3-methylglutaconic acid has been researched along with Child Development Deviations in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (33.33) | 18.2507 |
| 2000's | 2 (66.67) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Baric, I; Bennetts, B; Carpenter, K; Christodoulou, J; Kelley, R; Kirk, EP; Neas, K; White, R; Wilson, M | 1 |
| Bertini, E; Boenzi, S; Carrozzo, R; D'Amico, A; Deodato, F; Di Rosa, G; Dionisi-Vici, C; Loupatty, FJ; Maiorana, A; Rizzo, C; Santorelli, FM; Tozzi, G; Wanders, RJ | 1 |
| De Meirleir, L; Desprechins, B; Erasmus, E; Gerlo, E; Gibson, KM; Jooste, S; Mienie, LJ; Wappner, RS | 1 |
3 other study(ies) available for 3-methylglutaconic acid and Child Development Deviations
| Article | Year |
|---|---|
OPA3 mutation screening in patients with unexplained 3-methylglutaconic aciduria.
Topics: 5' Untranslated Regions; Adolescent; Alleles; Amino Acid Metabolism, Inborn Errors; Base Sequence; Child; Child, Preschool; Cohort Studies; Developmental Disabilities; DNA Mutational Analysis; Genetic Variation; Glutarates; Heterozygote; Homozygote; Humans; Infant, Newborn; Middle Aged; Molecular Sequence Data; Mutation; Phenotype; Proteins; Reverse Transcriptase Polymerase Chain Reaction; Syndrome | 2005 |
Hypertrophic cardiomyopathy, cataract, developmental delay, lactic acidosis: a novel subtype of 3-methylglutaconic aciduria.
Topics: Acidosis, Lactic; Amino Acid Metabolism, Inborn Errors; Brain; Cardiomyopathy, Hypertrophic; Cataract; Developmental Disabilities; Family Health; Female; Glutarates; Humans; Infant; Infant, Newborn; Magnetic Resonance Imaging; Male; Pedigree | 2006 |
Variable clinical presentation in three patients with 3-methylglutaconyl-coenzyme A hydratase deficiency.
Topics: Adolescent; Brain; Developmental Disabilities; Female; Glutarates; Humans; Hydro-Lyases; Infant; Leucine; Magnetic Resonance Imaging; Male; Metabolism, Inborn Errors | 1998 |