Retinitis Pigmentosa Latest Advances

Primary Bronchiectasis and Chronic Sinus Disease in Retinitis Pigmentosa.

Journal: CHEST pulmonary

Published: September 05, 2026

Pathological Retinal Oscillations across Retinal Diseases: Shared Circuit Mechanisms and Implications for Photopsia.

Journal: Biological & pharmaceutical bulletin

Published: September 02, 2026

Unique retinal phenotype may support pathogenicity of FSCN2 in inherited retinal degenerations: a case report and review of the literature.

Journal: Ophthalmic genetics

Published: August 27, 2026

Coexistence of Retinitis Pigmentosa and Coats-Like Vitreoretinopathy.

Journal: Turkish journal of ophthalmology

Published: August 26, 2026

Non-syndromic adult-onset rod-cone dystrophy.

Journal: Retina (Philadelphia, Pa.)

Published: August 21, 2026

Gene therapy clinical trials for inherited eye diseases: The pediatric perspective.

Journal: European journal of ophthalmology

Published: August 21, 2026

Bubble-Wrapped: An Unusual Developmental Cataract.

Journal: QJM : monthly journal of the Association of Physicians

Published: August 20, 2026

Association Between PS-OCT Derived Polarimetric Entropy and RPE Cellular Metrics Measured With Adaptive Optics Imaging in Retinitis Pigmentosa.

Journal: Investigative ophthalmology & visual science

Published: August 17, 2026

Inherited Retinal Dystrophy in an 11-month-old Infant with Yunis-Varon Syndrome and Homozygous FIG4 Mutation.

Journal: Retinal cases & brief reports

Published: August 14, 2026

Defining a Novel RPGR Phenotype of Sector Retinitis Pigmentosa With Cone Dystrophy.

Journal: Investigative ophthalmology & visual science

Published: August 10, 2026

WDR34 Deficiency Disrupts Retrograde Intraflagellar Transport and Induces Unfolded Protein Response-Driven Inflammation and Retinal Degeneration.

Journal: Investigative ophthalmology & visual science

Published: August 04, 2026

Identification of a Duplication in the RP17 Locus in an Individual With Pathogenic CEP290 Variants: Implications for RP17 Variant Classification.

Journal: Investigative ophthalmology & visual science

Published: August 03, 2026

Retinitis Pigmentosa Latest Advances

Find the Latest Research About Retinitis Pigmentosa

Primary Bronchiectasis and Chronic Sinus Disease in Retinitis Pigmentosa.

Primary Bronchiectasis and Chronic Sinus Disease in Retinitis Pigmentosa.

Pathological Retinal Oscillations across Retinal Diseases: Shared Circuit Mechanisms and Implications for Photopsia.

Pathological Retinal Oscillations across Retinal Diseases: Shared Circuit Mechanisms and Implications for Photopsia.

Unique retinal phenotype may support pathogenicity of FSCN2 in inherited retinal degenerations: a case report and review of the literature.

Unique retinal phenotype may support pathogenicity of FSCN2 in inherited retinal degenerations: a case report and review of the literature.

Coexistence of Retinitis Pigmentosa and Coats-Like Vitreoretinopathy.

Coexistence of Retinitis Pigmentosa and Coats-Like Vitreoretinopathy.

Non-syndromic adult-onset rod-cone dystrophy.

Non-syndromic adult-onset rod-cone dystrophy.

Gene therapy clinical trials for inherited eye diseases: The pediatric perspective.

Gene therapy clinical trials for inherited eye diseases: The pediatric perspective.

Bubble-Wrapped: An Unusual Developmental Cataract.

Bubble-Wrapped: An Unusual Developmental Cataract.

Association Between PS-OCT Derived Polarimetric Entropy and RPE Cellular Metrics Measured With Adaptive Optics Imaging in Retinitis Pigmentosa.

Association Between PS-OCT Derived Polarimetric Entropy and RPE Cellular Metrics Measured With Adaptive Optics Imaging in Retinitis Pigmentosa.

Inherited Retinal Dystrophy in an 11-month-old Infant with Yunis-Varon Syndrome and Homozygous FIG4 Mutation.

Inherited Retinal Dystrophy in an 11-month-old Infant with Yunis-Varon Syndrome and Homozygous FIG4 Mutation.

Defining a Novel RPGR Phenotype of Sector Retinitis Pigmentosa With Cone Dystrophy.

Defining a Novel RPGR Phenotype of Sector Retinitis Pigmentosa With Cone Dystrophy.

WDR34 Deficiency Disrupts Retrograde Intraflagellar Transport and Induces Unfolded Protein Response-Driven Inflammation and Retinal Degeneration.

WDR34 Deficiency Disrupts Retrograde Intraflagellar Transport and Induces Unfolded Protein Response-Driven Inflammation and Retinal Degeneration.

Identification of a Duplication in the RP17 Locus in an Individual With Pathogenic CEP290 Variants: Implications for RP17 Variant Classification.

Identification of a Duplication in the RP17 Locus in an Individual With Pathogenic CEP290 Variants: Implications for RP17 Variant Classification.