uracil has been researched along with Hyperammonemia in 3 studies
2,4-dihydroxypyrimidine: a urinary biomarker for bipolar disorder
Hyperammonemia: Elevated level of AMMONIA in the blood. It is a sign of defective CATABOLISM of AMINO ACIDS or ammonia to UREA.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Uracil and orotic acid concentrations were analyzed in three female patients with OTCD at both the hyperammonemia-attack and interval stages." | 3.73 | Urinary uracil in female patients with ornithine transcarbamylase deficiency. ( Ban, K; Imaeda, M; Ito, T; Ohkubo, Y; Sumi, S; Togari, H; Ueta, A, 2005) |
| "A presumptive diagnosis of ornithine transcarbamylase deficiency was made on the basis of the detection of orotic acid and uracil." | 1.32 | A suspected case of ornithine transcarbamylase deficiency in a cat. ( Matsumoto, I; Sawamura, M; Suzuki, T; Washizu, M; Washizu, T; Zhang, C, 2004) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (66.67) | 29.6817 |
| 2010's | 1 (33.33) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Auray-Blais, C | 1 |
| Maranda, B | 1 |
| Lavoie, P | 1 |
| Washizu, T | 1 |
| Washizu, M | 1 |
| Zhang, C | 1 |
| Matsumoto, I | 1 |
| Sawamura, M | 1 |
| Suzuki, T | 1 |
| Sumi, S | 1 |
| Imaeda, M | 1 |
| Ito, T | 1 |
| Ueta, A | 1 |
| Ban, K | 1 |
| Ohkubo, Y | 1 |
| Togari, H | 1 |
3 other studies available for uracil and Hyperammonemia
| Article | Year |
|---|---|
High-throughput tandem mass spectrometry multiplex analysis for newborn urinary screening of creatine synthesis and transport disorders, Triple H syndrome and OTC deficiency.
Topics: Biomarkers; Creatine; Creatinine; Filtration; Glycine; Humans; Hyperammonemia; Infant, Newborn; Orni | 2014 |
A suspected case of ornithine transcarbamylase deficiency in a cat.
Topics: Alanine Transaminase; Animals; Aspartate Aminotransferases; Bile Acids and Salts; Cat Diseases; Cats | 2004 |
Urinary uracil in female patients with ornithine transcarbamylase deficiency.
Topics: Child, Preschool; Female; Heterozygote; Humans; Hyperammonemia; Infant; Ornithine Carbamoyltransfera | 2005 |