fenofibrate has been researched along with Mitochondrial Diseases in 2 studies
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Mitochondrial Diseases: Diseases caused by abnormal function of the MITOCHONDRIA. They may be caused by mutations, acquired or inherited, in mitochondrial DNA or in nuclear genes that code for mitochondrial components. They may also be the result of acquired mitochondria dysfunction due to adverse effects of drugs, infections, or other environmental causes.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (50.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 1 (50.00) | 2.80 |
| Authors | Studies |
|---|---|
| Zhang, X | 1 |
| Chen, Y | 1 |
| Tong, N | 1 |
| Shao, Q | 1 |
| Zhou, Y | 1 |
| Mu, T | 1 |
| Yang, X | 1 |
| Zhang, Y | 1 |
| Brunmair, B | 1 |
| Lest, A | 1 |
| Staniek, K | 1 |
| Gras, F | 1 |
| Scharf, N | 1 |
| Roden, M | 1 |
| Nohl, H | 1 |
| Waldhäusl, W | 1 |
| Fürnsinn, C | 1 |
2 other studies available for fenofibrate and Mitochondrial Diseases
| Article | Year |
|---|---|
Maternally inherited diabetes and deafness coexists with lipoprotein lipase gene mutation-associated severe hyperlipidemia that was resistant to fenofibrate and atorvastatin, but sensitive to bezafibrate: A case report.
Topics: Atorvastatin; Bezafibrate; Deafness; Diabetes Mellitus, Type 2; Female; Fenofibrate; Humans; Hyperli | 2022 |
Fenofibrate impairs rat mitochondrial function by inhibition of respiratory complex I.
Topics: Animals; Electron Transport Complex I; Energy Metabolism; Fenofibrate; Hypolipidemic Agents; Male; M | 2004 |