Vogt Koyanagi Harada Disease
Mostrando 1-8 de 8 artigos, teses e dissertações.
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1. Conus medullaris syndrome in Vogt-Koyanagi-Harada disease: an unusual presentation
Arquivos de Neuro-Psiquiatria. Publicado em: 2022
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2. Análise morfológica e funcional ocular de pacientes com doença de Vogt-Koyanagi-Harada no estágio tardio / Structural and functional ocular analysis of patients with late-stage Vogt-Koyanagi-Harada disease
OBJETIVO: Caracterizar morfologicamente e funcionalmente as alterações observadas no fundo de olho de pacientes com a doença de Vogt-Koyanagi- Harada (VKH) no estágio tardio. MÉTODOS: Estudo prospectivo, transversal, com inclusão de 36 pacientes com diagnóstico de doença de VKH no estágio tardio (definido como 6 meses ou mais após o início da doen
IBICT - Instituto Brasileiro de Informação em Ciência e Tecnologia. Publicado em: 22/08/2011
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3. Aplicabilidade do critério diagnóstico revisado de 2001 em pacientes brasileiros com doença de Vogt-Koyanagi-Harada
OBJETIVO: Determinar a aplicabilidade do "Internacional revised diagnostic criteria for Vogt-Koyanagi-Harada disease". MÉTODOS: Estudo retrospectivo. Prontuários de 140 pacientes com diagnóstico de "Vogt-Koyanagi-Harada disease", do setor de uveítes da Universidade Federal de São Paulo (UNIFESP), foram revisados e classificados segundo o "Internacional
Arquivos Brasileiros de Oftalmologia. Publicado em: 2008-02
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4. Vogt-Koyanagi-Harada disease during pregnancy.
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5. Oligo-2',5'-adenylate synthetase activity in peripheral blood mononuclear leukocytes in various diseases.
Interferon induces oligo-2',5'-adenylate synthetase in cells. In various diseases, interferon was detectable in the circulation or was produced spontaneously from peripheral blood mononuclear leukocytes. The oligo-2',5'-adenylate synthetase activity in peripheral blood mononuclear leukocytes was examined in various diseases, including systemic lupus erythema
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6. HLA-DRB1 typing of Vogt-Koyanagi-Harada's disease by PCR-RFLP and the strong association with DRB1*0405 and DRB1*0410.
Vogt-Koyanagi-Harada's (VKH) disease is reported to be closely associated with the HLA class II antigen, HLA-DR4. Serologically defined DR4 is further divided into 11 alleles by molecular HLA genotyping. However, no study of HLA-DNA typing of VKH patients has been reported. To clarify molecular genetic mechanism underlying the susceptibility/resistance to VK
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7. Melanoma specific Th1 cytotoxic T lymphocyte lines in Vogt-Koyanagi-Harada disease.
AIMS/BACKGROUND: To determine the functional properties and cytokine production profiles of melanoma specific cytotoxic T lymphocytes (CTLs) induced from peripheral blood leucocytes of two patients with Vogt-Koyanagi-Harada disease (VKH). METHODS: Melanoma specific CTL lines were established by long term coculture with a human melanoma cell line (P-36). Cyto
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8. Increased D-arabinitol/creatinine ratio in sera of patients with Behçet's disease during an active phase.
The ratios of D-arabinitol (a major metabolite of Candida species) to creatinine were examined in 46 sera of 40 patients with ocular inflammatory disease and in 50 age-matched normal controls (25 men and 25 women). The mean ratio in patients with endogenous Candida endophthalmitis was higher than in the normal controls. Seven samples taken from patients with