3-methylglutaconic acid has been researched along with Auditory Processing Disorder, Central in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (33.33) | 18.7374 |
| 1990's | 1 (33.33) | 18.2507 |
| 2000's | 1 (33.33) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Buckel, W; Carpenter, K; Ensenauer, R; Gibson, KM; Hoffmann, GF; Liesert, M; Ly, TB; Mack, M; Peters, V; Wilcken, B; Zschocke, J | 1 |
| Gutman, A; Harel, S; Lerman-Sagie, T; Michelson, M | 1 |
| Beemer, FA; Divry, P; Gibson, KM; Lehnert, W; Narisawa, K; Nyhan, WL; Robinson, BH; Roth, KS; Sweetman, L; van Sprang, FJ | 1 |
3 other study(ies) available for 3-methylglutaconic acid and Auditory Processing Disorder, Central
| Article | Year |
|---|---|
Mutations in the AUH gene cause 3-methylglutaconic aciduria type I.
Topics: Amino Acid Metabolism, Inborn Errors; Carnitine; Child, Preschool; Exons; Genes, Recessive; Glutarates; Humans; Hydro-Lyases; Infant, Newborn; Intellectual Disability; Language Development Disorders; Male; Mutation; Neonatal Screening | 2003 |
Urinary organic acid screening in children with developmental language delay.
Topics: Child; Child, Preschool; Female; Fumarates; Glutarates; Humans; Language Development Disorders; Male; Malonates; Mass Screening; Meglutol | 1999 |
3-Methylglutaconic aciduria: a phenotype in which activity of 3-methylglutaconyl-coenzyme A hydratase is normal.
Topics: Chemical Phenomena; Chemistry; Female; Glutarates; Humans; Hydro-Lyases; Infant; Infant, Newborn; Language Development Disorders; Male; Motor Skills | 1988 |