thioctic acid has been researched along with Amino Acid Metabolism Disorders, Inborn 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.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 4 (80.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (20.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Tort, F | 1 |
| Ferrer-Cortès, X | 1 |
| Thió, M | 1 |
| Navarro-Sastre, A | 1 |
| Matalonga, L | 1 |
| Quintana, E | 1 |
| 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 | 1 |
| Ribes, A | 1 |
| da COSTA, S | 1 |
| da SILVA, J | 1 |
| CORREIA, JA | 1 |
| MALDONADO, FE | 1 |
| ROSSIER, A | 1 |
| CALDERA, R | 1 |
| ODIEVRE, M | 1 |
| Hiraga, K | 1 |
| Kochi, H | 1 |
| Hayasaka, K | 1 |
| Kikuchi, G | 1 |
| Nyhan, WL | 1 |
| Galamon, T | 1 |
| Szulc-Kuberska, J | 1 |
| Tronczyńska, J | 1 |
5 other studies available for thioctic acid and Amino Acid Metabolism Disorders, Inborn
| 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 |
[Metabolic significance of alpha-lipoic acid. V. Comparative action of alpha-lipoic acid, vitamin B 12 and cocarboxylase on metabolism of copper and iron and on aminoacidurias. (Further observations)].
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Copper; Corrinoids; Hematinics; Humans; Iron; Pro | 1963 |
[RECENT IDEAS ON CYSTINOSIS].
Topics: Amino Acid Metabolism, Inborn Errors; Blood Chemical Analysis; Citric Acid Cycle; Cystinosis; Dimerc | 1963 |
Defective glycine cleavage system in nonketotic hyperglycinemia. Occurrence of a less active glycine decarboxylase and an abnormal aminomethyl carrier protein.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acid Oxidoreductases; Aminomethyltransferase; Brain; Car | 1981 |
Studies on the effect of alpha-lipoic acid on disturbances in histidine metabolism.
Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Child; Decarboxylation; Histidine; Humans; Ketoglu | 1971 |