Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Batool Azadeh"'
Autor:
Maryam Taghdiri, Nooshin Nikzat, Niloofar Bazzazadegan, Zohreh Fattahi, Batool Azadeh, Haleh Habibi, Kimia Kahrizi, Hossein Najmabadi, Farahnaz Sabbagh-Kermani, Atie Kashef, Atefeh Khoshaeen, Faezeh Mojahedi
Publikováno v:
International Journal of Pediatric Otorhinolaryngology. 79:136-138
Objective Hereditary hearing loss is the most common neurosensory disorder in humans. Half of the cases have genetic etiology with extraordinary genetic heterogeneity. Mutations in one gene, GJB2, are the most common cause for autosomal recessive non
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::43f911245a71c02f427ea31d11087d98
https://doi.org/10.1016/j.ijporl.2014.11.024
https://doi.org/10.1016/j.ijporl.2014.11.024
Autor:
Farahnaz Sabbagh Kermani, Hossein Najmabadi, Narges Nouri, Atie Kashef, Shima Sahraian, Atefeh Khoshaeen, Faezeh Mojahedi, Mojgan Babanejad, Niloofar Bazazzadegan, Maryam Taghdiri, Kimia Kahrizi, Batool Azadeh, Payman Jamali, Hilda Yazdan, Richard J.H. Smith, Haleh Habibi, Zohreh Fattahi, Nicole C. Meyer, Farahnaz Reyhanifar, Nooshin Nikzat, Carla Nishimura
Publikováno v:
International Journal of Pediatric Otorhinolaryngology. 76:1164-1174
Objective Mutations in GJB2, encoding connexin 26 (CX26), are causally related to autosomal recessive form of non-syndromic hearing loss (NSHL) at the DFNB1 locus and autosomal dominant NSHL at the DFNA3 locus. In this study, we investigated the prev
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d9c0e2aeb3e8d0791170edd0a07206dc
https://doi.org/10.1016/j.ijporl.2012.04.026
https://doi.org/10.1016/j.ijporl.2012.04.026
Autor:
Hossein Najmabadi, A. Eliot Shearer, Kimia Kahrizi, Zohreh Fattahi, Seyed Navid Almadani, Sanaz Arzhangi, Batool Azadeh, Richard J.H. Smith, Niloofar Bazazzadegan, Mojgan Babanejad, Fatemehsadat Esteghamat, Khadijeh Jalalvand, Nooshin Nikzat, Rezvan Abtahi
Publikováno v:
American Journal of Medical Genetics Part A. :1857-1864
MYO15A is located at the DFNB3 locus on chromosome 17p11.2, and encodes myosin-XV, an unconventional myosin critical for the formation of stereocilia in hair cells of cochlea. Recessive mutations in this gene lead to profound autosomal recessive nons
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e84d6481b8539325e1667c4bf9e0c2d8
https://doi.org/10.1002/ajmg.a.34411
https://doi.org/10.1002/ajmg.a.34411
Autor:
Hossein Najmabadi, Jennifer Webster, Michael S. Hildebrand, Ali Anousheh, A. Eliot Shearer, Batool Azadeh, Kimia Kahrizi, Catherine J. Bromhead, Dietrich A. Stephan, Melanie Bahlo, William J. Kimberling, Richard J.H. Smith, Arash Nazeri
Publikováno v:
American Journal of Medical Genetics Part A. :555-558
To the Editor: Hearing impairment is the most common genetic sensory defect in humans worldwide. It is estimated that profound hearing loss occurs in 4 out of every 10,000 children [Morton 1991]. Seventy percent of hereditary SNHL is nonsyndromic (DF
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fad19c9edd16fd920eacc6bddc85082c
https://doi.org/10.1002/ajmg.a.32670
https://doi.org/10.1002/ajmg.a.32670