vigabatrin has been researched along with Genetic Diseases, Inborn in 1 studies
Genetic Diseases, Inborn: Diseases that are caused by genetic mutations present during embryo or fetal development, although they may be observed later in life. The mutations may be inherited from a parent's genome or they may be acquired in utero.
| 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 |
|---|---|
| McFarlane, MT | 1 |
| Wright, T | 1 |
| McCoy, B | 1 |
| Snead, OC | 1 |
| Westall, CA | 1 |
1 other study available for vigabatrin and Genetic Diseases, Inborn
| Article | Year |
|---|---|
Retinal defect in children with infantile spasms of varying etiologies: An observational study.
Topics: Anticonvulsants; Child, Preschool; Electroretinography; Female; Genetic Diseases, Inborn; Humans; Hy | 2020 |