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2. Abnormal eye movements in Gerstmann-Sträussler-Scheinker disease. Yee RD; Farlow MR; Suzuki DA; Betelak KF; Ghetti B Arch Ophthalmol; 1992 Jan; 110(1):68-74. PubMed ID: 1731725 [TBL] [Abstract][Full Text] [Related]
3. Diagnosis of Gerstmann-Sträussler syndrome in familial dementia with prion protein gene analysis. Collinge J; Harding AE; Owen F; Poulter M; Lofthouse R; Boughey AM; Shah T; Crow TJ Lancet; 1989 Jul; 2(8653):15-7. PubMed ID: 2567794 [TBL] [Abstract][Full Text] [Related]
4. 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]
8. [An autopsy case of Gerstmann-Sträussler-Scheinker's disease with family history]. Hashiguchi H; Shii H; Kitamoto T; Tateishi J Rinsho Shinkeigaku; 1988 Jun; 28(6):681-7. PubMed ID: 3233841 [No Abstract] [Full Text] [Related]
9. [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]
10. 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]