uric acid has been researched along with Phenylketonurias in 7 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.
Phenylketonurias: A group of autosomal recessive disorders marked by a deficiency of the hepatic enzyme PHENYLALANINE HYDROXYLASE or less frequently by reduced activity of DIHYDROPTERIDINE REDUCTASE (i.e., atypical phenylketonuria). Classical phenylketonuria is caused by a severe deficiency of phenylalanine hydroxylase and presents in infancy with developmental delay; SEIZURES; skin HYPOPIGMENTATION; ECZEMA; and demyelination in the central nervous system. (From Adams et al., Principles of Neurology, 6th ed, p952).
| Excerpt | Relevance | Reference |
|---|---|---|
| "Free triiodothyronine was higher in both patient groups than in control subjects, whereas free thyroxine was higher in the PKU patients only." | 1.31 | Antioxidant and thyroid hormone status in selenium-deficient phenylketonuric and hyperphenylalaninemic patients. ( Printzen, G; van Bakel, MM; Wermuth, B; Wiesmann, UN, 2000) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 3 (42.86) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (14.29) | 29.6817 |
| 2010's | 2 (28.57) | 24.3611 |
| 2020's | 1 (14.29) | 2.80 |
| Authors | Studies |
|---|---|
| Fernandez-Crespo, S | 1 |
| Vazquez-Agra, N | 1 |
| Marques-Afonso, AT | 1 |
| Cruces-Sande, A | 1 |
| Martinez-Olmos, MA | 1 |
| Araujo-Vilar, D | 1 |
| Hermida-Ameijeiras, A | 1 |
| Keshavarzi, F | 1 |
| Rastegar, M | 1 |
| Vessal, M | 1 |
| Rafiei Dehbidi, G | 1 |
| Khorsand, M | 1 |
| Ganjkarimi, AH | 1 |
| Takhshid, MA | 1 |
| Zhang, D | 1 |
| Li, W | 1 |
| Zhang, J | 1 |
| Tang, W | 1 |
| Qian, C | 1 |
| Feng, M | 1 |
| Chu, Q | 1 |
| Ye, J | 1 |
| van Bakel, MM | 1 |
| Printzen, G | 1 |
| Wermuth, B | 1 |
| Wiesmann, UN | 1 |
| Holtzman, NA | 1 |
| Rundle, AT | 1 |
| Fannin, CV | 1 |
| Wilson, JM | 1 |
2 reviews available for uric acid and Phenylketonurias
| Article | Year |
|---|---|
Dietary treatment of inborn errors of metabolism.
Topics: Ammonia; Carbohydrate Metabolism, Inborn Errors; Diet Therapy; Female; Fructose; Galactosemias; Glyc | 1970 |
Current trends and problems in health screening.
Topics: Autoanalysis; Blood Glucose; Clinical Laboratory Techniques; Costs and Cost Analysis; Female; Humans | 1973 |
5 other studies available for uric acid and Phenylketonurias
| Article | Year |
|---|---|
The value of waist circumference as a preditor of cardiovascular risk in adult patients with classic phenylketonuria.
Topics: Adult; Body Mass Index; Cardiovascular Diseases; Case-Control Studies; Cholesterol, HDL; Female; Hea | 2023 |
Serum ischemia modified albumin is a possible new marker of oxidative stress in phenylketonuria.
Topics: Adolescent; Biomarkers; Child; Child, Preschool; Female; Humans; Male; Malondialdehyde; Oxidative St | 2018 |
Study on urinary metabolic profile of phenylketonuria by micellar electrokinetic capillary chromatography with dual electrochemical detection--potential clinical application in fast diagnosis of phenylketonuria.
Topics: Chromatography, Micellar Electrokinetic Capillary; Electrochemical Techniques; Humans; Hydrogen-Ion | 2011 |
Antioxidant and thyroid hormone status in selenium-deficient phenylketonuric and hyperphenylalaninemic patients.
Topics: Adolescent; Adult; Antioxidants; Child; Child, Preschool; Diet, Protein-Restricted; Female; Glutathi | 2000 |
A survey of serum uric acid levels in mentally retarded patients.
Topics: Adolescent; Adult; Aged; Athetosis; Central Nervous System Diseases; Down Syndrome; Female; Humans; | 1966 |