fenofibrate has been researched along with Muscular Dystrophy, Oculopharyngeal in 1 studies
Muscular Dystrophy, Oculopharyngeal: An autosomal dominant hereditary disease that presents in late in life and is characterized by DYSPHAGIA and progressive ptosis of the eyelids. Mutations in the gene for POLY(A)-BINDING PROTEIN II have been associated with oculopharyngeal muscular dystrophy.
| 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 |
|---|---|
| Pasco, MY | 1 |
| Rotili, D | 1 |
| Altucci, L | 1 |
| Farina, F | 1 |
| Rouleau, GA | 1 |
| Mai, A | 1 |
| Néri, C | 1 |
1 other study available for fenofibrate and Muscular Dystrophy, Oculopharyngeal
| Article | Year |
|---|---|
Characterization of sirtuin inhibitors in nematodes expressing a muscular dystrophy protein reveals muscle cell and behavioral protection by specific sirtinol analogues.
Topics: Animals; Animals, Genetically Modified; Benzamides; Caenorhabditis elegans; Cell Movement; Green Flu | 2010 |