Results 281 to 290 of about 499,083 (318)
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RETINAL VESSELS WHITENING IN RETINITIS PIGMENTOSA
RetinaPurpose: To characterize retinal vessel whitening (RVW) in retinitis pigmentosa (RP). Methods: Single-center cross-sectional study. Review of clinical notes of clinically confirmed patients with RP was performed followed by grading ultra-widefield imaging.
Shaden H. Yassin +8 more
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Retinal Detachments in Patients With Cytomegalovirus Retinitis
Archives of Ophthalmology, 1991Retinal detachments are a recognized complication of cytomegalovirus retinitis. In a series of 145 patients with cytomegalovirus retinitis, 38 (26%) developed retinal detachments. The cumulative probability of a retinal detachment 1 year after the diagnosis of cytomegalovirus retinitis was 50%.
D A, Jabs +3 more
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Retina, 1984
A healthy-appearing male patient presented with signs of unilateral fibrinous iritis, necrotizing retinitis, retinal vasculitis, and vitritis, suggestive of a herpesvirus retinitis or acute retinal necrosis syndrome (ARN). The patient, an active homosexual, withheld the details of his sexual history, portraying himself as exclusively heterosexual. With
A D, Mendelsohn, L M, Jampol
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A healthy-appearing male patient presented with signs of unilateral fibrinous iritis, necrotizing retinitis, retinal vasculitis, and vitritis, suggestive of a herpesvirus retinitis or acute retinal necrosis syndrome (ARN). The patient, an active homosexual, withheld the details of his sexual history, portraying himself as exclusively heterosexual. With
A D, Mendelsohn, L M, Jampol
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Archivos de la Sociedad Española de Oftalmología (English Edition), 2017
The case is presented of a 16 year-old girl with unilateral congenital retinal macrovessel associated with peripheral telangiectasia and retinal ischaemia.Congenital retinal macrovessel is a rare finding. To the best of our knowledge this is the first report of this unusual presentation of congenital retinal macrovessel.
A, Medina-Tapia +6 more
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The case is presented of a 16 year-old girl with unilateral congenital retinal macrovessel associated with peripheral telangiectasia and retinal ischaemia.Congenital retinal macrovessel is a rare finding. To the best of our knowledge this is the first report of this unusual presentation of congenital retinal macrovessel.
A, Medina-Tapia +6 more
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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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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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The Lancet, 2006
Hereditary degenerations of the human retina are genetically heterogeneous, with well over 100 genes implicated so far. This Seminar focuses on the subset of diseases called retinitis pigmentosa, in which patients typically lose night vision in adolescence, side vision in young adulthood, and central vision in later life because of progressive loss of ...
Dyonne T, Hartong +2 more
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Hereditary degenerations of the human retina are genetically heterogeneous, with well over 100 genes implicated so far. This Seminar focuses on the subset of diseases called retinitis pigmentosa, in which patients typically lose night vision in adolescence, side vision in young adulthood, and central vision in later life because of progressive loss of ...
Dyonne T, Hartong +2 more
openaire +2 more sources
Giant retinal tears, retinal detachment and retinitis pigmentosa.
Canadian journal of ophthalmology. Journal canadien d'ophtalmologie, 1985A patient with retinitis pigmentosa and sensorineural deafness presented with bilateral giant retinal tears and a unilateral retinal detachment. The peripheral visual field loss could have been erroneously ascribed to the primary retinal dystrophy. A retinal detachment must be considered in patients with a sudden loss of visual acuity or field even if ...
M E, Johnston, J R, Gonder
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A foundation model for generalizable disease detection from retinal images
Nature, 2023Yukun Zhou +2 more
exaly
Ring Retinal Detachment in Retinitis Pigmentosa
Archives of Ophthalmology, 2006Shu-Yen, Lee, Sze-Guan, Ong
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