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Page 1
GJB2 mutations: passage through Iran.
Najmabadi H, Nishimura C, Kahrizi K, Riazalhosseini Y, Malekpour M, Daneshi A, Farhadi M, Mohseni M, Mahdieh N, Ebrahimi A, Bazazzadegan N, Naghavi A, Avenarius M, Arzhangi S, Smith RJ. Najmabadi H, et al. Among authors: farhadi m. Am J Med Genet A. 2005 Mar 1;133A(2):132-7. doi: 10.1002/ajmg.a.30576. Am J Med Genet A. 2005. PMID: 15666300
Functional brain abnormalities localized in 55 chronic tinnitus patients: fusion of SPECT coincidence imaging and MRI.
Farhadi M, Mahmoudian S, Saddadi F, Karimian AR, Mirzaee M, Ahmadizadeh M, Ghasemikian K, Gholami S, Ghoreyshi E, Beyty S, Shamshiri A, Madani S, Bakaev V, Moradkhani S, Raeisali G. Farhadi M, et al. J Cereb Blood Flow Metab. 2010 Apr;30(4):864-70. doi: 10.1038/jcbfm.2009.254. Epub 2010 Jan 13. J Cereb Blood Flow Metab. 2010. PMID: 20068582 Free PMC article.
Two Iranian families with a novel mutation in GJB2 causing autosomal dominant nonsyndromic hearing loss.
Bazazzadegan N, Sheffield AM, Sobhani M, Kahrizi K, Meyer NC, Van Camp G, Hilgert N, Abedini SS, Habibi F, Daneshi A, Nishimura C, Avenarius MR, Farhadi M, Smith RJ, Najmabadi H. Bazazzadegan N, et al. Among authors: farhadi m. Am J Med Genet A. 2011 May;155A(5):1202-11. doi: 10.1002/ajmg.a.33209. Epub 2011 Apr 11. Am J Med Genet A. 2011. PMID: 21484990 Free PMC article. Review.
Prognostic validity of dichotic multiple frequencies auditory steady-state responses versus distortion product otoacoustic emissions in hearing screening of high risk neonates.
Mahmoudian S, Farhadi M, Kadivar M, Ghalehbaghi B, Rahimi F, Hemami MR, Kamrava SK, Asghari A, Amintehran E, Mohagheghi P. Mahmoudian S, et al. Among authors: farhadi m. Int J Pediatr Otorhinolaryngol. 2011 Sep;75(9):1109-16. doi: 10.1016/j.ijporl.2011.05.026. Epub 2011 Jun 29. Int J Pediatr Otorhinolaryngol. 2011. PMID: 21719120
305 results