ethylmalonic acid has been researched along with glycine in 5 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (40.00) | 18.7374 |
| 1990's | 3 (60.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Gargus, JJ; O'Shea, JJ; Previs, SF; Rinaldo, P; Schmidt-Sommerfeld, E; Welch, RD; Zinn, AB | 1 |
| Jezyk, PF; Patterson, DF; Prochazka, M; Roderick, TH; Schiffer, SP; Yudkoff, M | 1 |
| Amendt, BA; Armstrong, D; Inoue, F; Millington, DS; Rhead, WJ; Wood, PA | 1 |
| Cyr, D; Giguère, R; Leblanc, D; Mitchell, G; Qureshi, IA | 1 |
| Clarke, JT; Fisher, L; Lehotay, DC; Nowaczyk, MJ; Phillips, H; Platt, BA; Tan, R | 1 |
5 other study(ies) available for ethylmalonic acid and glycine
| Article | Year |
|---|---|
Ethylmalonic/adipic aciduria: effects of oral medium-chain triglycerides, carnitine, and glycine on urinary excretion of organic acids, acylcarnitines, and acylglycines.
Topics: Acylation; Adipates; Administration, Oral; Carnitine; Child; Electron-Transferring Flavoproteins; Fatty Acid Desaturases; Female; Glycine; Humans; Iron-Sulfur Proteins; Malonates; Metabolism, Inborn Errors; Multienzyme Complexes; Oxidoreductases Acting on CH-NH Group Donors; Triglycerides | 1991 |
Organic aciduria and butyryl CoA dehydrogenase deficiency in BALB/cByJ mice.
Topics: Animals; Butyryl-CoA Dehydrogenase; Crosses, Genetic; Fatty Acid Desaturases; Female; Gas Chromatography-Mass Spectrometry; Genetic Variation; Glycine; Isoenzymes; Male; Malonates; Mice; Mice, Inbred BALB C; Phenotype; Sex Factors; Species Specificity | 1989 |
Short-chain acyl-coenzyme A dehydrogenase deficiency in mice.
Topics: Acyl-CoA Dehydrogenase; Animals; Carnitine; Disease Models, Animal; Fatty Acid Desaturases; Fatty Acids; Fatty Acids, Volatile; Gas Chromatography-Mass Spectrometry; Glycine; Malonates; Mice; Mice, Inbred BALB C; Oxidation-Reduction; Succinates | 1989 |
Breeding experiments to combine the X-linked sparse-fur (spf) mutation with the autosomal recessive BALB/cByJ strain: testing the biochemical phenotype of double-mutant mice as a model for ammonia: fatty acyl CoA synergism.
Topics: Acyl Coenzyme A; Acyl-CoA Dehydrogenases; Ammonia; Animals; Butyryl-CoA Dehydrogenase; Crosses, Genetic; Female; Genes, Recessive; Genetic Linkage; Glycine; Hair; Male; Malonates; Mice; Mice, Inbred BALB C; Mice, Mutant Strains; Mutation; Ornithine Carbamoyltransferase; Ornithine Carbamoyltransferase Deficiency Disease; Orotic Acid; Phenotype; Succinates; X Chromosome | 1993 |
Ethylmalonic and methylsuccinic aciduria in ethylmalonic encephalopathy arise from abnormal isoleucine metabolism.
Topics: Administration, Oral; Brain; Cells, Cultured; Child, Preschool; Female; Fibroblasts; Glycine; Humans; Isoleucine; Malonates; Metabolism, Inborn Errors; Oxidoreductases; Oxidoreductases Acting on CH-CH Group Donors; Succinates | 1998 |