Disease: Achromatopsia
- "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 diagnostic model based on color vision examination for dysthyroid optic neuropathy using Hardy-Rand-Rittler color plates
- AAV Serotypes and Their Suitability for Retinal Gene Therapy
- 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 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
- Canine and Feline Models of Inherited Retinal Diseases
- Center Deviation Measurement of Color Contact Lenses Based on a Deep Learning Model and Hough Circle Transform
- Chromatic vision and structural assessment in primary congenital glaucoma
- Clinical analysis of the Konan-Waggoner D15 color vision test using the Surface-Pro display
- 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
- Cone contrast test-HD: sensitivity and specificity in red-green dichromacy and the impact of age
- Contributed Session III: AAV-mediated gene therapy for PDE6C achromatopsia: Progress and challenges
- Detection of early bruises on apples using hyperspectral reflectance imaging coupled with optimal wavelengths selection and improved watershed segmentation algorithm
- Dyschromatopsia: a comprehensive analysis of mechanisms and cutting-edge treatments for color vision deficiency
- Dysthyroid Optic Neuropathy
- Effect of laser eye protection devices on color perception
- Electroretinography in congenital nystagmus patients with a normal fundus examination
- Elimination of the color discrimination impairment along the blue-yellow axis in patients with hypothyroidism after treatment with levothyroxine as assessed by the Farnsworth-Munsell 100 hue test
- Empirical tests of the effectiveness of EnChroma multi-notch filters for enhancing color vision in deuteranomaly
- 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
- Functional evaluation allows ACMG/AMP-based re-classification of CNGA3 variants associated with achromatopsia
- Ga<sub>2</sub>O<sub>3</sub> Bipolar Heterojunction-Based Optoelectronic Synapse Array with Visual Attention
- Generation of two human induced pluripotent stem cell lines (ABi001-A and ABi002-A) from cone dystrophy with supernormal rod response patients caused by KCNV2 mutation
- HIGH MYOPIA IS COMMON IN PATIENTS WITH X-LINKED RETINOPATHIES: Myopic Maculopathy Analysis
- 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 color vision deficiency on the quality of life in a sample of Indian population: Application of the CVD-QoL tool
- 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
- Modeling D15 test sequences in red-green anomalous trichromacy
- 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
- Morphological and Functional Aspects and Quality of Life in Patients with Achromatopsia
- Novel ATF6 homozygous variant in a Chinese patient with achromatopsia
- Ocular Survey in Kathmandu University Medical Students
- 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
- Reduced cone photoreceptor function and subtle systemic manifestations in two siblings with loss of SCLT1
- Retinal Dystrophies
- 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
- Screening for mild anomalous trichromacy using the Ishihara plates test
- 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
- Tests for Potential Vision
- The causal mutation in ARR3 gene for high myopia and progressive color vision defect
- 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 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
- The Verriest Lecture: Pathways to color in the eye and brain
- Unique Haplotypes in OPN1LW as a Common Cause of High Myopia With or Without Protanopia: A Potential Window Into Myopic Mechanism
- Unusual OCT findings in a patient with CABP4-associated cone-rod synaptic disorder
- Vision restoration: Little red booster
- Word and color impressions measured with normal and simulated deutan color stimulus sets in color vision normal and deuteranopic observers