Results 161 to 170 of about 49,907 (194)
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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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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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Archives of Ophthalmology, 1980
Analysis of 196 patients with retinal dialysis indicated that unilateral nasal and superior dialyses almost invariably were produced by trauma (87.5%). A traumatic cause is proposed for unilateral inferotemporal dialyses, which also had an inordinately high rate of trauma (56%).
V M, Zion, T C, Burton
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Analysis of 196 patients with retinal dialysis indicated that unilateral nasal and superior dialyses almost invariably were produced by trauma (87.5%). A traumatic cause is proposed for unilateral inferotemporal dialyses, which also had an inordinately high rate of trauma (56%).
V M, Zion, T C, Burton
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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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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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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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Cytomegalovirus Retinitis After Initiation of Highly Active Antiretroviral Therapy
Lancet, The, 1997Narsing A Rao +2 more
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Features of Retinitis-Like Lesions in Vitreoretinal Lymphoma
Ocular Immunology and Inflammation, 2021Alessandro Marchese +2 more
exaly
GOUTY RETINITIS, CHORIO-RETINITIS, AND NEURO-RETINITIS
The American Journal of the Medical Sciences, 1894openaire +1 more source