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uric acid and Lipid Metabolism, Inborn Error

uric acid has been researched along with Lipid Metabolism, Inborn Error 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's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's1 (25.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Ku, E1
Thomas, M1
Ho, CH1
Whipple, NS1
Abdul-Rahman, O1
Megason, GC1
Herrington, BL1
Carmody, JB1
Charlton, JR1
Niessen, KH1
Cole, DE1
Clarke, LA1
McPhee, MD1
Marie, MS1
Torsvik, H1
Gjone, E1
Norum, KR1

Reviews

1 review available for uric acid and Lipid Metabolism, Inborn Error

ArticleYear
[Diseases of the exocrine pancreas in infants and children. A review. 1. Organic pancreatic diseases].
    Fortschritte der Medizin, 1980, Feb-28, Volume: 98, Issue:8

    Topics: Amino Acid Metabolism, Inborn Errors; Amylases; Child, Preschool; Cholecystokinin; Cystic Fibrosis;

1980

Trials

1 trial available for uric acid and Lipid Metabolism, Inborn Error

ArticleYear
Familial plasma cholesterol ester deficiency. Clinical studies of a family.
    Acta medica Scandinavica, 1968, Volume: 183, Issue:4

    Topics: Acid Phosphatase; Adolescent; Adult; Aged; Anemia; Bone Marrow Cells; Child; Cholesterol; Clinical T

1968

Other Studies

2 other studies available for uric acid and Lipid Metabolism, Inborn Error

ArticleYear
Index of suspicion. Case 1: fever, diarrhea, jaundice, and confusion in an 18-year-old male. Case 2: severe anemia in a 6-month-old girl. Case 3: red urine in a 4-month-old boy.
    Pediatrics in review, 2014, Volume: 35, Issue:3

    Topics: Acyl-CoA Dehydrogenase, Long-Chain; Adolescent; Anemia; Anti-Inflammatory Agents; Confusion; Congeni

2014
Hyperuricemia in disorders of fatty acid oxidation.
    Clinical chemistry, 1988, Volume: 34, Issue:4

    Topics: Fatty Acids; Humans; Infant; Lipid Metabolism, Inborn Errors; Male; Oxidation-Reduction; Uric Acid

1988