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Síndrome Uveomeningeo Vogt-Koyanagi-Harada
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
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Vogt-Koyanagi-Harada Disease: A Case Report Through Poliosis and Inflammatory Relapses. [PDF]
Wang Z +4 more
europepmc +1 more source
Clinical and OCT Predictors of Refractory Vogt-Koyanagi-Harada Disease. [PDF]
Cho YC +8 more
europepmc +1 more source
Commentary: Treatment of refractory uveitis with Vogt Koyanagi Harada disease
Sivaraman Balamurugan, Somanath Anjana
doaj +1 more source
Recurrence of Vogt-Koyanagi-Harada Disease as Immune-Related Adverse Events Induced by an Immune Checkpoint Inhibitor. [PDF]
Fukushima A, Tabuchi H.
europepmc +1 more source
Late-onset optic disc swelling-type Vogt-Koyanagi-Harada disease: diagnostic value of longitudinal multimodal imaging. [PDF]
Goncharova T +6 more
europepmc +1 more source
Segmental choroidal vascularity in Acute Vogt-Koyanagi-Harada disease. [PDF]
Jacob N +7 more
europepmc +1 more source
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
Vogt-Koyanagi-Harada Disease with Oral Manifestations: A Rare Case Report. [PDF]
Rani N +4 more
europepmc +1 more source

