Results 51 to 60 of about 137,274 (148)
, 2018 Objective: To evaluate in which phase of Vogt-Koyanagi-Harada (VKH) syndrome the patients receive the first attendance in specialized service. Methods: A retrospective study was conduted to evaluate medical records of 14 patients with VKH in the ...
Giovanna Provenzano (5313341) +4 more
core +1 more source
Advanced Science, Volume 13, Issue 16, 18 March 2026.ABSTRACT Immune homeostasis is indispensable for preserving organismal integrity, orchestrated through complex molecular networks encompassing immune cell dynamics, microbial cues, and epigenetic regulation. Among these, the gut microbiota‐non‐coding RNA (ncRNA) axis has recently garnered substantial attention as a multifaceted modulator of host ...
Bonan Chen +12 more
wiley +1 more source
Vogt-Koyanagi-Harada syndrome and keratoconjunctivitis sicca
, 2004 PURPOSE: To discover a relationship between Vogt-Koyanagi- Harada (VKH) syndrome and Sjogren syndrome. DESIGN: Observational case-control study. METHODS: Sixteen Italian patients with VKH syndrome and 16 controls with diffuse uveitis underwent tear ...
PRIORI R. +4 more
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, 2022 Vogt-Koyanagi-Harada (VKH) syndrome is a rare disorder that affects several body systems. Here we take a broad look at the presentation and pathophysiology of VKH, with a more specific focus on the relevant eye findings. Since much is not known about VKH,
Shwetha Mudalegundi, Medical Student; Amanda D. Henderson, MD
core
, 2020 Purpose: To describe severe bilateral iris depigmentation and persistent ocular hypotony as end-stage manifestations of untreated Vogt–Koyanagi–Harada disease.
Cuevas M. +2 more
core +1 more source
The Role of Viral and Bacterial Infections in the Etiology of Behçet's Disease
Journal of Clinical Laboratory Analysis, Volume 40, Issue 1, January 2026.Bacterial and viral pathogens may play a key role in Behçet's disease (BD) pathogenesis by triggering autoimmunity, molecular mimicry, or microbiome disruption. These infectious agents could initiate inflammatory pathways, contributing to BD's diverse clinical manifestations.
Mohsen Moghoofei +4 more
wiley +1 more source
, 2017 peer reviewedWe present the case of a patient who had a decrease of the visual acuity associated with headaches, diagnosed as Vogt-Koyanagi-Harada syndrome. This is a rare multisystemic pathology that affects organs with high concentration of melanocytes.
DUCHATEAU, Edouard +2 more
core +1 more source
Vogt‐Koyanagi‐Harada disease in pregnancy: Case report and review of 32 patients in the literature
Clinical Case ReportsKey Clinical Message Systemic prednisolone including steroid pulse therapy would be safe in 32 pregnant women, who developed Vogt‐Koyanagi‐Harada disease in the literature.
Toshihiko Matsuo +2 more
doaj +1 more source
Bilateral betrayal: When imaging calls out Vogt–Koyanagi–Harada’s one-eyed act
Indian Journal of Ophthalmology. Case ReportsWe report a case of asymmetric Vogt-Koyanagi-Harada syndrome mimicking unilateral Central Serous Chorioretinopathy. This case highlights the diagnostic challenge for making a correct diagnosis between asymmetric Vogt-Koyanagi-Harada disease and Central ...
Shagun Korla +2 more
doaj +1 more source
Panuveite révélant une maladie de Vogt Koyanagi Harada (A propos de trois cas)
Journal de la Société Marocaine d’Ophtalmologie, 2015 Le syndrome de voght koyanagi harada (VKH) est une uvéo méningite bilatérale d’origine auto-immune, le diagnostic repose sur l’association variable de signes oculaires, méningés , auditifs et cutanés, le traitement repose sur les bolus de corticothérapie
G. El houari +9 more
doaj +1 more source