Purpose It is unknown which retinal cells are involved in the retina-to-sclera signaling cascade causing myopia. As inherited retinal dystrophies (IRD) are characterized by dysfunction of a single retinal cell type and have a high risk of refractive errors, a study investigating the affected cell type, causal gene, and refractive error in IRDs may provide insight herein. Design Case-control study. Methods STUDY POPULATION: Total of 302 patients with IRD from 2 ophthalmogenetic centers in the Netherlands. REFERENCE POPULATION: Population-based Rotterdam Study-III and Erasmus Rucphen Family Study (N = 5550). Distributions and mean spherical equivalent (SE) were calculated for main affected cell type and causal gene; and risks of myopia and hy...
Inherited retinal degenerative diseases are one of the leading causes of childhood blindness. While ...
Inherited retinal degenerative diseases are one of the leading causes of childhood blindness. While ...
International audienceOBJECTIVE:To determine the refractive error in patients with autosomal recessi...
Purpose It is unknown which retinal cells are involved in the retina-to-sclera signaling cascade cau...
markdownabstractPURPOSE: It is unknown which retinal cells are involved in the retina-to-sclera sign...
PURPOSE: It is unknown which retinal cells are involved in the retina-to-sclera signaling cascade ca...
PurposeTo illustrate the importance of systemic evaluation in retinal dystrophies through examples o...
Contains fulltext : 147477.pdf (publisher's version ) (Open Access)Defects in over...
Inherited retinal dystrophies (IRDs) are congenital retinal degenerative diseases that have various ...
Purpose: To describe the clinical and genetic spectrum of RP1-associated retinal dystrophies. Method...
International audiencePhenotypes observed in a large cohort of patients with cone and cone-rod dystr...
Retinal dystrophies comprise relatively rare but devastating causes of progressive vision loss. They...
This study aimed to identify novel genetic loci and genes responsible for a number of inherited reti...
Purpose: To describe the clinical and genetic spectrum of RP1-associated retinal dystrophies. Method...
Inherited retinal dystrophies (IRD) is a vast group of genetically determined diseases characterized...
Inherited retinal degenerative diseases are one of the leading causes of childhood blindness. While ...
Inherited retinal degenerative diseases are one of the leading causes of childhood blindness. While ...
International audienceOBJECTIVE:To determine the refractive error in patients with autosomal recessi...
Purpose It is unknown which retinal cells are involved in the retina-to-sclera signaling cascade cau...
markdownabstractPURPOSE: It is unknown which retinal cells are involved in the retina-to-sclera sign...
PURPOSE: It is unknown which retinal cells are involved in the retina-to-sclera signaling cascade ca...
PurposeTo illustrate the importance of systemic evaluation in retinal dystrophies through examples o...
Contains fulltext : 147477.pdf (publisher's version ) (Open Access)Defects in over...
Inherited retinal dystrophies (IRDs) are congenital retinal degenerative diseases that have various ...
Purpose: To describe the clinical and genetic spectrum of RP1-associated retinal dystrophies. Method...
International audiencePhenotypes observed in a large cohort of patients with cone and cone-rod dystr...
Retinal dystrophies comprise relatively rare but devastating causes of progressive vision loss. They...
This study aimed to identify novel genetic loci and genes responsible for a number of inherited reti...
Purpose: To describe the clinical and genetic spectrum of RP1-associated retinal dystrophies. Method...
Inherited retinal dystrophies (IRD) is a vast group of genetically determined diseases characterized...
Inherited retinal degenerative diseases are one of the leading causes of childhood blindness. While ...
Inherited retinal degenerative diseases are one of the leading causes of childhood blindness. While ...
International audienceOBJECTIVE:To determine the refractive error in patients with autosomal recessi...