Disease: Achromatopsia 1
- 100% visual inspection of tablets produced with continuous direct compression and coating
- A Bioengineered In Vitro Model to Assess AAV-Based Gene Therapies for Cyclic GMP-Related Disorders
- 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 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
- A Novel Smartphone-Based Color Test for Detection of Color Vision Defects in Age Related Macular Degeneration
- 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: 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
- 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
- Association Between Color Vision Deficiency and Myopia in Chinese Children Over a Five-Year Period
- 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
- 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
- Chromatic discrimination in fixed saturation levels from trichromats and subjects with congenital color vision deficiency
- Circumpapillary Retinal Nerve Fiber Layer OCT Imaging in a Parkinson's Disease Cohort-A Multidisciplinary Approach in a Clinical Research Hospital
- Clinical and Genetic Features of Korean Patients with Achromatopsia
- Clinically relevant colour album test for the colour defective medical student
- 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
- Color Vision Testing, Standards, and Visual Performance of the U.S. Military
- 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
- Congenital Colour Vision Deficiency among Patients Attending Outpatient Department of Ophthalmology in a Tertiary Care Centre: A Descriptive Cross-sectional Study
- Deficits in color detection in patients with Alzheimer disease
- Diagnosis of colour vision deficits using eye movements
- 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
- 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
- Identifiable universal fluorescent multiplex PCR equipped with capillary electrophoresis for genotyping of exons 1 to 5 in human red and green pigment genes
- Identification of the Transcriptional Biomarkers Panel Linked to Pathological Remodelling of the Eye Tissues in Various HD Mouse Models
- Impact of color vision deficiency on the quality of life in a sample of Indian population: Application of the CVD-QoL tool
- Implications of inherited color vision deficiency on occupations: A neglected entity!
- 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
- 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
- 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
- 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
- Ocular Survey in Kathmandu University Medical Students
- Poster Session II: Non-degenerating double cone opsin knockout mouse model of blue cone monochromacy
- 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
- Presumed topiramate-induced retinopathy in a 58-year-old woman
- Prevalence of Color Vision Anomalies among Dental Professionals
- 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
- Relatively mild blue cone monochromacy phenotype caused by various haplotypes in the L- and M-cone opsin genes
- Revisiting color vision standards and testing methods in various occupational groups
- 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
- Spheno-Orbital Meningioma and Vision Impairment-Case Report and Review of the Literature
- Stem cells for treating retinal degeneration
- Structural and functional characterization of an achromatopsia-associated mutation in a phototransduction channel
- Structural changes to primary visual cortex in the congenital absence of cone input in achromatopsia
- Systematic analysis of CNGA3 splice variants identifies different mechanisms of aberrant splicing
- Temporal dynamics of the neural representation of hue and luminance polarity
- Tests for Potential Vision
- The causal mutation in ARR3 gene for high myopia and progressive color vision defect
- 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
- Two-dimensional biocompatible plasmonic contact lenses for color blindness correction
- 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 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