Results 101 to 110 of about 137,343 (204)

Vogt-Koyanagi-Harada Syndrome: A case report

, 2015
The Vogt-Koyanagl-Harada Syndrome is characterized by bilateral panuveitis and exudative retinal detachments, in association with cutaneous and neurosensory manifestations. This syndrome is seen most commonly in darker pigmented races, such as Orientals,
Suhardjo, Suhardjo
core   +1 more source

Delayed cutaneous depigmentation in Vogt-Koyanagi-Harada disease. [PDF]

Skin Health Dis
Shanshal M, Khan S.
europepmc   +1 more source

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

, 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  

Enfermedad de Vogt-Koyanagi-Harada y rehabilitación visual

Revista Cubana de Oftalmología
La enfermedad de Vogt-Koyanagi-Harada es una entidad infrecuente, multisistémica, de etiología desconocida, presuntamente autoinmune, caracterizada por panuveítis granulomatosa crónica bilateral y difusa, acompañada de participación tegumentaria ...
Mayrelis Quintero Busutil, Daysi Caridad Vilches Lescalle, Yurania Bueno Arrieta, Susana Rodríguez Masó, Carlos Alberto Perea Ruíz, Miladis Paz Lorenzo   +5 more
doaj  

Vogt-Koyanagi-Harada Disease Presenting With Progressive Visual Loss and Multisystem Involvement: A Case Report. [PDF]

Am J Case Rep
Elshweikh SA, Almutairi AG, Thalib HI, Alolayan RW, Aly MM.   +4 more
europepmc   +1 more source

Vogt-Koyanagi-Harada Disease: A Case Report Through Poliosis and Inflammatory Relapses. [PDF]

Cureus
Wang Z, Comberg C, Makhoul D, Beun A, Le A.   +4 more
europepmc   +1 more source

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

Ophthalmol Sci
Cho YC, Mizuki Y, Nakamura J, Meguro A, Kanasashi S, Sakono T, Kawagoe T, Ohno S, Mizuki N.   +8 more
europepmc   +1 more source

Vogt-Koyanagi-Harada disease

, 2011
An 18-year-old female presented with bilateral visual loss following severe headache. She had bilateral serous retinal detachment in the fundus examination, multiple pinpoint leakage in fundus fluoresein angiography, and choroidal thickening in ...
Yaylalı, Volkan, Yaldızkaya, Filiz, Çetin, Ebru Nevin, Yıldırım, Cem   +3 more
core  

Recurrence of Vogt-Koyanagi-Harada Disease as Immune-Related Adverse Events Induced by an Immune Checkpoint Inhibitor. [PDF]

Cureus
Fukushima A, Tabuchi H.
europepmc   +1 more source

Immune Checkpoint Inhibitor-Induced Vogt-Koyanagi-Harada-like Disease Complicated by Inflammatory Macular Neovascularisation: A Case Report and Literature Review. [PDF]

Diagnostics (Basel)
Papavasileiou ME, Stavrakas P, Mitri P, Kalaitzakis P, Makris G, Ragkousis A.   +5 more
europepmc   +1 more source