3-methylglutaconic acid has been researched along with Brain Diseases, Metabolic, Familial in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| de Vries, MC; Engelke, UF; Heldt, K; Huizing, M; Jonckheere, A; Kluijtmans, LA; Morava, E; Rodenburg, RJ; Smeitink, JA; van den Heuvel, LP; Wendel, U; Wevers, RA; Wortmann, SB | 1 |
| Eriguchi, M; Hasegawa, Y; Kosugi, M; Kuroda, Y; Kurohara, K; Mizuta, H; Okada, R; Yakushiji, Y; Yamaguchi, S; Yukitake, M | 1 |
2 other study(ies) available for 3-methylglutaconic acid and Brain Diseases, Metabolic, Familial
| Article | Year |
|---|---|
Biochemical and genetic analysis of 3-methylglutaconic aciduria type IV: a diagnostic strategy.
Topics: Adenosine Triphosphatases; Brain; Brain Diseases, Metabolic, Inborn; Cardiomyopathies; Carrier Proteins; DNA Polymerase gamma; DNA-Directed DNA Polymerase; Facies; Female; Glutarates; Humans; Infant, Newborn; Magnetic Resonance Imaging; Magnetic Resonance Spectroscopy; Male; Membrane Proteins; Metabolism, Inborn Errors; Mitochondrial Diseases; Mitochondrial Proteins; Mitochondrial Proton-Translocating ATPases; Mutation; Phenotype; Ryanodine Receptor Calcium Release Channel | 2009 |
3-Methylglutaconic aciduria type I causes leukoencephalopathy of adult onset.
Topics: Amino Acid Metabolism, Inborn Errors; Brain; Brain Diseases, Metabolic, Inborn; Cognition Disorders; Dementia, Vascular; DNA Mutational Analysis; Enoyl-CoA Hydratase; Female; Glutarates; Humans; Magnetic Resonance Imaging; Middle Aged; Mutation; Nerve Fibers, Myelinated; Reflex, Abnormal; RNA-Binding Proteins | 2006 |