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dc.contributor.authorBell, Katy J.L.
dc.contributor.authorHayen, Andrew
dc.contributor.authorGlasziou, Paul
dc.contributor.authorMitchell, Andrew S
dc.contributor.authorFarris, Maria
dc.contributor.authorWright, Jonathan
dc.contributor.authorDuerr, Hans-Peter
dc.contributor.authorMitchell, Paul
dc.contributor.authorIrwig, Les
dc.date.accessioned2021-04-22T05:59:24Z
dc.date.available2021-04-22T05:59:24Z
dc.date.issued2017en
dc.identifier.urihttps://hdl.handle.net/2123/24970
dc.description.abstractOur primary purpose was to assess the clinical (predictive) validity of central retinal thickness (CRT) and best corrected visual acuity (BCVA) at 1 week and 1 month after starting treatment with ranibizumab for central retinal vein occlusion. The authors also assessed detectability of response to treatment.en
dc.language.isoenen
dc.publisherLippincott, Williams & Wilkinsen
dc.relation.ispartofRETINA, The Journal of Retinal and Vitreous Diseasesen
dc.rightsCreative Commons Attribution-NonCommercial-NoDerivatives 4.0en
dc.subjectvisual acuityen
dc.subjectoptical coherenceen
dc.subjecttomographyen
dc.subjectretinal vein occlusionen
dc.subjectmacular edemaen
dc.subjectintravitreal injectionsen
dc.titleEarly CRT monitoring using time-domain optical coherence tomography does not add to visual acuity for predicting visual loss in patients with central retinal vein occlusion treated with intravitreal Ranibizumaben
dc.typeArticleen
dc.subject.asrc1113 Ophthalmology and Optometryen
dc.subject.asrc1117 Public Health and Health Servicesen
dc.identifier.doi10.1097/IAE.0000000000001207
dc.relation.nhmrc1013390
dc.relation.nhmrc527500
dc.relation.nhmrc633003
usyd.facultySeS faculties schools::Faculty of Medicine and Health::Sydney School of Public Healthen
usyd.citation.volume37en
usyd.citation.issue3en
usyd.citation.spage509en
usyd.citation.epage514en
workflow.metadata.onlyNoen


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