betaxolol has been researched along with Eye Diseases, Hereditary in 1 studies
Eye Diseases, Hereditary: Transmission of gene defects or chromosomal aberrations/abnormalities which are expressed in extreme variation in the structure or function of the eye. These may be evident at birth, but may be manifested later with progression of the disorder.
| 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 |
|---|---|
| Örnek, N | 1 |
| Oğurel, R | 1 |
| Örnek, K | 1 |
1 other study available for betaxolol and Eye Diseases, Hereditary
| Article | Year |
|---|---|
Congenital hypothyroidism in Rieger Syndrome.
Topics: Adrenergic beta-1 Receptor Antagonists; Anterior Eye Segment; Betaxolol; Child; Congenital Hypothyro | 2016 |