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Síndrome Uveomeningeo Vogt-Koyanagi-Harada

open access: yes, 2017
El síndrome Vogt-Koyanagi-Harada es una panuveitis granulomatosa bilateral que cursa con desprendimiento de retina seroso y que puede acompañarse de afectación del sistema nervioso central, alteraciones dermatológicas y auditivas1.
Alejos Ramirez, Luis E.   +2 more
core  

Clinical and OCT Predictors of Refractory Vogt-Koyanagi-Harada Disease. [PDF]

open access: yesOphthalmol Sci
Cho YC   +8 more
europepmc   +1 more source

Commentary: Treatment of refractory uveitis with Vogt Koyanagi Harada disease

open access: yesIndian Journal of Ophthalmology. Case Reports, 2022
Sivaraman Balamurugan, Somanath Anjana
doaj   +1 more source

Late-onset optic disc swelling-type Vogt-Koyanagi-Harada disease: diagnostic value of longitudinal multimodal imaging. [PDF]

open access: yesJ Ophthalmic Inflamm Infect
Goncharova T   +6 more
europepmc   +1 more source

Segmental choroidal vascularity in Acute Vogt-Koyanagi-Harada disease. [PDF]

open access: yesInt J Retina Vitreous
Jacob N   +7 more
europepmc   +1 more source

Progressive Subretinal Fibrosis Complicating Vogt-Koyanagi-Harada Syndrome during Systemic Corticosteroid Treatment

open access: yes, 2009
We describe 2 patients with Vogt-Koyanagi-Harada syndrome in whom the development of markedly progressive subretinal fibrosis and telangiectasis over the optic disc showed peculiar manifestations.
CHEN, MUH-SHY, 陳慕師
core  

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