Results 61 to 70 of about 8,054 (126)
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
Neurological Behcet’s disease with transverse myelitis in an adolescent: A case report
SAGE Open Medical Case ReportsNeurological Behcet’s disease is a rare systemic vasculitis marked by recurrent oral or genital ulcers, eye manifestations of uveitis or retinal vasculitis, and skin lesions.
Jeanine McColl +2 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
doaj
Bilateral Hemophthalmus — the First Symptom of Behcet’s Disease (Clinical Case)
Oftalʹmologiâ, 2016 Behcet’s disease (BD) — a systemic chronic idiopathic inflammatory recurrent disease of unknown etiology. The development of the disease involve a combination of various factors, among them the most important is genetic and infectious.
O. Yu. Yatsenko +5 more
doaj +1 more source
Polymorphisms of MicroRNA-146a Gene in Behcet’s Disease in Iraqi Patients
Journal of Pure and Applied Microbiology, 2018 The present study was carried out to detect the association of miR-146a haplotypes polymorphisms with Behcet’s Disease in Iraqi patients, PCR-SSCP technique used in present study, blood was used to DNA extraction, the results show that there was strong
Israa Harjan Mohsen +4 more
doaj +1 more source
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
Juvenile Behсet's Disease: Clinical Observation
Вопросы современной педиатрии, 2016 Behcet's disease is a type of systemic vasculitis of unknown etiology characterized by recurrent erosive and ulcerative lesions of the mucous membrane in the mouth and genitals and pathological processes in the joints, central nervous system, and ...
Nikolai V. Sobotiuk +8 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
doaj
Early administration of adalimumab for paediatric uveitis due to Behçet’s disease
Pediatric Rheumatology Online Journal, 2019 Background Behçet’s disease is a chronic inflammatory multisystem disorder that is characterised by oral and/or genital ulcerations as well as intraocular inflammation.
Tomona Hiyama +3 more
doaj +1 more source
Journal of International Medical ResearchBehçet’s disease, also known as the oral–ocular–genital syndrome, is a chronic systemic vasculitis characterized by recurrent oral and genital ulcers as well as ocular manifestations such as uveitis and conjunctivitis.
Dou Yuan
doaj +1 more source