Gerstmann-Sträussler-Scheinker Disease
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Wiley-Blackwell
Reference61 articles.
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3. Phenotypic variability of Gerstmann-Sträussler-Scheinker disease is associated with prion protein heterogeneity;Piccardo;J Neuropathol Exp Neurol,1998
4. Protease K resistant prion protein isoforms in Gerstmann-Sträussler-Scheinker Disease (Indiana kindred);Piccardo;J Neuropathol Exp Neurol,1996
5. A 7-kDa prion protein (PrP) fragment, an integral component of the PrP region required for infectivity, is the major amyloid protein in Gerstmann-Straussler-Scheinker disease A117V;Tagliavini;J Biol Chem,2001
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1. Detection of tau in Gerstmann-Sträussler-Scheinker disease (PRNP F198S) by [18F]Flortaucipir PET;Acta Neuropathologica Communications;2018-10-29
2. An autopsy report of three kindred in a Gerstmann-Sträussler-Scheinker disease P105L family with a special reference to prion protein, tau, and beta-amyloid;Brain and Behavior;2018-09-21
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