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Page 1
Genetic Analysis of 13 Iranian Families With Leukocyte Adhesion Deficiency Type 1.
Teimourian S, De Boer M, Roos D, Isaian A, Bemanian MH, Lashkary S, Nabavi M, Arshi S, Nateghian A, Sayyahfar S, Sazgara F, Taheripak G, Alipour Fayez E. Teimourian S, et al. Among authors: isaian a. J Pediatr Hematol Oncol. 2019 Jan;41(1):e3-e6. doi: 10.1097/MPH.0000000000001221. J Pediatr Hematol Oncol. 2019. PMID: 29750748
BAK, BAX, and NBK/BIK proapoptotic gene alterations in Iranian patients with ataxia telangiectasia.
Isaian A, Bogdanova NV, Houshmand M, Movahadi M, Aghamohammadi A, Rezaei N, Atarod L, Sadeghi-Shabestari M, Tonekaboni SH, Chavoshzadeh Z, Hassani SM, Mirfakhrai R, Cheraghi T, Kalantari N, Ataei M, Dork-Bousset T, Sanati MH. Isaian A, et al. J Clin Immunol. 2010 Jan;30(1):132-7. doi: 10.1007/s10875-009-9340-6. Epub 2009 Nov 7. J Clin Immunol. 2010. PMID: 19898928
NPHS2 gene mutation in an Iranian family with familial steroid-resistant nephrotic syndrome.
Ameli S, Mazaheri M, Zare-Shahabadi A, Ozaltin F, Asgarian F, Monajemzadeh M, Bazargani B, Ataei N, Hajezadeh N, Madani A, Esfahani T, Isaian A, Zenker M, Rezaei N. Ameli S, et al. Among authors: isaian a. Nefrologia. 2012;32(5):674-6. doi: 10.3265/Nefrologia.pre2012.Jun.11428. Nefrologia. 2012. PMID: 23013956 Free article. No abstract available.
KRT5 and KRT14 Mutations in Epidermolysis Bullosa Simplex with Phenotypic Heterogeneity, and Evidence of Semidominant Inheritance in a Multiplex Family.
Vahidnezhad H, Youssefian L, Saeidian AH, Mozafari N, Barzegar M, Sotoudeh S, Daneshpazhooh M, Isaian A, Zeinali S, Uitto J. Vahidnezhad H, et al. Among authors: isaian a. J Invest Dermatol. 2016 Sep;136(9):1897-1901. doi: 10.1016/j.jid.2016.05.106. Epub 2016 Jun 7. J Invest Dermatol. 2016. PMID: 27283507 Free article. No abstract available.
14 results