methylmalonic acid has been researched along with Glycine Encephalopathy in 2 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 | 1 (50.00) | 29.6817 |
2010's | 1 (50.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Scalais, E | 1 |
Osterheld, E | 1 |
Weitzel, C | 1 |
De Meirleir, L | 1 |
Mataigne, F | 1 |
Martens, G | 1 |
Shaikh, TH | 1 |
Coughlin, CR | 1 |
Yu, HC | 1 |
Swanson, M | 1 |
Friederich, MW | 1 |
Scharer, G | 1 |
Helbling, D | 1 |
Wendt-Andrae, J | 1 |
Van Hove, JLK | 1 |
Randak, C | 1 |
Roschinger, W | 1 |
Rolinski, B | 1 |
Hadorn, HB | 1 |
Applegarth, DA | 1 |
Roscher, AA | 1 |
2 other studies available for methylmalonic acid and Glycine Encephalopathy
Article | Year |
---|---|
X-Linked Cobalamin Disorder (HCFC1) Mimicking Nonketotic Hyperglycinemia With Increased Both Cerebrospinal Fluid Glycine and Methylmalonic Acid.
Topics: Biomarkers; Brain; Diagnosis, Differential; Genetic Diseases, X-Linked; Glycine; Humans; Hyperglycin | 2017 |
Three siblings with nonketotic hyperglycinaemia, mildly elevated plasma homocysteine concentrations and moderate methylmalonic aciduria.
Topics: Child; Consanguinity; Female; Homocysteine; Humans; Hyperglycinemia, Nonketotic; Infant; Infant, New | 2000 |