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Treatment of Stargardt disease with dobesilate
Stargardt disease is a common inherited macular degeneration characterised by a significant loss in the central vision during the first or second decade of the life. Bilateral atrophic changes in the central retina are associated with degeneration of photoreceptors and underlying retinal pigment epi...
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| Yayımlandı: | BMJ Case Rep |
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| Asıl Yazarlar: | , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
BMJ Group
2012
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4544153/ https://ncbi.nlm.nih.gov/pubmed/23076703 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr-2012-007128 |
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