thioctic acid has been researched along with Lactic Acidosis in 5 studies
Thioctic Acid: An octanoic acid bridged with two sulfurs so that it is sometimes also called a pentanoic acid in some naming schemes. It is biosynthesized by cleavage of LINOLEIC ACID and is a coenzyme of oxoglutarate dehydrogenase (KETOGLUTARATE DEHYDROGENASE COMPLEX). It is used in DIETARY SUPPLEMENTS.
| Excerpt | Relevance | Reference |
|---|---|---|
| "PDHc deficiency was demonstrated in muscle and fibroblasts without detectable PDHA1 mutations." | 1.36 | Dihydrolipoamide dehydrogenase (DLD) deficiency in a Spanish patient with myopathic presentation due to a new mutation in the interface domain. ( Briones, P; Font, A; Pineda, M; Quintana, E; Ribes, A; Tort, F; Vilaseca, MA, 2010) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (20.00) | 18.7374 |
| 1990's | 1 (20.00) | 18.2507 |
| 2000's | 1 (20.00) | 29.6817 |
| 2010's | 2 (40.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Tort, F | 2 |
| Ferrer-Cortès, X | 1 |
| Thió, M | 1 |
| Navarro-Sastre, A | 1 |
| Matalonga, L | 1 |
| Quintana, E | 2 |
| Bujan, N | 1 |
| Arias, A | 1 |
| García-Villoria, J | 1 |
| Acquaviva, C | 1 |
| Vianey-Saban, C | 1 |
| Artuch, R | 1 |
| García-Cazorla, À | 1 |
| Briones, P | 2 |
| Ribes, A | 2 |
| Orsucci, D | 1 |
| Filosto, M | 1 |
| Siciliano, G | 1 |
| Mancuso, M | 1 |
| Pineda, M | 1 |
| Font, A | 1 |
| Vilaseca, MA | 1 |
| Yoshida, I | 1 |
| Sweetman, L | 1 |
| Kulovich, S | 1 |
| Nyhan, WL | 1 |
| Robinson, BH | 1 |
| Byrd, DJ | 1 |
| Krohn, HP | 1 |
| Winkler, L | 1 |
| Steinborn, C | 1 |
| Hadam, M | 1 |
| Brodehl, J | 1 |
| Hunneman, DH | 1 |
1 review available for thioctic acid and Lactic Acidosis
| Article | Year |
|---|---|
Electron transfer mediators and other metabolites and cofactors in the treatment of mitochondrial dysfunction.
Topics: Acidosis, Lactic; Animals; Antioxidants; Carnitine; Creatine; Dietary Supplements; Electron Transpor | 2009 |
4 other studies available for thioctic acid and Lactic Acidosis
| Article | Year |
|---|---|
Mutations in the lipoyltransferase LIPT1 gene cause a fatal disease associated with a specific lipoylation defect of the 2-ketoacid dehydrogenase complexes.
Topics: Acidosis, Lactic; Acyltransferases; Amino Acid Metabolism, Inborn Errors; Animals; Cells, Cultured; | 2014 |
Dihydrolipoamide dehydrogenase (DLD) deficiency in a Spanish patient with myopathic presentation due to a new mutation in the interface domain.
Topics: Acidosis, Lactic; Adult; Amino Acid Sequence; Base Sequence; Biomarkers; Blepharoptosis; Cells, Cult | 2010 |
Effect of lipoic acid in a patient with defective activity of pyruvate dehydrogenase, 2-oxoglutarate dehydrogenase, and branched-chain keto acid dehydrogenase.
Topics: 3-Hydroxybutyric Acid; 3-Methyl-2-Oxobutanoate Dehydrogenase (Lipoamide); Acidosis, Lactic; Acidosis | 1990 |
Neonatal pyruvate dehydrogenase deficiency with lipoate responsive lactic acidaemia and hyperammonaemia.
Topics: Acidosis, Lactic; Ammonia; Female; Humans; Infant, Newborn; Pyruvate Dehydrogenase Complex Deficienc | 1989 |