3-methylglutaconic acid has been researched along with Chorea Disorders in 4 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (25.00) | 29.6817 |
| 2010's | 3 (75.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Ryan, RO; Su, B | 1 |
| Anikster, Y; Blumkin, L; Carmi, N; Kivity, S; Lerman-Sagie, T; Leshinsky-Silver, E; Lev, D; Zerem, A | 1 |
| Christodoulou, J; Ho, G; Walter, JH | 1 |
| Anikster, Y; Barth, PG; Duran, M; Morava, E; Sperl, W; Wevers, RA; Wortmann, SB; Zschocke, J | 1 |
3 review(s) available for 3-methylglutaconic acid and Chorea Disorders
| Article | Year |
|---|---|
Metabolic biology of 3-methylglutaconic acid-uria: a new perspective.
Topics: Acetyl Coenzyme A; Acyl Coenzyme A; Animals; Cardiolipins; Chorea; Citric Acid Cycle; Glutarates; Humans; Metabolism, Inborn Errors; Mitochondrial Proteins; Optic Atrophy; Phosphatidylglycerols; Smith-Lemli-Opitz Syndrome; Spastic Paraplegia, Hereditary; Terpenes | 2014 |
Costeff optic atrophy syndrome: new clinical case and novel molecular findings.
Topics: Adolescent; Adolescent Development; Biomarkers; Chorea; Codon, Nonsense; DNA Mutational Analysis; Female; Genetic Predisposition to Disease; Glutarates; Heterozygote; Homozygote; Humans; Metabolism, Inborn Errors; Optic Atrophy; Pedigree; Phenotype; Proteins; Spastic Paraplegia, Hereditary | 2008 |
Inborn errors of metabolism with 3-methylglutaconic aciduria as discriminative feature: proper classification and nomenclature.
Topics: Abnormalities, Multiple; Barth Syndrome; Cardiomyopathy, Dilated; Cerebellar Ataxia; Chorea; Diagnosis, Differential; Glutarates; Humans; Metabolism, Inborn Errors; Optic Atrophy; Spastic Paraplegia, Hereditary; Terminology as Topic | 2013 |
1 other study(ies) available for 3-methylglutaconic acid and Chorea Disorders
| Article | Year |
|---|---|
Atypical presentation of Costeff syndrome-severe psychomotor involvement and electrical status epilepticus during slow wave sleep.
Topics: Basal Ganglia Diseases; Child, Preschool; Chorea; Consanguinity; Electroencephalography; Female; Glutarates; Humans; Jews; Metabolism, Inborn Errors; Muscle Spasticity; Optic Atrophy; Proteins; Psychomotor Agitation; Seizures; Sleep; Spastic Paraplegia, Hereditary; Status Epilepticus | 2015 |