urea has been researched along with Lipid Metabolism, Inborn Error in 3 studies
pseudourea: clinical use; structure
isourea : A carboximidic acid that is the imidic acid tautomer of urea, H2NC(=NH)OH, and its hydrocarbyl derivatives.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (33.33) | 18.7374 |
| 1990's | 1 (33.33) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (33.33) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Tan, JQ | 1 |
| Chen, DY | 1 |
| Li, ZT | 1 |
| Huang, JW | 1 |
| Yan, TZ | 1 |
| Cai, R | 1 |
| Snyderman, SE | 1 |
| Imamura, Y | 1 |
| Saheki, T | 1 |
| Arakawa, H | 1 |
| Noda, T | 1 |
| Koizumi, T | 1 |
| Nikaido, H | 1 |
| Hayakawa, J | 1 |
1 review available for urea and Lipid Metabolism, Inborn Error
| Article | Year |
|---|---|
The dietary therapy of inherited metabolic disease.
Topics: Alkaptonuria; Amino Acid Metabolism, Inborn Errors; Carbohydrate Metabolism, Inborn Errors; Child; C | 1975 |
2 other studies available for urea and Lipid Metabolism, Inborn Error
| Article | Year |
|---|---|
[An analysis of clinical characteristics and gene mutation in two patients with medium- and short-chain acyl-CoA dehydrogenase deficiency].
Topics: Acyl-CoA Dehydrogenase; Carnitine; Female; Humans; Infant; Infant, Newborn; Lipid Metabolism, Inborn | 2016 |
Urea cycle disorder in C3H-H-2 degree mice with juvenile steatosis of viscera.
Topics: Ammonia; Animals; Fatty Liver; Gene Expression Regulation, Enzymologic; Homozygote; Lipid Metabolism | 1990 |