ureidosuccinic acid has been researched along with Ornithine Carbamoyltransferase Deficiency Disease in 1 studies
ureidosuccinic acid: RN given refers to (DL)-isomer
N-carbamoylaspartic acid : An N-carbamoylamino acid that is aspartic acid with one of its amino hydrogens replaced by a carbamoyl group.
Ornithine Carbamoyltransferase Deficiency Disease: An inherited urea cycle disorder associated with deficiency of the enzyme ORNITHINE CARBAMOYLTRANSFERASE, transmitted as an X-linked trait and featuring elevations of amino acids and ammonia in the serum. Clinical features, which are more prominent in males, include seizures, behavioral alterations, episodic vomiting, lethargy, and coma. (Menkes, Textbook of Child Neurology, 5th ed, pp49-50)
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (100.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Inoue, Y | 1 |
| Ohkura, T | 1 |
| Matsumoto, I | 1 |
| Rudewicz, PJ | 1 |
1 other study available for ureidosuccinic acid and Ornithine Carbamoyltransferase Deficiency Disease
| Article | Year |
|---|---|
Fast atom bombardment tandem mass spectrometric analysis of N-carbamoylamino acids.
Topics: Amino Acids; Aspartic Acid; beta-Alanine; Carbamates; Humans; Ornithine Carbamoyltransferase Deficie | 1991 |