Blue Cone Monochromatism Latest Advances

Find the Latest Research About Blue Cone Monochromatism

Last Updated: 04/28/2026

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Found 146 publications

Advanced therapeutic approaches for inherited retinal diseases: an umbrella review.

Advanced therapeutic approaches for inherited retinal diseases: an umbrella review.

Journal: BMJ open
Published: February 27, 2026

Blue Cone Monochromatism.

Blue Cone Monochromatism.

Journal: Advances in experimental medicine and biology
Published: July 30, 2025

Review of Four Refined Clinical Entities in Hereditary Retinal Disorders from Japan.

Review of Four Refined Clinical Entities in Hereditary Retinal Disorders from Japan.

Journal: International journal of molecular sciences
Published: March 19, 2025

Natural course of refractive errors in early onset inherited retinal diseases.

Natural course of refractive errors in early onset inherited retinal diseases.

Journal: Eye (London, England)
Published: March 06, 2025

Whole exome sequencing reveals pathogenic variants in CNGA3, CACNA1F, and RPGRIP1 in consanguineous Pakistani families with diverse retinal phenotypes.

Whole exome sequencing reveals pathogenic variants in CNGA3, CACNA1F, and RPGRIP1 in consanguineous Pakistani families with diverse retinal phenotypes.

Journal: PloS one
Published: October 28, 2024

Frequency and Genetic Spectrum of Inherited Retinal Dystrophies in a Large Dutch Pediatric Cohort: The RD5000 Consortium.

Frequency and Genetic Spectrum of Inherited Retinal Dystrophies in a Large Dutch Pediatric Cohort: The RD5000 Consortium.

Journal: Investigative ophthalmology & visual science
Published: August 27, 2024

The construction of genetics teaching resources related to colour blindness and their application in genetics teaching.

The construction of genetics teaching resources related to colour blindness and their application in genetics teaching.

Journal: Yi chuan = Hereditas
Published: April 17, 2024

Congenital Stationary Night Blindness: Structure, Function and Genotype-Phenotype Correlations in a Cohort of 122 Patients.

Congenital Stationary Night Blindness: Structure, Function and Genotype-Phenotype Correlations in a Cohort of 122 Patients.

Journal: Ophthalmology. Retina
Published: February 02, 2024

HIGH MYOPIA IS COMMON IN PATIENTS WITH X-LINKED RETINOPATHIES: Myopic Maculopathy Analysis.

HIGH MYOPIA IS COMMON IN PATIENTS WITH X-LINKED RETINOPATHIES: Myopic Maculopathy Analysis.

Journal: Retina (Philadelphia, Pa.)
Published: December 20, 2023

Colour vision impairments in bipolar disorder: A systematic review.

Colour vision impairments in bipolar disorder: A systematic review.

Journal: Neuroscience applied
Published: December 08, 2023

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 syndromes.

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 syndromes.

Journal: Progress in retinal and eye research
Published: October 26, 2023

Unusual OCT findings in a patient with CABP4-associated cone-rod synaptic disorder.

Unusual OCT findings in a patient with CABP4-associated cone-rod synaptic disorder.

Journal: Documenta ophthalmologica. Advances in ophthalmology
Published: August 25, 2023
Showing 1-12 of 146

Last Updated: 04/28/2026