fenofibrate has been researched along with Color Vision Defects in 1 studies
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Color Vision Defects: Defects of color vision are mainly hereditary traits but can be secondary to acquired or developmental abnormalities in the CONES (RETINA). Severity of hereditary defects of color vision depends on the degree of mutation of the ROD OPSINS genes (on X CHROMOSOME and CHROMOSOME 3) that code the photopigments for red, green and blue.
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 1 (100.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
de Moraes, G | 1 |
Layton, CJ | 1 |
1 review available for fenofibrate and Color Vision Defects
Article | Year |
---|---|
Therapeutic targeting of diabetic retinal neuropathy as a strategy in preventing diabetic retinopathy.
Topics: Animals; Color Vision Defects; Contrast Sensitivity; Dark Adaptation; Diabetic Neuropathies; Diabeti | 2016 |