Results 91 to 100 of about 1,278,456 (199)

Vogt-Koyanagi-Harada Syndrome: A Case Report

Neuropsychiatric Investigation, 2008
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Filiz Koç, Hacer Bozdemir
doaj  

Brain abscess caused by nocardia farcinica in a patient with Vogt-Koyanagi-Harada syndrome

Egyptian Journal of Neurosurgery
Background Nocardia brain abscess is extremely rare. Vogt-Koyanagi-Harada disease is an autoimmune driven inflammation of ocular, auditory and meningeal structures that all contain melanocyes, treated by high dose systemic steroid drugs and ...
Ravishankar S. Goel, Vikram Dua, Sachin Gupta, Reemu Bansal, Neha Rathor   +4 more
doaj   +1 more source

Le syndrome de Vogt-Koyanagi Harada dans sa forme purement oculaire: à propos d'un cas

The Pan African Medical Journal, 2014
Le syndrome de Vogt-Koyanagi-Harada (VKH) est une affection systémique rare, sévère mettant en jeu le pronostic visuel malgré les traitements agressifs, caractérisée par l'association de plusieurs symptômes: oculaires, méningés, auditifs et cutanés ...
Shamil Louaya, Youssef Bennouk, Mohamed Kriet, Abdelbarre Oubaaz   +3 more
doaj   +1 more source

Clinical and epidemiologic characterization of non-infectious uveitis in a university hospital in Paraguay

Medicina Clínica y Social
Objective: To determine the clinical and epidemiological characteristics of patients with noninfectious uveitis at a university hospital in Paraguay.
Abel Esteban Figueredo Rojas, Guillermo Raul Vera-Duarte, Claudia Leticia Delgado-Herrera , Martin Fernando Arrúa Caballero, Luis González Sanabria   +4 more
doaj   +1 more source

A case of Vogt-Koyanagi-Harada

, 2017
Vogt-Koyanagi-Harada syndrome (VKH) is often not recognized. The diagnosis of VKH is based upon the clinical presentation; there are no serologic tests or specific histological ...
Florentina Berianu; Juan Maya
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Management of ocular complications of Vogt-Koyanagi-Harada syndrome

, 2009
Background: Vogt-Koyanagi-Harada syndrome (VKH) is a multisystem disorder, characterized by the T-cell-mediated autoimmune process directed against melanocytic antigens in the ocular, nervous, auditory and integumentary systems.
Cakir, Hanefi, Kaya, Vedat, Yilmaz, Omer Faruk, YILDIRIM, CANAN ASLI, Perente, Irfan, Tutkun, Ilknur Tugal   +5 more
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Uveitis and dermal depigmentation (Vogt-Koyanagi-Harada-1 ike syndrome) in Akita dogs. I. Clinical aspects

, 1991
A síndrome de Vogt-Koyanagi-Harada, caracterizada pela associação de uveite e alteraçõe cutaneas e de meninge, de causa desconhecida é bastante estudada na oftalmologia humana. Foi primeiro descrita no Japão uma síndrome semelhante em cães da raça Akita,
Safatle, Angélica Mendonça Vaz, Malerba, Telma Aparecida, Barros, Paulo Sergio de Moraes, Larsson, Maria Helena Matiko Akao, Yrio, Kenji, Alvarenga, José   +5 more
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Le syndrome de Vogt-Koyanagi Harada dans sa forme purement oculaire: à propos d'un cas [PDF]

, 2016
Le syndrome de Vogt-Koyanagi-Harada (VKH) est une affection systémique rare, sévère mettant en jeu le pronostic visuel malgré les traitements agressifs, caractérisée par l'association de plusieurs symptômes: oculaires, méningés, auditifs et cutanés ...
Bennouk, Youssef, Oubaaz, Abdelbarre, Louaya, Shamil, Kriet, Mohamed   +3 more
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Surdité brutale révélant un syndrome de Vogt-Koyanagi-Harada

The Pan African Medical Journal, 2015
Le syndrome de Vogt-Koyanagi-Harada est une affection rare, caractérisée par l'association de manifestations oculaires, méningées, auditives et cutanées. L'atteinte cochléo-vestibulaire se voit dans 33 à 75% des cas.
Madiha Mahfoudhi, Khaled Khamassi
doaj   +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
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