Results 71 to 80 of about 2,441 (231)
Case Reports in Ophthalmology, 2023 I report a case with ocular Behçet disease presenting as hypopyon-anterior uveitis refractory to conventional immunosuppressive drugs who was safely and effectively managed for 20 years by nonstop infusions of a modern anti-TNF agent, infliximab.
Cem Evereklioglu
doaj +1 more source
Glucocorticoid sensitivity in Behcet's disease [PDF]
, 2012 WOS: 000209773300007PubMed ID: 23781311Objective: Glucocorticoid (GC) sensitivity is highly variable among individuals and has been associated with susceptibility to develop (auto-) inflammatory disorders.
Ben-Chetrit, E +15 more
core +1 more source
Frontiers in Molecular Biosciences, 2022 Background: Behçet’s disease (BD) is a chronic autoimmune disease. The early diagnosis of BD is very important to avoid serious and/or fatal complications such as eye damage, severe neurological involvement, and large vessel occlusion.
Shereen Rashad Mohammed +8 more
doaj +1 more source
IL10 Low-Frequency Variants in Behçet's Disease Patients [PDF]
, 2014 To explain the missing heritability after the genome-wide association studies era, sequencing studies allow the identification of low-frequency variants with a stronger effect on disease risk.
Abdollahi, B +18 more
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Vascular Behçet’s Disease: A Case of Arterial Occlusion and Successful Medical Management
Case Reports in Medicine, Volume 2026, Issue 1, 2026.Behçet’s disease is a rare, chronic, multisystem vasculitis that can involve arteries and veins of all sizes, with vascular manifestations representing some of its most severe and potentially life‐threatening complications. Arterial involvement is uncommon but clinically significant, particularly in young patients.
Alhareth M. Amro +5 more
wiley +1 more source
Síndrome de Budd-Chiari em associação com a doença de Behçet: revisão de literatura [PDF]
, 2011 The risk that patients with Behçet's disease may develop various thrombotic complications has been previously described. Although vascular complications from Budd-Chiari syndrome associated with Behçet's disease have been described, the pathogenic ...
CARVALHO, Daniela +3 more
core +1 more source
Autoimmune diseases and pregnancy: analysis of a series of cases [PDF]
, 2015 BACKGROUND: An autoimmune disease is characterized by tissue damage, caused by self-reactivity of different effector mechanisms of the immune system, namely antibodies and T cells.
Alexandra Mesquita +31 more
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Clinical Dermatology ReviewIntroduction: Pyoderma gangrenosum (PG) is a neutrophilic dermatosis of uncertain etiology characterized by rapidly progressive, painful skin ulcers, and is often difficult to diagnose.
J P Prathibha +3 more
doaj +1 more source
Kikuchi–Fujimoto Disease Presenting With Complex Neurological Manifestations: A Case Report
Case Reports in Neurological Medicine, Volume 2026, Issue 1, 2026.Kikuchi–Fujimoto Disease (KFD) is a rare, typically self‐limiting inflammatory condition primarily associated with fever, cervical lymphadenopathy, and occasionally small‐vessel vasculitis. Central nervous system (CNS) involvement in KFD is exceedingly rare and has been described in isolated cases, including encephalitis, aseptic meningitis, and ...
Yusuf Kagzi +5 more
wiley +1 more source
CC chemokine receptor 5 polymorphism in Italian patients with Behcet's disease. [PDF]
, 2012 Objective. To evaluate the potential role of CC chemokine receptor 5 (CCR5)Δ32 polymorphism in the susceptibility to and clinical expression of Behçet's disease (BD) in a cohort of Italian patients.Methods.
Atzeni, F +14 more
core +2 more sources