pyruvic acid has been researched along with Muscular Dystrophy in 2 studies
Pyruvic Acid: An intermediate compound in the metabolism of carbohydrates, proteins, and fats. In thiamine deficiency, its oxidation is retarded and it accumulates in the tissues, especially in nervous structures. (From Stedman, 26th ed)
pyruvic acid : A 2-oxo monocarboxylic acid that is the 2-keto derivative of propionic acid. It is a metabolite obtained during glycolysis.
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 2 (100.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
LICHY, J | 1 |
HORAK, M | 1 |
JICHA, J | 1 |
ZDRAHAL, L | 1 |
Prick, MJ | 1 |
Gabreƫls, FJ | 1 |
Trijbels, JM | 1 |
Janssen, AJ | 1 |
le Coultre, R | 1 |
van Dam, K | 1 |
Jaspar, HH | 1 |
Ebels, EJ | 1 |
Op de Coul, AA | 1 |
2 other studies available for pyruvic acid and Muscular Dystrophy
Article | Year |
---|---|
[The transaminase of glutmic-pyruvic acid (GPT) in myopathies].
Topics: Humans; Muscular Diseases; Muscular Dystrophies; Pyruvic Acid; Transaminases | 1961 |
Progressive poliodystrophy (Alpers' disease) with a defect in cytochrome aa3 in muscle: a report of two unrelated patients.
Topics: Atrophy; Brain; Child; Child, Preschool; Cytochrome a Group; Cytochrome-c Oxidase Deficiency; Cytoch | 1983 |