glycine has been researched along with Cranial Nerve II Diseases in 1 studies
| Excerpt | Relevance | Reference |
|---|---|---|
| "Perry syndrome is a rare form of autosomal dominant Parkinsonism with respiratory failure recently defined as being due to mutations in the DCTN1 gene." | 1.36 | Perry syndrome due to the DCTN1 G71R mutation: a distinctive levodopa responsive disorder with behavioral syndrome, vertical gaze palsy, and respiratory failure. ( Fish, M; Hack, M; Majounie, E; Morris, HR; Newsway, V; Rohrer, JD; Warren, JD; Williams, N, 2010) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Newsway, V | 1 |
| Fish, M | 1 |
| Rohrer, JD | 1 |
| Majounie, E | 1 |
| Williams, N | 1 |
| Hack, M | 1 |
| Warren, JD | 1 |
| Morris, HR | 1 |
1 other study available for glycine and Cranial Nerve II Diseases
| Article | Year |
|---|---|
Perry syndrome due to the DCTN1 G71R mutation: a distinctive levodopa responsive disorder with behavioral syndrome, vertical gaze palsy, and respiratory failure.
Topics: Arginine; Behavioral Symptoms; DNA Mutational Analysis; Dopamine Agents; Dynactin Complex; Glycine; | 2010 |