Results 1 to 10 of about 1,141,952 (120)

Calculation of Similarity Between 26 Autoimmune Diseases Based on Three Measurements Including Network, Function, and Semantics [PDF]

Frontiers in Genetics, 2021
Autoimmune diseases (ADs) are a broad range of diseases in which the immune response to self-antigens causes damage or disorder of tissues, and the genetic susceptibility is regarded as the key etiology of ADs.
Yanjun Ding, Yanjun Ding, Mintian Cui, Jun Qian, Chao Wang, Qi Shen, Hongbiao Ren, Liangshuang Li, Fengmin Zhang, Ruijie Zhang   +9 more
doaj   +2 more sources

Acute interstitial nephritis and probable Vogt–Koyanagi–Harada disease following COVID-19 infection: a case report [PDF]

Journal of Medical Case Reports
Introduction Vogt–Koyanagi–Harada disease is an autoimmune inflammatory disease characterized by bilateral serous retinal detachment, which viral infections might induce.
Nahid Aslani, Mohammad Malekahmadi, Alireza Merrikhi, Alaleh Gheisari, Aida Mardani, Kimia Afshar   +5 more
doaj   +2 more sources

Fingerprint sign in Vogt-Koyanagi-Harada disease: a case series

International Journal of Retina and Vitreous, 2022
Background The tomographic finding, which has been called the "fingerprint sign" in en face reconstructions, seems to be the result of a variety of processes that cause distension of the outer plexiform layer (OPL) and the Henle fiber layer (HFL).
Ruy Felippe Brito Gonçalves Missaka, Mauro Goldbaum, Cleide Guimarães Machado, Emmett T. Cunningham, Fernanda Maria Silveira Souto, Marcelo Mendes Lavezzo, Priscilla Figueiredo Campos da Nóbrega, Viviane Mayumi Sakata, Maria Kiyoko Oyamada, Carlos Eduardo Hirata, Joyce Hisae Yamamoto   +10 more
doaj   +1 more source

Vogt-Koyanagi-Harada disease: the step-by-step approach to a better understanding of clinicopathology, immunopathology, diagnosis, and management: a brief review

Journal of Ophthalmic Inflammation and Infection, 2022
Background Appraisals of Vogt-Koyanagi-Harada disease (VKH) have become progressively more complete, since its first description in 1906. The availability of new investigational methods has improved our knowledge of the immunopathology, clinicopathology,
Cristhian A. Urzua, Carl P. Herbort, Masaru Takeuchi, Ariel Schlaen, Luz E. Concha-del-Rio, Yoshihiko Usui, Loreto Cuitino, Ioannis Papasavvas   +7 more
doaj   +1 more source

A dor de cabeça como primeiro sintoma da síndrome de Vogt-Koyanagi-Harada: uma revisão sistemática

Headache Medicine, 2020
Introdução A Síndrome de Vogt-Koyanagi-Harada (VKH) é uma panuveíte associada a perda visual grave e variados sintomas sistêmicos, que prevalece em mulheres asiática e latinoamericanas, com idades entre 15-78 anos.
Ariane Jurno
doaj   +1 more source

Clinical characteristics of Vogt⁃Koyanagi⁃Harada syndrome combing with meningitis/ encephalitis

Chinese Journal of Contemporary Neurology and Neurosurgery
Objective To summarize the clinical characteristics of Vogt-Koyanagi-Harada syndrome (VKHS) combing with meningitis/encephalitis patients. Methods and Results The clinical data of the inpatients of Beijing Tongren Hospital, Capital Medical University ...
PENG Yu-jing, SHI Xiao-hong, WANG Jia-wei   +2 more
doaj   +1 more source

Bacillary layer detachment in acute Vogt-Koyanagi-Harada disease: an early predictor of long-term complications in a Brazilian cohort

International Journal of Retina and Vitreous
Background Long-term complications occur in some patients with Vogt-Koyanagi-Harada disease (VKHD).This study aimed to evaluate the presence of bacillary layer detachment (BALAD) at presentation as an early predictor of long-term structural and ...
Ruy Felippe Brito Gonçalves Missaka, Mauro Goldbaum, Cleide Guimarães Machado, Emmett T. Cunningham, Fernanda Maria Silveira Souto, Marcelo Mendes Lavezzo, Priscilla Figueiredo Campos da Nóbrega, Camillo Carneiro Gusmão, Viviane Mayumi Sakata, Maria Kiyoko Oyamada, Carlos Eduardo Hirata, Joyce Hisae Yamamoto   +11 more
doaj   +1 more source

Vogt-Koyanagi-Harada's disease: literature review

International Archives of Otorhinolaryngology, 2008
Introduction: Vogt-Koyanagi-Harada's disease is a rare syndrome that affects tissues with melanocytes like eyes, central nervous system, skin and inner ear. It affects primarily Asians, Indians and Latin Americans and also women.
Pereira, Talita Valleska de Campos, Ferreira, Thaís Oliveira, Nunes, Cláudio Tobias Acatauassú, Palheta Neto, Francisco Xavier, Palheta, Angélica Cristina Pezzin, Silva, Dorivaldo Lopes da, Carneiro, Stephanie Gonçalves, Monteiro, Viviane Cristina dos Santos   +7 more
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Estudio preliminar de la frecuencia fenotípica y génica de los antígenos HLA en la enfermedad de Voght-Koyanagi-Harada Preliminary study of the phenotypical and genic frequency of HLA antigens in Voght-Koyanagi-Harada’s disease

Revista Cubana de Hematología, Inmunología y Hemoterapia, 2001
Se determinó la frecuencia de 67 antígenos HLA de clase I (loci A, B y C) y 18 de clase II en 15 pacientes portadores del síndrome de Voght-Koyanagi-Harada, diagnosticados en los servicios de Oftalmología del Hospital General “Enrique Cabrera”
Luz M Morera Barrios, Tomás Verdura González, Rosa Ricardo Lorenzo, Daysy Vilches, Zoila C Martínez Legón, Ana M Guerreiro Hernández   +5 more
doaj  

A 47-year-old man with sudden onset of blindness, pleocytosis, and temporary hearing loss. Vogt-Koyanagi-Harada syndrome (Uveomeningoencephalitic syndrome).

Archives of pathology & laboratory medicine, 2006
The clinicopathologic findings of this patient were typical for Vogt-Koyanagi-Harada syndrome. Clinically, the patient had sudden onset of blindness, pleocytosis, and temporary hearing loss, with no history of eye trauma or surgery. Histopathologically, the choroid and iris showed chronic inflammation, loss of choroidal melanocytes, and dense ...
Thaer, Khoury, Federico, Gonzalez-Fernandez, Fredrick E, Munschauer, Peter, Ostrow   +3 more
openaire   +1 more source