Results 191 to 200 of about 82,030 (241)
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Retinal Metastasis Simulating Cytomegalovirus Retinitis
Ophthalmic Surgery, Lasers and Imaging Retina, 2012A 62-year-old man with lung cancer presented with a 2-week history of decreased vision and clinical features of cytomegalovirus retinitis. The patient was empirically treated for viral retinitis, but microbiological testing of the vitreous fluid was negative.
John F, Payne +3 more
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Retinal remodeling during retinal degeneration
Experimental Eye Research, 2005Retinal degenerations, regardless of the initiating event or gene defect, often result in a loss of photoreceptors. This formal deafferentation of the neural retina eliminates the intrinsic glutamatergic drive of the sensory retina and, perhaps more importantly, removes coordinated Ca++-coupled signaling to the neural retina.
Bryan W, Jones, Robert E, Marc
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Retinitis Pigmentosa and Retinal Neovascularization
Ophthalmology, 1986Four patients with retinitis pigmentosa and either disc or peripheral retinal neovascularization with recurrent vitreous hemorrhage are described. One patient with peripheral retinal neovascularization also had rubeosis and neovascular glaucoma. The effects of relative hyperoxia on the retinal microcirculation in retinitis pigmentosa as well as ...
A E, Uliss, Z J, Gregor, A C, Bird
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Medical Journal of Australia, 1980
The appearances of cytomegalovirus retinitis are described in a body who was receiving maintenance immunosuppressive therapy for lymphatic leukaemia. The retinitis improved on cessation of the treatment and settled completely after an injection of lymphocyte dialysable transfer factor.
C G, Keith, J, La Nauze
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The appearances of cytomegalovirus retinitis are described in a body who was receiving maintenance immunosuppressive therapy for lymphatic leukaemia. The retinitis improved on cessation of the treatment and settled completely after an injection of lymphocyte dialysable transfer factor.
C G, Keith, J, La Nauze
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Survey of Ophthalmology, 1976
The authors review the symptomatic and genetic aspects of the various entities of isolated retinitis pigmentosa (R.P), both in its typical form and in the forms associated with the affection of other ocular tissues. Syndromes in which R. P. is associated with the affection of other organs and systemic disorders are also cconsidered.
S, Merin, E, Auerbach
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The authors review the symptomatic and genetic aspects of the various entities of isolated retinitis pigmentosa (R.P), both in its typical form and in the forms associated with the affection of other ocular tissues. Syndromes in which R. P. is associated with the affection of other organs and systemic disorders are also cconsidered.
S, Merin, E, Auerbach
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Ocular Immunology and Inflammation, 2018
Purpose: To study demography, seasonal variation, clinical presentation, and treatment outcome of "retinitis post febrile illness." (RpFI) Method: Case records of patients diagnosed as RpFI, from July 2009 to May 2017 were studied retrospectively. Patients with complete follow up were evaluated for treatment and visual outcomes.
Ankush Kawali +4 more
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Purpose: To study demography, seasonal variation, clinical presentation, and treatment outcome of "retinitis post febrile illness." (RpFI) Method: Case records of patients diagnosed as RpFI, from July 2009 to May 2017 were studied retrospectively. Patients with complete follow up were evaluated for treatment and visual outcomes.
Ankush Kawali +4 more
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Current Opinion in Ophthalmology, 2003
Retinal vasculitis represents a group of diseases characterized by inflammation affecting the retinal vasculature. It is an uncommon disorder that may occur as an isolated disease or more commonly in association with other ocular diseases or a variety of systemic diseases. With a wide variety of disease associations, a search for an underlying etiology
R Christopher, Walton, Emily D, Ashmore
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Retinal vasculitis represents a group of diseases characterized by inflammation affecting the retinal vasculature. It is an uncommon disorder that may occur as an isolated disease or more commonly in association with other ocular diseases or a variety of systemic diseases. With a wide variety of disease associations, a search for an underlying etiology
R Christopher, Walton, Emily D, Ashmore
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International Ophthalmology Clinics, 1999
Phototoxic retinal lesions are a product of advances in operative technology. Use of more powerful light sources in both anterior and posterior segment cases and an increase in surgical complexity requiring longer operative times (especially during ophthalmic training) have rendered photic injury a real danger for all surgeons.
W A, Solley, P, Sternberg
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Phototoxic retinal lesions are a product of advances in operative technology. Use of more powerful light sources in both anterior and posterior segment cases and an increase in surgical complexity requiring longer operative times (especially during ophthalmic training) have rendered photic injury a real danger for all surgeons.
W A, Solley, P, Sternberg
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Survey of Ophthalmology, 1988
Retinitis pigmentosa is a clinically and genetically heterogeneous group of hereditary disorders in which there is progressive loss of photoreceptor and pigment epithelial function. The prevalence of retinitis pigmentosa is between 1/3000 and 1/5000 making it one of the most common causes of visual impairment in all age groups.
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Retinitis pigmentosa is a clinically and genetically heterogeneous group of hereditary disorders in which there is progressive loss of photoreceptor and pigment epithelial function. The prevalence of retinitis pigmentosa is between 1/3000 and 1/5000 making it one of the most common causes of visual impairment in all age groups.
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Documenta Ophthalmologica, 1981
Retinal dysplasia is defined as an abnormal growth and differentiation of embryonic retina being more a secondary lesion rather than a disease. Clinically, the disorder may present itself in a surprisingly wide range of severity or of degree from retinal folds to vascularized masses in the vitreous cavity.
V, Godel, P, Nemet, M, Lazar
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Retinal dysplasia is defined as an abnormal growth and differentiation of embryonic retina being more a secondary lesion rather than a disease. Clinically, the disorder may present itself in a surprisingly wide range of severity or of degree from retinal folds to vascularized masses in the vitreous cavity.
V, Godel, P, Nemet, M, Lazar
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