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Rahul N. Khurana

Researcher at University of California, San Francisco

Publications -  93
Citations -  2024

Rahul N. Khurana is an academic researcher from University of California, San Francisco. The author has contributed to research in topics: Visual acuity & Macular edema. The author has an hindex of 20, co-authored 85 publications receiving 1331 citations. Previous affiliations of Rahul N. Khurana include University of Southern California & University of California.

Papers
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Journal ArticleDOI

Efficacy and safety of dexamethasone intravitreal implant for persistent uveitic cystoid macular edema.

TL;DR: A single DEX Implant produced sustained improvements in both visual acuity and retinal thickness in the majority of eyes with persistent uveitic CME; however, close posttreatment monitoring is recommended.
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Factors Predicting Visual Acuity Outcome in Intermediate, Posterior, and Panuveitis: The Multicenter Uveitis Steroid Treatment (MUST) Trial

John H. Kempen, +490 more
TL;DR: Intermediate, posterior, and panuveitis have a similarly favorable prognosis with both systemic and fluocinolone acetonide implant treatment and the results indicate the value of implementing best practices in managing inflammation.
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Prospective evaluation of a sustained-release dexamethasone intravitreal implant for cystoid macular edema in quiescent uveitis.

TL;DR: Dexamethasone intravitreal implant may be an effective treatment for patients with persistent cystoid macular edema in quiescent uveitis.
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The association of epiretinal membrane with macular hole formation after rhegmatogenous retinal detachment repair.

TL;DR: The epiretinal membrane may play a role in the pathogenesis of secondary macular hole formation after rhegmatogenous retinal detachment (RRD) repair and is associated with an epireTinal membrane.
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Bartonella henselae infection presenting as a unilateral panuveitis simulating Vogt-Koyanagi-Harada syndrome

TL;DR: Ocular manifestations of cat scratch disease can include diffuse thickening of the choroid and may manifest with angiographic features suggestive of Vogt-Koyanagi-Harada disease.