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Page 1
Characterising the spectrum of autosomal recessive hereditary hearing loss in Iran.
Sloan-Heggen CM, Babanejad M, Beheshtian M, Simpson AC, Booth KT, Ardalani F, Frees KL, Mohseni M, Mozafari R, Mehrjoo Z, Jamali L, Vaziri S, Akhtarkhavari T, Bazazzadegan N, Nikzat N, Arzhangi S, Sabbagh F, Otukesh H, Seifati SM, Khodaei H, Taghdiri M, Meyer NC, Daneshi A, Farhadi M, Kahrizi K, Smith RJ, Azaiez H, Najmabadi H. Sloan-Heggen CM, et al. Among authors: daneshi a. J Med Genet. 2015 Dec;52(12):823-9. doi: 10.1136/jmedgenet-2015-103389. Epub 2015 Oct 7. J Med Genet. 2015. PMID: 26445815 Free PMC article.
Three familial cases of Michel's aplasia.
Daneshi A, Farhadi M, Asghari A, Emamjomeh H, Abbasalipour P, Hasanzadeh S. Daneshi A, et al. Otol Neurotol. 2002 May;23(3):346-8. doi: 10.1097/00129492-200205000-00020. Otol Neurotol. 2002. PMID: 11981393
Cochlear implantation in Mondini dysplasia.
Daneshi A, Hassanzadeh S, Abasalipour P, Emamdjomeh H, Farhadi M. Daneshi A, et al. ORL J Otorhinolaryngol Relat Spec. 2003 Jan-Feb;65(1):39-44. doi: 10.1159/000068656. ORL J Otorhinolaryngol Relat Spec. 2003. PMID: 12624505
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: daneshi a. 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
Sensorineural deafness and male infertility: a contiguous gene deletion syndrome.
Zhang Y, Malekpour M, Al-Madani N, Kahrizi K, Zanganeh M, Lohr NJ, Mohseni M, Mojahedi F, Daneshi A, Najmabadi H, Smith RJ. Zhang Y, et al. Among authors: daneshi a. J Med Genet. 2007 Apr;44(4):233-40. doi: 10.1136/jmg.2006.045765. Epub 2006 Nov 10. J Med Genet. 2007. PMID: 17098888 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: daneshi a. 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.
Sensorineural deafness and male infertility: a contiguous gene deletion syndrome.
Zhang Y, Malekpour M, Al-Madani N, Kahrizi K, Zanganeh M, Mohseni M, Mojahedi F, Daneshi A, Najmabadi H, Smith RJ. Zhang Y, et al. Among authors: daneshi a. BMJ Case Rep. 2009;2009:bcr08.2008.0645. doi: 10.1136/bcr.08.2008.0645. Epub 2009 Jan 23. BMJ Case Rep. 2009. PMID: 21686705 Free PMC article.
Complications in a series of 4400 paediatric cochlear implantation.
Daneshi A, Ajalloueyan M, Ghasemi MM, Hashemi BS, Emamjome H, Farhadi M, Ajalloueyan Z. Daneshi A, et al. Int J Pediatr Otorhinolaryngol. 2015 Sep;79(9):1401-3. doi: 10.1016/j.ijporl.2015.05.035. Epub 2015 Jun 19. Int J Pediatr Otorhinolaryngol. 2015. PMID: 26139509
99 results