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- 2011
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Mark
Alteration of rod and cone function in children with Usher syndrome.
(
- Contribution to journal › Article
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Mark
Morphological and functional changes in multifocal vitelliform retinopathy and biallelic mutations in BEST1.
(
- Contribution to journal › Article
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Mark
Phenotypes in Defined Genotypes Including Siblings with Usher Syndrome.
(
- Contribution to journal › Article
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Mark
Anterior Segment Abnormalities and Angle-Closure Glaucoma in a Family with a Mutation in the BEST1 Gene and Best Vitelliform Macular Dystrophy.
(
- Contribution to journal › Article
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Mark
Electrophysiological studies in newly onset type 2 diabetes without visible vascular retinopathy.
(
- Contribution to journal › Article
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Mark
Electrophysiological evaluation of retinal function in children receiving vigabatrin medication
(
- Contribution to journal › Article
- 2010
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Mark
Using multifocal electroretinography hard exudates affect macular function in eyes with diabetic retinopathy
(
- Contribution to journal › Article
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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
Long-term 12 year follow-up of X-linked congenital retinoschisis.
(
- Contribution to journal › Article
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Mark
Improved retinal function after trabeculectomy in glaucoma patients.
(
- Contribution to journal › Article