carbamates has been researched along with Ornithine Carbamoyltransferase Deficiency Disease in 3 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)
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (66.67) | 18.7374 |
| 1990's | 1 (33.33) | 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 |
|---|---|
| Gelehrter, TD | 1 |
| Rosenberg, LE | 1 |
| Oberholzer, VG | 1 |
| Palmer, T | 1 |
| Inoue, Y | 1 |
| Ohkura, T | 1 |
| Matsumoto, I | 1 |
| Rudewicz, PJ | 1 |
3 other studies available for carbamates and Ornithine Carbamoyltransferase Deficiency Disease
| Article | Year |
|---|---|
Ornithine transcarbamylase deficiency. Unsuccessful therapy of neonatal hyperammonemia with N-carbamyl-L-glutamate and L-arginine.
Topics: Ammonia; Arginine; Carbamates; Catheterization; Drug Therapy, Combination; Glutamates; Humans; Infan | 1975 |
Increased excretion of N-carbamoyl compounds in patients with urea cycle defects.
Topics: Alanine; Argininosuccinate Synthase; Argininosuccinic Aciduria; Aspartic Acid; Carbamates; Child; Ch | 1976 |
Fast atom bombardment tandem mass spectrometric analysis of N-carbamoylamino acids.
Topics: Amino Acids; Aspartic Acid; beta-Alanine; Carbamates; Humans; Ornithine Carbamoyltransferase Deficie | 1991 |