Page last updated: 2024-10-20

uric acid and Constitutional Liver Dysfunction

uric acid has been researched along with Constitutional Liver Dysfunction 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.

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19902 (66.67)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's1 (33.33)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Higashi, Y1
Maruhashi, T1
Noma, K1
Kihara, Y1
van Waeg, G1
Niklasson, F1
de Verdier, CH1
Gattereau, A1
Vinay, P1
Restellini, A1

Reviews

1 review available for uric acid and Constitutional Liver Dysfunction

ArticleYear
Oxidative stress and endothelial dysfunction: clinical evidence and therapeutic implications.
    Trends in cardiovascular medicine, 2014, Volume: 24, Issue:4

    Topics: Animals; Bilirubin; Endothelium, Vascular; Gilbert Disease; Humans; Hypertension, Renovascular; NADP

2014

Other Studies

2 other studies available for uric acid and Constitutional Liver Dysfunction

ArticleYear
Deamination of guanine to xanthine: a metabolic pathway of underestimated importance in human purine catabolism?
    Advances in experimental medicine and biology, 1986, Volume: 195 Pt A

    Topics: Allopurinol; Female; Gilbert Disease; Guanine; Humans; Kinetics; Liver Cirrhosis, Biliary; Male; Ref

1986
[Coexistence of constitutional hyperbilirubinemia and familial hypouricemia of renal origin in a Quebec family].
    L'union medicale du Canada, 1985, Volume: 114, Issue:3

    Topics: Adult; Female; Gilbert Disease; Humans; Hyperbilirubinemia, Hereditary; Kidney Diseases; Male; Middl

1985