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- 2010
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Mark
Phenotype associated with mutation in the recently identified autosomal dominant retinitis pigmentosa KLHL7 gene.
(
- Contribution to journal › Article
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Mark
Multifocal electroretinogram for functional evaluation of retinal injury following ischemia-reperfusion in pigs.
(
- Contribution to journal › Article
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Mark
Electrophysiological Assessment of Retinal Function During 6 Months of Bevacizumab Treatment in Neovascular Age-Related Macular Degeneration
(
- Contribution to journal › Article
- 2009
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Mark
Dose-related changes in retinal function and PKC-alpha expression in rabbits on vigabatrin medication : Effect of vigabatrin in the rabbit eye.
(
- Contribution to journal › Article
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Mark
The porcine retinal vasculature can be accessed using an endovascular approach, a new experimental model for retinal ischemia.
(
- Contribution to journal › Article
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Mark
Rifabutin accumulates in the lens and reduces retinal function in the rabbit eye
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- Contribution to journal › Article
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Mark
Macular Dysfunction and Morphology in Spinocerebellar Ataxia Type 7 (SCA 7)
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- Contribution to journal › Article
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Mark
Mutations in a BTB-Kelch Protein, KLHL7, Cause Autosomal-Dominant Retinitis Pigmentosa
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- Contribution to journal › Article
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Mark
A homologous genetic basis of the murine cpfl1 mutant and human achromatopsia linked to mutations in the PDE6C gene
(
- Contribution to journal › Article
- 2008
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Mark
Autosomal dominant inheritance in pericentral retinal dystrophy, an atypical form of retinitis pigmentosa (Abstracts of the XXXVIII Nordic Congress of Ophthalmology 14-17 June 2008)
(
- Contribution to journal › Published meeting abstract