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uric acid and Labhart-Willi Syndrome

uric acid has been researched along with Labhart-Willi Syndrome in 1 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 (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (100.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Asanuma, H1
Nagatsuma, K1
Baba, S1
Murai, M1

Other Studies

1 other study available for uric acid and Labhart-Willi Syndrome

ArticleYear
[A case of Prader-Willi syndrome accompanied with a renal stone].
    Hinyokika kiyo. Acta urologica Japonica, 1998, Volume: 44, Issue:1

    Topics: Adult; Humans; Kidney Calculi; Male; Prader-Willi Syndrome; Uric Acid

1998