Page last updated: 2024-10-20

uric acid and BCKD Deficiency

uric acid has been researched along with BCKD Deficiency in 5 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 (5)

TimeframeStudies, this research(%)All Research%
pre-19903 (60.00)18.7374
1990's0 (0.00)18.2507
2000's1 (20.00)29.6817
2010's0 (0.00)24.3611
2020's1 (20.00)2.80

Authors

AuthorsStudies
Yıldız, Y1
Akcan Yıldız, L1
Dursun, A1
Tokatlı, A1
Coşkun, T1
Tekşam, Ö1
Sivri, HS1
Barschak, AG1
Marchesan, C1
Sitta, A1
Deon, M1
Giugliani, R1
Wajner, M1
Vargas, CR1
Chodorowski, Z1
Schulman, JD1
Lustberg, TJ1
Kennedy, JL1
Museles, M1
Seegmiller, JE1
Jolley, RL1
Scott, CD1

Reviews

1 review available for uric acid and BCKD Deficiency

ArticleYear
[Selected phsiopathological and clinical aspects of purine metabolism].
    Polski tygodnik lekarski (Warsaw, Poland : 1960), 1976, Oct-04, Volume: 31, Issue:40

    Topics: Alkalosis, Respiratory; Diabetes Mellitus; Diuresis; Female; Fructose Intolerance; Glomerular Filtra

1976

Other Studies

4 other studies available for uric acid and BCKD Deficiency

ArticleYear
Predictors of acute metabolic decompensation in children with maple syrup urine disease at the emergency department.
    European journal of pediatrics, 2020, Volume: 179, Issue:7

    Topics: Acid-Base Equilibrium; Acute Disease; Adolescent; Biomarkers; Child; Child, Preschool; Disease Progr

2020
Maple syrup urine disease in treated patients: biochemical and oxidative stress profiles.
    Clinical biochemistry, 2008, Volume: 41, Issue:4-5

    Topics: Antioxidants; Cholesterol; Cholesterol, HDL; Cholesterol, LDL; Creatine; Glucose; Humans; Hydro-Lyas

2008
A new variant of maple syrup urine disease (branched chain ketoaciduria). Clinical and biochemical evaluation.
    The American journal of medicine, 1970, Volume: 49, Issue:1

    Topics: Amino Acids; Carboxy-Lyases; Creatinine; Diet Therapy; Enzyme Induction; Female; Fibroblasts; Humans

1970
Preliminary results from high-resolution analyses of ultraviolet-absorbing and carbohydrate constituents in several pathologic body fluids.
    Clinical chemistry, 1970, Volume: 16, Issue:8

    Topics: Adolescent; Adult; Alkaptonuria; Allopurinol; Amniotic Fluid; Athetosis; Carbohydrates; Chorea; Chro

1970