pyruvic acid has been researched along with Congenital Myotonic Dystrophy in 1 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 | 1 (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 |
|---|---|
| KUHN, E | 1 |
| WOERNER, W | 1 |
1 other study available for pyruvic acid and Congenital Myotonic Dystrophy
| Article | Year |
|---|---|
[Studies of intermediate metabolism in myotonic dystrophy (lactic acid, pyruvic acid, lactic dehydrogenase and malic acid dehydrogenase)].
Topics: Humans; Lactates; Lactic Acid; Malate Dehydrogenase; Malates; Myotonic Dystrophy; Oxidoreductases; P | 1961 |