methionine has been researched along with Encephalopathy, Subacute Spongiform, Gerstmann-Straussler Type in 3 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 1 (33.33) | 18.2507 |
2000's | 1 (33.33) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 1 (33.33) | 2.80 |
Authors | Studies |
---|---|
Agrimi, U; Bruno, R; Cardone, F; D'Agostino, C; De Cecco, E; Di Bari, MA; Gambetti, P; Legname, G; Nonno, R; Pirisinu, L; Riccardi, G | 1 |
Dickson, DW; Golbe, LI; Jones, CK; Lazzarini, A; Lennox, A; McLachlan, DC; Piccardo, P; St George-Hyslop, P; Young, K; Zimmerman, TR | 1 |
Beavis, RC; Bugiani, O; Frangione, B; Ghetti, B; Giaccone, G; Lievens, PM; Mohr, M; Perini, F; Piccardo, P; Prelli, F; Rossi, G; Salmona, M; Tagliavini, F; Tranchant, C; Warter, JM | 1 |
3 other study(ies) available for methionine and Encephalopathy, Subacute Spongiform, Gerstmann-Straussler Type
Article | Year |
---|---|
Gerstmann-Sträussler-Scheinker Disease with F198S Mutation Induces Independent Tau and Prion Protein Pathologies in Bank Voles.
Topics: Animals; Arvicolinae; Codon; Gerstmann-Straussler-Scheinker Disease; Humans; Isoleucine; Methionine; Mutation; Phenylalanine; Presenilin-1; Prion Proteins; Prions; Serine | 2022 |
Gerstmann-Sträussler-Scheinker disease with mutation at codon 102 and methionine at codon 129 of PRNP in previously unreported patients.
Topics: Adult; Base Sequence; Codon; Female; Gerstmann-Straussler-Scheinker Disease; Humans; Male; Methionine; Middle Aged; Molecular Sequence Data; Mutation; Prions | 1995 |
A 7-kDa prion protein (PrP) fragment, an integral component of the PrP region required for infectivity, is the major amyloid protein in Gerstmann-Sträussler-Scheinker disease A117V.
Topics: Adult; Alleles; Amyloid; Cerebral Cortex; Gerstmann-Straussler-Scheinker Disease; Heterozygote; Humans; Male; Methionine; Peptide Fragments; Prion Proteins; Prions; Protein Precursors; Sequence Analysis, Protein; Syndrome; Valine | 2001 |