beta-resorcylic acid has been researched along with Mitochondrial Diseases in 2 studies
beta-resorcylic acid: RN given refers to parent cpd; structure
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 | 0 (0.00) | 29.6817 |
| 2010's | 2 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Luna-Sánchez, M | 1 |
| Díaz-Casado, E | 1 |
| Barca, E | 1 |
| Tejada, MÁ | 1 |
| Montilla-García, Á | 1 |
| Cobos, EJ | 1 |
| Escames, G | 1 |
| Acuña-Castroviejo, D | 1 |
| Quinzii, CM | 1 |
| López, LC | 1 |
| Freyer, C | 1 |
| Stranneheim, H | 1 |
| Naess, K | 1 |
| Mourier, A | 1 |
| Felser, A | 1 |
| Maffezzini, C | 1 |
| Lesko, N | 1 |
| Bruhn, H | 1 |
| Engvall, M | 1 |
| Wibom, R | 1 |
| Barbaro, M | 1 |
| Hinze, Y | 1 |
| Magnusson, M | 1 |
| Andeer, R | 1 |
| Zetterström, RH | 1 |
| von Döbeln, U | 1 |
| Wredenberg, A | 1 |
| Wedell, A | 1 |
2 other studies available for beta-resorcylic acid and Mitochondrial Diseases
| Article | Year |
|---|---|
The clinical heterogeneity of coenzyme Q10 deficiency results from genotypic differences in the Coq9 gene.
Topics: Animals; Ataxia; Disease Models, Animal; Genetic Variation; Genotype; Hydroxybenzoates; Mammals; Mic | 2015 |
Rescue of primary ubiquinone deficiency due to a novel COQ7 defect using 2,4-dihydroxybensoic acid.
Topics: Amino Acid Sequence; Ataxia; Child; Child, Preschool; Chromatography, Liquid; DNA Mutational Analysi | 2015 |