glycine has been researched along with Hemiplegia in 2 studies
Hemiplegia: Severe or complete loss of motor function on one side of the body. This condition is usually caused by BRAIN DISEASES that are localized to the cerebral hemisphere opposite to the side of weakness. Less frequently, BRAIN STEM lesions; cervical SPINAL CORD DISEASES; PERIPHERAL NERVOUS SYSTEM DISEASES; and other conditions may manifest as hemiplegia. The term hemiparesis (see PARESIS) refers to mild to moderate weakness involving one side of the body.
| 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 |
|---|---|
| Ito, T | 1 |
| Narugami, M | 1 |
| Egawa, K | 1 |
| Yamamoto, H | 1 |
| Asahina, N | 1 |
| Kohsaka, S | 1 |
| Ishii, A | 1 |
| Hirose, S | 1 |
| Shiraishi, H | 1 |
| Alonso, I | 1 |
| Barros, J | 1 |
| Tuna, A | 1 |
| Coelho, J | 1 |
| Sequeiros, J | 1 |
| Silveira, I | 1 |
| Coutinho, P | 1 |
2 other studies available for glycine and Hemiplegia
| Article | Year |
|---|---|
Long-term follow up of an adult with alternating hemiplegia of childhood and a p.Gly755Ser mutation in the ATP1A3 gene.
Topics: Adult; Female; Glycine; Hemiplegia; Humans; Longitudinal Studies; Mutation; Neuroimaging; Phenotype; | 2018 |
Phenotypes of spinocerebellar ataxia type 6 and familial hemiplegic migraine caused by a unique CACNA1A missense mutation in patients from a large family.
Topics: Adolescent; Adult; Alanine; Child; Cysteine; Female; Genetic Linkage; Glycine; Hemiplegia; Humans; L | 2003 |