3-methylglutaconic acid has been researched along with Cataract 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 | 1 (50.00) | 29.6817 |
| 2010's | 1 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Bekheirnia, MR; Dhar, SU; Eble, T; Scaglia, F; Shaibani, A; Willis, A; Wong, LJ; Zhang, W | 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 |
2 other study(ies) available for 3-methylglutaconic acid and Cataract
| Article | Year |
|---|---|
POLG mutation in a patient with cataracts, early-onset distal muscle weakness and atrophy, ovarian dysgenesis and 3-methylglutaconic aciduria.
Topics: Age of Onset; Amino Acid Metabolism, Inborn Errors; Cataract; DNA Mutational Analysis; DNA Polymerase gamma; DNA-Directed DNA Polymerase; Female; Glutarates; Humans; Models, Molecular; Muscle Weakness; Muscular Atrophy; Mutation; Ovarian Diseases; Ovary; Young Adult | 2012 |
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 |