glycine 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 | 0 (0.00) | 29.6817 |
| 2010's | 2 (66.67) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Simpson, M | 1 |
| Johanssen, V | 1 |
| Boyd, A | 1 |
| Klug, G | 1 |
| Masters, CL | 1 |
| Li, QX | 1 |
| Pamphlett, R | 1 |
| McLean, C | 1 |
| Lewis, V | 1 |
| Collins, SJ | 1 |
| Jansen, C | 1 |
| Parchi, P | 1 |
| Capellari, S | 1 |
| Strammiello, R | 1 |
| Dopper, EG | 1 |
| van Swieten, JC | 1 |
| Kamphorst, W | 1 |
| Rozemuller, AJ | 1 |
| Tagliavini, F | 1 |
| Prelli, F | 1 |
| Ghiso, J | 1 |
| Bugiani, O | 1 |
| Serban, D | 1 |
| Prusiner, SB | 1 |
| Farlow, MR | 1 |
| Ghetti, B | 1 |
| Frangione, B | 1 |
3 other studies available for glycine and Encephalopathy, Subacute Spongiform, Gerstmann-Straussler Type
| Article | Year |
|---|---|
Unusual clinical and molecular-pathological profile of gerstmann-Sträussler-Scheinker disease associated with a novel PRNP mutation (V176G).
Topics: Creutzfeldt-Jakob Syndrome; Female; Genetic Predisposition to Disease; Gerstmann-Straussler-Scheinke | 2013 |
A second case of Gerstmann-Sträussler-Scheinker disease linked to the G131V mutation in the prion protein gene in a Dutch patient.
Topics: Adult; Brain; Genetic Predisposition to Disease; Genome-Wide Association Study; Gerstmann-Straussler | 2011 |
Amyloid protein of Gerstmann-Sträussler-Scheinker disease (Indiana kindred) is an 11 kd fragment of prion protein with an N-terminal glycine at codon 58.
Topics: Amino Acid Sequence; Amyloid; Animals; Basal Ganglia; Cerebral Cortex; Chromatography, Gel; Codon; G | 1991 |