ethylmalonic acid has been researched along with Intellectual Disability 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 |
|---|---|
| Fu, X; Hahn, SH; Kodama, H; Packman, S; Rinaldo, P | 1 |
| Bennett, MJ; Bertini, E; Burlina, AB; Dionisi-Vici, C; Gibson, KM; Hale, DE; Sabetta, G; Schmidt-Sommerfeld, E; Servidei, S; Zacchello, F | 1 |
2 other study(ies) available for ethylmalonic acid and Intellectual Disability
| Article | Year |
|---|---|
Mutation analysis of copper transporter genes in patients with ethylmalonic encephalopathy, mitochondriopathies and copper deficiency phenotypes.
Topics: Blotting, Northern; Brain Diseases, Metabolic; Cation Transport Proteins; Cells, Cultured; Child; Copper; Copper Transporter 1; DNA Mutational Analysis; DNA, Complementary; Fatty Acids; Female; Fibroblasts; Humans; Intellectual Disability; Lipid Metabolism, Inborn Errors; Lymphocytes; Male; Malonates; Mitochondrial Encephalomyopathies; Molecular Chaperones; Oxidation-Reduction; Phenotype | 2003 |
A new syndrome with ethylmalonic aciduria and normal fatty acid oxidation in fibroblasts.
Topics: Acyl-CoA Dehydrogenase; Brain; Chronic Disease; Cyanosis; Diarrhea; Fatty Acid Desaturases; Fatty Acids; Fibroblasts; Humans; Infant; Intellectual Disability; Isoleucine; Male; Malonates; Oxidation-Reduction; Paralysis; Purpura; Syndrome | 1994 |