Results 91 to 100 of about 1,359,849 (169)

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

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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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
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Association of Vogt Koyanagi Harada Syndrome and Seronegative Rheumatoid Arthritis [PDF]

, 2016
Background: Vogt Koyanagi Harada (VKH) Syndrome is a rarely-seen multi-systemic, autoimmune and inflammatory disease. It observed frequently with neurologic, auditory and skin manifestations and characterized with bilateral, chronic and diffused ...
Taspinar, Ozgur, Guneser, Meryem, Keskin, Yasar, Aydin, Teoman   +3 more
core   +1 more source

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

Evolución severa en Enfermedad de Vogt-Koyanagi-Harada

, 1986
We present the severe evolution of Vogt-Koyanagi-Harada disease with corticotherapy and immunosuppresive treatment.Presentamos la evolución severa de la enfermedad de Vogt-KoyanagiHarada a pesar del tratamiento corticoideo e inmunosupresor ...
Herrera Piñero, R., Castellano Solanes, Jorge, Gil Hernández, María A., Hernández Brito, Ana María, Abreu Reyes, Pedro   +4 more
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Vogt-Koyanagi-Harada Disease: Presentation and Implications in Undocumented Immigrants

, 2013
Vogt-Koyanagi-Harada syndrome is an autoimmune disease involving pigmented tissue in the eyes, auditory system, skin, and central nervous system. It often presents as bilateral chronic granulomatous panuveitis.
Manizate, Fotini, Hassen, Getaw Worku, Baksh, Farnaz, Kalantari, Hossein, MD   +3 more
core   +1 more source

Macular Abnormalities in Vogt-Koyanagi-Harada Disease

, 2019
Purpose: To investigate the prevalence of macular abnormalities in Chinese Vogt-Koyanagi-Harada (VKH) patients. Methods: Clinical characteristics, therapeutic effectiveness and visual outcome were reviewed and analyzed.
Yang, Peizeng, Qi, Jian, Liang, Liang, Wang, Chaokui, Cao, Qingfeng, Xu, Jing, Du, Liping, Wu, Lili, Zhou, Chunjian, Zhou, Qingyun, Ye, Zi, Kijlstra, Aize   +11 more
core   +1 more source

VOGT, KOYANAGI, HARADA (VKH) SYNDROME

Journal of Nepal Medical Association, 2003
D N Shah, PCD Karmacharya, S Koirala, M P Upadhayay   +3 more
doaj   +1 more source