monomethyl succinate has been researched along with Lipid Metabolism, Inborn Error in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (33.33) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 2 (66.67) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Cheon, CK; Kim, GH; Kim, YM; Ko, JM; Lee, KA; Park, KH; Park, S; Yoo, HW | 1 |
| Abdenur, JE; Barshop, BA; Cederbaum, SD; Chang, E; Deignan, JL; Dorrani, N; Feuchtbaum, L; Gallant, NM; Leydiker, K; Lorey, F; Neidich, J; Puckett, R; Tang, H; Wang, RY | 1 |
| Amendt, BA; Cloherty, J; Greene, C; Moon, A; Rhead, WJ; Shih, V; Sweetman, L; Teel, L | 1 |
3 other study(ies) available for monomethyl succinate and Lipid Metabolism, Inborn Error
| Article | Year |
|---|---|
Novel and Recurrent ACADS Mutations and Clinical Manifestations Observed in Korean Patients with Short-chain Acyl-coenzyme a Dehydrogenase Deficiency.
Topics: Acyl-CoA Dehydrogenase; Asian People; Child; Child, Preschool; Disease Progression; Female; Follow-Up Studies; Humans; Infant; Lipid Metabolism, Inborn Errors; Male; Malonates; Mutation; Republic of Korea; Succinates; Treatment Outcome | 2016 |
Biochemical, molecular, and clinical characteristics of children with short chain acyl-CoA dehydrogenase deficiency detected by newborn screening in California.
Topics: Acyl Coenzyme A; Acyl-CoA Dehydrogenase; California; Carnitine; Female; Follow-Up Studies; Humans; Infant, Newborn; Lipid Metabolism, Inborn Errors; Male; Malonates; Neonatal Screening; Sequence Deletion; Succinates | 2012 |
Short-chain acyl-coenzyme A dehydrogenase deficiency. Clinical and biochemical studies in two patients.
Topics: 3-Hydroxybutyric Acid; Acyl-CoA Dehydrogenases; Adipates; Adult; Butyrates; Butyric Acid; Female; Fibroblasts; Humans; Hydroxybutyrates; Lactates; Lactic Acid; Lipid Metabolism, Inborn Errors; Malonates; Succinates | 1987 |