3-hydroxyisobutyric acid has been researched along with Hyperoxaluria, Primary in 1 studies
3-hydroxyisobutyric acid: RN given refers to cpd without isomeric designation
3-hydroxyisobutyric acid : A 4-carbon, branched hydroxy fatty acid and intermediate in the metabolism of valine.
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.
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 |
---|---|
Konkoľová, J | 1 |
Chandoga, J | 1 |
Kováčik, J | 1 |
Repiský, M | 1 |
Kramarová, V | 1 |
Paučinová, I | 1 |
Böhmer, D | 1 |
1 other study available for 3-hydroxyisobutyric 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- | 2017 |