Results 101 to 110 of about 1,278,456 (199)

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

open access: yes, 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   +3 more
core  

VOGT, KOYANAGI, HARADA (VKH) SYNDROME

open access: yesJournal of Nepal Medical Association, 2003
D N Shah   +3 more
doaj   +1 more source

Sindrom Vogt-Koyanagi Harada Laporan Kasus

open access: yes, 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

Intravitreal triamcinolone for intraocular inflammation and associated macular edema

open access: yesClinical Ophthalmology, 2008
Steven M Couch, Sophie J BakriMayo Clinic Department of Ophthalmology, Mayo Clinic, Rochester, MN, USAAbstract: Triamcinolone acetonide (TA) is a corticosteroid that has many uses in the treatment of ocular diseases because of its potent anti ...
Steven M Couch, Sophie J Bakri
doaj  

A unique case of VKH in HIV patient

open access: yesIndian 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

Intravascular lymphoma masquerading as Vogt-Koyanagi-Harada syndrome

open access: yes, 2009
PURPOSE: To describe the clinical course of a case of intravascular lymphoma. DESIGN: Case report. METHODS: Retrospective chart review. RESULTS: A 56-year-old man presented with blurry vision associated with fever and decreased hearing.
Zabar, Yuval   +8 more
core   +1 more source

Vogt–Koyanagi–Harada (VKH)—What Do We Know About the Disease, and Can We Recognize It?

open access: yesDiagnostics
Background: Vogt–Koyanagi–Harada (VKH) is a multisystem autoimmune disease that ophthalmologists often encounter first. The condition is caused by an immune response against tyrosinase-related proteins in pigment cells (melanocytes) of the uvea, inner ...
Maria Boyadzhieva   +5 more
doaj   +1 more source

Successive onset of Vogt-Koyanagi-Harada syndrome in father and son. [PDF]

open access: yesBMC Ophthalmol, 2023
Li H   +5 more
europepmc   +1 more source

Vogt-Koyanagi-Harada Syndrome in Two Patients with Immunoglobulin A Nephropathy

open access: yes
We describe herein 2 patients who developed Vogt-Koyanagi-Harada syndrome in the course of renal biopsy-proven immunoglobulin A (IgA) nephropathy. A 61-year-old man with an 11-year history of IgA nephropathy and a 16-year history of thyroiditis, and a 56-
Ota, Kosuke   +5 more
core  

Ocular syphilis mimicking Vogt-Koyanagi-Harada syndrome: a diagnostic dilemma. [PDF]

open access: yesProc (Bayl Univ Med Cent), 2023
Abdelnabi M   +4 more
europepmc   +1 more source

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