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 *

304 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.