urea has been researched along with alpha-Galactosidase A Deficiency 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 | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 2 (66.67) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Andreotti, G | 1 |
| Citro, V | 1 |
| Correra, A | 1 |
| Cubellis, MV | 1 |
| Marin-Medina, A | 1 |
| Brambila-Tapia, AJ | 1 |
| Picos-Cárdenas, VJ | 1 |
| Gallegos-Arreola, MP | 1 |
| Figuera, LE | 1 |
| Moser, HW | 1 |
| Batshaw, ML | 1 |
| Murray, C | 1 |
| Braine, H | 1 |
| Brusilow, SW | 1 |
3 other studies available for urea and alpha-Galactosidase A Deficiency
| Article | Year |
|---|---|
A thermodynamic assay to test pharmacological chaperones for Fabry disease.
Topics: alpha-Galactosidase; Animals; Chlorocebus aethiops; COS Cells; Fabry Disease; HEK293 Cells; Humans; | 2014 |
eNOS gene Glu298Asp and 4b/a polymorphisms are associated with renal function parameters in Mexican patients with Fabry disease.
Topics: Adult; Creatinine; Fabry Disease; Genetic Association Studies; Genetic Predisposition to Disease; Ge | 2016 |
Management of heritable disorders of the urea cycle and of Refsum's and Fabry's diseases.
Topics: Adult; Amino Acid Metabolism, Inborn Errors; Arginine; Benzoates; Carbamoyl-Phosphate Synthase (Ammo | 1979 |