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- 2016
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Mark
Characterization of macular structure and function in two swedish families with genetically identified autosomal dominant retinitis pigmentosa
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- Contribution to journal › Article
- 2014
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Mark
Retinal Function and Morphology in the Rabbit Eye after Intravitreal Injection of the TNF Alpha Inhibitor Adalimumab.
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- Contribution to journal › Article
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Mark
Attenuation of the retinal nerve fibre layer and reduced retinal function assessed by optical coherence tomography and full-field electroretinography in patients exposed to vigabatrin medication.
(
- Contribution to journal › Article
- 2013
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Mark
Intravitreal Injection of Triamcinolone Acetonide into Healthy Rabbit Eyes Alters Retinal Function and Morphology
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- Contribution to journal › Article
- 2012
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Mark
Retinal function and morphology in rabbit after intravitreal injection of VEGF inhibitors.
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- Contribution to journal › Article
- 2011
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Mark
Electrophysiological studies in newly onset type 2 diabetes without visible vascular retinopathy.
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- 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.
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- Contribution to journal › Article
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Mark
Phenotypes in Defined Genotypes Including Siblings with Usher Syndrome.
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- Contribution to journal › Article
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Mark
Morphological and functional changes in multifocal vitelliform retinopathy and biallelic mutations in BEST1.
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- Contribution to journal › Article
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Mark
Alteration of rod and cone function in children with Usher syndrome.
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- Contribution to journal › Article
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Mark
Electrophysiological evaluation of retinal function in children receiving vigabatrin medication
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- Contribution to journal › Article
- 2010
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Mark
Using multifocal electroretinography hard exudates affect macular function in eyes with diabetic retinopathy
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- Contribution to journal › Article
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Mark
Long-term 12 year follow-up of X-linked congenital retinoschisis.
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- Contribution to journal › Article
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Mark
Electrophysiological evaluation and visual outcome in patients with central retinal vein occlusion, primary open-angle glaucoma and neovascular glaucoma.
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- 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