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dc.contributor.authorBernstein, Steven L.
dc.contributor.authorWoo, Kwang Min
dc.contributor.authorGuo, Yan, M.D.
dc.contributor.authorMehrabyan, Zara
dc.date.accessioned2024-05-23T15:59:30Z
dc.date.available2024-05-23T15:59:30Z
dc.date.issued2024-05-04
dc.identifier.urihttp://hdl.handle.net/10713/22435
dc.descriptionAssociation for Vision and Ophthalmology (ARVO) convention. May 4, 2024.en_US
dc.description.abstractCurrent approaches to treatment of nonarteritic anterior ischemic optic neuropathy (NAION) rely on early retinal ganglion cell (RGC) neuroprotection. However, current neuroprotective approaches have been ineffective when administered late (>1d) after induction in rodent and primate NAION models. This is particularly problematic clinically, since nearly all patients are diagnosed at least a day post-symptom onset. We report on the success of a new neuroregenerative approach using TXA127, a pharmaceutical formulation of angiotensin (1-7) currently in Phase II for ischemic stroke.en_US
dc.language.isoen_USen_US
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subject.meshOptic Nerveen_US
dc.subject.meshOptic Neuropathy, Ischemicen_US
dc.subject.meshNeuroprotectionen_US
dc.titleEffective NAION neuroregenerative treatment using TXA127en_US
dc.typePoster/Presentationen_US
refterms.dateFOA2024-05-23T15:59:31Z


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Attribution-NonCommercial-NoDerivatives 4.0 International
Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivatives 4.0 International