Electroretinography

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  Subject Areas on Research

  • A contact lens electrode with built-in high intensity white light-emitting diodes. A contact lens electrode with built-in white LEDs. 
  • A shot of adrenaline. 
  • Abnormal cone ERGs in a family with congenital nystagmus and photophobia harboring a p.X423Lfs mutation in the PAX6 gene. 
  • Absence of synaptic regulation by phosducin in retinal slices. 
  • Aclacinomycin A in the treatment of experimental proliferative vitreoretinopathy. Efficacy and toxicity in the rabbit eye. 
  • Acquired subretinal flecks secondary to hypovitaminosis A in a patient with hepatitis C. 
  • Age-related changes in visual function in cystathionine-beta-synthase mutant mice, a model of hyperhomocysteinemia. 
  • An intravitreal sustained-release triamcinolone and 5-fluorouracil codrug in the treatment of experimental proliferative vitreoretinopathy. 
  • An unusual X-linked retinoschisis phenotype and biochemical characterization of the W112C RS1 mutation. 
  • 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. 
  • Autosomal recessive best vitelliform macular dystrophy: report of a family and management of early-onset neovascular complications. 
  • Autosomal-dominant retinitis pigmentosa associated with an Arg-135-Trp point mutation of the rhodopsin gene. Clinical features and longitudinal observations. 
  • Bilateral paraneoplastic optic neuropathy and unilateral retinal compromise in association with prostate cancer: a differential diagnostic challenge in a patient with unexplained visual loss. 
  • Biomarkers of Diabetic Retinopathy. 
  • Bull's-eye maculopathy associated with quinacrine therapy for malaria. 
  • Characterization of Fatty Acid Binding Protein 7 (FABP7) in the Murine Retina. 
  • Characterization of a Case of Pigmentary Retinopathy in Sanfilippo Syndrome Type IIIA Associated with Compound Heterozygous Mutations in the SGSH Gene. 
  • Characterization of intraocular immunopathology following intracameral inoculation with alloantigen. 
  • Clinical and functional findings in choroideremia due to complete deletion of the CHM gene. 
  • Correlation between Goldmann perimetry and maximal electroretinogram response in retinitis pigmentosa. 
  • Correlation between retinal oscillatory potentials and retinal vascular caliber in type 2 diabetes. 
  • Correlation of structural and electrophysiological changes in the retina of young high myopes. 
  • Cross-modal selective attention effects on retinal, myogenic, brainstem, and cerebral evoked potentials. 
  • Disease expression of RP1 mutations causing autosomal dominant retinitis pigmentosa. 
  • Dispase facilitates posterior vitreous detachment during vitrectomy in young pigs. 
  • Dominant late-onset retinal degeneration with regional variation of sub-retinal pigment epithelium deposits, retinal function, and photoreceptor degeneration. 
  • ERG responses and microarray analysis of gene expression in a multifactorial murine model of age-related retinal degeneration. 
  • EVALUATION OF FULL-FIELD ELECTRORETINOGRAM REDUCTIONS AFTER OCRIPLASMIN TREATMENT: Results of the OASIS Trial ERG Substudy. 
  • Early retinal neurodegeneration and impaired Ran-mediated nuclear import of TDP-43 in progranulin-deficient FTLD. 
  • Effect of Anti-C5a Therapy in a Murine Model of Early/Intermediate Dry Age-Related Macular Degeneration. 
  • Effect of INS37217, a P2Y(2) receptor agonist, on experimental retinal detachment and electroretinogram in adult rabbits. 
  • Effects of intravitreous injection of preserved and non-preserved triamcinolone in rabbit retina. 
  • Effects of simvastatin on retinal structure and function of a high-fat atherogenic mouse model of thickened Bruch's membrane. 
  • Efficacy of low-release-rate fluocinolone acetonide intravitreal implants to treat experimental uveitis. 
  • Electrophysiologic monitoring of diabetic retinopathy in pregnancy. 
  • Electroretinographic abnormalities in parents of patients with Leber congenital amaurosis who have heterozygous GUCY2D mutations. 
  • Electroretinographic alterations in the Laurence-Moon-Bardet-Biedl phenotype. 
  • Electroretinographic findings in sickle cell retinopathy. 
  • Elovl4 5-bp-deletion knock-in mice develop progressive photoreceptor degeneration. 
  • Evaluation of a delivery system providing long-term release of cyclosporine. 
  • Evidence for a two pigment visual system in the fiddler crab, Uca thayeri. 
  • Expression of human complement factor H prevents age-related macular degeneration-like retina damage and kidney abnormalities in aged Cfh knockout mice. 
  • Fluocinolone acetonide sustained drug delivery device to treat severe uveitis. 
  • Fluvastatin downregulates VEGF-A expression in TNF-α-induced retinal vessel tortuosity. 
  • Frequency characteristics in the visual system of Drosophila: genetic dissection of electroretinogram components. 
  • Functionally rodless mice: transgenic models for the investigation of cone function in retinal disease and therapy. 
  • Fundus albipunctatus in a 6-year old girl due to compound heterozygous mutations in the RDH5 gene. 
  • GABA, picrotoxin and retinal sensitivity. 
  • Genetic dissection of rod and cone pathways in the dark-adapted mouse retina. 
  • Genetically engineered large animal model for studying cone photoreceptor survival and degeneration in retinitis pigmentosa. 
  • Haploinsufficient Bmp4 ocular phenotypes include anterior segment dysgenesis with elevated intraocular pressure. 
  • Impact of the revised american academy of ophthalmology guidelines regarding hydroxychloroquine screening on actual practice. 
  • Impaired photoreceptor protein transport and synaptic transmission in a mouse model of Bardet-Biedl syndrome. 
  • Increased proteasomal activity supports photoreceptor survival in inherited retinal degeneration. 
  • Intraretinal pH in diabetic cats. 
  • Intravitreal sustained-release cyclosporine in the treatment of experimental uveitis. 
  • Intravitreal sustained-release dexamethasone device in the treatment of experimental uveitis. 
  • Jalili Syndrome: Cross-sectional and Longitudinal Features of Seven Patients With Cone-Rod Dystrophy and Amelogenesis Imperfecta. 
  • Light and vision in the deep-sea benthos: II. Vision in deep-sea crustaceans. 
  • Long-term retinal toxicity of intravitreal commercially available preserved triamcinolone acetonide (Kenalog) in rabbit eyes. 
  • Low-noise electroretinogram recording techniques in retinitis pigmentosa. 
  • Mechanistic basis for the failure of cone transducin to translocate: why cones are never blinded by light. 
  • Multifocal electroretinogram in rhodopsin P347L transgenic pigs. 
  • N,N-dimethyladriamycin for treatment of experimental proliferative vitreoretinopathy: efficacy and toxicity on the rabbit retina. 
  • N-3-pyridylmethyl-N'-p-nitrophenylurea ocular toxicity in man and rabbits. 
  • Nonsyndromic Retinitis Pigmentosa in the Ashkenazi Jewish Population: Genetic and Clinical Aspects. 
  • Numerical solution of the bioelectric field of the e.r.g. 
  • Ocular toxicity of daunomycin: effects of subdivided doses on the rabbit retina after vitreous gas compression. 
  • PPARβ/δ selectively regulates phenotypic features of age-related macular degeneration. 
  • Pattern electroretinogram and psychophysical tests of visual function for discriminating between healthy and glaucoma eyes. 
  • Pharmacologically defined components of the normal porcine multifocal ERG. 
  • Phenotypic expression of Bardet-Biedl syndrome in patients homozygous for the common M390R mutation in the BBS1 gene. 
  • Phosducin regulates transmission at the photoreceptor-to-ON-bipolar cell synapse. 
  • Photoreceptor synapses degenerate early in experimental choroidal neovascularization. 
  • Pigmented paravenous retinochoroidal atrophy. Discordant expression in monozygotic twins. 
  • Porcine global flash multifocal electroretinogram: possible mechanisms for the glaucomatous changes in contrast response function. 
  • Prevention of experimental proliferative vitreoretinopathy with a biodegradable intravitreal implant for the sustained release of fluorouracil. 
  • Primary retinal pathology in multiple sclerosis as detected by optical coherence tomography. 
  • Quantification of Ellipsoid Zone Changes in Retinitis Pigmentosa Using en Face Spectral Domain-Optical Coherence Tomography. 
  • RGS9 knockout causes a short delay in light responses of ON-bipolar cells. 
  • RanBP2 modulates Cox11 and hexokinase I activities and haploinsufficiency of RanBP2 causes deficits in glucose metabolism. 
  • Reduced blue cone electroretinogram in cocaine-withdrawn patients. 
  • Regular examinations for toxic maculopathy in long-term chloroquine or hydroxychloroquine users. 
  • Reply to abnormalities on the multifocal electroretinogram may precede clinical signs of hydroxychloroquine retinotoxicity. 
  • Rescue from light-induced retinal degeneration by human fetal retinal transplantation in minipigs. 
  • Retinal dysfunction as an initial ophthalmic sign in AIDS. 
  • Retinal effects of 6 months of daily use of tadalafil or sildenafil. 
  • Retinal phenotype of an X-linked pseudo-Usher syndrome in association with the G173R mutation in the RPGR gene. 
  • Retinal phenotypes in patients homozygous for the G1961E mutation in the ABCA4 gene. 
  • Retinal rod photoreceptor-specific gene mutation perturbs cone pathway development. 
  • Retinal toxicity of cyanoacrylate tissue adhesive in the rabbit. 
  • Retinitis pigmentosa associated with rhodopsin mutations: Correlation between phenotypic variability and molecular effects. 
  • Reversal of retinal ganglion cell dysfunction after surgical reduction of intraocular pressure. 
  • Rod differentiation factor NRL activates the expression of nuclear receptor NR2E3 to suppress the development of cone photoreceptors. 
  • Role for the target enzyme in deactivation of photoreceptor G protein in vivo. 
  • SAFETY PROFILE OF OCRIPLASMIN FOR SYMPTOMATIC VITREOMACULAR ADHESION: A Comprehensive Analysis of Premarketing and Postmarketing Experiences. 
  • Safety and pharmacokinetics of an intraocular fluocinolone acetonide sustained delivery device. 
  • Safety and pharmokinetics of triamcinolone hexacetonide in rabbit eyes. 
  • Spectral sensitivity, spatial resolution and temporal resolution and their implications for conspecific signalling in cleaner shrimp. 
  • Spontaneous retinal reattachment in incontinentia pigmenti. 
  • Targeted inactivation of synaptic HRG4 (UNC119) causes dysfunction in the distal photoreceptor and slow retinal degeneration, revealing a new function. 
  • 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. 
  • The Prevalence of Hydroxychloroquine Retinopathy and Toxic Dosing, and the Role of the Ophthalmologist in Reducing Both. 
  • The impact of intraocular pressure reduction on retinal ganglion cell function measured using pattern electroretinogram in eyes receiving latanoprost 0.005% versus placebo. 
  • The isolated perfused frog eye: a useful preparation for the investigation of drug effects on retinal function. 
  • The lack of toxicity of intravitreally administered triamcinolone acetonide. 
  • The ocular phenotype of the Bardet-Biedl syndrome. Comparison to non-syndromic retinitis pigmentosa. 
  • The oral iron chelator deferiprone protects against iron overload-induced retinal degeneration. 
  • The oral iron chelator deferiprone protects against systemic iron overload-induced retinal degeneration in hepcidin knockout mice. 
  • The role of cystoid macular edema as a marker in the progression of non-paraneoplastic autoimmune retinopathy. 
  • Transducin gamma-subunit sets expression levels of alpha- and beta-subunits and is crucial for rod viability. 
  • Transformation of cone precursors to functional rod photoreceptors by bZIP transcription factor NRL. 
  • Treatment of adult-onset acute macular retinoschisis in enhanced s-cone syndrome with oral acetazolamide. 
  • Uniocular vascular occlusion in a paraplegic hybrid monkey. A clinicopathologic study. 
  • Usher syndrome: correlation between visual field size and maximal ERG response b-wave amplitude. 
  • Variations in opsin coding sequences cause x-linked cone dysfunction syndrome with myopia and dichromacy. 
  • Visual physiology underlying orientation and diel behavior in the sand beach amphipod Talorchestia longicornis. 
  • Whole-exome sequencing implicates UBE3D in age-related macular degeneration in East Asian populations. 
  • X-linked high myopia associated with cone dysfunction. 
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  Keywords of People

  • Bowes Rickman, Catherine, Professor of Ophthalmology, Cell Biology
  • Hogan, Brigid L. M., George Barth Geller Professor, Cell Biology