pyruvic acid has been researched along with Hereditary Optic Atrophy 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 | 0 (0.00) | 18.7374 |
1990's | 2 (100.00) | 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 |
---|---|
Cornelissen, JC | 1 |
Wanders, RJ | 1 |
Bolhuis, PA | 1 |
Bleeker-Wagemakers, E | 1 |
Oostra, RJ | 1 |
Wijburg, FA | 1 |
Ninomiya, T | 1 |
Yamazaki, H | 1 |
Munakata, S | 1 |
Yoshino, H | 1 |
Sato, T | 1 |
1 trial available for pyruvic acid and Hereditary Optic Atrophy
Article | Year |
---|---|
Respiratory chain function in Leber's hereditary optic neuropathy: lack of correlation with clinical disease.
Topics: Adolescent; Adult; Aged; DNA; Electron Transport; Female; Fibroblasts; Humans; Lactates; Lactic Acid | 1993 |
1 other study available for pyruvic acid and Hereditary Optic Atrophy
Article | Year |
---|---|
A case of Leber's hereditary optic neuropathy with elevated blood levels of lactate and pyruvate.
Topics: Adult; Humans; Lactic Acid; Male; Optic Atrophies, Hereditary; Pyruvic Acid | 1997 |