• A case of schizophrenia with congenital color vision deficiency: From the perspective of color universal design to promote medication adherence
• A demonstration of cone function plasticity after gene therapy in achromatopsia
• A diagnostic model based on color vision examination for dysthyroid optic neuropathy using Hardy-Rand-Rittler color plates
• A new mutation in the <em>PDE6C</em> gene in achromatopsia
• Achromatic and chromatic contrast discrimination in patients with type 2 diabetes
• Achromatopsia : Clinical aspects, diagnostics, genes, brain and quality of life
• Achromatopsia Showing Compound Heterozygous Mutations in <em>ATF6</em> by Whole Exome Sequencing: A Rare Case Report
• Achromatopsia-Visual Cortex Stability and Plasticity in the Absence of Functional Cones
• Achromatopsia: Genetics and Gene Therapy
• Achromatopsia: Long term visual performance and clinical characteristics
• Alterations in choroidal circulatory dynamics and choroidal thickness before and after treatment in posterior scleritis
• Ametropia and Emmetropization in CNGB3 Achromatopsia
• An early onset cone dystrophy due to CEP290 mutation: a case report
• Analysis of Suspected Achromatopsia by Multimodal Diagnostic Testing
• Application of patient-derived induced pluripotent stem cells and organoids in inherited retinal diseases
• Assessing the impact of color blindness on the ability of identifying benign and malignant skin lesions by naked-eye examination
• Association between cognition and color discrimination among Lebanese patients with schizophrenia
• Awareness for glaucoma in the general population
• Axial Length Distributions in Patients With Genetically Confirmed Inherited Retinal Diseases
• Azole-Induced Color Vision Deficiency Associated with Thyroid Hormone Signaling: An Integrated <em>In Vivo</em>, <em>In Vitro</em>, and <em>In Silico</em> Study
• Central retina plays a decisive role in the suppression of pupillary escape
• Clinical and Genetic Features of Korean Patients with Achromatopsia
• Clinical and Molecular Characterization of Achromatopsia Patients: A Longitudinal Study
• Coats-like vasculopathy in inherited retinal disease: prevalence, characteristics, genetics and management
• Coats-like Vasculopathy in Inherited Retinal Disease: Prevalence, Characteristics, Genetics, and Management
• Color perception on Ishihara plates with red lenses in subjects with low vision due to retinal diseases
• Color Vision Deficiency Survey in Anatomic Pathology
• Color Vision in Blue Cone Monochromacy: Outcome Measures for a Clinical Trial
• Colour perception deficits after posterior stroke: Not so rare after all?
• Coloured filters can simulate colour deficiency in normal vision but cannot compensate for congenital colour vision deficiency
• Comparing Retinal Structure in Patients with Achromatopsia and Blue Cone Monochromacy Using OCT
• Comparison of Two Printed Pseudoisochromatic Tests for Color Vision Assessment
• Comprehensive variant spectrum of the CNGA3 gene in patients affected by achromatopsia
• Deep Phenotyping of PDE6C-Associated Achromatopsia
• Development of a Chromatic Pupillography Protocol for the First Gene Therapy Trial in Patients With CNGA3-Linked Achromatopsia
• Diagnosis and Treatment Options for Achromatopsia: A Review of the Literature
• ELECTRONEGATIVE ELECTRORETINOGRAM IN ACHROMATOPSIA
• Embryonic mercury exposure in zebrafish: Alteration of metabolites and gene expression, related to visual and behavioral impairments
• Endoplasmic reticulum stress: molecular mechanism and therapeutic targets
• First-in-Human Gene Therapy Trial of AAV8-hCARp.hCNGB3 in Adults and Children With CNGB3-associated Achromatopsia
• Foveal Cone Structure in Patients With Blue Cone Monochromacy
• Foveal hypoplasia in a patient with achromatopsia
• Frequency-dependent retinal responsiveness to sinusoidal electrical stimulation in achromatopsia
• Genetic and Clinical Characterization of Danish Achromatopsia Patients
• Genotypic and Phenotypic Spectrum of Foveal Hypoplasia: A Multicenter Study
• Glaucomatous optic nerve damage in the contralateral eye of a patient with peripapillary retinoschisis: a case report
• HIGH MYOPIA IS COMMON IN PATIENTS WITH X-LINKED RETINOPATHIES: Myopic Maculopathy Analysis
• High visibility colored fabrics for normal trichromats and individuals with color vision defects in a sunset-simulated environment
• High-Efficiency CRISPR/Cas9-Mediated Correction of a Homozygous Mutation in Achromatopsia-Patient-Derived iPSCs
• Impact of color vision deficiency on the quality of life in a sample of Indian population: Application of the CVD-QoL tool
• In vivo imaging of a cone mosaic in a patient with achromatopsia associated with a GNAT2 variant
• Increased H3K27 trimethylation contributes to cone survival in a mouse model of cone dystrophy
• Inhibition of Ryanodine Receptor 1 Reduces Endoplasmic Reticulum (ER) Stress and Promotes ER Protein Degradation in Cyclic Nucleotide-Gated Channel Deficiency
• Keratoconus, Dry Eye Syndrome, Overnight Orthokeratology, Achromatopsia and Uveitis in Children
• Longitudinal Evaluation of Changes in Retinal Architecture Using Optical Coherence Tomography in Achromatopsia
• Macular Pseudocoloboma in Achromatopsia
• Mitochondria and Endoplasmic Reticulum Stress in Retinal Organoids from Patients with Vision Loss
• Molecular and Clinical Characterization of <em>CNGA3</em> and <em>CNGB3</em> Genes in Brazilian Patients Affected with Achromatopsia
• Morphological and Functional Aspects and Quality of Life in Patients with Achromatopsia
• Mouse Models of Achromatopsia in Addressing Temporal "Point of No Return" in Gene-Therapy
• Multiexon deletion alleles of ATF6 linked to achromatopsia
• Multimodal imaging including semiquantitative short-wavelength and near-infrared autofluorescence in achromatopsia
• New pathogenic variants of ALMS1 gene in two Chinese families with Alström Syndrome
• Nonlinear cortical encoding of color predicts enhanced McCollough effects in anomalous trichromats
• Novel <em>OPN1LW/OPN1MW</em> Exon 3 Haplotype-Associated Splicing Defect in Patients with X-Linked Cone Dysfunction
• Novel Bi-allelic PDE6C Variant Leads to Congenital Achromatopsia
• Novel mutations in the gene for α-subunit of retinal cone cyclic nucleotide-gated channels in a Japanese patient with congenital achromatopsia
• Ocular Survey in Kathmandu University Medical Students
• Optical Gap Biomarker in Cone-Dominant Retinal Dystrophy
• Oscillatory Potentials in Achromatopsia as a Tool for Understanding Cone Retinal Functions
• Outer retinal transduction by AAV2-7m8 following intravitreal injection in a sheep model of CNGA3 achromatopsia
• Paternal Uniparental Isodisomy of Chromosome 2 in a Patient with <em>CNGA3</em>-Associated Autosomal Recessive Achromatopsia
• Poster Session II: Non-degenerating double cone opsin knockout mouse model of blue cone monochromacy
• Prenylation is essential for the enrichment of cone phosphodiesterase-6 (PDE6) in outer segments and efficient cone phototransduction
• Presumed topiramate-induced retinopathy in a 58-year-old woman
• Quantitative and qualitative characterization of retinal dystrophies in canine models of inherited retinal diseases using spectral domain optical coherence tomography (SD-OCT)
• Reduced cone photoreceptor function and subtle systemic manifestations in two siblings with loss of SCLT1
• Refractive errors among commercial drivers
• REPEATABILITY AND LONGITUDINAL ASSESSMENT OF FOVEAL CONE STRUCTURE IN CNGB3-ASSOCIATED ACHROMATOPSIA
• Residual Foveal Cone Structure in CNGB3-Associated Achromatopsia
• Rod Monochromatism (Achromatopsia)
• Safety and Efficacy of Adeno-Associated Viral Gene Therapy in Patients With Retinal Degeneration: A Systematic Review and Meta-Analysis
• Seeing color following gene augmentation therapy in achromatopsia
• Six Years and Counting: Restoration of Photopic Retinal Function and Visual Behavior Following Gene Augmentation Therapy in a Sheep Model of <em>CNGA3</em> Achromatopsia
• Spheno-Orbital Meningioma and Vision Impairment-Case Report and Review of the Literature
• Stem cells for treating retinal degeneration
• Systematic analysis of CNGA3 splice variants identifies different mechanisms of aberrant splicing
• Tests for Potential Vision
• The causal mutation in ARR3 gene for high myopia and progressive color vision defect
• The Clinical Phenotype of CNGA3-Related Achromatopsia: Pretreatment Characterization in Preparation of a Gene Replacement Therapy Trial
• The impact of display saturation on visual search performance in congenital colour vision deficiency
• The landscape of submicroscopic structural variants at the <em>OPN1LW/OPN1MW</em> gene cluster on Xq28 underlying blue cone monochromacy
• The VA-CAL Test Quantifies Improvement of Visual Acuity in Achromatopsia by Means of Short-Wave Cutoff Filter Glasses in Daily Living Conditions
• Their loss is our gain: regressive evolution in vertebrates provides genomic models for uncovering human disease loci
• Three-year results of phase I retinal gene therapy trial for CNGA3-mutated achromatopsia: results of a non randomised controlled trial
• Unique Haplotypes in OPN1LW as a Common Cause of High Myopia With or Without Protanopia: A Potential Window Into Myopic Mechanism
• UV/blue/green converted efficient red-NIR photoluminescence in Cr incorporated MgAl₂O₄nanocrystals: Site selective emission tailored through cation inversion and intrinsic defects
• Vision-Related Quality of Life in Primary Angle-Closure Glaucoma Patients with or without Visual Field Dysfunction
• Visual Characteristics of Adults with Long-Standing History of Dietary Exposure to Mercury in Grassy Narrows First Nation, Canada
• Word and color impressions measured with normal and simulated deutan color stimulus sets in color vision normal and deuteranopic observers