3-methylglutaconic acid has been researched along with Carbamoyl Phosphate Synthase (Ammonia) Deficiency Disease in 1 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Alhaddad, B; Carrozzo, R; Ciara, E; Dionisi-Vici, C; Gan, CS; Haack, TB; Haidar, R; Jabłońska, E; Kovacs-Nagy, R; Krajewska-Walasek, M; Muthukumarasamy, P; Ołtarzewski, M; Pajdowska, M; Piekutowska-Abramczuk, D; Pronicka, E; Pronicki, M; Rizzo, C; Rokicki, D; Semeraro, M; Sikora, R; Sthaneswar, P; Taurisano, R; Thong, MK; Trubicka, J; Verrigni, D; Wortmann, SB | 1 |
1 other study(ies) available for 3-methylglutaconic acid and Carbamoyl Phosphate Synthase (Ammonia) Deficiency Disease
| Article | Year |
|---|---|
3-Methylglutaconic aciduria, a frequent but underrecognized finding in carbamoyl phosphate synthetase I deficiency.
Topics: Carbamoyl-Phosphate Synthase I Deficiency Disease; Female; Glutarates; Humans; Infant, Newborn; Male; Mutation; Pedigree | 2017 |