Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Fatemeh Atashrazm"'
Autor:
Javad Nazari, Faezeh Shahba, Negin Jafariaghdam, Saleh Mohebbi, Saba Arshi, Mohammad Hassan Bemanian, Morteza Fallahpour, Sima Shokri, Fatemeh Atashrazm, Saeed Amini, Maryam Roomiani, Mahnaz Jamee, Pegah Babaheidarian, Majid Khoshmirsafa, Mohammad Nabavi
Publikováno v:
Allergy, Asthma & Clinical Immunology, Vol 20, Iss 1, Pp 1-10 (2024)
Abstract Background Chronic Rhinosinusitis (CRS) is a paranasal sinus inflammatory disease and is divided into two subgroups defined as CRS with nasal polyps (CRSwNP) and CRS without nasal polyps (CRSsNP). CRSwNP displays a T helper (Th)2 biased phen
Externí odkaz:
https://doaj.org/article/33c3b558be114abcbb913f0d47e06879
Autor:
Mohammad Nabavi, Faezeh Mohammadi, Saba Arshi, Mohammad Hasan Bemanian, Morteza Fallahpour, Fatemeh Atashrazm, Sima Shokri
Publikováno v:
Iranian Journal of Allergy, Asthma and Immunology, Vol 21, Iss 5 (2022)
Coronavirus disease 2019 (COVID-19) affects millions of people worldwide. Clinical manifestations range from asymptomatic to severe viral pneumonia. CVID patients with COVID-19 infection are not adequately studied. In some studies, CVID patients had
Externí odkaz:
https://doaj.org/article/ee0b0bc2aae84e4c9c805d73939d97f2
Autor:
Mohammad Nabavi, Afshin Rezaeifar, Morteza Fallahpour, Saba Arshi, Mohammad Hassan Bemanian, Sima Shokri, Fatemeh Atashrazm, Sima Bahrami, Mehrnaz Asadi Gharabaghi, Parisa Rezaeifar, Zahra Vakilazad
Publikováno v:
Clinical Case Reports, Vol 9, Iss 6, Pp n/a-n/a (2021)
Abstract Good's syndrome is a rare adult‐onset thymoma‐associated immunodeficiency with unknown pathogenesis. Therefore, it should be carefully managed as soon as possible when complications are presented. Because of variety of immunodeficiency,
Externí odkaz:
https://doaj.org/article/e041653d699648199cb7ce75494df060
Autor:
Mohammad Hassan Bemanian, Saba Arshi, Mohammad Nabavi, Mohammad Vafaee-Shahi, Morteza Fallahpour, Sima Shokri, Afshin Rezaeifar, Hossein Shahzadi, Fatemeh Atashrazm
Publikováno v:
Iranian Journal of Allergy, Asthma and Immunology, Vol 20, Iss 2 (2021)
Immunodeficiency, centromeric instability, and facial anomalies (ICF) syndrome is a rare primary immunodeficiency disorder characterized by recurrent infections and low immunoglobulin levels due to variable combined immunodeficiency, and centromeric
Externí odkaz:
https://doaj.org/article/e9f9c4e763e64b26b2ea20b0d1a7380f
Descriptive Study of 123 Symptomatic Patients with IgA Deficiency, a Retrospective Case Series Study
Autor:
Mohammad Hassan Bemanian, Saba Arshi, Mohammad Nabavi, Morteza Fallahpour, Sima Shokri, Ali Alimohammadi, Nahid Chezanisharahi, Fatemeh Atashrazm, Vahid Bakrani, Javad Nazari
Publikováno v:
Immunology and Genetics Journal.
Background: IgA deficiency (IgAD) is the most common primary immunodeficiency, which is caused by a defect in IgA antibody production. Most of the patients are asymptomatic. However, patients can present various manifestations. This study was designe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2de57fb2804adf5bc69091db64051165
https://doi.org/10.18502/igj.v4i2.9987
https://doi.org/10.18502/igj.v4i2.9987
Autor:
Mohammad Nabavi, Saba Arshi, Mohammad Hassan Bemanian, Morteza Fallahpour, Sima Shokri, Sofia Sabouri, Fatima Moosavian, Javad Nazari, Vahid Bakrani, Fatemeh Atashrazm
Publikováno v:
American Journal of Rhinology & Allergy. :194589242311540
Background Chronic rhinosinusitis with nasal polyps (CRSwNP) is a complex disorder and effective treatment remains a major challenge. Some antibiotics with anti-inflammatory properties are reported to have potential to be used as an adjunct therapy i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::607ece4b1872670a36e2a9615c2e5054
https://doi.org/10.1177/19458924231154066
https://doi.org/10.1177/19458924231154066
Autor:
Parisa Rezaeifar, Mohammad Nabavi, Mohammad Hassan Bemanian, Afshin Rezaeifar, Saba Arshi, Mehrnaz Asadi Gharabaghi, Morteza Fallahpour, Fatemeh Atashrazm, Zahra Vakilazad, Sima Shokri, Sima Bahrami
Publikováno v:
Clinical Case Reports, Vol 9, Iss 6, Pp n/a-n/a (2021)
Good's syndrome is a rare adult‐onset thymoma‐associated immunodeficiency with unknown pathogenesis. Therefore, it should be carefully managed as soon as possible when complications are presented. Because of variety of immunodeficiency, this synd
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d0f945e614f3f9052c73c24307999d4e
https://doi.org/10.1002/ccr3.4136
https://doi.org/10.1002/ccr3.4136