uric acid has been researched along with Retinitis Pigmentosa 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.
Retinitis Pigmentosa: Hereditary, progressive degeneration of the retina due to death of ROD PHOTORECEPTORS initially and subsequent death of CONE PHOTORECEPTORS. It is characterized by deposition of pigment in the retina.
| Excerpt | Relevance | Reference |
|---|---|---|
| "The content of uric acid was measured in the blood of patients suffering from retinitis pigmentosa, as well as in the blood, retina, brain, liver and urine of rats with inherited retinal degeneration in the course of postnatal development." | 7.66 | [Changes in the blood uric acid levels in patients with retinitis pigmentosa and in rats with hereditary retinal degeneration]. ( Chusova, GG; Eliseeva, RF; Ostapenko, IA; Shabanova, ME, 1982) |
| "The content of uric acid was measured in the blood of patients suffering from retinitis pigmentosa, as well as in the blood, retina, brain, liver and urine of rats with inherited retinal degeneration in the course of postnatal development." | 3.66 | [Changes in the blood uric acid levels in patients with retinitis pigmentosa and in rats with hereditary retinal degeneration]. ( Chusova, GG; Eliseeva, RF; Ostapenko, IA; Shabanova, ME, 1982) |
| " In 2 cases a mild diabetes mellitus, in 7 cases uric acid level in serum was raised." | 3.65 | [Clinical-neurological and electromyographical studies of inpatients isolated with selective pigmentary retinopathy]. ( Eickhoff, W; Hellner, KA; Müller-Jensen, A, 1975) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 5 (100.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Bresler, VM | 1 |
| Ostapenko, IA | 2 |
| Rebane, EN | 1 |
| Chusova, GG | 2 |
| Shabanova, ME | 1 |
| Eliseeva, RF | 1 |
| Müller-Jensen, A | 2 |
| Eickhoff, W | 1 |
| Hellner, KA | 2 |
| Goldstein, JL | 1 |
| Fialkow, PJ | 1 |
5 other studies available for uric acid and Retinitis Pigmentosa
| Article | Year |
|---|---|
[The system of active transport of organic acids in the proximal tubules of rats with hereditary retinal degeneration (Campbell strain)].
Topics: Adenosine; Adenosine Monophosphate; Animals; Bile Acids and Salts; Biological Transport, Active; Dis | 1983 |
[Changes in the blood uric acid levels in patients with retinitis pigmentosa and in rats with hereditary retinal degeneration].
Topics: Animals; Brain; Disease Models, Animal; Genetic Diseases, Inborn; Genetic Testing; Humans; Liver; Ra | 1982 |
[Clinical-neurological and electromyographical studies of inpatients isolated with selective pigmentary retinopathy].
Topics: Adolescent; Adult; Aged; Child; Child, Preschool; Diabetes Mellitus; Diabetic Retinopathy; Electroen | 1975 |
[Pigmentary degeneration of the retina: neurological and biochemical findings (author's transl)].
Topics: Adolescent; Adult; Aged; Body Constitution; Child; Diabetes Complications; Electroencephalography; E | 1975 |
The Alström syndrome. Report of three cases with further delineation of the clinical, pathophysiological, and genetic aspects of the disorder.
Topics: Adolescent; Adult; Albuminuria; Blood Cell Count; Blood Urea Nitrogen; Child; Complement System Prot | 1973 |