methylmalonic acid has been researched along with Late Onset Diseases in 1 studies
Methylmalonic Acid: A malonic acid derivative which is a vital intermediate in the metabolism of fat and protein. Abnormalities in methylmalonic acid metabolism lead to methylmalonic aciduria. This metabolic disease is attributed to a block in the enzymatic conversion of methylmalonyl CoA to succinyl CoA.
methylmalonic acid : A dicarboxylic acid that is malonic acid in which one of the methylene hydrogens is substituted by a methyl group.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Their physical examination showed sensory ataxia." | 1.51 | Isolated subacute combined degeneration in late-onset cobalamin C deficiency in children: Two case reports and literature review. ( Cui, J; Cui, X; Wang, L; Wang, Y; Zhang, H; Zheng, H, 2019) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Cui, J | 1 |
| Wang, Y | 1 |
| Zhang, H | 1 |
| Cui, X | 1 |
| Wang, L | 1 |
| Zheng, H | 1 |
1 other study available for methylmalonic acid and Late Onset Diseases
| Article | Year |
|---|---|
Isolated subacute combined degeneration in late-onset cobalamin C deficiency in children: Two case reports and literature review.
Topics: Adolescent; Ataxia; Brain; Carrier Proteins; Child; Female; Homocysteine; Homocystinuria; Humans; In | 2019 |