urea has been researched along with Genetic Diseases, X-Chromosome Linked in 8 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 (12.50) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (25.00) | 29.6817 |
| 2010's | 5 (62.50) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Cailleaux, A | 1 |
| Mahieu, F | 1 |
| Heinrichs, C | 2 |
| Adams, B | 1 |
| Ismaili, K | 1 |
| Brachet, C | 2 |
| Bardanzellu, F | 1 |
| Pintus, MC | 1 |
| Masile, V | 1 |
| Fanos, V | 1 |
| Marcialis, MA | 1 |
| Pey, AL | 2 |
| Vandergheynst, F | 1 |
| Decaux, G | 1 |
| Mesa-Torres, N | 1 |
| Chiarelli, LR | 1 |
| Valentini, G | 1 |
| CONOLLY, ME | 1 |
| ELLIS, H | 1 |
| McBride, KL | 1 |
| Miller, G | 1 |
| Carter, S | 1 |
| Karpen, S | 1 |
| Goss, J | 1 |
| Lee, B | 1 |
| Suriano, G | 1 |
| Azevedo, L | 1 |
| Novais, M | 1 |
| Boscolo, B | 1 |
| Seruca, R | 1 |
| Amorim, A | 1 |
| Ghibaudi, EM | 1 |
2 reviews available for urea and Genetic Diseases, X-Chromosome Linked
| Article | Year |
|---|---|
Focus on neonatal and infantile onset of nephrogenic syndrome of inappropriate antidiuresis: 12 years later.
Topics: Age of Onset; Antidiuretic Hormone Receptor Antagonists; Clinical Trials as Topic; Diuretics, Osmoti | 2019 |
Long-term treatment of hyponatremic patients with nephrogenic syndrome of inappropriate antidiuresis: personal experience and review of published case reports.
Topics: Adult; Aged; Diuretics; Furosemide; Genetic Diseases, X-Linked; Humans; Hyponatremia; Inappropriate | 2012 |
6 other studies available for urea and Genetic Diseases, X-Chromosome Linked
| Article | Year |
|---|---|
[Nephrogenic syndrome of inappropriate antidiuresis: Early diagnosis avoids severe hyponatremia complications].
Topics: Early Diagnosis; Genetic Diseases, X-Linked; Humans; Hyponatremia; Inappropriate ADH Syndrome; Infan | 2017 |
The interplay between protein stability and dynamics in conformational diseases: the case of hPGK1 deficiency.
Topics: Amino Acid Substitution; Enzyme Stability; Genetic Diseases, X-Linked; Humans; Metabolism, Inborn Er | 2013 |
Structural and energetic basis of protein kinetic destabilization in human phosphoglycerate kinase 1 deficiency.
Topics: Adenosine Diphosphate; Adenosine Triphosphate; Calorimetry, Differential Scanning; Enzyme Stability; | 2013 |
ANURIA DUE TO URIC ACID CRYSTALLURIA: AN UNUSUAL COMPLICATION OF THERAPY IN THE RETICULOSES.
Topics: Abdominal Neoplasms; Anuria; Blood; Genetic Diseases, X-Linked; Humans; Kidney Diseases; Leukemia, H | 1964 |
Developmental outcomes with early orthotopic liver transplantation for infants with neonatal-onset urea cycle defects and a female patient with late-onset ornithine transcarbamylase deficiency.
Topics: Ammonia; Carbamoyl-Phosphate Synthase I Deficiency Disease; Child Development; Child, Preschool; Com | 2004 |
In vitro demonstration of intra-locus compensation using the ornithine transcarbamylase protein as model.
Topics: Alleles; Amino Acid Substitution; Animals; Cell Line; Genetic Diseases, X-Linked; Humans; Hyperammon | 2007 |