thioctic acid has been researched along with Muscle Weakness in 2 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.
Muscle Weakness: A vague complaint of debility, fatigue, or exhaustion attributable to weakness of various muscles. The weakness can be characterized as subacute or chronic, often progressive, and is a manifestation of many muscle and neuromuscular diseases. (From Wyngaarden et al., Cecil Textbook of Medicine, 19th ed, p2251)
| 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 | 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 |
|---|---|
| Kishita, Y | 1 |
| Pajak, A | 1 |
| Bolar, NA | 1 |
| Marobbio, CM | 1 |
| Maffezzini, C | 1 |
| Miniero, DV | 1 |
| Monné, M | 1 |
| Kohda, M | 1 |
| Stranneheim, H | 1 |
| Murayama, K | 1 |
| Naess, K | 1 |
| Lesko, N | 1 |
| Bruhn, H | 1 |
| Mourier, A | 1 |
| Wibom, R | 1 |
| Nennesmo, I | 1 |
| Jespers, A | 1 |
| Govaert, P | 1 |
| Ohtake, A | 1 |
| Van Laer, L | 1 |
| Loeys, BL | 1 |
| Freyer, C | 1 |
| Palmieri, F | 1 |
| Wredenberg, A | 1 |
| Okazaki, Y | 1 |
| Wedell, A | 1 |
| Quintana, E | 1 |
| Pineda, M | 1 |
| Font, A | 1 |
| Vilaseca, MA | 1 |
| Tort, F | 1 |
| Ribes, A | 1 |
| Briones, P | 1 |
2 other studies available for thioctic acid and Muscle Weakness
| Article | Year |
|---|---|
Intra-mitochondrial Methylation Deficiency Due to Mutations in SLC25A26.
Topics: Amino Acid Sequence; Amino Acid Transport Systems; Calcium-Binding Proteins; Child, Preschool; DNA M | 2015 |
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 |