Disease: Macular dystrophy- concentric annular
- Bull's eye maculopathy caused by a novel IMPG-1 mutation
- BULL'S EYE MACULOPATHY POSSIBLY DUE TO IRON OVERLOAD IN A CHILD WITH THALASSEMIA MAJOR: A CASE OF POSSIBLE "FERRITIN RETINOPATHY"
- BULL'S EYE MACULOPATHY WITH MUTATIONS IN RDS/PRPH2 AND ROM-1
- Bull's-Eye Maculopathy Associated with Hydroxychloroquine
- Chloroquine retinopathy
- Early onset monocular hydroxychloroquine maculopathy in a systemic lupus erythematosus patient with history of central retinal artery occlusion: a case report
- Genotypic Profile and Clinical Characteristics of CRX-Associated Retinopathy in Koreans
- Heterozygous <em>CRX</em> R90W mutation-associated adult-onset macular dystrophy with phenotype analogous to benign concentric annular macular dystrophy
- Heterozygous CRX R90W mutation-associated adult-onset macular dystrophy with phenotype analogous to benign concentric annular macular dystrophy
- Hydroxychloroquine Causes Early Inner Retinal Toxicity and Affects Autophagosome-Lysosomal Pathway and Sphingolipid Metabolism in the Retina
- Lenses and Spectacles to Prevent Myopia Worsening in Children [Internet]
- MACULAR ATROPHY AND PHENOTYPIC VARIABILITY IN AUTOSOMAL DOMINANT STARGARDT-LIKE MACULAR DYSTROPHY DUE TO PROM1 MUTATION
- Multimodal imaging of benign concentric annular macular dystrophy
- Pathogenic variants in <em>IMPG1</em> cause autosomal dominant and autosomal recessive retinitis pigmentosa
- Presumed veterinary niclosamide-induced retinal toxicity in a human: a case report
- PRPH2 mutation c.582-1G>A causing adult-onset macular dystrophy with a benign concentric annular macular dystrophy phenotype in a family
- PRPH2 mutation c.582-1G>A causing adult-onset macular dystrophy with a benign concentric annular macular dystrophy phenotype in a family
- Quantitative Fundus Autofluorescence in Systemic Chloroquine/Hydroxychloroquine Therapy: One Year Follow-Up
- Retinal dystrophies with bull's-eye maculopathy along with negative ERGs