calconcarboxylic acid has been researched along with Hyperoxaluria, Primary in 1 studies
*Hyperoxaluria, Primary: A genetic disorder characterized by excretion of large amounts of OXALATES in urine; NEPHROLITHIASIS; NEPHROCALCINOSIS; early onset of RENAL FAILURE; and often a generalized deposit of CALCIUM OXALATE. There are subtypes classified by the enzyme defects in glyoxylate metabolism. [MeSH]
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Díaz-Gavilán, M; Fernandes, MX; Franco-Montalbán, F; Gómez-Vidal, JA; Martín Higueras, C; Moya-Garzón, MD; Peñalver, P; Romera, M; Salido, E | 1 |
1 other study(ies) available for calconcarboxylic acid and Hyperoxaluria, Primary
| Article | Year |
|---|---|
Salicylic Acid Derivatives Inhibit Oxalate Production in Mouse Hepatocytes with Primary Hyperoxaluria Type 1.
Topics: Alcohol Oxidoreductases; Animals; Cells, Cultured; Computer Simulation; Drug Design; Hepatocytes; Humans; Hyperoxaluria, Primary; Male; Mice, Inbred C57BL; Mice, Mutant Strains; Molecular Docking Simulation; Oxalates; Salicylates; Structure-Activity Relationship; Transaminases | 2018 |