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PROGRESSIVE MACULOPATHY IN A CHILD RESULTING FROM VITREOPAPILLARY TRACTION ON A CONGENITALLY ANOMALOUS NERVE. [PDF]
Retin Cases Brief RepKennamer-Chapman RM +2 more
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Gene Therapy for Inherited Retinal Disease: Current Strategies, Personalized Medicine, and Future Implications-A Comprehensive Review. [PDF]
J Pers MedButt FR +8 more
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Characteristics of Myopic Traction Maculopathy in the Aier-SERI High Myopia Adult Cohort Study. [PDF]
Ophthalmol SciCheong KX +11 more
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Acta Ophthalmologica, 1981
Four generations of a family with congenital retinoschisis are described. Six male members in the second generation suffer from this disease. The fundus changes in these patients were advanced with marked chorioretinal atrophy. Schisis of the retina was only seen in one of them.
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Four generations of a family with congenital retinoschisis are described. Six male members in the second generation suffer from this disease. The fundus changes in these patients were advanced with marked chorioretinal atrophy. Schisis of the retina was only seen in one of them.
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COMPLICATED CONGENITAL RETINOSCHISIS
RETINAL Cases & Brief Reports, 2017Purpose: To describe the treatment and natural history of a patient with complicated congenital retinoschisis. Methods: A retrospective case report. A 10-month-old boy with congenital retinoschisis presented with tractional retinal detachments and foveal schisis in both eyes.
Brian T, Savoie, Philip J, Ferrone
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Archives of Ophthalmology, 1977
Three young women, offspring of a nonconsanguineous marriage of normal parents, manifested mild visual loss associated with a bilateral foveal dystrophy that resembled the macular involvement in juvenile sex-linked retinoschisis. Electrophysiologic and psychophysiologic tests showed less severe involvement than the gonosomal equivalent.
R A, Lewis +4 more
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Three young women, offspring of a nonconsanguineous marriage of normal parents, manifested mild visual loss associated with a bilateral foveal dystrophy that resembled the macular involvement in juvenile sex-linked retinoschisis. Electrophysiologic and psychophysiologic tests showed less severe involvement than the gonosomal equivalent.
R A, Lewis +4 more
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Ophthalmic Surgery, Lasers and Imaging Retina, 2007
<P>A 34-year-old woman with a refraction of -11 diopters in both eyes presented with a central scotoma and metamorphopsia in her right eye related to a juxtafoveal hemorrhage. Fluorescein angiography ruled out choroidal neovascularization and lacquer cracks.
M Rosa, Sanabria, Rosa M, Coco
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<P>A 34-year-old woman with a refraction of -11 diopters in both eyes presented with a central scotoma and metamorphopsia in her right eye related to a juxtafoveal hemorrhage. Fluorescein angiography ruled out choroidal neovascularization and lacquer cracks.
M Rosa, Sanabria, Rosa M, Coco
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Archives of Ophthalmology, 1981
• Secondary retinoschisis is an unusual complication of chronic peripheral uveitis. Photocoagulation can be used to confirm the diagnosis.
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• Secondary retinoschisis is an unusual complication of chronic peripheral uveitis. Photocoagulation can be used to confirm the diagnosis.
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