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1 Gerstmann-Straussler-Scheinker (GSS) disease is a domina
2 Gerstmann-Straussler-Scheinker disease (GSS) is an inher
3 Gerstmann-Straussler-Scheinker disease (GSS) is characte
4 Gerstmann-Straussler-Scheinker syndrome (GSS) is a genet
5 Gerstmann-Straussler-Scheinker syndrome (GSS) with the P
6 n = 17, fatal familial insomnia (FFI) n = 9, Gerstmann-Straussler-Scheinker syndrome (GSS)) n = 4), p
10 o the Y145Stop PrP variant associated with a Gerstmann-Straussler-Scheinker-like prion disease) spont
12 sporadic Creutzfeldt-Jakob disease (CJD) and Gerstmann-Straussler-Scheinker F198S disease brains all
13 disease, Creutzfeldt-Jakob disease (CJD) and Gerstmann-Straussler-Scheinker syndrome have been attrib
15 enetic Creutzfeldt-Jakob disease (gCJD), and Gerstmann-Straussler-Scheinker (GSS) syndrome are neurod
17 have been identified: prion mutations cause Gerstmann Straussler syndrome and hereditary Creuzfeldt-
19 on disease, Creutzfeldt-Jakob disease (CJD), Gerstmann-Straussler-Scheinker syndrome, and fatal famil
20 onally have been classified as familial CJD, Gerstmann-Straussler-Scheinker syndrome, or fatal famili
21 nd a low sensitivity limited to variant CJD, Gerstmann-Straussler-Scheinker syndrome and fatal famili
23 ssociated with neuropathologically confirmed Gerstmann-Straussler-Scheinker disease displaying a some
26 hat include Kuru, Creutzfeldt-Jakob disease, Gerstmann-Straussler-Scheinker syndrome (GSS), and fatal
27 in genetic Creutzfeldt-Jakob disease-E200K, Gerstmann-Straussler-Scheinker-P102L and fatal familial
29 inherited prion disease P102L, historically Gerstmann-Straussler-Scheinker syndrome, originates from
31 on, sensory symptoms and loss of reflexes in Gerstmann-Straussler-Scheinker syndrome can be explained
32 symptoms and loss of lower limb reflexes in Gerstmann-Straussler-Scheinker syndrome is due to pathol
33 sing inherited prion disease (IPD) including Gerstmann-Straussler-Scheinker (GSS) disease phenotypes
34 n presentation of inherited prion disease is Gerstmann-Straussler-Scheinker syndrome, typically prese
37 cular-neuropathological profile of a case of Gerstmann-Straussler-Scheinker disease associated with a
41 (specifically mutated PrP(A116V)) plaques of Gerstmann-Straussler-Scheinker disease (GSS) and compare
43 tients with various mutations causing CJD or Gerstmann-Straussler-Scheinker syndrome, 6 had positive
45 with an inherited prion disease [also termed Gerstmann-Straussler-Scheinker (GSS) syndrome] with unus
46 to noncyclic aliphatic residues such as the Gerstmann-Straussler-Scheinker-linked leucines can promo
47 re model and in the human brain carrying the Gerstmann-Straussler-Scheinker disease Q217R mutation.
48 eposits and neuronal loss, by expressing the Gerstmann-Straussler-Scheinker haplotype Q217R-129V in h
49 -state folding behavior was observed for the Gerstmann-Straussler-Scheinker disease-associated F198S
50 ude the hydrophobic domain implicated in the Gerstmann-Straussler-Scheinker (GSS) mutation (P102L).
51 The clinicopathological phenotype of the Gerstmann-Straussler-Scheinker disease (GSS) variant lin
52 102 (P102L), classically associated with the Gerstmann-Straussler-Scheinker (GSS) phenotype, also sho
53 containing point mutations corresponding to Gerstmann-Straussler-Scheinker disease (P102L), Creutzfe
54 genic (Tg) mice overexpressing PrP linked to Gerstmann-Straussler Scheinker syndrome, and the failure
55 P102L in the human PrP gene, associated with Gerstmann-Straussler syndrome (GSS), has been introduced
56 y was observed for mutations associated with Gerstmann-Straussler-Scheinker syndrome and fatal famili
57 pathogenic mutation A116V is associated with Gerstmann-Straussler-Scheinker syndrome, but no accumula