Chorioretinal degeneration

OXYS rats are characterized by early development of cataract and chorioretinal degeneration with clinical manifestations similar… (More)

Sveinsson's chorioretinal atrophy (SCRA) is an autosomal dominant eye disease characterized by bilateral chorioretinal… (More)

PURPOSE To report extensive chorioretinal atrophy during the long-term course of Vogt-Koyanagi-Harada (VKH) disease not treated… (More)

PURPOSE To study the early changes in the outer retina of myopic eyes, we performed fundus reflection foveal cone densitometry in… (More)

PURPOSE To describe the ophthalmologic findings and electroretinograms in patients with microcephaly and chorioretinal… (More)

Deficiency of ornithine–δ–aminotransferase (OAT) in humans causes hyperornithinaemia and gyrate atrophy (GA), a blinding… (More)

Deficiency of ornithine-delta-aminotransferase (OAT) in humans causes hyperornithinaemia and gyrate atrophy (GA), a blinding… (More)

We recorded full-field electroretinograms from a family with two daughters with microcephaly and chorioretinal degeneration and a… (More)

A light and electron microscopic study of an eye from a 79-year-old woman diagnosed as having sector retinitis pigmentosa is… (More)

In the same family the author found: a. Fives males with chorioretinal degeneration. b. Seven heterozygous females with a golden… (More)