edaravone has been researched along with Mannosidase Deficiency Diseases in 1 studies
Mannosidase Deficiency Diseases: Diseases caused by the loss of one or more enzymes involved in the hydrolysis of mannoside linkages (MANNOSIDASES). The defects in enzyme activity are primarily associated with genetic mutation of the genes that codes for a particular mannosidase isoenzyme.
| 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 |
|---|---|
| Sowell, J | 1 |
| Wood, T | 1 |
1 other study available for edaravone and Mannosidase Deficiency Diseases
| Article | Year |
|---|---|
Towards a selected reaction monitoring mass spectrometry fingerprint approach for the screening of oligosaccharidoses.
Topics: Antipyrine; Chromatography, High Pressure Liquid; Edaravone; Fucosidosis; Glycogen Storage Disease T | 2011 |