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Subject Areas on Research
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A contact lens electrode with built-in high intensity white light-emitting diodes. A contact lens electrode with built-in white LEDs.
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A shot of adrenaline.
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Abnormal cone ERGs in a family with congenital nystagmus and photophobia harboring a p.X423Lfs mutation in the PAX6 gene.
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Absence of synaptic regulation by phosducin in retinal slices.
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Aclacinomycin A in the treatment of experimental proliferative vitreoretinopathy. Efficacy and toxicity in the rabbit eye.
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Acquired subretinal flecks secondary to hypovitaminosis A in a patient with hepatitis C.
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Activation of Rod Input in a Model of Retinal Degeneration Reverses Retinal Remodeling and Induces Formation of Functional Synapses and Recovery of Visual Signaling in the Adult Retina.
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An intravitreal sustained-release triamcinolone and 5-fluorouracil codrug in the treatment of experimental proliferative vitreoretinopathy.
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An unusual X-linked retinoschisis phenotype and biochemical characterization of the W112C RS1 mutation.
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Ankyrin-B is required for coordinated expression of beta-2-spectrin, the Na/K-ATPase and the Na/Ca exchanger in the inner segment of rod photoreceptors.
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Autosomal recessive best vitelliform macular dystrophy: report of a family and management of early-onset neovascular complications.
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Autosomal-dominant retinitis pigmentosa associated with an Arg-135-Trp point mutation of the rhodopsin gene. Clinical features and longitudinal observations.
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Baseline Visual Field Findings in the RUSH2A Study: Associated Factors and Correlation With Other Measures of Disease Severity.
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Bilateral paraneoplastic optic neuropathy and unilateral retinal compromise in association with prostate cancer: a differential diagnostic challenge in a patient with unexplained visual loss.
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Biomarkers of Diabetic Retinopathy.
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Bull's-eye maculopathy associated with quinacrine therapy for malaria.
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Characterization of Fatty Acid Binding Protein 7 (FABP7) in the Murine Retina.
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Characterization of a Case of Pigmentary Retinopathy in Sanfilippo Syndrome Type IIIA Associated with Compound Heterozygous Mutations in the SGSH Gene.
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Characterization of intraocular immunopathology following intracameral inoculation with alloantigen.
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Clinical and functional findings in choroideremia due to complete deletion of the CHM gene.
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Correlation between Goldmann perimetry and maximal electroretinogram response in retinitis pigmentosa.
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Correlation between retinal oscillatory potentials and retinal vascular caliber in type 2 diabetes.
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Correlation of structural and electrophysiological changes in the retina of young high myopes.
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Cross-modal selective attention effects on retinal, myogenic, brainstem, and cerebral evoked potentials.
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Disease expression of RP1 mutations causing autosomal dominant retinitis pigmentosa.
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Dispase facilitates posterior vitreous detachment during vitrectomy in young pigs.
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Dominant late-onset retinal degeneration with regional variation of sub-retinal pigment epithelium deposits, retinal function, and photoreceptor degeneration.
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ERG responses and microarray analysis of gene expression in a multifactorial murine model of age-related retinal degeneration.
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EVALUATION OF FULL-FIELD ELECTRORETINOGRAM REDUCTIONS AFTER OCRIPLASMIN TREATMENT: Results of the OASIS Trial ERG Substudy.
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Early retinal neurodegeneration and impaired Ran-mediated nuclear import of TDP-43 in progranulin-deficient FTLD.
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Effect of Anti-C5a Therapy in a Murine Model of Early/Intermediate Dry Age-Related Macular Degeneration.
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Effect of Ciliary Neurotrophic Factor on Retinal Neurodegeneration in Patients with Macular Telangiectasia Type 2: A Randomized Clinical Trial.
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Effect of INS37217, a P2Y(2) receptor agonist, on experimental retinal detachment and electroretinogram in adult rabbits.
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Effects of intravitreous injection of preserved and non-preserved triamcinolone in rabbit retina.
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Effects of organophosphates on the visual system of rats.
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Effects of simvastatin on retinal structure and function of a high-fat atherogenic mouse model of thickened Bruch's membrane.
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Efficacy of low-release-rate fluocinolone acetonide intravitreal implants to treat experimental uveitis.
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Electrophysiologic monitoring of diabetic retinopathy in pregnancy.
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Electroretinographic abnormalities in parents of patients with Leber congenital amaurosis who have heterozygous GUCY2D mutations.
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Electroretinographic alterations in the Laurence-Moon-Bardet-Biedl phenotype.
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Electroretinographic findings in sickle cell retinopathy.
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Elovl4 5-bp-deletion knock-in mice develop progressive photoreceptor degeneration.
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Evaluation of a delivery system providing long-term release of cyclosporine.
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Evidence for a two pigment visual system in the fiddler crab, Uca thayeri.
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Expression of human complement factor H prevents age-related macular degeneration-like retina damage and kidney abnormalities in aged Cfh knockout mice.
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Fluocinolone acetonide sustained drug delivery device to treat severe uveitis.
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Fluvastatin downregulates VEGF-A expression in TNF-α-induced retinal vessel tortuosity.
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Frequency characteristics in the visual system of Drosophila: genetic dissection of electroretinogram components.
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Functionally rodless mice: transgenic models for the investigation of cone function in retinal disease and therapy.
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Fundus albipunctatus in a 6-year old girl due to compound heterozygous mutations in the RDH5 gene.
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GABA, picrotoxin and retinal sensitivity.
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GPR158 in the Visual System: Homeostatic Role in Regulation of Intraocular Pressure.
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Genetic dissection of rod and cone pathways in the dark-adapted mouse retina.
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Genetically engineered large animal model for studying cone photoreceptor survival and degeneration in retinitis pigmentosa.
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Haploinsufficient Bmp4 ocular phenotypes include anterior segment dysgenesis with elevated intraocular pressure.
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Impact of the revised american academy of ophthalmology guidelines regarding hydroxychloroquine screening on actual practice.
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Impaired photoreceptor protein transport and synaptic transmission in a mouse model of Bardet-Biedl syndrome.
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Increased proteasomal activity supports photoreceptor survival in inherited retinal degeneration.
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Intraretinal pH in diabetic cats.
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Intravitreal sustained-release cyclosporine in the treatment of experimental uveitis.
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Intravitreal sustained-release dexamethasone device in the treatment of experimental uveitis.
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Light and vision in the deep-sea benthos: II. Vision in deep-sea crustaceans.
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Long-term retinal toxicity of intravitreal commercially available preserved triamcinolone acetonide (Kenalog) in rabbit eyes.
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Low-noise electroretinogram recording techniques in retinitis pigmentosa.
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Mechanistic basis for the failure of cone transducin to translocate: why cones are never blinded by light.
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Multifocal electroretinogram in rhodopsin P347L transgenic pigs.
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N,N-dimethyladriamycin for treatment of experimental proliferative vitreoretinopathy: efficacy and toxicity on the rabbit retina.
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N-3-pyridylmethyl-N'-p-nitrophenylurea ocular toxicity in man and rabbits.
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Nonsyndromic Retinitis Pigmentosa in the Ashkenazi Jewish Population: Genetic and Clinical Aspects.
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Ocular toxicity of daunomycin: effects of subdivided doses on the rabbit retina after vitreous gas compression.
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PPARβ/δ selectively regulates phenotypic features of age-related macular degeneration.
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Pattern electroretinogram and psychophysical tests of visual function for discriminating between healthy and glaucoma eyes.
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Pharmacologically defined components of the normal porcine multifocal ERG.
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Phenotypic and Genetic Spectrum of Autosomal Recessive Bestrophinopathy and Best Vitelliform Macular Dystrophy.
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Phenotypic expression of Bardet-Biedl syndrome in patients homozygous for the common M390R mutation in the BBS1 gene.
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Phosducin regulates transmission at the photoreceptor-to-ON-bipolar cell synapse.
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Photoreceptor synapses degenerate early in experimental choroidal neovascularization.
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Photoreceptors in a mouse model of Leigh syndrome are capable of normal light-evoked signaling.
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Pigmented paravenous retinochoroidal atrophy. Discordant expression in monozygotic twins.
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Porcine global flash multifocal electroretinogram: possible mechanisms for the glaucomatous changes in contrast response function.
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Prevention of experimental proliferative vitreoretinopathy with a biodegradable intravitreal implant for the sustained release of fluorouracil.
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Primary retinal pathology in multiple sclerosis as detected by optical coherence tomography.
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Quantification of Ellipsoid Zone Changes in Retinitis Pigmentosa Using en Face Spectral Domain-Optical Coherence Tomography.
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RGS9 knockout causes a short delay in light responses of ON-bipolar cells.
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RanBP2 modulates Cox11 and hexokinase I activities and haploinsufficiency of RanBP2 causes deficits in glucose metabolism.
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Reduced blue cone electroretinogram in cocaine-withdrawn patients.
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Regular examinations for toxic maculopathy in long-term chloroquine or hydroxychloroquine users.
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Reply to abnormalities on the multifocal electroretinogram may precede clinical signs of hydroxychloroquine retinotoxicity.
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Retinal Degeneration After Accidental Intravitreal Injection of Ropivacaine During Strabismus Surgery.
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Retinal dysfunction as an initial ophthalmic sign in AIDS.
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Retinal effects of 6 months of daily use of tadalafil or sildenafil.
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Retinal phenotype of an X-linked pseudo-Usher syndrome in association with the G173R mutation in the RPGR gene.
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Retinal phenotypes in patients homozygous for the G1961E mutation in the ABCA4 gene.
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Retinal rod photoreceptor-specific gene mutation perturbs cone pathway development.
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Retinal toxicity of cyanoacrylate tissue adhesive in the rabbit.
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Retinitis pigmentosa associated with rhodopsin mutations: Correlation between phenotypic variability and molecular effects.
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Reversal of retinal ganglion cell dysfunction after surgical reduction of intraocular pressure.
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Role for the target enzyme in deactivation of photoreceptor G protein in vivo.
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Safety and pharmacokinetics of an intraocular fluocinolone acetonide sustained delivery device.
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Safety and pharmokinetics of triamcinolone hexacetonide in rabbit eyes.
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Spectral sensitivity, spatial resolution and temporal resolution and their implications for conspecific signalling in cleaner shrimp.
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Spontaneous retinal reattachment in incontinentia pigmenti.
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Targeted inactivation of synaptic HRG4 (UNC119) causes dysfunction in the distal photoreceptor and slow retinal degeneration, revealing a new function.
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Targeting age-related macular degeneration with Alzheimer's disease based immunotherapies: anti-amyloid-beta antibody attenuates pathologies in an age-related macular degeneration mouse model.
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The NLRP3 Inflammasome May Contribute to Pathologic Neovascularization in the Advanced Stages of Diabetic Retinopathy.
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The Prevalence of Hydroxychloroquine Retinopathy and Toxic Dosing, and the Role of the Ophthalmologist in Reducing Both.
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The RUSH2A Study: Best-Corrected Visual Acuity, Full-Field Electroretinography Amplitudes, and Full-Field Stimulus Thresholds at Baseline.
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The impact of intraocular pressure reduction on retinal ganglion cell function measured using pattern electroretinogram in eyes receiving latanoprost 0.005% versus placebo.
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The isolated perfused frog eye: a useful preparation for the investigation of drug effects on retinal function.
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The lack of toxicity of intravitreally administered triamcinolone acetonide.
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The ocular phenotype of the Bardet-Biedl syndrome. Comparison to non-syndromic retinitis pigmentosa.
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The oral iron chelator deferiprone protects against iron overload-induced retinal degeneration.
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The oral iron chelator deferiprone protects against systemic iron overload-induced retinal degeneration in hepcidin knockout mice.
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The role of cystoid macular edema as a marker in the progression of non-paraneoplastic autoimmune retinopathy.
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Transducin gamma-subunit sets expression levels of alpha- and beta-subunits and is crucial for rod viability.
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Treatment of adult-onset acute macular retinoschisis in enhanced s-cone syndrome with oral acetazolamide.
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Uniocular vascular occlusion in a paraplegic hybrid monkey. A clinicopathologic study.
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Usher syndrome: correlation between visual field size and maximal ERG response b-wave amplitude.
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Variations in opsin coding sequences cause x-linked cone dysfunction syndrome with myopia and dichromacy.
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Visual contrast sensitivity in major depressive disorder.
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Visual physiology underlying orientation and diel behavior in the sand beach amphipod Talorchestia longicornis.
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Whole-exome sequencing implicates UBE3D in age-related macular degeneration in East Asian populations.
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X-linked high myopia associated with cone dysfunction.
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