Clinical research in families with inherited retinal degeneration
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- 2017
-
Mark
Central retinal vein occlusion in younger Swedish adults : Case reports and review of the literature
- Contribution to journal › Article
-
Mark
Genotype and Phenotype in an unusual form of Laurence-Moon-Bardet-Biedl syndrome
- Contribution to journal › Article
-
Mark
The clinical phenotype of CNGA3-related achromatopsia : Pretreatment characterization in preparation of a gene replacement therapy trial
- Contribution to journal › Article
-
Mark
Ataxia-pancytopenia syndrome with SAMD9L mutations
- Contribution to journal › Article
-
Mark
Reduction of rod and cone function in 6.5-year-old children born extremely preterm
- Contribution to journal › Article
- 2009
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Mark
Rifabutin accumulates in the lens and reduces retinal function in the rabbit eye
- Contribution to journal › Article
- 2004
-
Mark
Alterations in electroretinograms and retinal morphology in rabbits treated with vigabatrin
- Contribution to journal › Article
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