Zobrazeno 1 - 10
of 722
pro vyhledávání: '"M. Moin"'
Autor:
M. Gharagozlou, F.A. Ebrahimi, A. Farhoudi, A. Aghamohammadi, M.-H. Bemanian, Z. Chavoshzadeh, M. Heidarzadeh, M. Mehdizadeh, M. Moin, M. Movahedi, M. Nabavi, Z. Pourpak, N. Rezaei
Publikováno v:
Monaldi Archives for Chest Disease, Vol 65, Iss 2 (2016)
Background. Primary hypogammaglobulinemia disorders are a group of heterogeneous immunodeficiency syndromes with an increased susceptibility to pulmonary complications. Methods. The aim of this study was to evaluate the extent of lung abnormalities i
Externí odkaz:
https://doaj.org/article/2d304865851342f791cbf221c1f27c23
Autor:
A. Aghamohammadi, A. Farhoudi, M. Moin, Zahra Pourpak, N. Rezaei, M. Nikzad, M. Movahedi, M. Gharagozlou, Lida Atarod, Akefeh Ahmadi Afshar, Nasrin Bazargan, K. Abolmaali Maryam Mahmoudi
Publikováno v:
Iranian Journal of Allergy, Asthma and Immunology, Vol 2, Iss 3 (2003)
Long-term intravenous immunoglobulin (IVIG) infusion is an effective treatment for children with humoral immunodeficiencies, already be complicated by systemic ad¬verse effects. In order to determine the adverse effects of intravenous immunoglobulin
Externí odkaz:
https://doaj.org/article/14ddfcd3961f47f8acb5b3ab2655d9c1
Autor:
Lida Atarod, Azita Raissi, A. Aghamoliammadi, A. Farhoudi, A. Khodadad, M. Moin, Zahra Pourpak, M. Movaliedi, M. Gliaragozlou, N. Rezaei
Publikováno v:
Iranian Journal of Allergy, Asthma and Immunology, Vol 2, Iss 2 (2003)
One of the most prevalent manifestations of primary antibody deficiencies is gastrointestinal disorders. In this study we reviewed 83 patients including 25 with X-Linked agamma¬globulinemia. 40 with common variable immunodeficiency, 14 with IgA defi
Externí odkaz:
https://doaj.org/article/73445997beb142c39882d09d6bab863b
Autor:
M. Movahedi, A. Aghamohammadi, A. Farhondi, M. Moin, Zahra Pourpak, M. Gharagozlou, D. Mansoiiri, A. Babaei Jandaghi, N. Shahnavaz, N. Rezaei, K. Abolmaali, Sh. Alizadeh Arasi, J. Bakhshaei, M. Vaziri
Publikováno v:
Iranian Journal of Allergy, Asthma and Immunology, Vol 2, Iss 1 (2003)
Chronic granulomatous disease represents a group of inherited disorders of phagocytic system wherein recurrent infections are seen at different sites especially in the respiratory system. To determine the clinical spectrum of respiratory manifestatio
Externí odkaz:
https://doaj.org/article/727921d58de349d7a7c4eaf5e8448ecd
Publikováno v:
Iranian Journal of Allergy, Asthma and Immunology, Vol 1, Iss 1 (2000)
Helicobacter pylori, the most important cause of gastritis and peptic ulcer, has recently been associated with several extradigestive diseases. The aim of this study was to assess the prevalence of Helicobacter pylori infection and effects of bacteri
Externí odkaz:
https://doaj.org/article/51d635199e124111bf9a75a4f4becbf4
Publikováno v:
Iranian Journal of Allergy, Asthma and Immunology, Vol 1, Iss 1 (2000)
The prevalence of allergic diseases is high in the general population, and the high prevalence of these diseases not only leads to considerable mortality and morbidity, but also has economic importance. In this study 400 patients were evaluated in Te
Externí odkaz:
https://doaj.org/article/62f4e09ad34a488cbdb17e5ac256a8c4
Publikováno v:
Iranian Journal of Allergy, Asthma and Immunology, Vol 1, Iss 1 (2000)
Ataxia-telangiectasia (AT) is an autosomal recessive disease characterized by telangiectasia, progressive ataxia, sinopulmonary infection, hypersensitivity to ionizing radiation, and a combined immunodeficiency, usually consisting of selective IgA an
Externí odkaz:
https://doaj.org/article/f5b5b5bb0e6c44048638e4e09bf4d723
Autor:
N. Mojdehi, M. Moin
Publikováno v:
Acta Medica Iranica, Vol 1, Iss 4, Pp 259-265 (1957)
A case of Tropical Eosinophylia which seems to be an independent disease is described. The patient was admitted because of fever, loss of weight- ~and some respiratory disorders. The blood examination shows a high percentage of eosinophylia in severa
Externí odkaz:
https://doaj.org/article/d718f90485ca4897bc668f2d50896d64
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Akademický článek
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