Results 11 to 20 of about 9,989 (122)
Blepharoptosis in Behçet's Disease [PDF]
Archives of Aesthetic Plastic Surgery, 2016 Behçet's disease is a systemic chronic disease that occurs in tissues such as eyes, joints, organs and nerves, and it has been noted that symptoms may be observed in a variety of tissues.
So-Min Hwang +4 more
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The acquisition of trisomy 8 associated with Behçet's-like disease in myelodysplastic syndrome
Leukemia Research Reports, 2020 A relationship has been reported between myelodysplastic syndrome (MDS) and autoimmune disease. Behçet's disease is a multisystem inflammatory disorder with mucocutaneous, articular, gastrointestinal, neurological, and vascular manifestations.
Satoko Oka, Kazuo Ono, Masaharu Nohgawa
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Hints for Genetic and Clinical Differentiation of Adult-Onset Monogenic Autoinflammatory Diseases
Mediators of Inflammation, 2019 Monogenic autoinflammatory diseases (mAIDs) are inherited errors of innate immunity characterized by systemic inflammation recurring with variable frequency and involving the skin, serosal membranes, synovial membranes, joints, the gastrointestinal tube,
Carla Gaggiano +11 more
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Egyptian Rheumatology and Rehabilitation, 2018 Background Insulin resistance is found in Behçet’s disease and associated with the development of metabolic syndrome. Our study explored whether amylin, which is involved in insulin resistance and development of metabolic syndrome, is observed in ...
Shimaa M Abdelwhab +3 more
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Could Mean Platelet Volume Be Used as A Marker for Oral Aphthae and Activity of Behçet’s Disease?
İstanbul Medical Journal, 2016 Objective: Behçet’s disease is a common inflammatory disease in our country. We aimed to determine whether mean platelet volume can be used as a marker for oral aphthae and the activity of Behçet’s disease.Methods: Between 04/01/2010 and 30/07/2010, 78 ...
Okan Dikker +5 more
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Low Level Laser Therapy to Reduce Recurrent Oral Ulcers in Behçet’s Disease
Case Reports in Dentistry, 2016 Behçet’s disease (BD) is a chronic, relapsing multisystemic vascular condition. Behçet’s disease was described by Hulusi Behçet in 1937. This rare multisystem relapsing-remitting inflammatory disease is poorly understood but is thought to be an ...
D. B. Gandhi Babu +4 more
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Journal of Medical Case Reports, 2011 Introduction The risk that patients with Behçet's disease will develop thrombotic complications has been previously described. Although it is distributed worldwide, Behçet's disease is rare in the Americas and Europe.
Évora Paulo RB +4 more
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Behçet's Disease (Adamantiades-Behçet's Disease)
Clinical and Developmental Immunology, 2011 Adamantiades-Behçet's disease (ABD) is characterized by starting with oral aphthous ulceration and developing of the systemic involvements. The pathogenesis of ABD is closely correlated with the genetic factors and the triggering factors which acquire ...
Fumio Kaneko +7 more
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Acta Medica Iranica, 2005 Behçet’s disease (BD) which is classified among vasculitides is a systemic disease with various manifestations. Its clinical course is characterized by attacks and remissions.
F. Davatchi +3 more
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Spontaneous resolution of unilateral Behcet's associated neuroretinitis
American Journal of Ophthalmology Case Reports, 2020 Purpose: Behcet's disease is an immune-mediated condition which can commonly have ocular involvement. We present a case of Behcet's associated neuroretinitis, which is a rare ocular manifestation of Behcet's disease. Observations: The patient experienced
George Skopis, Sneha Padidam, Brian Do
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