pyruvic acid has been researched along with Benign Infantile Myoclonic Epilepsy 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.
Excerpt | Relevance | Reference |
---|---|---|
"The disorders causing myoclonus have been compared to those in which myoclonus has been reported." | 2.37 | Myoclonus and mitochondrial myopathy. ( Hopkins, LC; Rosing, HS, 1986) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 1 (50.00) | 18.7374 |
1990's | 1 (50.00) | 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 |
---|---|
van Hellenberg Hubar, JL | 1 |
Gabreƫls, FJ | 1 |
Ruitenbeek, W | 1 |
Sengers, RC | 1 |
Renier, WO | 1 |
Thijssen, HO | 1 |
ter Laak, HJ | 1 |
Hopkins, LC | 1 |
Rosing, HS | 1 |
2 reviews available for pyruvic acid and Benign Infantile Myoclonic Epilepsy
Article | Year |
---|---|
MELAS syndrome. Report of two patients, and comparison with data of 24 patients derived from the literature.
Topics: Biopsy; Child; Child, Preschool; Electroencephalography; Electromyography; Energy Metabolism; Enzyme | 1991 |
Myoclonus and mitochondrial myopathy.
Topics: Adolescent; Brain Diseases, Metabolic; Central Nervous System Diseases; Electroencephalography; Epil | 1986 |