2-ethylhydracrylic 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 |
|---|---|
| Böhmer, D; Chandoga, J; Konkoľová, J; Kováčik, J; Kramarová, V; Paučinová, I; Repiský, M | 1 |
1 other study(ies) available for 2-ethylhydracrylic acid and Hyperoxaluria, Primary
| Article | Year |
|---|---|
Severe child form of primary hyperoxaluria type 2 - a case report revealing consequence of GRHPR deficiency on metabolism.
Topics: Alcohol Oxidoreductases; Aminoisobutyric Acids; DNA Mutational Analysis; Female; Gas Chromatography-Mass Spectrometry; Humans; Hydroxybutyrates; Hyperoxaluria, Primary; Infant; Lactic Acid; Urolithiasis; Valerates | 2017 |