methylmalonic acid has been researched along with Acid beta-Glucosidase Deficiency in 3 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.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (66.67) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 1 (33.33) | 2.80 |
| Authors | Studies |
|---|---|
| Basgalupp, SP | 1 |
| Siebert, M | 1 |
| Ferreira, C | 1 |
| Behringer, S | 1 |
| Spiekerkoetter, U | 1 |
| Hannibal, L | 1 |
| Schwartz, IVD | 1 |
| Sasaki, M | 1 |
| Sakuragawa, N | 1 |
| Gielchinsky, Y | 1 |
| Elstein, D | 1 |
| Green, R | 1 |
| Miller, JW | 1 |
| Elstein, Y | 1 |
| Algur, N | 1 |
| Lahad, A | 1 |
| Shinar, E | 1 |
| Abrahamov, A | 1 |
| Zimran, A | 1 |
1 review available for methylmalonic acid and Acid beta-Glucosidase Deficiency
| Article | Year |
|---|---|
[Inherited metabolic disorders accompanied with epileptic manifestations].
Topics: Epilepsy; Gangliosidoses, GM2; Gaucher Disease; Humans; Infant; Infant, Newborn; Leukodystrophy, Glo | 2002 |
2 other studies available for methylmalonic acid and Acid beta-Glucosidase Deficiency
| Article | Year |
|---|---|
Assessment of cellular cobalamin metabolism in Gaucher disease.
Topics: beta-Glucosidase; Cell Culture Techniques; Female; Fibroblasts; Gaucher Disease; Glucosylceramidase; | 2020 |
High prevalence of low serum vitamin B12 in a multi-ethnic Israeli population.
Topics: Adult; Arabs; Blood Donors; Case-Control Studies; Chi-Square Distribution; Female; Gaucher Disease; | 2001 |