 8411733
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [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]  

  • 17. Genetic prion disease: Experience of a rapidly progressive dementia center in the United States and a review of the literature.
    Takada LT; Kim MO; Cleveland RW; Wong K; Forner SA; Gala II; Fong JC; Geschwind MD
    Am J Med Genet B Neuropsychiatr Genet; 2017 Jan; 174(1):36-69. PubMed ID: 27943639
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Differential overexpression of SERPINA3 in human prion diseases.
    Vanni S; Moda F; Zattoni M; Bistaffa E; De Cecco E; Rossi M; Giaccone G; Tagliavini F; Haïk S; Deslys JP; Zanusso G; Ironside JW; Ferrer I; Kovacs GG; Legname G
    Sci Rep; 2017 Nov; 7(1):15637. PubMed ID: 29142239
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Molecular genetics in Creutzfeldt-Jakob disease].
    Kitamoto T
    Rinsho Shinkeigaku; 1994 Dec; 34(12):1222-3. PubMed ID: 7774117
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Prion disease].
    Mizusawa H
    Rinsho Shinkeigaku; 2010 Nov; 50(11):797-802. PubMed ID: 21921445
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.