n(delta)-(phosphonoacetyl)-l-ornithine has been researched along with Ornithine Carbamoyltransferase Deficiency Disease in 1 studies
*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) [MeSH]
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (100.00) | 18.7374 |
| 1990's | 0 (0.00) | 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 |
|---|---|
| Briand, P; Cathelineau, L | 1 |
1 other study(ies) available for n(delta)-(phosphonoacetyl)-l-ornithine and Ornithine Carbamoyltransferase Deficiency Disease
| Article | Year |
|---|---|
Sparse-fur mutation: a model for some human ornithine transcarbamylase deficiencies.
Topics: Amino Acid Metabolism, Inborn Errors; Animals; Chromatography, Gel; Electrophoresis, Polyacrylamide Gel; Epoxy Compounds; Hair; Immunodiffusion; Male; Mice; Mice, Mutant Strains; Mitochondria, Liver; Mutation; Ornithine; Ornithine Carbamoyltransferase; Ornithine Carbamoyltransferase Deficiency Disease; Phosphates; Valine | 1982 |