نتایج جستجو برای: major β

تعداد نتایج: 787041  

Journal: :archives of cardiovascular imaging 0
marzieh nikparvar assistant professor of cardiology, fellow of echocardiography, cardiovascular research center, hormozgan university of medical sciences, bandar abbas, ir iran nehzat akiash assistant professor of cardiology, fellow of echocardiography, atherosclerosis research center, ahvaz jundishapur university of medical sciences, ahvaz, ir iran; atherosclerosis research center, ahvaz jundishapur university of medical sciences, ahvaz, ir iran nader fayazi assistant professor of pulmonology, hormozgan university of medical sciences, bandar abbas, ir iran sepideh fouladi general physician, hormozgan university of medical sciences, bandar abbas, ir iran fatemeh jafary general physician, hormozgan university of medical sciences, bandar abbas, ir iran mahboubeh pazoki fellow of echocardiography, rasul akram general hospital, iran university of medical sciences, tehran, ir iran

conclusions the etiology of pah in thalassemia is multifactorial such as inflammatory mediators. also, the absence of the spleen plays an important role in developing a high trv and pah. results average age of the patients was 21.15 ± 6.68 years. no significant difference was observed in the pap between the 2 groups of thalassemia major and intermedia and also the 2 sex groups. indeed, 6.6% of ...

Journal: :International Journal of Andrology 1996

Journal: :Asian Journal of Transfusion Science 2009

Ali Akbar Amirzargar, Ardeshir Ghavamzadeh Batoul Moradi Behrouz Nikbin, Bita Ansaripour Farideh Khosravi Kamran Alimoghadam Morteza Bagheri

Background: β-thalassemia as a hereditary disease is defined as defective synthesis of   β-globin chains, resulting in erythropoiesis abnormalities and severe anemia. Different studies have shown that cytokines and cytokine gene polymorphisms play a major role in the pathogenesis of   β-thalassemia. Single nucleotide polymorphisms (SNPs) within the promoter region or other regulatory sequences ...

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