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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_AU
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_AU
dc.language.isoenen_AU
dc.publisherLippincott, Williams & Wilkinsen_AU
dc.relation.ispartofRETINA, The Journal of Retinal and Vitreous Diseasesen_AU
dc.rightsCreative Commons Attribution-NonCommercial-NoDerivatives 4.0en_AU
dc.subjectvisual acuityen_AU
dc.subjectoptical coherenceen_AU
dc.subjecttomographyen_AU
dc.subjectretinal vein occlusionen_AU
dc.subjectmacular edemaen_AU
dc.subjectintravitreal injectionsen_AU
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_AU
dc.typeArticleen_AU
dc.subject.asrc1113 Ophthalmology and Optometryen_AU
dc.subject.asrc1117 Public Health and Health Servicesen_AU
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_AU
usyd.citation.volume37en_AU
usyd.citation.issue3en_AU
usyd.citation.spage509en_AU
usyd.citation.epage514en_AU
workflow.metadata.onlyNoen_AU


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