aminoimidazole carboxamide has been researched along with Aura in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (50.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 1 (50.00) | 2.80 |
| Authors | Studies |
|---|---|
| Billiemaz, K; Ceballos, I; Denommé-Pichon, AS; Héron, B; Imbard, A; Kuentz, P; Marie, S; Piraud, M; Ramond, F; Rio, M; Touraine, R; Vincent, MF | 1 |
| Bosschaart, AN; Duran, M; Hageman, G; Tien Poll-The, B; van den Bergh, FA | 1 |
2 other study(ies) available for aminoimidazole carboxamide and Aura
| Article | Year |
|---|---|
AICA-ribosiduria due to ATIC deficiency: Delineation of the phenotype with three novel cases, and long-term update on the first case.
Topics: Aminoimidazole Carboxamide; Child; Child, Preschool; Congenital Abnormalities; Epilepsy; Female; Humans; Hydroxymethyl and Formyl Transferases; Infant; Infant, Newborn; Intellectual Disability; Male; Multienzyme Complexes; Mutation; Nucleotide Deaminases; Phenotype; Ribonucleosides | 2020 |
Adenylosuccinase deficiency with neonatal onset severe epileptic seizures and sudden death.
Topics: Adenosine; Adenylosuccinate Lyase; Aminoimidazole Carboxamide; Anticonvulsants; Death, Sudden; Epilepsy; Humans; Infant, Newborn; Male; Purine-Pyrimidine Metabolism, Inborn Errors; Ribonucleotides | 1998 |