ethylmalonic acid has been researched along with Liver Dysfunction in 2 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 1 (50.00) | 18.2507 |
2000's | 1 (50.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Bok, LA; Corydon, MJ; Duran, M; Gregersen, N; Vreken, P; Wanders, RJ; Waterham, HR; Wijburg, FA | 1 |
Elias, E; Gray, RG; Green, A; Poulton, K | 1 |
2 other study(ies) available for ethylmalonic acid and Liver Dysfunction
Article | Year |
---|---|
Short-chain Acyl-CoA dehydrogenase deficiency: studies in a large family adding to the complexity of the disorder.
Topics: Amino Acid Substitution; Anemia, Hemolytic; Butyryl-CoA Dehydrogenase; Carnitine; Consanguinity; DNA Mutational Analysis; Female; Humans; Infant, Newborn; Infant, Premature; Liver Diseases; Male; Malonates; Mutation, Missense; Pedigree; Point Mutation; Polymorphism, Genetic; Pregnancy; Pregnancy Complications; Syndrome; Thrombocytopenia | 2003 |
Ethylmalonic adipic aciduria--a treatable hepatomuscular disorder in two adult brothers.
Topics: Adipates; Adult; Humans; Lipid Metabolism, Inborn Errors; Liver Diseases; Male; Malonates; Muscular Diseases; Reye Syndrome | 1997 |