Items where Author is "Arzhangi, S."

Article

Mohseni, M. and Babanejad, M. and Booth, K.T. and Jamali, P. and Jalalvand, K. and Davarnia, B. and Ardalani, F. and Khoshaeen, A. and Arzhangi, S. and Ghodratpour, F. and Beheshtian, M. and Jahanshad, F. and Otukesh, H. and Bahrami, F. and Seifati, S.M. and Bazazzadegan, N. and Habibi, F. and Behravan, H. and Mirzaei, S. and Keshavarzi, F. and Nikzat, N. and Mehrjoo, Z. and Thiele, H. and Nothnagel, M. and Azaiez, H. and Smith, R.J. and Kahrizi, K. and Najmabadi, H. (2021) Exome sequencing utility in defining the genetic landscape of hearing loss and novel-gene discovery in Iran. Clinical Genetics, 100 (1). pp. 59-78.

Mehrjoo, Z. and Kahrizi, K. and Mohseni, M. and Akbari, M. and Arzhangi, S. and Jalalvand, K. and Najmabadi, H. and Farhadi, M. and Mohseni, M. and Asghari, A. and Mohebbi, S. and Daneshi, A. (2020) Limbic system associated membrane protein mutation in an iranian family diagnosed with ménière's disease. Archives of Iranian Medicine, 23 (5). pp. 319-325.

Beheshtian, M. and Babanejad, M. and Azaiez, H. and Bazazzadegan, N. and Kolbe, D. and Sloan-Heggen, C. and Arzhangi, S. and Booth, K. and Mohseni, M. and Frees, K. and Azizi, M.H. and Daneshi, A. and Farhadi, M. and Kahrizi, K. and Smith, R.J.H. and Najmabadi, H. (2016) Heterogeneity of hereditary hearing loss in Iran: A comprehensive review. Archives of Iranian Medicine, 19 (10). pp. 724-732.

Sloan-Heggen, C.M. and Babanejad, M. and Beheshtian, M. and Simpson, A.C. and Booth, K.T. and Ardalani, F. and Frees, K.L. and Mohseni, M. and Mozafari, R. and Mehrjoo, Z. and Jamali, L. and Vaziri, S. and Akhtarkhavari, T. and Bazazzadegan, N. and Nikzat, N. and Arzhangi, S. and Sabbagh, F. and Otukesh, H. and Seifati, S.M. and Khodaei, H. and Taghdiri, M. and Meyer, N.C. and Daneshi, A. and Farhadi, M. and Kahrizi, K. and Smith, R.J.H. and Azaiez, H. and Najmabadi, H. (2015) Characterising the spectrum of autosomal recessive hereditary hearing loss in Iran. Journal of Medical Genetics, 52 (12). pp. 823-829.

Daneshi, A. and Hassanzadeh, S. and Emamdjomeh, H. and Mohammadi, S.H. and Arzhangi, S. and Farhadi, M. and Najmabadi, H. (2011) Prevalence of GJB2-associated deafness and outcomes of cochlear implantation in Iran. Journal of Laryngology and Otology, 125 (5). pp. 455-459.

Najmabadi, H. and Nishimura, C. and Kahrizi, K. and Riazalhosseini, Y. and Malekpour, M. and Daneshi, A. and Farhadi, M. and Mohseni, M. and Mahdieh, N. and Ebrahimi, A. and Bazazzadegan, N. and Naghavi, A. and Avenarius, M. and Arzhangi, S. and Smith, R.J.H. (2005) GJB2 mutations: Passage through Iran. American Journal of Medical Genetics, 133 A (2). pp. 132-137.