Disease: Achromatopsia 3
- A case of schizophrenia with congenital color vision deficiency: From the perspective of color universal design to promote medication adherence
- A Computer-Based Farnsworth-Munsell 100-Hue (CFM-100) Test in Pilots' Medical Assessments
- A demonstration of cone function plasticity after gene therapy in achromatopsia
- A new mutation in the <em>PDE6C</em> gene in achromatopsia
- 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
- An early onset cone dystrophy due to CEP290 mutation: a case report
- Analysis of Suspected Achromatopsia by Multimodal Diagnostic Testing
- Association Between Color Vision Deficiency and Myopia in Chinese Children Over a Five-Year Period
- Burden of ocular morbidities and color blindness among school-attending children in a foothill town of Uttarakhand State
- Central retina plays a decisive role in the suppression of pupillary escape
- Circumpapillary Retinal Nerve Fiber Layer OCT Imaging in a Parkinson's Disease Cohort-A Multidisciplinary Approach in a Clinical Research Hospital
- Clinical analysis of the Konan-Waggoner D15 color vision test using the Surface-Pro display
- Clinical and Genetic Features of Korean Patients with Achromatopsia
- Clinically relevant colour album test for the colour defective medical student
- Color Vision Testing, Standards, and Visual Performance of the U.S. Military
- Colour perception deficits after posterior stroke: Not so rare after all?
- ColourSpot, a novel gamified tablet-based test for accurate diagnosis of color vision deficiency in young children
- 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
- Cone contrast test-HD: sensitivity and specificity in red-green dichromacy and the impact of age
- Congenital Colour Vision Deficiency among Patients Attending Outpatient Department of Ophthalmology in a Tertiary Care Centre: A Descriptive Cross-sectional Study
- Detection of early bruises on apples using hyperspectral reflectance imaging coupled with optimal wavelengths selection and improved watershed segmentation algorithm
- Diagnosis of colour vision deficits using eye movements
- Dissociation between red and white stimulus perception: A perimetric quantification of protanopic color vision deficiencies
- Effect of laser eye protection devices on color perception
- Electrophysiology-Guided Genetic Characterisation Maximises Molecular Diagnosis in an Irish Paediatric Inherited Retinal Degeneration Population
- 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
- Ethambutol optic neuropathy in the extended anti-tubercular therapy regime: A systematic review
- First-in-Human Gene Therapy Trial of AAV8-hCARp.hCNGB3 in Adults and Children With CNGB3-associated 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
- HIGH MYOPIA IS COMMON IN PATIENTS WITH X-LINKED RETINOPATHIES: Myopic Maculopathy Analysis
- High-Efficiency CRISPR/Cas9-Mediated Correction of a Homozygous Mutation in Achromatopsia-Patient-Derived iPSCs
- HIGH-RESOLUTION SPECTRAL-DOMAIN OPTICAL COHERENCE TOMOGRAPHY OF MULTIPLE EVANESCENT WHITE DOT SYNDROME
- Identifiable universal fluorescent multiplex PCR equipped with capillary electrophoresis for genotyping of exons 1 to 5 in human red and green pigment genes
- Impact of color vision deficiency on the quality of life in a sample of Indian population: Application of the CVD-QoL tool
- IMPAIRMENTS OF L-CONE/M-CONE AND S-CONE-MEDIATED COLOR DISCRIMINATION IN MACULAR TELANGIECTASIA TYPE II
- Intermixing the <em>OPN1LW</em> and <em>OPN1MW</em> Genes Disrupts the Exonic Splicing Code Causing an Array of Vision Disorders
- Keratoconus, Dry Eye Syndrome, Overnight Orthokeratology, Achromatopsia and Uveitis in Children
- Lanthony D15 for Occupational Testing: Short-term Repeatability
- Limitation of standard pseudoisochromatic plates in identifying colour vision deficiencies when compared with genetic testing
- Longitudinal Evaluation of Changes in Retinal Architecture Using Optical Coherence Tomography in Achromatopsia
- Macular Pseudocoloboma in Achromatopsia
- Mapping Visual Field Defects With fMRI - Impact of Approach and Experimental Conditions
- MFN1 augmentation prevents retinal degeneration in a Charcot-Marie-Tooth type 2A mouse model
- Mitochondria and Endoplasmic Reticulum Stress in Retinal Organoids from Patients with Vision Loss
- 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
- 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
- Non-syndromic inherited retinal diseasesĀ in Poland: Genes, mutations, and phenotypes
- Novel <em>OPN1LW/OPN1MW</em> Exon 3 Haplotype-Associated Splicing Defect in Patients with X-Linked Cone Dysfunction
- Ocular Survey in Kathmandu University Medical Students
- 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
- Poster Session II: XR-based personalized active aid for color deficient observers
- Potential value of color vision aids for varying degrees of color vision deficiency
- Prenylation is essential for the enrichment of cone phosphodiesterase-6 (PDE6) in outer segments and efficient cone phototransduction
- Preservation of endoplasmic reticulum (ER) Ca<sup>2+</sup> stores by deletion of inositol-1,4,5-trisphosphate receptor type 1 promotes ER retrotranslocation, proteostasis, and protein outer segment localization in cyclic nucleotide-gated chann
- Presumed topiramate-induced retinopathy in a 58-year-old woman
- Prevalence and awareness levels of color blindness among students of faculty of dentistry and dental prosthesis technology program
- Prevalence and predictors of colour vision defects among Egyptian university students
- Prevalence of Color Vision Anomalies among Dental Professionals
- Prevalence of color vision deficiency among school-going boys in South India
- Prevalence of Congenital Color Vision Deficiency in Southern Taiwan and Detection of Female Carriers by Visual Pigment Gene Analysis
- Prevalence of refractive errors and color vision deficiency in a population of industry-workers in Abhar, Iran
- Quantitative and qualitative characterization of retinal dystrophies in canine models of inherited retinal diseases using spectral domain optical coherence tomography (SD-OCT)
- Reduced ability to discriminate colours - an under-recognised feature of depressive disorders? A pilot study
- Reduced cone photoreceptor function and subtle systemic manifestations in two siblings with loss of SCLT1
- Refractive errors among commercial drivers
- Relatively mild blue cone monochromacy phenotype caused by various haplotypes in the L- and M-cone opsin genes
- Risk assessment of chemical mixtures by benchmark dose-principle component analysis approach in occupational exposure
- Screening for mild anomalous trichromacy using the Ishihara plates test
- Seeing color following gene augmentation therapy in achromatopsia
- Silent progressive bilateral papillitis after COVID-19 vaccination: A case report
- Sleep and circadian phenotype in people without cone-mediated vision: a case series of five <em>CNGB3</em> and two <em>CNGA3</em> patients
- Spheno-Orbital Meningioma and Vision Impairment-Case Report and Review of the Literature
- Systematic analysis of CNGA3 splice variants identifies different mechanisms of aberrant splicing
- Tackling the Challenges of Product Development Through a Collaborative Rare Disease Network: The Foundation Fighting Blindness Consortium
- Tests for Potential Vision
- The impact of display saturation on visual search performance in congenital colour vision deficiency
- The safety and efficacy of gene therapy treatment for monogenic retinal and optic nerve diseases: A systematic review
- 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
- Three-year results of phase I retinal gene therapy trial for CNGA3-mutated achromatopsia: results of a non randomised controlled trial
- Two Novel Disease-Causing Variants in the PDE6C Gene Underlying Achromatopsia
- 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 MgAl<sub>2</sub>O<sub>4</sub>nanocrystals: 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 and ocular findings in a family with X-linked cone dysfunction and protanopia
- Visual field defects due to optic nerve drusen in Afro-Caribbean patients: A case series of 16 eyes
- Word and color impressions measured with normal and simulated deutan color stimulus sets in color vision normal and deuteranopic observers