lysine has been researched along with Encephalopathy, Subacute Spongiform, Gerstmann-Straussler Type in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (50.00) | 29.6817 |
| 2010's | 1 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Cai, X; Long, L; Lu, Z; Shu, Y | 1 |
| Hayashi, Y; Kitamoto, N; Kitamoto, T; Kutomi, T; Muramoto, T; Sano, C; Tanaka, T; Yutani, C | 1 |
2 other study(ies) available for lysine and Encephalopathy, Subacute Spongiform, Gerstmann-Straussler Type
| Article | Year |
|---|---|
A family with hereditary cerebellar ataxia finally confirmed as Gerstmann-Straussler-Scheinker syndrome with P102L mutation in PRNP gene.
Topics: Cerebellar Ataxia; Family Health; Female; Gerstmann-Straussler-Scheinker Disease; Humans; Lysine; Magnetic Resonance Imaging; Middle Aged; Mutation; Prion Proteins; Proline | 2017 |
Analyses of Gerstmann-Straussler syndrome with 102Leu219Lys using monoclonal antibodies that specifically detect human prion protein with 219Glu.
Topics: Amino Acid Substitution; Animals; Antibodies, Monoclonal; Epitope Mapping; Gerstmann-Straussler-Scheinker Disease; Glutamic Acid; Humans; Immunohistochemistry; Leucine; Lysine; Mice; Mice, Inbred BALB C; Polymorphism, Genetic; Prions | 2000 |