glycine has been researched along with Creutzfeldt-Jakob Syndrome in 5 studies
Creutzfeldt-Jakob Syndrome: A rare transmissible encephalopathy most prevalent between the ages of 50 and 70 years. Affected individuals may present with sleep disturbances, personality changes, ATAXIA; APHASIA, visual loss, weakness, muscle atrophy, MYOCLONUS, progressive dementia, and death within one year of disease onset. A familial form exhibiting autosomal dominant inheritance and a new variant CJD (potentially associated with ENCEPHALOPATHY, BOVINE SPONGIFORM) have been described. Pathological features include prominent cerebellar and cerebral cortical spongiform degeneration and the presence of PRIONS. (From N Engl J Med, 1998 Dec 31;339(27))
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (20.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (20.00) | 29.6817 |
| 2010's | 2 (40.00) | 24.3611 |
| 2020's | 1 (20.00) | 2.80 |
| Authors | Studies |
|---|---|
| Chen, Z | 1 |
| Nan, H | 1 |
| Kong, Y | 1 |
| Chu, M | 1 |
| Liu, L | 1 |
| Zhang, J | 1 |
| Wang, L | 1 |
| Wu, L | 1 |
| 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 |
| Liu, Z | 1 |
| Jia, L | 1 |
| Piao, Y | 1 |
| Lu, D | 1 |
| Wang, F | 1 |
| Lv, H | 1 |
| Lu, Y | 1 |
| Jia, J | 1 |
| Vey, M | 1 |
| Baron, H | 1 |
| Weimer, T | 1 |
| Gröner, A | 1 |
| Kimberlin, RH | 1 |
| Walker, CA | 1 |
| Millson, GC | 1 |
| Taylor, DM | 1 |
| Robertson, PA | 1 |
| Tomlinson, AH | 1 |
| Dickinson, AG | 1 |
5 other studies available for glycine and Creutzfeldt-Jakob Syndrome
| Article | Year |
|---|---|
Amino Acid Substitution within Seven-Octapeptide Repeat Insertions in the Prion Protein Gene Associated with Short-Term Course.
Topics: Amino Acid Substitution; Codon; Creutzfeldt-Jakob Syndrome; Curriculum; Disease Progression; Glutama | 2022 |
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 |
Creutzfeldt-Jakob disease with PRNP G114V mutation in a Chinese family.
Topics: 14-3-3 Proteins; Adult; Aged; Asian People; Cerebral Cortex; Creutzfeldt-Jakob Syndrome; DNA Mutatio | 2010 |
Purity of spiking agent affects partitioning of prions in plasma protein purification.
Topics: Animals; Blood Proteins; Brain Chemistry; Chemical Precipitation; Creutzfeldt-Jakob Syndrome; Cricet | 2002 |
Disinfection studies with two strains of mouse-passaged scrapie agent. Guidelines for Creutzfeldt-Jakob and related agents.
Topics: Animals; Creutzfeldt-Jakob Syndrome; Disinfection; Glycine; Humans; Hypochlorous Acid; Mice; Mice, I | 1983 |