Items where Author is "Arshi, S."

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Number of items: 12.

Article

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.

Teimourian, S. and De Boer, M. and Roos, D. and Isaian, A. and Bemanian, M.H. and Lashkary, S. and Nabavi, M. and Arshi, S. and Nateghian, A. and Sayyahfar, S. and Sazgara, F. and Taheripak, G. and Alipour fayez, E. (2018) Genetic Analysis of 13 Iranian Families With Leukocyte Adhesion Deficiency Type 1. Journal of Pediatric Hematology/Oncology.

Teimourian, S. and De Boer, M. and Roos, D. and Isaian, A. and Bemanian, M.H. and Lashkary, S. and Nabavi, M. and Arshi, S. and Nateghian, A. and Sayyahfar, S. and Sazgara, F. and Taheripak, G. and Alipour fayez, E. (2018) Genetic Analysis of 13 Iranian Families With Leukocyte Adhesion Deficiency Type 1. Journal of Pediatric Hematology/Oncology.

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.

Arshi, S. and Nabavi, M. and Bemanian, M.H. and Shakeri, R. and Taghvaei, B. and Ghalebaghi, B. and Babaie, D. and Bahrami, A. and Fallahpour, M. and Esmaeilzadeh, H. and Rekabi, M. and Amadian, J. and Eslami, N. and Shokri, S. and Jalali, F. and Akbarpour, N. and Molatefi, R. and Rezaei, N. (2016) Phenotyping and follow up of forty-seven Iranian patients with common variable immunodeficiency. Allergologia et Immunopathologia, 44 (3). pp. 226-231.

Esmaeilzadeh, H. and Nabavi, M. and Aryan, Z. and Arshi, S. and Bemanian, M.H. and Fallahpour, M. and Mortazavi, N. (2015) Aspirin desensitization for patients with aspirin-exacerbated respiratory disease: A randomized double-blind placebo-controlled trial. Clinical Immunology, 160 (2). pp. 349-357.

Bemanin, M.H. and Fallahpour, M. and Arshi, S. and Nabavi, M. and Yousofi, T. and Shariatifar, A. (2015) First report of asthma prevalence in Afghanistan using international standardized methods Premier rapport sur l�asthme en Afghanistan utilisant des méthodes internationales normalisées. Eastern Mediterranean Health Journal, 21 (3). pp. 194-198.

Esmaeilzadeh, H. and Bemanian, M.H. and Nabavi, M. and Arshi, S. and Fallahpour, M. and Fuchs, I. and zur Stadt, U. and Warnatz, K. and Ammann, S. and Ehl, S. and Lehmberg, K. and Rezaei, N. (2015) Novel Patient with Late-Onset Familial Hemophagocytic Lymphohistiocytosis with STXBP2 Mutations Presenting with Autoimmune Hepatitis, Neurological Manifestations and Infections Associated with Hypogammaglobulinemia. Journal of Clinical Immunology, 35 (1). pp. 22-25.

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.

Oshaghi, M.A. and Vatandoost, H. and Gorouhi, A. and Abai, M.R. and Madjidpour, A. and Arshi, S. and Sadeghi, H. and Nazari, M. and Mehravaran, A. (2011) Anopheline species composition in borderline of Iran-Azerbaijan. Acta Tropica, 119 (1). pp. 44-49.

This list was generated on Mon Dec 16 03:08:28 2019 +0330.