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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
Familial ankyloglossia (tongue-tie): a case report.
Morowati S, Yasini M, Ranjbar R, Peivandi AA, Ghadami M. Morowati S, et al. Among authors: ghadami m. Acta Med Iran. 2010 Mar-Apr;48(2):123-4. Acta Med Iran. 2010. PMID: 21133006 Free article.
Mutations in the histamine N-methyltransferase gene, HNMT, are associated with nonsyndromic autosomal recessive intellectual disability.
Heidari A, Tongsook C, Najafipour R, Musante L, Vasli N, Garshasbi M, Hu H, Mittal K, McNaughton AJ, Sritharan K, Hudson M, Stehr H, Talebi S, Moradi M, Darvish H, Arshad Rafiq M, Mozhdehipanah H, Rashidinejad A, Samiei S, Ghadami M, Windpassinger C, Gillessen-Kaesbach G, Tzschach A, Ahmed I, Mikhailov A, Stavropoulos DJ, Carter MT, Keshavarz S, Ayub M, Najmabadi H, Liu X, Ropers HH, Macheroux P, Vincent JB. Heidari A, et al. Among authors: ghadami m. Hum Mol Genet. 2015 Oct 15;24(20):5697-710. doi: 10.1093/hmg/ddv286. Epub 2015 Jul 23. Hum Mol Genet. 2015. PMID: 26206890 Free PMC 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: ghadami m. Arch Iran Med. 2015 Nov;18(11):760-4. Arch Iran Med. 2015. PMID: 26497373
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
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
Variable Clinical Manifestations of COVID-19: Viral and Human Genomes Talk.
Imani-Saber Z, Vaseghi H, Mahdian M, Safari F, Ghadami M. Imani-Saber Z, et al. Among authors: ghadami m. Iran J Allergy Asthma Immunol. 2020 Oct 18;19(5):456-470. doi: 10.18502/ijaai.v19i5.4461. Iran J Allergy Asthma Immunol. 2020. PMID: 33463113 Free article. Review.
94 results