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Page 1
Clinical, immunologic, and genetic spectrum of 696 patients with combined immunodeficiency.
Abolhassani H, Chou J, Bainter W, Platt CD, Tavassoli M, Momen T, Tavakol M, Eslamian MH, Gharagozlou M, Movahedi M, Ghadami M, Hamidieh AA, Azizi G, Yazdani R, Afarideh M, Ghajar A, Havaei A, Chavoshzadeh Z, Mahdaviani SA, Cheraghi T, Behniafard N, Amin R, Aleyasin S, Faridhosseini R, Jabbari-Azad F, Nabavi M, Bemanian MH, Arshi S, Molatefi R, Sherkat R, Mansouri M, Mesdaghi M, Babaie D, Mohammadzadeh I, Ghaffari J, Shafiei A, Kalantari N, Ahanchian H, Khoshkhui M, Soheili H, Dabbaghzadeh A, Shirkani A, Nasiri Kalmarzi R, Mortazavi SH, Tafaroji J, Khalili A, Mohammadi J, Negahdari B, Joghataei MT, Al-Ramadi BK, Picard C, Parvaneh N, Rezaei N, Chatila TA, Massaad MJ, Keles S, Hammarström L, Geha RS, Aghamohammadi A. Abolhassani H, et al. Among authors: hamidieh aa. J Allergy Clin Immunol. 2018 Apr;141(4):1450-1458. doi: 10.1016/j.jaci.2017.06.049. Epub 2017 Sep 12. J Allergy Clin Immunol. 2018. PMID: 28916186
Inheritance pattern and clinical aspects of 93 Iranian patients with chronic granulomatous disease.
Fattahi F, Badalzadeh M, Sedighipour L, Movahedi M, Fazlollahi MR, Mansouri SD, Khotaei GT, Bemanian MH, Behmanesh F, Hamidieh AA, Bazargan N, Mamishi S, Zandieh F, Chavoshzadeh Z, Mohammadzadeh I, Mahdaviani SA, Tabatabaei SA, Kalantari N, Tajik S, Maddah M, Pourpak Z, Moin M. Fattahi F, et al. Among authors: hamidieh aa. J Clin Immunol. 2011 Oct;31(5):792-801. doi: 10.1007/s10875-011-9567-x. Epub 2011 Jul 26. J Clin Immunol. 2011. PMID: 21789723
Different pattern of gene mutations in Iranian patients with severe congenital neutropenia (including 2 new mutations).
Alizadeh Z, Fazlollahi MR, Houshmand M, Maddah M, Chavoshzadeh Z, Hamidieh AA, Shamsian BS, Eshghi P, Bolandghamat Pour S, Sadaaie Jahromi H, Mansouri M, Movahedi M, Nayebpour M, Pourpak Z, Moin M. Alizadeh Z, et al. Among authors: hamidieh aa. Iran J Allergy Asthma Immunol. 2013 Mar;12(1):86-92. Iran J Allergy Asthma Immunol. 2013. PMID: 23454784 Free article.
Investigation of ITGB2 gene in 12 new cases of leukocyte adhesion deficiency-type I revealed four novel mutations from Iran.
Taghizade Mortezaee F, Esmaeli B, Badalzadeh M, Ghadami M, Fazlollahi MR, Alizade Z, Hamidieh AA, Chavoshzadeh Z, Movahedi M, Heydarzadeh M, Sadeghi Shabestari M, Tavassoli M, Nabavi M, Nasiri Kalmarzi R, Pourpak Z. Taghizade Mortezaee F, et al. Among authors: hamidieh aa. Arch Iran Med. 2015 Nov;18(11):760-4. Arch Iran Med. 2015. PMID: 26497373
183 results