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Purpose To identify the causative paired box 6 (PAX6) mutation in a family with autosomal dominant aniridia. Methods A family… Expand UNLABELLED
PURPOSE. To identify the risk factors for development of myopic choroidal neovascularization (mCNV), a major cause of… Expand Ninety patients (163 eyes) with tilted disc syndrome were examined in order to show possible chorioretinal degenerative lesions… Expand PURPOSE
To report extensive chorioretinal atrophy during the long-term course of Vogt-Koyanagi-Harada (VKH) disease not treated… Expand PURPOSE
To describe the ophthalmologic findings and electroretinograms in patients with microcephaly and chorioretinal… Expand We studied 354 eyes with myopic chorioretinal degeneration by means of standard clinical evaluation and fluorescein angiography… Expand A light and electron microscopic study of an eye from a 79-year-old woman diagnosed as having sector retinitis pigmentosa is… Expand The vitreous condition in retinitis pigmentosa, high myopia, peripheral uveitis, and Wagner's disease and in normal eyes was… Expand Four patients with gyrate atrophy of the choroid and retina were studied, all of whom exhibited the hyperornithinemia… Expand Gyrate atrophy of the choroid and retina is an inherited form of chorioretinal degeneration associated with hyperornithinemia. We… Expand