uric acid has been researched along with Hyperbilirubinemia, Hereditary in 3 studies
Uric Acid: An oxidation product, via XANTHINE OXIDASE, of oxypurines such as XANTHINE and HYPOXANTHINE. It is the final oxidation product of purine catabolism in humans and primates, whereas in most other mammals URATE OXIDASE further oxidizes it to ALLANTOIN.
uric acid : An oxopurine that is the final oxidation product of purine metabolism.
6-hydroxy-1H-purine-2,8(7H,9H)-dione : A tautomer of uric acid having oxo groups at C-2 and C-8 and a hydroxy group at C-6.
7,9-dihydro-1H-purine-2,6,8(3H)-trione : An oxopurine in which the purine ring is substituted by oxo groups at positions 2, 6, and 8.
Hyperbilirubinemia, Hereditary: Inborn errors of bilirubin metabolism resulting in excessive amounts of bilirubin in the circulating blood, either because of increased bilirubin production or because of delayed clearance of bilirubin from the blood.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 3 (100.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Manzke, H | 1 |
| Koke, HG | 1 |
| Kruse, K | 1 |
| Gattereau, A | 1 |
| Vinay, P | 1 |
| Restellini, A | 1 |
| Dipalma, JR | 1 |
3 other studies available for uric acid and Hyperbilirubinemia, Hereditary
| Article | Year |
|---|---|
Purine metabolites, uracil and cAMP during exchange transfusion.
Topics: Cyclic AMP; Exchange Transfusion, Whole Blood; Female; Humans; Hyperbilirubinemia, Hereditary; Infan | 1984 |
[Coexistence of constitutional hyperbilirubinemia and familial hypouricemia of renal origin in a Quebec family].
Topics: Adult; Female; Gilbert Disease; Humans; Hyperbilirubinemia, Hereditary; Kidney Diseases; Male; Middl | 1985 |
Pharmacogenetics.
Topics: Abnormalities, Drug-Induced; Allopurinol; Barbiturates; Chromosome Aberrations; Drug-Related Side Ef | 1974 |