Results 111 to 120 of about 1,359,849 (169)

Common practice patterns in the diagnosis and management of Vogt-Koyanagi-Harada syndrome: a survey study of uveitis specialists. [PDF]

Front Ophthalmol (Lausanne), 2023
Choo CH, Acharya NR, Shantha JG.
europepmc   +1 more source

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
core   +1 more source

A unique case of VKH in HIV patient

Indian Journal of Ophthalmology. Case Reports
A 49-year-female with known human immunodeficiency virus on highly active antiretroviral therapy presented with diminution of vision and mild pain in both eyes of 2 weeks duration, preceded by alopecia, headache, and tinnitus.
Arpitha Ramesh, C K Minija, Nidhi Dubey
doaj   +1 more source

Vogt‐Koyanagi‐Harada disease‐like uveitis induced by nivolumab in metastatic renal cell carcinoma

Introduction Nivolumab can cause various immune‐related adverse events; it rarely induces Vogt‐Koyanagi‐Harada‐disease‐like uveitis. Vogt‐Koyanagi‐Harada‐disease is reported to be closely associated with human leukocyte antigen‐DR4.
Kei Yaginuma, Hidenori Akaihata, Seiji Hoshi, Hitomi Imai, Yuki Harigane, Satoru Meguro, Junya Hata, Soichiro Ogawa, Tomoyuki Koguchi, Yoshiyuki Kojima   +9 more
core   +1 more source

Rare Association Between Lichen Planus and Vogt-Koyanagi-Harada Syndrome: A Case Report. [PDF]

Cureus, 2023
Al-Haddab M, Alsharif S, Alsehli T, Altukhaim F.   +3 more
europepmc   +1 more source

Síndrome Uveomeningeo Vogt-Koyanagi-Harada

, 2017
El síndrome Vogt-Koyanagi-Harada es una panuveitis granulomatosa bilateral que cursa con desprendimiento de retina seroso y que puede acompañarse de afectación del sistema nervioso central, alteraciones dermatológicas y auditivas1.
Alejos Ramirez, Luis E., Garzarán Tejeiro, Ana, Pastor Espuig, M.   +2 more
core  

Sindrom Vogt-Koyanagi Harada Laporan Kasus

, 1998
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,
Perpustakaan UGM, i-lib
core   +1 more source

Vogt-Koyanagi-Harada disease and HLA type in Italian patients

, 1996
PURPOSE: To study the frequencies of human leukocyte antigen (HLA) specificities in Italian patients with Vogt-Koyanagi-Harada disease and to correlate the presence of each specificity to the clinical features.
Massimo Accorinti, R. A. M. Colabelli Gisoldi, M. P. Pirraglia, PIVETTI, Paola   +3 more
core  

Vogt-Koyanagi-Harada Syndrome: Clinical Features, Immunogenetic Predisposition and PD-1 Inhibitor-Induced Forms-A Comprehensive Review. [PDF]

J Clin Med
Orłowska SM, Bednarczyk Ł, Morshed K, Tyniec M, Olczyk P.   +4 more
europepmc   +1 more source

Bilateral Iris depigmentation, transillumination defects and hypotony in Vogt–Koyanagi–Harada disease

Indian Journal of Ophthalmology, 2022
Mohit Garg, Dipankar Das, Harsha Bhattacharjee, Kanika Godani, Madhusmita Mahapatra, Riddhi Raichura   +5 more
doaj   +1 more source