نتایج جستجو برای: behçet
تعداد نتایج: 781 فیلتر نتایج به سال:
Vascular involvement is one of the major causes of mortality and morbidity in Behçet disease (BD). There are no controlled studies for the management of vascular BD (VBD), and according to the EULAR recommendations, only immunosuppressive (IS) agents are recommended. In this study, we aimed to investigate the therapeutic approaches chosen by Turkish physicians during the initial event and relap...
OBJECTIVE To investigate the long-term efficacy and safety of low-dose and dose-escalating therapy of interferon alfa-2a in the treatment of Behçet uveitis. METHODS This study included 37 patients with refractory Behçet panuveitis unresponsive to conventional immunosuppressive therapy. Induction interferon alfa-2a therapy was given as a daily dose of 3.0 million IU (MIU) subcutaneously for 14...
Background: The etiology of the Behçet disease (BD) has remained obscured. There have been studies to show the association of BD to infections like herpes simplex, hepatitis, and parvovirus B19 however, the findings are rather controversial.Materials and Methods: We selected 55 patients with the best matched symptoms of BD and measured the loads of B19 DNA in their plasma by quantitative real t...
Nosocomial invasive infections due to Acinetobacter species are gradually increasing in the health care settings especially in intensive care units (ICUs).1 This retrospective study is designed to investigate risk factors associated with Acinetobacter bacteremia among children hospitalized in Dr. Behçet Uz Children’s Hospital, during 2005–2011. Nosocomial bacteremia was defined as isolation of ...
Behçet's disease (BD) was described as a three-symptom complex comprising uveitis, oral aphthae, and genital ulcerations. It is a multisystemic, recurrent, inflammatory disorder and it is of unknown cause. Neuro-Behçet (NB) is present in 5%-7% of BD. Movement disorders have rarely been reported in NB. Here, we report a case of chronic parenchymal NB presenting with chorea.
A 28 year old non smoker male with Behçet syndrome presented recurrent oral genital ulcers and erythema nodosum, giant pulmonary arterial saccular aneurysms (Figure 1 D) hemoptysis a nodule biopsy suggestive of necrotizing vasculitis.
Les syndromes myélodysplasiques (SMD) sont des maladies hématologiques clonales. Il existe aussi une composante dysimmunitaire, dirigée contre le clone médullaire pathologique via l’implication lymphocytes T (CD8 et régulateurs) sensibilité accrue à l’apoptose. Des manifestations dysimmunitaires satellites du SMD peuvent être observées, sans qu’aucune corrélation phénotype–caryotype n’ait pu mi...
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