pamidronate 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 |
|---|---|
| Munns, CF | 1 |
| Fahiminiya, S | 1 |
| Poudel, N | 1 |
| Munteanu, MC | 1 |
| Majewski, J | 1 |
| Sillence, DO | 1 |
| Metcalf, JP | 1 |
| Biggin, A | 1 |
| Glorieux, F | 1 |
| Fassier, F | 1 |
| Rauch, F | 1 |
| Hinsdale, ME | 1 |
1 other study available for pamidronate and Eye Diseases, Hereditary
| Article | Year |
|---|---|
Homozygosity for frameshift mutations in XYLT2 result in a spondylo-ocular syndrome with bone fragility, cataracts, and hearing defects.
Topics: Base Sequence; Cataract; Craniofacial Abnormalities; Diphosphonates; Exome; Eye Diseases, Hereditary | 2015 |