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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]
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]
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]