Search Results - "Kiaee, F."

T-Cell Abnormalities in Common Variable Immunodeficiency by Azizi, G, Rezaei, N, Kiaee, F, Tavakolinia, N, Yazdani, R, Mirshafiey, A, Aghamohammadi, A

“…Common variable immunodeficiency (CVID) is the most common clinical primary immunodeficiency. It is characterized by a defect in B-cell differentiation to…”
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Epidemiology and pathophysiology of malignancy in common variable immunodeficiency? by Tak Manesh, A, Azizi, G, Heydari, A, Kiaee, F, Shaghaghi, M, Hossein-Khannazer, N, Yazdani, R, Abolhassani, H, Aghamohammadi, A

“…Common variable immunodeficiency (CVID) is a diagnostic category of primary immunodeficiency (PID) which may present with heterogeneous disorders including…”
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Analysis of Lymphocyte and Clinical Profile in Nonmonogenic Common Variable Immunodeficiency Patients With and Without Class Switch Recombination Defect by Tofighi Zavareh, F, Mirshafiey, A, Yazdani, R, Keshtkar, A A, Abolhassani, H, Kiaee, F, Parvaneh, N, Shariat, M, Rezaei, N, Aghamohammadi, A

“…Common variable immunodeficiency (CVID) is a heterogeneous inborn error of immunity characterized by various clinical manifestations. Class switch…”
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Rheumatologic complications in a cohort of 227 patients with common variable immunodeficiency by Azizi, G., Kiaee, F., Hedayat, E., Yazdani, R., Dolatshahi, E., Alinia, T., Sharifi, L., Mohammadi, H., Kavosi, H., Jadidi‐Niaragh, F., Ziaee, V., Abolhassani, H., Aghamohammadi, A.

“…Common variable immunodeficiency (CVID) is the most prevalent symptomatic type of human primary immunodeficiency diseases (PID). Clinically, CVID is…”
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Evaluation of pulmonary complications in patients with primary immunodeficiency disorders by Reisi, M, Azizi, G, Kiaee, F, Masiha, F, Shirzadi, R, Momen, T, Rafiemanesh, H, Tavakolinia, N, Modaresi, M, Aghamohammadi, A

“…Primary immunodeficiencies (PIDs) are inherited disorders in which one or several components of immune system are defected. Moreover, affected patients are at…”
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Fourth Update on the Iranian National Registry of Primary Immunodeficiencies: Integration of Molecular Diagnosis by Abolhassani, Hassan, Kiaee, Fatemeh, Tavakol, Marzieh, Chavoshzadeh, Zahra, Mahdaviani, Seyed Alireza, Momen, Tooba, Yazdani, Reza, Azizi, Gholamreza, Habibi, Sima, Gharagozlou, Mohammad, Movahedi, Masoud, Hamidieh, Amir Ali, Behniafard, Nasrin, Nabavi, Mohammamd, Bemanian, Mohammad Hassan, Arshi, Saba, Molatefi, Rasol, Sherkat, Roya, Shirkani, Afshin, Amin, Reza, Aleyasin, Soheila, Faridhosseini, Reza, Jabbari-Azad, Farahzad, Mohammadzadeh, Iraj, Ghaffari, Javad, Shafiei, Alireza, Kalantari, Arash, Mansouri, Mahboubeh, Mesdaghi, Mehrnaz, Babaie, Delara, Ahanchian, Hamid, Khoshkhui, Maryam, Soheili, Habib, Eslamian, Mohammad Hossein, Cheraghi, Taher, Dabbaghzadeh, Abbas, Tavassoli, Mahmoud, Kalmarzi, Rasoul Nasiri, Mortazavi, Seyed Hamidreza, Kashef, Sara, Esmaeilzadeh, Hossein, Tafaroji, Javad, Khalili, Abbas, Zandieh, Fariborz, Sadeghi-Shabestari, Mahnaz, Darougar, Sepideh, Behmanesh, Fatemeh, Akbari, Hedayat, Zandkarimi, Mohammadreza, Abolnezhadian, Farhad, Fayezi, Abbas, Moghtaderi, Mojgan, Ahmadiafshar, Akefeh, Shakerian, Behzad, Sajedi, Vahid, Taghvaei, Behrang, Safari, Mojgan, Heidarzadeh, Marzieh, Ghalebaghi, Babak, Fathi, Seyed Mohammad, Darabi, Behzad, Bazregari, Saeed, Bazargan, Nasrin, Fallahpour, Morteza, Khayatzadeh, Alireza, Javahertrash, Naser, Bashardoust, Bahram, Zamani, Mohammadali, Mohsenzadeh, Azam, Ebrahimi, Sarehsadat, Sharafian, Samin, Vosughimotlagh, Ahmad, Tafakoridelbari, Mitra, Rahimi, Maziar, Ashournia, Parisa, Razaghian, Anahita, Rezaei, Arezou, Mamishi, Setareh, Parvaneh, Nima, Rezaei, Nima, Hammarström, Lennart, Aghamohammadi, Asghar

“…Background The number of inherited diseases and the spectrum of clinical manifestations of primary immunodeficiency disorders (PIDs) are ever-expanding…”
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Clinical, immunologic, molecular analyses and outcomes of iranian patients with LRBA deficiency: A longitudinal study by Azizi, Gholamreza, Abolhassani, Hassan, Mahdaviani, Seyed Alireza, Chavoshzadeh, Zahra, Eshghi, Peyman, Yazdani, Reza, Kiaee, Fatemeh, Shaghaghi, Mohammadreza, Mohammadi, Javad, Rezaei, Nima, Hammarström, Lennart, Aghamohammadi, Asghar

“…Background LPS‐responsive beige‐like anchor protein (LRBA) deficiency is a combined immunodeficiency caused by mutation in LRBA gene. The patients have a…”
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Analysis of Lymphocyte and Clinical Profile among Non-monogenic Common Variable Immunodeficiency Patients with and without Class Switch Recombination Defect by Zavareh, FT, Mirshafiey, A, Yazdani, R, Keshtkar, AA, Abolhassani, H, Kiaee, F, Parvaneh, N, Shariat, M, Rezaei, N, Aghamohammadi, A

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Autoimmunity in a cohort of 471 patients with primary antibody deficiencies by Azizi, Gholamreza, Tavakol, Marzieh, Rafiemanesh, Hosein, Kiaee, Fatemeh, Yazdani, Reza, Heydari, Amin, Abouhamzeh, Kosar, Anvari, Pardis, Mohammadikhajehdehi, Sara, Sharifia, Laleh, Bagheri, Yasser, Mohammadi, Hamed, Abolhassani, Hassan, Aghamohammadi, Asghar

“…The aim of this study was to evaluate the frequency of autoimmunity in primary antibody deficiency (PAD). A total of 471 patients with PADs enrolled in this…”
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Comparison of clinical and immunological features and mortality in common variable immunodeficiency and agammaglobulinemia patients by Bagheri, Yasser, Vosughi, Ahmad, Azizi, Gholamreza, Yazdani, Reza, kiaee, Fatemeh, Hafezi, Nasim, Alimorad, Shahriar, Khoshmirsafa, Majid, Seif, Farhad, Hassanpour, Gholamreza, Abolhassani, Hassan, Aghamohammadi, Asghar

“…•1. Infections were the most prevalent clinical manifestations in both groups of patients. 2. Respiratory infections were the most common complication and…”
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G2-lymphocyte chromosomal radiosensitivity in patients with LPS responsive beige-like anchor protein (LRBA) deficiency by Mozdarani, Hossein, Kiaee, Fatemeh, Fekrvand, Saba, Azizi, Gholamreza, Yazdani, Reza, Zaki-Dizaji, Majid, Mozdarani, Sahar, Mozdarani, Sohail, Nosrati, Hassan, Abolhassani, Hassan, Aghamohammadi, Asghar

“…Lipopolysaccharide-responsive, beige-like anchor protein (LRBA) deficiency is an autosomal recessive primary immunodeficiency disease characterized by a…”
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Comparison of Common Monogenic Defects in a Large Predominantly Antibody Deficiency Cohort by Yazdani, Reza, Abolhassani, Hassan, Kiaee, Fatemeh, Habibi, Sima, Azizi, Gholamreza, Tavakol, Marzieh, Chavoshzadeh, Zahra, Mahdaviani, Seyed Alireza, Momen, Tooba, Gharagozlou, Mohammad, Movahedi, Masoud, Hamidieh, Amir Ali, Behniafard, Nasrin, Nabavi, Mohammamd, Bemanian, Mohammad Hassan, Arshi, Saba, Molatefi, Rasol, Sherkat, Roya, Shirkani, Afshin, Amin, Reza, Aleyasin, Soheila, Faridhosseini, Reza, Jabbari-Azad, Farahzad, Mohammadzadeh, Iraj, Ghaffari, Javad, Shafiei, Alireza, Kalantari, Arash, Mansouri, Mahboubeh, Mesdaghi, Mehrnaz, Babaie, Delara, Ahanchian, Hamid, Khoshkhui, Maryam, Soheili, Habib, Eslamian, Mohammad Hossein, Cheraghi, Taher, Dabbaghzadeh, Abbas, Tavassoli, Mahmoud, Kalmarzi, Rasoul Nasiri, Mortazavi, Seyed Hamidreza, Kashef, Sara, Esmaeilzadeh, Hossein, Tafaroji, Javad, Khalili, Abbas, Zandieh, Fariborz, Sadeghi-Shabestari, Mahnaz, Darougar, Sepideh, Behmanesh, Fatemeh, Akbari, Hedayat, Zandkarimi, Mohammadreza, Abolnezhadian, Farhad, Fayezi, Abbas, Moghtaderi, Mojgan, Ahmadiafshar, Akefeh, Shakerian, Behzad, Sajedi, Vahid, Taghvaei, Behrang, Safari, Mojgan, Heidarzadeh, Marzieh, Ghalebaghi, Babak, Fathi, Seyed Mohammad, Darabi, Behzad, Bazregari, Saeed, Bazargan, Nasrin, Fallahpour, Morteza, Khayatzadeh, Alireza, Javahertrash, Naser, Bashardoust, Bahram, Zamani, Mohammadali, Mohsenzadeh, Azam, Ebrahimi, Sarehsadat, Sharafian, Samin, Vosughimotlagh, Ahmad, Tafakoridelbari, Mitra, Rahim, Maziar, Ashournia, Parisa, Razaghian, Anahita, Rezaei, Arezou, Samavat, Ashraf, Mamishi, Setareh, Khazaei, Hossein Ali, Mohammadi, Javad, Negahdari, Babak, Parvaneh, Nima, Rezaei, Nima, Lougaris, Vassilios, Giliani, Silvia, Plebani, Alessandro, Ochs, Hans D., Hammarström, Lennart, Aghamohammadi, Asghar

“…Predominantly antibody deficiencies (PADs) are the most common primary immunodeficiencies, characterized by hypogammaglobulinemia and inability to generate…”
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Genetic mutations and immunological features of severe combined immunodeficiency patients in Iran by Shahbazi, Zahra, Yazdani, Reza, Shahkarami, Sepideh, Shahbazi, Shirin, Hamid, Mohammad, Sadeghi-Shabestari, Mahnaz, Momen, Tooba, Aleyasin, Soheila, Esmaeilzadeh, Hossein, Darougar, Sepideh, Delavari, Sama, Mahdaviani, Seyed Alireza, Ahanchian, Hamid, Behmanesh, Fatemeh, Kiaee, Fatemeh, Chavoshzade, Zahra, Shariat, Mansoureh, Keramatipour, Mohammad, Rezaei, Nima, Abolhassani, Hassan, Parvaneh, Nima, Mahdian, Reza, Aghamohammadi, Asghar

“…•Detecting genetic defects in a large number of SCID patients.•Molecular diagnosis is a critical step for genetic counseling, carrier detection, and prenatal…”
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Evaluation of Radiation Sensitivity in Patients with Hyper IgM Syndrome by Fekrvand, Saba, Mozdarani, Hossein, Delavari, Samaneh, Sohani, Mahsa, Nazari, Farzad, Kiaee, Fatemeh, Bagheri, Yasser, Azizi, Gholamreza, Hassanpour, Gholamreza, Mozdarani, Sohail, Abolhassani, Hassan, Aghamohammadi, Asghar, Yazdani, Reza

“…HIGM syndrome is a rare form of primary immunodeficiencies characterized by normal/increased amounts of serum IgM and decreased serum levels of other switched…”
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Evaluation of infectious and non-infectious complications in patients with primary immunodeficiency by Bazregari, Saeed, Azizi, Gholamreza, Tavakol, Marzieh, Asgardoon, Mohammad Hosein, Kiaee, Fatemeh, Tavakolinia, Naeimeh, Valizadeh, Amir, Abolhassani, Hassan, Aghamohammadi, Asghar

“…Primary immunodeficiency diseases (PIDs) are a heterogeneous group of genetic immune disorders. PID patients suffer from a variety of complications. The aim of…”
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Measurement of Health-Related Quality of Life in Primary Antibody-Deficient Patients by Ataeinia, Bahar, Montazeri, Ali, Tavakol, Marzieh, Azizi, Gholamreza, Kiaee, Fatemeh, Tavakolinia, Naiimeh, Negahdari, Babak, Mohammadi, Javad, Abolhassani, Hassan, Rezaei, Nima, Aghamohammadi, Asghar

“…Background: Primary immunodeficiency diseases are a group of disorders that result from a variety of defects of the immune system. Primary antibody…”
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The Clinical and Immunological Features of Patients with Primary Antibody Deficiencies by Azizi, Gholamreza, Bagheri, Yasser, Tavakol, Marzieh, Askarimoghaddam, Forough, Porrostami, Kumars, Rafiemanesh, Hosein, Yazdani, Reza, Kiaee, Fatemeh, Habibi, Sima, Abouhamzeh, Kosar, Mohammadi, Hamed, Qorbani, Mostafa, Abolhassani, Hassan, Aghamohammadi, Asghar

“…Primary antibody deficiency (PAD) comprises a range of diseases from early to late terminal B cells defects and is associated with the various clinical…”
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Infectious Complications Reporting in Common Variable Immunodeficiency: A Systematic Review and Meta-Analysis by Zainaldain , Hamed, Mohammadi , Sara, Babaie , Farhad, Yazdani , Reza, Azizi , Gholamreza, Mohammadi , Hamed, Jamee , Mahnaz, Rizvi , Fatema Sadaat, Alizadeh , Mahla, Kiaee , Fatemeh, Abolhassani , Hassan, Aghamohammadi , Asghar, Rafiemanesh , Hosein

“…Objectives: Common variable immunodeficiency (CVID) is a heterogeneous disorder characterized by hypogammaglobulinemia and increased susceptibility to…”
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Dystonia in Ataxia Telangiectasia: A Case Report with Novel Mutations by Tajdini , Mohammad, Zaki-Dizaji , Majid, Badv , Reza Shervin, Kiaee , Fatemeh, Abolhassani , Hassan, Aghamohammadi , Asghar, Shojaaldini , Hossein

“…ataxia telangiectasia (a-T) is a common, genetically inherited cause of early childhoodonset ataxia that is classically characterized by progressive cerebellar…”
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Comparison of Bone Mineral Density in Common Variable Immunodeficiency and X-Linked Agammaglobulinaemia Patients by Mohebbi, Ali, Azizi, Gholamreza, Tavakolinia, Naeimeh, Abbasi, Farzaneh, Sayarifard, Fatemeh, Karimipour, Mehdi, Kiaee, Fatemeh, Yazdani, Reza, Ebrahimi, Sareh Sadat, Ebrahimi, Mehran, Rafiemanesh, Hosein, Tafaroji, Javad, Ziaee, Vahid, Abolhassani, Hassan, Aghamohammadi, Asghar

“…Primary antibody deficiency (PAD) is the most common group of primary immunodeficiency disorders, resulting from different defects in the development and…”
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