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Argus II retinal prosthesis system: a review of patient selection criteria, surgical considerations, and post-operative outcomes
Retinitis pigmentosa (RP) is a group of heterogeneous inherited retinal degenerative disorders characterized by progressive rod and cone dysfunction and ensuing photoreceptor loss. Many patients suffer from legal blindness by their 40s or 50s. Artificial vision is considered once patients have lost...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Dove Medical Press
2018
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6005308/ https://www.ncbi.nlm.nih.gov/pubmed/29942114 http://dx.doi.org/10.2147/OPTH.S137525 |