Results 61 to 70 of about 9,989 (122)
Decreasing Serum Adropin Levels in Patients With Systemic Lupus Erythematosus: A Case‐Control Study
Health Science Reports, Volume 9, Issue 3, March 2026.ABSTRACT Introduction Systematic lupus erythematosus is a complex fundamental autoimmune disease with relapsing‐remitting course and spectrum of disease ranging from mild to life‐threatening illness. Approximately half of women diagnosed with systemic lupus erythematosus (SLE) are affected by obesity, with rates reaching up to 50%.
Mehrzad Hajialilo +5 more
wiley +1 more source
Long-Term Effectiveness of Secukinumab in Patients with Axial Spondyloarthritis
Mediators of Inflammation, 2020 Objectives. The primary aim of our study was to evaluate long-term efficacy of secukinumab (SCK) in patients with axial spondyloarthritis (axSpA); secondary aims were to evaluate drug retention rate and to identify differences in the clinical and ...
Stefano Gentileschi +10 more
doaj +1 more source
Dupilumab Treatment in Pemphigus: A Report of Three Cases and Literature Review
JEADV Clinical Practice, Volume 5, Issue 1, Page 254-257, March 2026.Capsule summary Pemphigus vulgaris and foliaceus are rare autoimmune blistering diseases traditionally treated with corticosteroids, immunosuppressants, intravenous immunoglobulins, and rituximab. A subset of patients remains refractory or has contraindications to these conventional therapies. We present three cases of pemphigus treated with dupilumab.
José Javier Mateos Rico +5 more
wiley +1 more source
Journal of Medical Case Reports, 2012 Introduction Behçet’s disease commonly presents with recurrent oral and genital mucocutaneous ulcerations, uveitis and various skin manifestations. Other clinical symptoms include gastrointestinal ulcerations, arthritis, venous thrombosis, arterial ...
Wagner Claudia +3 more
doaj +1 more source
MEFV Gene Mutations in Behçet’s Disease
Eurasian Journal of Medicine, 2019 Behçet's disease is a chronic inflammatory multisystemic disorder of unknown cause, characterized by orogenital ulcers, uveitis, skin lesions, vascular, locomotor, pulmoner, gastrointestinal, and central nervous system manifestations.
Fazile Hatipoğlu Erdem
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Vision-Threatening Behcet’s Disease: Severity of Ocular Involvement Predictors
Journal of Ophthalmology, 2018 Purpose. To examine and spot systemic findings commonly associated with a serious form of ocular Behcet’s disease. This could potentially help ophthalmologists categorize their patients based on future risk and plan treatment accordingly.
Mohammed A. Hussein +2 more
doaj +1 more source
Respirology Case ReportsBehcet's disease is a chronic, multisystem variable vessel vasculitis characterised by recurrent oral and genital ulcers, ocular inflammation and a wide range of systemic manifestations.
Rinoosha Rachel +4 more
doaj +1 more source
Antistreptolysin O Levels in Patients with Behcet’s Disease
Eurasian Journal of Medicine, 2011 Objective: Behcet’s disease is a multisystem inflammatory disorder, and its etiology has not been defined clearly yet. In this study, we aimed to investigate the antistreptolysin O (ASO) levels of patients with Behcet’s disease.
Hulya Uzkeser +4 more
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A Rare Case of Vasculitis Patched Necrosis of Cecum due to Behçet’s Disease
Case Reports in Surgery, 2017 Isolated cecal necrosis is a rare form of acute ischemic colitis and a rare cause of surgical abdomen. Behçet’s disease is a multisystemic autoimmune condition which can induce vasculitis.
Ehsan Shahverdi +4 more
doaj +1 more source
TWO CASES COMBINED WITH BEHCET’S DISEASE AND RHEUMATIC VALVULAR HEART DISEASE WERE DIAGNOSED
Eurasian Journal of Medicine, 2019 Recent studies have revealed that streptococci play an important role in the etiology of Behcet's disease. As it is known, rheumatic valvular heart disease results from carditis occuring after group A streptococcal infections.
Engin Bozkurt +2 more
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