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retinal vein occlusion/potasio

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[Warfarin potassium for impending central retinal vein occlusion].

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OBJECTIVE We reviewed the records of 10 patients who had impending central retinal vein occlusion in order judge whether anticoagulant treatment with warfarin potassium (Warfarin) was indicated. METHODS 6 men and 4 women, ranging in age from 25 to 83 (average 55) years were studied. RESULTS Of 6

[Effects of anticoagulant therapy on retinal vein occlusion].

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The combined effect of prostaglandin E1, stellate ganglion block, warfarin potassium and photocoagulation on 66 cases (eyes) of retinal vein occlusion was investigated immediately after, and 3 months and 6 months after final treatment. The time between onset and treatment was 2 months or less.
BACKGROUND To investigate the effect of induced arteriolar constriction (AC) on alterations in gene expression of factors implicated in the development of edema in branch retinal vein occlusion (BRVO). METHODS In Brown-Norway rats, BRVO was induced by laser photocoagulation of the veins in one half

Effects of intravitreal triamcinolone acetonide on retinal gene expression in a rat model of central retinal vein occlusion.

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OBJECTIVE The aim of this study was to investigate the effects of intravitreal triamcinolone acetonide on the alterations in retinal gene expression in a rat model of central retinal vein occlusion (CRVO). METHODS In one eye of adult Brown Norway rats (n = 77) CRVO was induced with laser

Retinal gene expression and Müller cell responses after branch retinal vein occlusion in the rat.

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OBJECTIVE In a rat model of branch retinal vein occlusion (BRVO), changes in gene expression of factors implicated in the development of retinal edema and alterations in the properties of Müller cells were determined. METHODS In adult Long-Evans rats, BRVO was induced by laser photocoagulation of

Neuronal degeneration and associated alterations in cytokine and protein in an experimental branch retinal venous occlusion model.

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The mechanisms of neuronal degeneration and associated acute alterations in intraretinal cytokine and protein levels remain poorly understood in variable ischaemic retinopathies such as in branch retinal vein occlusion (BRVO). Herein we investigate neuronal damage and alterations in retinal
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