pd 173074 has been researched along with Muscular Atrophy, Spinal in 1 studies
Muscular Atrophy, Spinal: A group of disorders marked by progressive degeneration of motor neurons in the spinal cord resulting in weakness and muscular atrophy, usually without evidence of injury to the corticospinal tracts. Diseases in this category include Werdnig-Hoffmann disease and later onset SPINAL MUSCULAR ATROPHIES OF CHILDHOOD, most of which are hereditary. (Adams et al., Principles of Neurology, 6th ed, p1089)
| 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 |
|---|---|
| Hensel, N | 1 |
| Stockbrügger, I | 1 |
| Rademacher, S | 1 |
| Broughton, N | 1 |
| Brinkmann, H | 1 |
| Grothe, C | 1 |
| Claus, P | 1 |
1 other study available for pd 173074 and Muscular Atrophy, Spinal
| Article | Year |
|---|---|
Bilateral crosstalk of rho- and extracellular-signal-regulated-kinase (ERK) pathways is confined to an unidirectional mode in spinal muscular atrophy (SMA).
Topics: Actin Cytoskeleton; Amides; Animals; Cell Line; Cell Proliferation; Enzyme Inhibitors; Extracellular | 2014 |