Items where Author is "Chavoshzadeh, Z."

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Number of items: 6.

Article

Teimourian, S. and Sazgara, F. and de Boer, M. and van Leeuwen, K. and Roos, D. and Lashkary, S. and Chavoshzadeh, Z. and Nabavi, M. and Bemanian, M.H. and Isaian, A. (2018) Characterization of 4 New Mutations in the CYBB Gene in 10 Iranian Families With X-linked Chronic Granulomatous Disease. Journal of Pediatric Hematology/Oncology.

Teimourian, S. and Sazgara, F. and De Boer, M. and Van Leeuwen, K. and Roos, D. and Lashkary, S. and Chavoshzadeh, Z. and Nabavi, M. and Bemanian, M.H. and Isaian, A. (2018) Characterization of 4 new mutations in the CYBB gene in 10 Iranian families with x-linked chronic granulomatous disease. Journal of Pediatric Hematology/Oncology, 40 (5). e268-e272.

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.

Karami, Z. and Mesdaghi, M. and Karimzadeh, P. and Mansouri, M. and Taghdiri, M.M. and Kayhanidoost, Z. and Jebelli, B. and Shekarriz Foumani, R. and Babaie, D. and Chavoshzadeh, Z. (2016) Evaluation of lymphocyte transformation test results in patients with delayed hypersensitivity reactions following the use of anticonvulsant drugs. International Archives of Allergy and Immunology, 170 (3). pp. 158-162.

Mortezaee, F.T. and Esmaeli, B. and Badalzadeh, M. and Ghadami, M. and Fazlollahi, M.R. and Alizade, Z. and Hamidieh, A.A. and Chavoshzadeh, Z. and Mova-Hedi, M. and Heydarzadeh, M. and Shabestari, M.S. and Tavassoli, M. and Nabavi, M. and Kalmarzi, R.N. and Pourpak, Z. (2015) Investigation of ITGB2 gene in 12 new cases of leukocyte adhesion deficiency-type I revealed four novel mutations from Iran. Archives of Iranian Medicine, 18 (11). pp. 760-764.

This list was generated on Fri Jan 17 17:17:42 2020 +0330.