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thioctic acid and Amino Acid Metabolism Disorders, Inborn

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.

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19904 (80.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's1 (20.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Tort, F1
Ferrer-Cortès, X1
Thió, M1
Navarro-Sastre, A1
Matalonga, L1
Quintana, E1
Bujan, N1
Arias, A1
García-Villoria, J1
Acquaviva, C1
Vianey-Saban, C1
Artuch, R1
García-Cazorla, À1
Briones, P1
Ribes, A1
da COSTA, S1
da SILVA, J1
CORREIA, JA1
MALDONADO, FE1
ROSSIER, A1
CALDERA, R1
ODIEVRE, M1
Hiraga, K1
Kochi, H1
Hayasaka, K1
Kikuchi, G1
Nyhan, WL1
Galamon, T1
Szulc-Kuberska, J1
Tronczyńska, J1

Other Studies

5 other studies available for thioctic acid and Amino Acid Metabolism Disorders, Inborn

ArticleYear
Mutations in the lipoyltransferase LIPT1 gene cause a fatal disease associated with a specific lipoylation defect of the 2-ketoacid dehydrogenase complexes.
    Human molecular genetics, 2014, Apr-01, Volume: 23, Issue:7

    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)].
    Arquivo de patologia, 1963, Volume: 35

    Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Copper; Corrinoids; Hematinics; Humans; Iron; Pro

1963
[RECENT IDEAS ON CYSTINOSIS].
    Bulletins et memoires de la Societe medicale des hopitaux de Paris, 1963, Nov-15, Volume: 114

    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.
    The Journal of clinical investigation, 1981, Volume: 68, Issue:2

    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.
    Polish medical journal, 1971, Volume: 10, Issue:1

    Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Child; Decarboxylation; Histidine; Humans; Ketoglu

1971