Results 241 to 250 of about 70,682 (288)
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Posterior Choroidal Involvement in Letterer-Siwe Disease
Journal of Pediatric Ophthalmology & Strabismus, 1978A five-year-old child with Letterer-Siwe disease in remission was found to have decreased vision in on eye produced by a choroidal mass and secondary retinal detachment with cystic degeneration. Echography confirmed a vascularized disciform-like mass with possible involvement of the optic nerve.
L K, Angell, T C, Burton
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Hereditary Retinal and Choroidal Disease,
Archives of Ophthalmology, 1973The recent tragic death of Alex Krill was a grave shock to the ophthalmologic community. To many of us who knew him as a friend the loss is all the more severe, while to those who knew him through his multiple articles in the ophthalmic literature the field has lost a prolific and thoughtful contributor.
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Choroidal physiology and primary angle closure disease
Survey of Ophthalmology, 2015Primary angle closure disease (PACD), prevalent in Asian countries, is generally associated with a shallower anterior chamber, a shorter axial length, thicker lens, hyperopia, and female sex. Other physiologic factors, however, may be important, especially with regard to triggering acute primary angle closure.
Xiulan Zhang +4 more
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Choroidal Folds in Vogt-Koyanagi-Harada Disease
American Journal of Ophthalmology, 2007To analyze choroidal folds in Vogt-Koyanagi-Harada (VKH) disease by fluorescein angiography (FA), indocyanine green angiography (ICGA), and optical coherence tomography (OCT).Retrospective, consecutive case series.Records of 95 patients diagnosed with VKH disease from October 2001 to July 2006 were reviewed.
Weiju, Wu +4 more
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Pigment Epithelial Diseases with Abnormal Choroidal Perfusion
American Journal of Ophthalmology, 1980Sixteen patients, seen during the first week of their disease, had swelling of the retinal pigment epithelium and angiographic evidence of a widespread abnormality of choroidal filling. The patients fell into three groups: In Group 1 there were multifocal pigment epithelial lesions identical to those of acute posterior multifocal placoid pigment ...
N J, Young, A C, Bird, K, Sehmi
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Retinal and Choroidal Vascular Diseases
2018The diagnosis and monitoring of retinal and choroidal vascular diseases has evolved significantly over the last two decades with the advent of new imaging techniques such as enhanced depth optical coherence tomography, ultrawide field imaging and angiography, optical coherence tomography angiography, and more.
Wenlan Zhang, Dilraj S. Grewal
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CHOROIDAL THICKNESS IN PATIENTS WITH STARGARDT DISEASE
Retina, 2018Purpose: To investigate the relationship between choroidal thicknesses (CT), central foveal thicknesses, multifocal electroretinography (mf-ERG) responses, and best-corrected visual acuity levels in patients with Stargardt disease (STGD).
Esra, Vural +6 more
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Choroidal Folding in Orbital Disease
1978Choroidal folds are lines or grooves of the posterior pole of the eye which appear as approximately parallel alternating light and dark lines, usually radiating from the disc across the macula. These folds are seen in a variety of orbital and ocular conditions, including orbital inflammation and tumors, hyperopia, scleritis, choroidal tumors, hypotony,
John D. Bullock, Robert R. Waller
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Hereditary Retinal and Choroidal Diseases.
Archives of Internal Medicine, 1974This text is the first of a planned two-volume series. It deals with the diagnostic evolution of hereditary retinal and choroidal disorders. Initially, basic genetic principles are reviewed as well as the latest terminology necessary for the understanding of the various inheritance patterns.
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Gene therapy for retinal and choroidal diseases
Expert Opinion on Biological Therapy, 2002The eye is a small compartment separated from the systemic circulation by the blood-ocular barriers, providing advantages for intraocular gene transfer - an approach which is being investigated for several types of retinal and choroidal diseases.
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