نتایج جستجو برای: behcet s disease

تعداد نتایج: 2133708  

Journal: :Bosnian journal of basic medical sciences 2011
Maja Zivkovic Marko Zlatanovic Gordana Zlatanovic Jasmina Djordjevic-Jocic Sonja Cekic

The aims of this study are to determine anticardiolipin antibodies in patients with Sy Behcet and to determine correlation between the levels of anticardiolipin antibodies in serum in patients with clinic systemic and ocular manifestations. The study was conducted on 11 patients with Behcet disease (group I), and on 11 healthy subjects (group II). Anticardiolipin antibodies -aCL were determined...

پناهی, محمدمسعود,

Behcet’s syndrome is a generalized vasculitis with unknown cause. Acute recurrent iritis , retinal vasculitis , retinal hemorrhage , macular edema , retinal necrosis , ischemic optic neuropathy and vitritis are the most common ophthalmologic involvement. The aim of this study was to determine the frequency of ophthalmologic involvement in patients with Behcet synd...

Journal: :Turk Kardiyoloji Dernegi arsivi : Turk Kardiyoloji Derneginin yayin organidir 2012
Selen Yurdakul Vefa Aslı Erdemir Özlem Yıldırımtürk Mehmet Salih Gürel Saide Aytekin

OBJECTIVES Behcet's disease (BD) is a chronic inflammatory disease characterized by recurrent oral and genital ulcerations and ocular lesions. This multisystemic disorder primarily affects the vascular system. In the present study, we aimed to evaluate vascular endothelial function in patients with Behcet' s disease without vascular involvement. STUDY DESIGN We studied 40 patients with BD (44...

Background & Aims: Behcet’s disease (BD) is an inflammatory vasculitis of unclear etiology. MCP-1 gene is a member of the C-C chemokines family that is a chemotactic factor for monocytes. The results obtained have shown that the -2518A/G polymorphism of MCP-1 gene is associated with BD. The aim of this study was to evaluate the possible involvement of this polymorphism and Behcet&rsq...

Journal: :acta medica iranica 0
amira hamzaoui department of internal medicine, fattouma bourguiba hospital, monastir, tunisia. rim klii department of internal medicine, fattouma bourguiba hospital, monastir, tunisia. olfa harzallah department of internal medicine, fattouma bourguiba hospital, monastir, tunisia. touhami mahjoub department of internal medicine, fattouma bourguiba hospital, monastir, tunisia. silvia mahjoub department of genetic, university of pharmacology, monastir, tunisia.

to assess the association between polymorphisms of the il-6 -174 g/c and behçet's disease (bd) in tunisian patients. dna was extracted from blood samples taken from 43 tunisian patients and 43 healthy controls. the polymorphisms were analyzed by pcr with the pcr-rflp. no significant association was found between patients and controls concerning polymorphism of il6 -174 g/c between the (allelic ...

Journal: :acta medica iranica 0
amira hamzaoui department of internal medicine, la rabta hospital, tunis, tunisia. fatima jaziri department of internal medicine, la rabta hospital, tunis, tunisia. thouraya ben salem department of internal medicine, la rabta hospital, tunis, tunisia. fatma said imed ben ghorbel department of internal medicine, la rabta hospital, tunis, tunisia. mounir lamloum department of internal medicine, la rabta hospital, tunis, tunisia. monia smiti khanfir department of internal medicine, la rabta hospital, tunis, tunisia.

behcet's disease (bd) is a multisystemic inflammatory disease that occurs most often between the second and fourth decade of life. patients have been reported during the first months of life and after 70 years. our objective was to determine the clinical, paraclinical and genetic characteristics of bd in patients aged < 20 and > 40 years. we conducted a comparative retrospective study including...

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