Search Results - "Babaha, F"

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    Monogenic Primary Immunodeficiency Disorder Associated with Common Variable Immunodeficiency and Autoimmunity by Asgardoon, Mohammad Hossein, Azizi, Gholamreza, Yazdani, Reza, Sohani, Mahsa, Pashangzadeh, Salar, Kalantari, Arash, Shariat, Mansoureh, Shafiei, Alireza, Salami, Fereshte, Jamee, Mahnaz, Rasouli, Seyed Erfan, Mohammadi, Javad, Hassanpour, Gholamreza, Tavakol, Marziyeh, Chavoshzadeh, Zahra, Mahdaviani, Seyed Alireza, Momen, Tooba, Behniafard, Nasrin, Nabavi, Mohammad, Bemanian, Mohammad Hassan, Arshi, Saba, Molatefi, Rasol, Sherkat, Roya, Shirkani, Afshin, Alyasin, Soheila, Jabbari-Azad, Farahzad, Ghaffari, Javad, Mesdaghi, Mehrnaz, Ahanchian, Hamid, Khoshkhui, Maryam, Eslamian, Mohammad Hossein, Cheraghi, Taher, Dabbaghzadeh, Abbas, Nasiri Kalmarzi, Rasoul, Esmaeilzadeh, Hossein, Tafaroji, Javad, Khalili, Abbas, Sadeghi-Shabestari, Mahnaz, Darougar, Sepideh, Moghtaderi, Mojgan, Ahmadiafshar, Akefeh, Shakerian, Behzad, Heidarzadeh, Marzieh, Ghalebaghi, Babak, Fathi, Seyed Mohammad, Darabi, Behzad, Fallahpour, Morteza, Mohsenzadeh, Azam, Ebrahimi, Sarehsadat, Sharafian, Samin, Vosughimotlagh, Ahmad, Tafakoridelbari, Mitra, Rahimi Haji-Abadi, Maziyar, Ashournia, Parisa, Razaghian, Anahita, Rezaei, Arezou, Delavari, Samaneh, Shirmast, Paniz, Babaha, Fateme, Samavat, Ashraf, Mamishi, Setareh, Khazaei, Hossein Ali, Negahdari, Babak, Rezaei, Nima, Abolhassani, Hassan, Aghamohammadi, Asghar

    “…Common variable immunodeficiency (CVID) is the most frequent primary immunodeficiency disorder mainly characterized by recurrent bacterial infections besides…”
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    Journal Article
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    IL-10 induces TGF-β secretion, TGF-β receptor II upregulation, and IgA secretion in B cells by Bagheri, Yasser, Babaha, Fateme, Falak, Reza, Yazdani, Reza, Azizi, Gholamreza, Sadri, Maryam, Abolhassani, Hassan, Shekarabi, Mehdi, Aghamohammadi, Asghar

    Published in European cytokine network (01-09-2019)
    “…Interleukin-10 (IL-10) is a pleiotropic cytokine, which has both regulatory and stimulatory effects on different immune cell types. Different studies have…”
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    Journal Article
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    PIK3R1 Mutation Associated with Hyper IgM (APDS2 Syndrome): A Case Report and Review of the Literature by Yazdani, Reza, Hamidi, Zahra, Babaha, Fateme, Azizi, Gholamreza, Fekrvand, Saba, Abolhassani, Hassan, Aghamohammadi, Asghar

    “…APDS [Activated phosphoinositide 3-kinase (PI3K) δ Syndrome] is a newly found special form of primary immunodeficiency caused by mutations in genes encoding…”
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    Journal Article