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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: ghadami m. Arch Iran Med. 2015 Nov;18(11):760-4. Arch Iran Med. 2015. PMID: 26497373
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: ghadami m. 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
The first cohort of Iranian patients with hyper immunoglobulin E syndrome: A long-term follow-up and genetic analysis.
Tavassoli M, Abolhassani H, Yazdani R, Ghadami M, Azizi G, Abdolrahim Poor Heravi S, Moeini Shad T, Kokabee M, Movahedi M, Abdshahzadeh H, Gharagozlou M, Rezaei N, Esmaeilzadeh H, Aleyasin S, Aghamohammadi A. Tavassoli M, et al. Among authors: ghadami m. Pediatr Allergy Immunol. 2019 Jun;30(4):469-478. doi: 10.1111/pai.13043. Epub 2019 May 15. Pediatr Allergy Immunol. 2019. PMID: 30801830
RPE65 and retinal dystrophy: Report of new and recurrent mutations.
Safari S, Zare-Abdollahi D, Bushehri A, Safari MR, Dehghani A, Tahmasebi Z, Khorram Khorshid HR, Ghadami M. Safari S, et al. Among authors: ghadami m. J Gene Med. 2020 Mar;22(3):e3154. doi: 10.1002/jgm.3154. Epub 2020 Jan 19. J Gene Med. 2020. PMID: 31957135
Demethylation and alterations in the expression level of the cell cycle-related genes as possible mechanisms in arsenic trioxide-induced cell cycle arrest in human breast cancer cells.
Moghaddaskho F, Eyvani H, Ghadami M, Tavakkoly-Bazzaz J, Alimoghaddam K, Ghavamzadeh A, Ghaffari SH. Moghaddaskho F, et al. Among authors: ghadami m. Tumour Biol. 2017 Feb;39(2):1010428317692255. doi: 10.1177/1010428317692255. Tumour Biol. 2017. PMID: 28218039 Free article.
Association of SP-B gene 9306 A/G polymorphism (rs7316) and risk of RDS.
Fatahi N, Niknafs N, Kalani M, Dalili H, Shariat M, Amini E, Esmaeilnia Shirvani T, Hardani AK, Taheritafti R, Ghasemi-Fakhr N, Ghadami M, Tavakkoly-Bazzaz J, Rashidi-Nezhad R, Nayeri F, Rashidi-Nezhad A. Fatahi N, et al. Among authors: ghadami m. J Matern Fetal Neonatal Med. 2018 Nov;31(22):2965-2970. doi: 10.1080/14767058.2017.1359829. Epub 2017 Aug 7. J Matern Fetal Neonatal Med. 2018. PMID: 28738720 Free article.
94 results