• "Congenital Stationary Night Blindness: Structure, Function and Genotype - Phenotype Correlations in a cohort of 122 patients."
• "The Saddest Waste" - Disability, Heredity, and the Artist's Eye
• 3D Printing of Multimaterial Contact Lenses
• A Binocular Color Line-Scanning Stereo Vision System for Heavy Rail Surface Detection and Correction Method of Motion Distortion
• A Comparative Study of the Sensitivity and Specificity of the Ishihara Test With Various Displays
• A Study of Visual Functions Amongst Primary Open-Angle Glaucoma Patients in Abuja, Nigeria
• AAV Serotypes and Their Suitability for Retinal Gene Therapy
• 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 Showing Compound Heterozygous Mutations in ATF6 by Whole Exome Sequencing: A Rare Case Report
• Achromatopsia-Visual Cortex Stability and Plasticity in the Absence of Functional Cones
• Achromatopsia: Long term visual performance and clinical characteristics
• Alterations in choroidal circulatory dynamics and choroidal thickness before and after treatment in posterior scleritis
• An early onset cone dystrophy due to CEP290 mutation: a case report
• Analysis of Suspected Achromatopsia by Multimodal Diagnostic Testing
• Analysis of suspected Achromatopsia by multimodal Diagnostics
• Application of patient-derived induced pluripotent stem cells and organoids in inherited retinal diseases
• Awareness for glaucoma in the general population
• Center Deviation Measurement of Color Contact Lenses Based on a Deep Learning Model and Hough Circle Transform
• Chromatic Pupillometry as a Putative Screening Tool for Heritable Retinal Disease in Rhesus Macaques
• Chromatic vision and structural assessment in primary congenital glaucoma
• Chromatic visual evoked potentials: A review of physiology, methods and clinical applications
• Clinical characterizations and molecular genetic study of two co-segregating variants in PDZD7 and PDE6C genes leading simultaneously to non-syndromic hearing loss and achromatopsia
• Clinical correlates of pareidolias and color discrimination deficits in idiopathic REM sleep behavior disorder and Parkinson's disease
• 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 in the Mountains
• Colors in the mind's eye
• Colour perception develops throughout childhood with increased risk of deficiencies in children born prematurely
• Colour vision deficiency in teaching dermatology
• Comparison of Two Printed Pseudoisochromatic Tests for Color Vision Assessment
• Compensatory Cone-Mediated Mechanisms in Inherited Retinal Degeneration Mouse Models: A Functional and Gene Expression Analysis
• Congenital Stationary Night Blindness Structure, Function and Genotype-Phenotype Correlations in a Cohort of 122 Patients
• Contributed Session III: AAV-mediated gene therapy for PDE6C achromatopsia: Progress and challenges
• Dyschromatopsia: a comprehensive analysis of mechanisms and cutting-edge treatments for color vision deficiency
• Dysthyroid Optic Neuropathy
• Electroretinography in congenital nystagmus patients with a normal fundus examination
• Empirical tests of the effectiveness of EnChroma multi-notch filters for enhancing color vision in deuteranomaly
• Endoplasmic reticulum stress: molecular mechanism and therapeutic targets
• Evaluation of contrast sensitivity in patients with congenital red-green color vision deficiency
• fMRI and gene therapy in adults with CNGB3 mutation
• Functional evaluation allows ACMG/AMP-based re-classification of CNGA3 variants associated with achromatopsia
• Ga₂O₃ Bipolar Heterojunction-Based Optoelectronic Synapse Array with Visual Attention
• HIGH MYOPIA IS COMMON IN PATIENTS WITH X-LINKED RETINOPATHIES: Myopic Maculopathy Analysis
• How the orientation of the color gamut of natural scenes influences color discrimination in red-green dichromacy
• Identifying missing pieces in color vision defects: a genome-wide association study in Silk Road populations
• Idiopathic hypertrophic pachymeningitis in a patient with a history of diffuse large B cell lymphoma
• Image Data-Centric Visual Feature Selection on Roll-to-Roll Slot-Die Coating Systems for Edge Wave Coating Defect Detection
• Impact of blur on clinical and occupational colour vision test results
• Inhibition of Ryanodine Receptor 1 Reduces Endoplasmic Reticulum (ER) Stress and Promotes ER Protein Degradation in Cyclic Nucleotide-Gated Channel Deficiency
• Investigation of the color discrimination ability using the Farnsworth-Munsell 100-hue test and structural changes by SS-OCT in patients with transfusion-dependent beta-thalassemia
• Keratoconus, Dry Eye Syndrome, Overnight Orthokeratology, Achromatopsia and Uveitis in Children
• Longitudinal Assessment of OCT-Based Measures of Foveal Cone Structure in Achromatopsia
• Molecular and Clinical Characterization of <em>CNGA3</em> and <em>CNGB3</em> Genes in Brazilian Patients Affected with Achromatopsia
• Molecular and Clinical Characterization of CNGA3 and CNGB3 Genes in Brazilian Patients Affected with Achromatopsia
• Molecular Mechanisms Governing Sight Loss in Inherited Cone Disorders
• Morphological and Functional Aspects and Quality of Life in Patients with Achromatopsia
• Novel ATF6 homozygous variant in a Chinese patient with achromatopsia
• Ocular findings in Jansen metaphyseal chondrodysplasia
• Optic Neuropathy Associated with POLG Mutations: A Case Series and Literature Review
• Phenotype and genotype of 15 Saudi patients with achromatopsia: A case series
• Phenotypic characteristics of Danish patients with achromatopsia
• Phenotyping and genotyping inherited retinal diseases: Molecular genetics, clinical and imaging features, and therapeutics of macular dystrophies, cone and cone-rod dystrophies, rod-cone dystrophies, Leber congenital amaurosis, and cone dysfunction syndro
• Portable Multi-focal Visual Evoked Potential Diagnostics for Multiple Sclerosis/Optic Neuritis patients
• Poster Session II: Non-degenerating double cone opsin knockout mouse model of blue cone monochromacy
• Poster Session II: XR-based personalized active aid for color deficient observers
• Pre-Descemet's endothelial keratoplasty with glued intraocular lens implantation with pinhole pupilloplasty in a case of ocular comorbidity in achromatopsia
• Predicted effectiveness of EnChroma multi-notch filters for enhancing color perception in anomalous trichromats
• 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
• Prevalence and genotypic frequency of color vision defects among primary schoolchildren in Adama Town, Eastern Ethiopia
• Prevalence of Congenital Color Vision Deficiency in Southern Taiwan and Detection of Female Carriers by Visual Pigment Gene Analysis
• Pro-Con Debate: Perioperative Research Should Be Color-Blind
• Rapid measurement and machine learning classification of colour vision deficiency
• Rationally blind? Rationality polarizes policy support for colour blindness versus multiculturalism
• Research on defect detection of bottle cap interior based on low-angle and large divergence angle vision system
• Retinal Dystrophies
• S-cone contribution to oscillatory potentials in patients with blue cone monochromacy
• Safety and Efficacy of Adeno-Associated Viral Gene Therapy in Patients With Retinal Degeneration: A Systematic Review and Meta-Analysis
• Screening for colour vision deficiency is needed in all children, not just those born prematurely
• Seeing color following gene augmentation therapy in achromatopsia
• Should Colour Vision Deficiency be a Factor for Considering Admission to Nursing Education Programs?
• Should medicine be colour blind?
• Sirolimus Induced Toxic Optic Neuropathy
• Sstr2 Defines the Cone Differentiation-Competent Late-Stage Retinal Progenitor Cells in the Developing Mouse Retina
• Statistical Evaluation of ERG Responses: A New Method to Validate Cycle-by-Cycle Recordings in Advanced Retinal Degenerations
• Structural and functional rescue of cones carrying the most common cone opsin C203R missense mutation
• SUBCLINICAL OPTIC NEURITIS
• Test time affects Farnsworth D15 outcomes in practiced, but not unpracticed, subjects with color vision deficiency
• Tests for Potential Vision
• The construction of genetics teaching resources related to colour blindness and their application in genetics teaching
• The endoplasmic reticulum: Homeostasis and crosstalk in retinal health and disease
• The genetic basis of clinically-suspected achromatopsia in the United Arab Emirates
• The impact of display saturation on visual search performance in congenital colour vision deficiency
• The VA-CAL Test Quantifies Improvement of Visual Acuity in Achromatopsia by Means of Short-Wave Cutoff Filter Glasses in Daily Living Conditions
• Unusual OCT findings in a patient with CABP4-associated cone-rod synaptic disorder
• Vision restoration: Little red booster
• Vision-related quality of life, photoaversion, and optical rehabilitation in achromatopsia
• Visual evoked potentials in patients with congenital color vision deficiency