ethylmalonic acid has been researched along with Complex IV Deficiency in 4 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 4 (100.00) | 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 |
|---|---|
| Lehnert, W; Ruitenbeek, W | 1 |
| Carrara, F; Colamaria, V; Garavaglia, B; Rimoldi, M; Tonin, P; Uziel, G | 1 |
| Arenas, J; Campos, Y; Garavaglia, B; García-Silva, MT; Ribes, A | 1 |
| Eber, SW; Hanefeld, F; Hoffmann, GF; Hunneman, DH; Jakobs, C; Rating, D; Reichmann, H; Wilichowski, E | 1 |
4 other study(ies) available for ethylmalonic acid and Complex IV Deficiency
| Article | Year |
|---|---|
Ethylmalonic aciduria associated with progressive neurological disease and partial cytochrome c oxidase deficiency.
Topics: Child; Child, Preschool; Cytochrome-c Oxidase Deficiency; Female; Humans; Male; Malonates; Muscles; Nervous System Diseases | 1993 |
Muscle cytochrome c oxidase deficiency in two Italian patients with ethylmalonic aciduria and peculiar clinical phenotype.
Topics: Cytochrome-c Oxidase Deficiency; Fatal Outcome; Humans; Infant; Infant, Newborn; Italy; Male; Malonates; Muscles; Phenotype | 1994 |
Syndrome of encephalopathy, petechiae, and ethylmalonic aciduria.
Topics: Brain; Cytochrome-c Oxidase Deficiency; DNA, Mitochondrial; Humans; Infant; Leigh Disease; Male; Malonates; Muscle, Skeletal; Purpura | 1997 |
Progressive fatal pancytopenia, psychomotor retardation and muscle carnitine deficiency in a child with ethylmalonic aciduria and ethylmalonic acidaemia.
Topics: Carnitine; Cytochrome-c Oxidase Deficiency; DNA, Mitochondrial; Fatty Acid Desaturases; Female; Humans; Infant, Newborn; Malonates; Metabolism, Inborn Errors; Mitochondria; Muscles; NADH Dehydrogenase; Pancytopenia; Psychomotor Disorders | 1990 |