Items where Author is "Aghamohammadi, A."

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Number of items: 36.

Article

Fekrvand, S. and Abolhassani, H. and Delavari, S. and Yazdani, R. and Aghamohammadi, A. (2020) Are asthma and allergic diseases phenotypic markers for patients with common variable immunodeficiency? Annals of Allergy, Asthma and Immunology, 124 (6). p. 636.

Aghamohammadi, A. and Shaghaghi, M. and Abolhassani, H. and Yazdani, R. and Zahraie, S.M. and Goya, M.M. and Mahmoudi, S. and Rezaei, N. and Shahmahmoodi, S. (2020) Establishment of national primary immunodeficiency network, requisite of health organization and final stage of polio eradication: Review article. Tehran University Medical Journal, 78 (1). pp. 1-8.

Fekrvand, S. and Yazdani, R. and Olbrich, P. and Azizi, G. and Shirzadi, R. and Modaresi, M. and Sohani, M. and Delavari, S. and Kalantari, A. and Shariat, M. and Shafiei, A. and Lu, N. and Hassanpour, G. and Rahimi Hajiabadi, M. and Ashournia, P. and Razaghian, A. and Asgharyan, M. and Shahraki-Ghadimi, Z. and Rouhani, R. and Hoda Fallah, F. and Rezaei, N. and Abolhassani, H. and Aghamohammadi, A. (2020) Evaluation of respiratory complications in patients with X-linked and autosomal recessive agammaglobulinemia. Pediatric Allergy and Immunology, 31 (4). pp. 405-417.

Fekrvand, S. and Yazdani, R. and Olbrich, P. and Gennery, A. and Rosenzweig, S.D. and Condino-Neto, A. and Azizi, G. and Rafiemanesh, H. and Hassanpour, G. and Rezaei, N. and Abolhassani, H. and Aghamohammadi, A. (2020) Primary Immunodeficiency Diseases and Bacillus Calmette-Guérin (BCG)-Vaccine�Derived Complications: A Systematic Review. Journal of Allergy and Clinical Immunology: In Practice, 8 (4). pp. 1371-1386.

Tafakori Delbari, M. and Cheraghi, T. and Yazdani, R. and Fekrvand, S. and Delavari, S. and Azizi, G. and Chavoshzadeh, Z. and Mahdaviani, S.A. and Ahanchian, H. and Khoshkhui, M. and Behmanesh, F. and Aleyasin, S. and Esmaeilzadeh, H. and Jabbari-Azad, F. and Fallahpour, M. and Zamani, M. and Madani, S.P. and Moazzami, B. and Habibi, S. and Rezaei, A. and Lotfalikhani, A. and Movahed, M. and Shariat, M. and Kalantari, A. and Babaei, D. and Darabi, M. and Parvaneh, N. and Rezaei, N. and Abolhassani, H. and Aghamohammadi, A. (2019) Clinical Manifestations, Immunological Characteristics and Genetic Analysis of Patients with Hyper-Immunoglobulin M Syndrome in Iran. International Archives of Allergy and Immunology.

Yazdani, R. and Abolhassani, H. and Kiaee, F. and Habibi, S. and Azizi, G. and Tavakol, M. and Chavoshzadeh, Z. and Mahdaviani, S.A. and Momen, T. and Gharagozlou, M. and Movahedi, M. and Hamidieh, A.A. and Behniafard, N. and Nabavi, M. and Bemanian, M.H. and Arshi, S. and Molatefi, R. and Sherkat, R. and Shirkani, A. and Amin, R. and Aleyasin, S. and Faridhosseini, R. and Jabbari-Azad, F. and Mohammadzadeh, I. and Ghaffari, J. and Shafiei, A. and Kalantari, A. and Mansouri, M. and Mesdaghi, M. and Babaie, D. and Ahanchian, H. and Khoshkhui, M. and Soheili, H. and Eslamian, M.H. and Cheraghi, T. and Dabbaghzadeh, A. and Tavassoli, M. and Kalmarzi, R.N. and Mortazavi, S.H. and Kashef, S. and Esmaeilzadeh, H. and Tafaroji, J. and Khalili, A. and Zandieh, F. and Sadeghi-Shabestari, M. and Darougar, S. and Behmanesh, F. and Akbari, H. and Zandkarimi, M. and Abolnezhadian, F. and Fayezi, A. and Moghtaderi, M. and Ahmadiafshar, A. and Shakerian, B. and Sajedi, V. and Taghvaei, B. and Safari, M. and Heidarzadeh, M. and Ghalebaghi, B. and Fathi, S.M. and Darabi, B. and Bazregari, S. and Bazargan, N. and Fallahpour, M. and Khayatzadeh, A. and Javahertrash, N. and Bashardoust, B. and Zamani, M. and Mohsenzadeh, A. and Ebrahimi, S. and Sharafian, S. and Vosughimotlagh, A. and Tafakoridelbari, M. and Rahim, M. and Ashournia, P. and Razaghian, A. and Rezaei, A. and Samavat, A. and Mamishi, S. and Khazaei, H.A. and Mohammadi, J. and Negahdari, B. and Parvaneh, N. and Rezaei, N. and Lougaris, V. and Giliani, S. and Plebani, A. and Ochs, H.D. and Hammarström, L. and Aghamohammadi, A. (2019) Comparison of Common Monogenic Defects in a Large Predominantly Antibody Deficiency Cohort. Journal of Allergy and Clinical Immunology: In Practice, 7 (3). 864-878.e9.

Bagheri, Y. and Vosughi, A. and Azizi, G. and Yazdani, R. and kiaee, F. and Hafezi, N. and Alimorad, S. and Khoshmirsafa, M. and Seif, F. and Hassanpour, G. and Abolhassani, H. and Aghamohammadi, A. (2019) Comparison of clinical and immunological features and mortality in common variable immunodeficiency and agammaglobulinemia patients. Immunology Letters, 210. pp. 55-62.

Sanaei, R. and Rezaei, N. and Aghamohammadi, A. and Delbandi, A.-A. and Tavasolian, P. and Tajik, N. (2019) Disturbed Transcription of TLRs� Negative Regulators and Cytokines Secretion among TLR4- and 9-Activated PBMCs of Agammaglobulinemic Patients. Immunological Investigations.

Sanaei, R. and Rezaei, N. and Aghamohammadi, A. and Delbandi, A.-A. and Teimourian, S. and Yazdani, R. and Tavasolian, P. and Kiaee, F. and Tajik, N. (2019) Evaluation of the TLR negative regulatory network in CVID patients. Genes and Immunity, 20 (3). pp. 198-206.

Yazdani, R. and Shapoori, S. and Rezaeepoor, M. and Sanaei, R. and Ganjalikhani-Hakemi, M. and Azizi, G. and Rae, W. and Aghamohammadi, A. and Rezaei, N. (2019) Features and roles of T helper 9 cells and interleukin 9 in immunological diseases. Allergologia et Immunopathologia, 47 (1). pp. 90-104.

Bagheri, Y. and Sanaei, R. and Yazdani, R. and Shekarabi, M. and Falak, R. and Mohammadi, J. and Abolhassani, H. and Aghamohammadi, A. (2019) The Heterogeneous Pathogenesis of Selective Immunoglobulin A Deficiency. International Archives of Allergy and Immunology. pp. 232-246.

Azizi, G. and Bagheri, Y. and Yazdani, R. and Zaki-Dizaji, M. and Jamee, M. and Jadidi-Niaragh, F. and Kamali, A.N. and Abolhassani, H. and Aghamohammadi, A. (2019) The profile of IL-4, IL-5, IL-10 and GATA3 in patients with LRBA deficiency and CVID with no known monogenic disease: Association with disease severity. Allergologia et Immunopathologia, 47 (2). pp. 172-178.

Abolhassani, H. and Chou, J. and Bainter, W. and Platt, C.D. and Tavassoli, M. and Momen, T. and Tavakol, M. and Eslamian, M.H. and Gharagozlou, M. and Movahedi, M. and Ghadami, M. and Hamidieh, A.A. and Azizi, G. and Yazdani, R. and Afarideh, M. and Ghajar, A. and Havaei, A. and Chavoshzadeh, Z. and Mahdaviani, S.A. and Cheraghi, T. and Behniafard, N. and Amin, R. and Aleyasin, S. and Faridhosseini, R. and Jabbari-Azad, F. and Nabavi, M. and Bemanian, M.H. and Arshi, S. and Molatefi, R. and Sherkat, R. and Mansouri, M. and Mesdaghi, M. and Babaie, D. and Mohammadzadeh, I. and Ghaffari, J. and Shafiei, A. and Kalantari, N. and Ahanchian, H. and Khoshkhui, M. and Soheili, H. and Dabbaghzadeh, A. and Shirkani, A. and Nasiri Kalmarzi, R. and Mortazavi, S.H. and Tafaroji, J. and Khalili, A. and Mohammadi, J. and Negahdari, B. and Joghataei, M.-T. and al-Ramadi, B.K. and Picard, C. and Parvaneh, N. and Rezaei, N. and Chatila, T.A. and Massaad, M.J. and Keles, S. and Hammarström, L. and Geha, R.S. and Aghamohammadi, A. (2018) Clinical, immunologic, and genetic spectrum of 696 patients with combined immunodeficiency. Journal of Allergy and Clinical Immunology, 141 (4). pp. 1450-1458.

Abolhassani, H. and Chou, J. and Bainter, W. and Platt, C.D. and Tavassoli, M. and Momen, T. and Tavakol, M. and Eslamian, M.H. and Gharagozlou, M. and Movahedi, M. and Ghadami, M. and Hamidieh, A.A. and Azizi, G. and Yazdani, R. and Afarideh, M. and Ghajar, A. and Havaei, A. and Chavoshzadeh, Z. and Mahdaviani, S.A. and Cheraghi, T. and Behniafard, N. and Amin, R. and Aleyasin, S. and Faridhosseini, R. and Jabbari-Azad, F. and Nabavi, M. and Bemanian, M.H. and Arshi, S. and Molatefi, R. and Sherkat, R. and Mansouri, M. and Mesdaghi, M. and Babaie, D. and Mohammadzadeh, I. and Ghaffari, J. and Shafiei, A. and Kalantari, N. and Ahanchian, H. and Khoshkhui, M. and Soheili, H. and Dabbaghzadeh, A. and Shirkani, A. and Nasiri Kalmarzi, R. and Mortazavi, S.H. and Tafaroji, J. and Khalili, A. and Mohammadi, J. and Negahdari, B. and Joghataei, M.-T. and al-Ramadi, B.K. and Picard, C. and Parvaneh, N. and Rezaei, N. and Chatila, T.A. and Massaad, M.J. and Keles, S. and Hammarström, L. and Geha, R.S. and Aghamohammadi, A. (2018) Clinical, immunologic, and genetic spectrum of 696 patients with combined immunodeficiency. Journal of Allergy and Clinical Immunology, 141 (4). pp. 1450-1458.

Sanaei, R. and Rezaei, N. and Aghamohammadi, A. and Delbandi, A.-A. and Teimourian, S. and Yazdani, R. and Tavasolian, P. and Kiaee, F. and Tajik, N. (2018) Evaluation of the TLR negative regulatory network in CVID patients. Genes and Immunity. pp. 1-9.

Sanaei, R. and Rezaei, N. and Aghamohammadi, A. and Delbandi, A.-A. and Teimourian, S. and Yazdani, R. and Tavasolian, P. and Kiaee, F. and Tajik, N. (2018) Evaluation of the TLR negative regulatory network in CVID patients. Genes and Immunity. pp. 1-9.

Yazdani, R. and Shapoori, S. and Rezaeepoor, M. and Sanaei, R. and Ganjalikhani-Hakemi, M. and Azizi, G. and Rae, W. and Aghamohammadi, A. and Rezaei, N. (2018) Features and roles of T helper 9 cells and interleukin 9 in immunological diseases. Allergologia et Immunopathologia.

Yazdani, R. and Shapoori, S. and Rezaeepoor, M. and Sanaei, R. and Ganjalikhani-Hakemi, M. and Azizi, G. and Rae, W. and Aghamohammadi, A. and Rezaei, N. (2018) Features and roles of T helper 9 cells and interleukin 9 in immunological diseases. Allergologia et Immunopathologia.

Sharifi, L. and Mohsenzadegan, M. and Aghamohammadi, A. and Rezaei, N. and Zavareh, F.T. and Bokaie, S. and Moshiri, M. and Aghazadeh, Z. and Norouzbabaie, Z. and Azizi, G. and Mirshafiey, A. (2018) Immunomodulatory effect of G2013 (α-L-guluronic acid) on the TLR2 and TLR4 in human mononuclear cells. Current Drug Discovery Technologies, 15 (2). pp. 123-131.

Sharifi, L. and Mohsenzadegan, M. and Aghamohammadi, A. and Rezaei, N. and Zavareh, F.T. and Bokaie, S. and Moshiri, M. and Aghazadeh, Z. and Norouzbabaie, Z. and Azizi, G. and Mirshafiey, A. (2018) Immunomodulatory effect of G2013 (α-L-guluronic acid) on the TLR2 and TLR4 in human mononuclear cells. Current Drug Discovery Technologies, 15 (2). pp. 123-131.

Sharifi, L. and Aghamohammadi, A. and Rezaei, N. and Yazdani, R. and Mahmoudi, M. and Amiri, M.M. and Masoumi, F. and Bokaie, S. and Tavasolian, P. and Sanaei, R. and Moshiri, M. and Tavakolinia, N. and Alinia, T. and Azizi, G. and Mirshafiey, A. (2018) The Profile of Toll-like Receptor 2 (TLR2), TLR4 and Their Cytosolic Downstream Signaling Pathway in Common Variable Immunodeficiency (CVID) Patients. Iranian Journal of Allergy, Asthma and Immunology, 17 (2). 188-200..

Sharifi, L. and Aghamohammadi, A. and Rezaei, N. and Yazdani, R. and Mahmoudi, M. and Amiri, M.M. and Masoumi, F. and Bokaie, S. and Tavasolian, P. and Sanaei, R. and Moshiri, M. and Tavakolinia, N. and Alinia, T. and Azizi, G. and Mirshafiey, A. (2018) The Profile of Toll-like Receptor 2 (TLR2), TLR4 and Their Cytosolic Downstream Signaling Pathway in Common Variable Immunodeficiency (CVID) Patients. Iranian Journal of Allergy, Asthma and Immunology, 17 (2). 188-200..

Behniafard, N. and Amirzargar, A.A. and Gharagozlou, M. and Delavari, F. and Hosseinverdi, S. and Sotoudeh, S. and Farhadi, E. and Mahmoudi, M. and Khaledi, M. and Moghaddam, Z.G. and Aghamohammadi, A. and Rezaei, N. (2018) Single nucleotide polymorphisms of the genes encoding IL-10 and TGF-β1 in Iranian children with atopic dermatitis. Allergologia et Immunopathologia, 46 (2). pp. 155-159.

Behniafard, N. and Amirzargar, A.A. and Gharagozlou, M. and Delavari, F. and Hosseinverdi, S. and Sotoudeh, S. and Farhadi, E. and Mahmoudi, M. and Khaledi, M. and Moghaddam, Z.G. and Aghamohammadi, A. and Rezaei, N. (2018) Single nucleotide polymorphisms of the genes encoding IL-10 and TGF-β1 in Iranian children with atopic dermatitis. Allergologia et Immunopathologia, 46 (2). pp. 155-159.

Azizi, G. and Bagheri, Y. and Tavakol, M. and Askarimoghaddam, F. and Porrostami, K. and Rafiemanesh, H. and Yazdani, R. and Kiaee, F. and Habibi, S. and Abouhamzeh, K. and Mohammadi, H. and Qorbani, M. and Abolhassani, H. and Aghamohammadi, A. (2018) The clinical and immunological features of patients with primary antibody deficiencies. Endocrine, Metabolic and Immune Disorders - Drug Targets, 18 (5). pp. 537-545.

Azizi, G. and Bagheri, Y. and Yazdani, R. and Zaki-Dizaji, M. and Jamee, M. and Jadidi-Niaragh, F. and Kamali, A.N. and Abolhassani, H. and Aghamohammadi, A. (2018) The profile of IL-4, IL-5, IL-10 and GATA3 in patients with LRBA deficiency and CVID with no known monogenic disease: Association with disease severity. Allergologia et Immunopathologia.

Shokri, S. and Nabavi, M. and Hirschmugl, T. and Aghamohammadi, A. and Arshi, S. and Bemanian, M.H. and Fallahpour, M. and Molatefi, R. and Rekabi, M. and Eslami, N. and Ahmadian, J. and Darabi, K. and Sedighi, G.R. and Monajemzadeh, M. and Modaresi, M. and Parvaneh, N. and Boztug, K. and Rezaei, N. (2016) LPS-responsive beige-like anchor gene mutation associated with possible bronchiolitis obliterans organizing pneumonia associated with hypogammaglobulinemia and normal IgM phenotype and low number of B. Acta Medica Iranica, 54 (10). pp. 620-623.

Shokri, S. and Nabavi, M. and Hirschmugl, T. and Aghamohammadi, A. and Arshi, S. and Bemanian, M.H. and Fallahpour, M. and Molatefi, R. and Rekabi, M. and Eslami, N. and Ahmadian, J. and Darabi, K. and Sedighi, G.R. and Monajemzadeh, M. and Modaresi, M. and Parvaneh, N. and Boztug, K. and Rezaei, N. (2016) LPS-responsive beige-like anchor gene mutation associated with possible bronchiolitis obliterans organizing pneumonia associated with hypogammaglobulinemia and normal IgM phenotype and low number of B. Acta Medica Iranica, 54 (10). pp. 620-623.

Nabavi, M. and Arshi, S. and Bemanian, M.H. and Aghamohammadi, A. and Mansouri, D. and Hedayat, M. and Nateghian, A. and Noorbakhsh, S. and Ehsanipour, F. and Faranoush, M. and Shakeri, R. and Mesdaghi, M. and Taghvaei, B. and Ghalebaghi, B. and Babaie, D. and Bahrami, A. and Fallahpour, M. and Esmaeilzadeh, H. and Ali Hamidieh, A. and Rekabi, M. and Ahmadian, J. and Eslami, N. and Shokri, S. and Afshar, M. and Jalali, F. and Akbarpour, N. and Molatefi, R. and Rezaei, N. (2016) Long-term follow-up of ninety eight Iranian patients with primary immune deficiency in a single tertiary centre. Allergologia et Immunopathologia, 44 (4). pp. 322-330.

Gharagozlou, M. and Behniafard, N. and Amirzargar, A.A. and Hosseinverdi, S. and Sotoudeh, S. and Farhadi, E. and Khaledi, M. and Aryan, Z. and Moghaddam, Z.G. and Mahmoudi, M. and Aghamohammadi, A. and Rezaei, N. (2015) Association between single nucleotide polymorphisms of the interleukin-4 gene and atopic dermatitis. Acta Dermatovenerologica Croatica, 23 (2). pp. 96-100.

Mohammadinejad, P. and Pourhamdi, S. and Abolhassani, H. and Mirminachi, B. and Havaei, A. and Masoom, S.N. and Sadeghi, B. and Ghajar, A. and Afarideh, M. and Parvaneh, N. and Mirsaeed-Ghazi, B. and Movahedi, M. and Gharagozlou, M. and Chavoushzadeh, Z. and Mahdaviani, A. and Zandieh, F. and Sherkat, R. and Sadeghi-Shabestari, M. and Faridhosseini, R. and Jabbari-Azad, F. and Ahanchian, H. and Zandkarimi, M. and Cherghi, T. and Fayezi, A. and Mohammadzadeh, I. and Amin, R. and Aleyasin, S. and Moghtaderi, M. and Ghaffari, J. and Bemanian, M. and Shafiei, A. and Kalantari, N. and Ahmadiafshar, A. and Khazaei, H.A. and Mohammadi, J. and Nabavi, M. and Rezaei, N. and Aghamohammadi, A. (2015) Primary antibody deficiency in a tertiary referral hospital: A 30-year experiment. Journal of Investigational Allergology and Clinical Immunology, 25 (6). pp. 416-425.

Nemati, S. and Amirzargar, A.A. and Farhadi, E. and Hirbod-Mobarakeh, A. and Nabavi, M. and Soltani, S. and Mahdaviani, S.A. and Shahinpour, S. and Arshi, S. and Mirahmadian, M. and Nicknam, M.H. and Aghamohammadi, A. and Rezaei, N. (2015) RAD50 single-nucleotide polymorphism in predominantly antibody deficiency. Journal of Investigational Allergology and Clinical Immunology, 25 (4). pp. 299-301.

Movahedi, M. and Tavakol, M. and Hirbod-Mobarakeh, A. and Gharagozlou, M. and Aghamohammadi, A. and Tavakol, Z. and Momenzadeh, K. and Nabavi, M. and Dabbaghzade, A. and Mosallanejad, A. and Rezaei, N. (2015) Vitamin D deficiency in chronic idiopathic urticaria. Iranian Journal of Allergy, Asthma and Immunology, 14 (2). pp. 222-227.

Movahedi, M. and Tavakol, M. and Mohammadinejad, P. and Baiardini, I. and Braido, F. and Gharagozlou, M. and Aghamohammadi, A. and Nabavi, M. and Dabbaghzade, A. and Tavakol, Z. and Afarideh, M. and Rezaei, N. (2014) The persian version of the chronic urticaria quality of life questionnaire: Factor analysis, validation, and initial clinical findings. Iranian Journal of Allergy, Asthma and Immunology, 13 (4). pp. 278-285. ISSN 1735-1502

Rezaei, N. and Pourpak, Z. and Aghamohammadi, A. and Farhoudi, A. and Movahedi, M. and Gharagozlou, M. and MirSaeid Ghazi, B. and Atarod, L. and Abolmaali, K. and Mahmoudi, M. and Mansouri, D. and Arshi, S. and Tarash, N.J. and Sherkat, R. and Amin, R. and Kashef, S. and Hosseini, R.F. and Mohammadzadeh, I. and Shabestari, M.S. and Nabavi, M. and Moin, M. (2006) Consanguinity in primary immunodeficiency disorders; the report from Iranian primary immunodeficiency registry. American Journal of Reproductive Immunology, 56 (2). pp. 145-151.

Moin, M. and Farhoudi, A. and Movahedi, M. and Rezaei, N. and Pourpak, Z. and Yeganeh, M. and Gharagozlou, M. and Mirsaeid Ghazi, B. and Arshi, S. and Mansouri, D. and Sherkat, R. and Kashef, S. and Mahmoudi, M. and Nabavi, M. and Aghamohammadi, A. (2006) The clinical and laboratory survey of Iranian patients with Hyper-IgE syndrome. Scandinavian Journal of Infectious Diseases, 38 (10). pp. 898-903.

This list was generated on Tue Apr 20 03:48:05 2021 +0430.