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Cell Free Tumoral DNA Versus Paraffin Block Epidermal Growth Factor Receptor Mutation Detection in Patients with Non-Small Cell Lung Cancer.
Mirtavoos-Mahyari H, Ghadami M, Khosravi A, Esfahani-Monfared Z, Seifi S, Motevaseli E, Pourabdollah M, Modarressi M. Mirtavoos-Mahyari H, et al. Among authors: ghadami m. Asian Pac J Cancer Prev. 2019 Dec 1;20(12):3591-3596. doi: 10.31557/APJCP.2019.20.12.3591. Asian Pac J Cancer Prev. 2019. PMID: 31870098 Free PMC article.
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.
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
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
Association of SP-C gene codon 186 polymorphism (rs1124) and risk of RDS.
Fatahi N, Dalili H, Kalani M, Niknafs N, Shariat M, Tavakkoly-Bazzaz J, Amini E, Esmaeilnia Shirvani T, Hardani AK, Taheritafti R, Ghasemi-Fakhr N, Ghadami M, Nayeri F, Rashidi-Nezhad A. Fatahi N, et al. Among authors: ghadami m. J Matern Fetal Neonatal Med. 2017 Nov;30(21):2585-2589. doi: 10.1080/14767058.2016.1256994. Epub 2016 Nov 24. J Matern Fetal Neonatal Med. 2017. PMID: 27884070
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
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
94 results