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.
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 3 (60.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (20.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 1 (20.00) | 2.80 |
Authors | Studies |
---|---|
Yıldız, Y | 1 |
Akcan Yıldız, L | 1 |
Dursun, A | 1 |
Tokatlı, A | 1 |
Coşkun, T | 1 |
Tekşam, Ö | 1 |
Sivri, HS | 1 |
Barschak, AG | 1 |
Marchesan, C | 1 |
Sitta, A | 1 |
Deon, M | 1 |
Giugliani, R | 1 |
Wajner, M | 1 |
Vargas, CR | 1 |
Chodorowski, Z | 1 |
Schulman, JD | 1 |
Lustberg, TJ | 1 |
Kennedy, JL | 1 |
Museles, M | 1 |
Seegmiller, JE | 1 |
Jolley, RL | 1 |
Scott, CD | 1 |
1 review available for uric acid and BCKD Deficiency
Article | Year |
---|---|
[Selected phsiopathological and clinical aspects of purine metabolism].
Topics: Alkalosis, Respiratory; Diabetes Mellitus; Diuresis; Female; Fructose Intolerance; Glomerular Filtra | 1976 |
4 other studies available for uric acid and BCKD Deficiency
Article | Year |
---|---|
Predictors of acute metabolic decompensation in children with maple syrup urine disease at the emergency department.
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.
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.
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.
Topics: Adolescent; Adult; Alkaptonuria; Allopurinol; Amniotic Fluid; Athetosis; Carbohydrates; Chorea; Chro | 1970 |