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uric acid and Deficiency, Hexosediphosphatase

uric acid has been researched along with Deficiency, Hexosediphosphatase in 4 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 (4)

TimeframeStudies, this research(%)All Research%
pre-19903 (75.00)18.7374
1990's1 (25.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Steinmann, B2
Baerlocher, K1
Gitzelmann, R2
Burlina, AB1
Poletto, M1
Shin, YS1
Zacchello, F1
Velázquez, A1
DeCéspedes, C1
DeVivo, DC1
Costin, G1
Shaw, KN1

Other Studies

4 other studies available for uric acid and Deficiency, Hexosediphosphatase

ArticleYear
[Hereditary disorders of fructose metabolism. Loading tests with fructose, sorbitol and dihydroxyacetone].
    Nutrition and metabolism, 1975, Volume: 18 Suppl 1

    Topics: Bicarbonates; Blood Glucose; Carbohydrate Metabolism, Inborn Errors; Depression, Chemical; Dihydroxy

1975
[Fructose and sorbitol in infusion solutions are not always harmless].
    Internationale Zeitschrift fur Vitamin- und Ernahrungsforschung. Beiheft, 1976, Volume: 15

    Topics: Blood Glucose; Carbohydrate Metabolism, Inborn Errors; Female; Fructose; Fructose Intolerance; Fruct

1976
Clinical and biochemical observations on three cases of fructose-1,6-diphosphatase deficiency.
    Journal of inherited metabolic disease, 1990, Volume: 13, Issue:3

    Topics: Acidosis, Lactic; Child, Preschool; Fructose-1,6-Diphosphatase Deficiency; Glycerol; Humans; Hypogly

1990
Hepatic metabolites and uric acid excretion in fructose-1,6-diphosphatase deficiency.
    Journal of inherited metabolic disease, 1988, Volume: 11, Issue:3

    Topics: Blood Chemical Analysis; Female; Fructose Metabolism, Inborn Errors; Fructose-1,6-Diphosphatase Defi

1988