pyruvic acid has been researched along with Encephalomyopathies, Mitochondrial in 5 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 | 5 (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 |
|---|---|
| Jackson, MJ | 1 |
| Schaefer, JA | 1 |
| Johnson, MA | 1 |
| Morris, AA | 1 |
| Turnbull, DM | 1 |
| Bindoff, LA | 1 |
| Agsteribbe, E | 1 |
| Huckriede, A | 1 |
| Veenhuis, M | 1 |
| Ruiters, MH | 1 |
| Niezen-Koning, KE | 1 |
| Skjeldal, OH | 1 |
| Skullerud, K | 1 |
| Gupta, RS | 1 |
| Hallberg, R | 1 |
| van Diggelen, OP | 1 |
| Ozawa, M | 1 |
| Goto, Y | 1 |
| Sakuta, R | 1 |
| Tanno, Y | 1 |
| Tsuji, S | 1 |
| Nonaka, I | 1 |
| Chen, RS | 1 |
| Huang, CC | 1 |
| Chu, NS | 1 |
| Dionisi-Vici, C | 1 |
| Ruitenbeek, W | 1 |
| Fariello, G | 1 |
| Bentlage, H | 1 |
| Wanders, RJ | 1 |
| Schägger, H | 1 |
| Bosman, C | 1 |
| Piantadosi, C | 1 |
| Sabetta, G | 1 |
| Bertini, E | 1 |
1 trial available for pyruvic acid and Encephalomyopathies, Mitochondrial
| Article | Year |
|---|---|
Coenzyme Q10 treatment in mitochondrial encephalomyopathies. Short-term double-blind, crossover study.
Topics: Activities of Daily Living; Adolescent; Adult; Aged; Coenzymes; Cross-Over Studies; Double-Blind Met | 1997 |
4 other studies available for pyruvic acid and Encephalomyopathies, Mitochondrial
| Article | Year |
|---|---|
Presentation and clinical investigation of mitochondrial respiratory chain disease. A study of 51 patients.
Topics: Adolescent; Adult; Alanine; Brain; Child; Creatine Kinase; DNA, Mitochondrial; Electroencephalograph | 1995 |
A fatal, systemic mitochondrial disease with decreased mitochondrial enzyme activities, abnormal ultrastructure of the mitochondria and deficiency of heat shock protein 60.
Topics: Cells, Cultured; Female; Fibroblasts; Glucose; Heat-Shock Proteins; Humans; Infant, Newborn; Lactate | 1993 |
The 8,344 mutation in mitochondrial DNA: a comparison between the proportion of mutant DNA and clinico-pathologic findings.
Topics: Adolescent; Adult; Base Sequence; Child; Child, Preschool; DNA Mutational Analysis; DNA, Mitochondri | 1995 |
New familial mitochondrial encephalopathy with macrocephaly, cardiomyopathy, and complex I deficiency.
Topics: Cardiomyopathies; Electrophoresis, Gel, Two-Dimensional; Family Health; Fatal Outcome; Fibroblasts; | 1997 |