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Page 1
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.
101 results