beta-resorcylic acid has been researched along with Electron Transport Chain Deficiencies, Mitochondrial in 2 studies
beta-resorcylic acid: RN given refers to parent cpd; structure
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 Electron Transport Chain Deficiencies, Mitochondrial
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 |