Results 11 to 20 of about 4,851,513 (185)
Anti-Tumor Necrosis Factor Therapy in Intestinal Behçet’s Disease
Gut and Liver, 2018 Intestinal Behçet’s disease is a rare, immune-mediated chronic intestinal inflammatory disease; therefore, clinical trials to optimize the management and treatment of patients are scarce.
Jihye Park, Jae Hee Cheon
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Behçet's Disease (Adamantiades-Behçet's Disease) [PDF]
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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Different Aspects of Behçet's Disease [PDF]
, 2020 The aim of this book is to give readers a different review of Behçet's disease, which has very rich mucocutaneous and systemic characteristics and can be confused with many diseases. This book has a total of five chapters. The first two chapters focus on
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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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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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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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Regarding neutrophil and lymphocyte responses to oralStreptococcusin AdamantiadesâBehçet's disease [PDF]
FEMS Immunology & Medical Microbiology, 2006 Dear Editor, I read the recent study of Kurauchi et al. entitled ‘Neutrophil and lymphocyte responses to oral Streptococcus in Adamantiades–Behcet's disease’ ( FEMS Immunol Med Microbiol 43: 125–131) with great interest. The authors evaluated neutrophil reactions and cytokine production levels by lymphocytes after stimulation with Streptococcus ...
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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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Concurrence of Incontinentia Pigmenti and Behçet's Disease [PDF]
, 2010 We report here a rare case of incontinentia pigmenti (IP) in a 10-year-old girl who developed Behçet's disease. IP was diagnosed in infancy and Behçet's disease was diagnosed at 10 years of age.
Lin-Shien Fu +3 more
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Case Report - Familial Behçet's disease [PDF]
, 2007 There are very few reports of Behçet's disease from India. Familial aggregation of Behçet's disease has been reported with restricted geographical distribution.
Singh, Sanjay +4 more
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