نتایج جستجو برای: behcet disease

تعداد نتایج: 1490306  

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1997
N Mizuki M Ota M Kimura S Ohno H Ando Y Katsuyama M Yamazaki K Watanabe K Goto S Nakamura S Bahram H Inoko

A member of a novel family of the human major histocompatibility complex (MHC) class I genes termed MIC (MHC class I chain-related genes), MICA, has been recently identified near the HLA-B gene on the short arm of human chromosome 6. The predicted amino acid sequence of the MICA chain suggests that it folds similarly to typical class I chains and may have the capacity to bind peptides or other ...

Journal: :the journal of tehran university heart center 0
seyedebrahim kassaian tehran heart center, tehran university of medical sciences, tehran, iran. kyomars abbasi tehran heart center, tehran university of medical sciences, tehran, iran. mahmood shirzad tehran heart center, tehran university of medical sciences, tehran, iran. maryam sotoudeh-anvari tehran heart center, tehran university of medical sciences, tehran, iran. maryam shahrzad tehran heart center, tehran university of medical sciences, tehran, iran. behnam molavi dr. shariati hospital, tehran university of medical sciences, tehran, iran.

behcet’s disease is a rare immune mediated systemic vasculitis which besides it’s more frequent involvement of eyes and skin,   sometimes present with aortic pseudo aneurysm and more rarely cardiac inflammatory masses.a 51-year-old patient with behçet’s disease presented with two symptomatic aortic pseudoaneurysms concomitant with a right atrial mass. computed tomography (ct) revealed one supra...

 Background: Behçet’s disease (BD) is a multi-system inflammatory vascular disorder with auto immunity background. It is a genetic disease that may be affected by environmental factors. Behçet’s disease may involve different organs like urogenital, skin, eyes and gastrointestinal system. According to geographic area and genetic predisposition, prevalence of the disease is different. The aim of...

2013
Y Shinar G Breuer A Livneh P Hashkes

Case Report We confirmed the Muckle-Wells syndrome phenotype of CAPS by NLRP3 genetic testing in a three generation family of Turkish Jewish origin, previously diagnosed with familial Behcet disease due to the presence of mucosal ulcers in several family members with the finding of the HLA-B51 antigen in at least one family member. Eight family members including a deceased grandfather, 4 of his...

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