baclofen has been researched along with ARG1 Deficiency in 1 studies
| Excerpt | Relevance | Reference |
|---|---|---|
| "Arginineemia, also known as arginase deficiency, is a rare autosomal recessive metabolic disease." | 1.56 | A novel compound heterozygous mutation in the arginase-1 gene identified in a Chinese patient with argininemia: A case report. ( Cao, L; Cui, D; Hu, L; Jin, L; Liu, Y, 2020) |
| 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 | 0 (0.00) | 24.3611 |
| 2020's | 1 (100.00) | 2.80 |
| Authors | Studies |
|---|---|
| Cui, D | 1 |
| Liu, Y | 1 |
| Jin, L | 1 |
| Hu, L | 1 |
| Cao, L | 1 |
1 other study available for baclofen and ARG1 Deficiency
| Article | Year |
|---|---|
A novel compound heterozygous mutation in the arginase-1 gene identified in a Chinese patient with argininemia: A case report.
Topics: Arginase; Baclofen; Botulinum Toxins; Cerebral Palsy; Child; China; Diet, Protein-Restricted; Humans | 2020 |