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Carla Nishimura

Showing results (11-20 of 23) with videos related to

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Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 4, 2022
De novo variants are a common cause of genetic hearing lossMiles J Klimara, Carla Nishimura, Donghong Wang, et al.
Archives of Otolaryngology--Head & Neck Surgery|February 21, 2007
The influence of mutations in the SLC26A4 gene on the temporal bone in a population with enlarged vestibular aqueductColm Madden, Mark Halsted, Jareen Meinzen-Derr, et al.
European Journal of Pediatrics|September 25, 2008
Identification of SLC26A4 gene mutations in Iranian families with hereditary hearing impairmentKimia Kahrizi, Marzieh Mohseni, Carla Nishimura, et al.
International Journal of Pediatric Otorhinolaryngology|December 17, 2011
Spectrum of GJB2 (Cx26) gene mutations in Iranian Azeri patients with nonsyndromic autosomal recessive hearing lossBehzad Davarnia, Mojgan Babanejad, Zohreh Fattahi, et al.
American Journal of Medical Genetics. Part A|August 21, 2012
A comprehensive study to determine heterogeneity of autosomal recessive nonsyndromic hearing loss in IranMojgan Babanejad, Zohreh Fattahi, Niloofar Bazazzadegan, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|May 19, 2012
The genetics of the alternative pathway of complement in the pathogenesis of HELLP syndromeFrancesca Crovetto, Nicolò Borsa, Barbara Acaia, et al.
American Journal of Medical Genetics. Part A|January 25, 2005
GJB2 mutations: passage through IranHossein Najmabadi, Carla Nishimura, Kimia Kahrizi, et al.
American Journal of Medical Genetics. Part A|October 16, 2007
Molecular characterization of a novel X-linked syndrome involving developmental delay and deafnessMichael S Hildebrand, Michelle G de Silva, Tiong Yang Tan, et al.
American Journal of Medical Genetics. Part A|April 13, 2011
Two Iranian families with a novel mutation in GJB2 causing autosomal dominant nonsyndromic hearing lossNiloofar Bazazzadegan, Abraham M Sheffield, Masoomeh Sobhani, et al.
American Journal of Human Genetics|September 25, 2018
Genomic Landscape and Mutational Signatures of Deafness-Associated GenesHela Azaiez, Kevin T Booth, Sean S Ephraim, et al.
Pageof 3

Showing results (11-20 of 23) with videos related to

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Pageof 3
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 4, 2022
De novo variants are a common cause of genetic hearing lossMiles J Klimara, Carla Nishimura, Donghong Wang, et al.
Archives of Otolaryngology--Head & Neck Surgery|February 21, 2007
The influence of mutations in the SLC26A4 gene on the temporal bone in a population with enlarged vestibular aqueductColm Madden, Mark Halsted, Jareen Meinzen-Derr, et al.
European Journal of Pediatrics|September 25, 2008
Identification of SLC26A4 gene mutations in Iranian families with hereditary hearing impairmentKimia Kahrizi, Marzieh Mohseni, Carla Nishimura, et al.
International Journal of Pediatric Otorhinolaryngology|December 17, 2011
Spectrum of GJB2 (Cx26) gene mutations in Iranian Azeri patients with nonsyndromic autosomal recessive hearing lossBehzad Davarnia, Mojgan Babanejad, Zohreh Fattahi, et al.
American Journal of Medical Genetics. Part A|August 21, 2012
A comprehensive study to determine heterogeneity of autosomal recessive nonsyndromic hearing loss in IranMojgan Babanejad, Zohreh Fattahi, Niloofar Bazazzadegan, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|May 19, 2012
The genetics of the alternative pathway of complement in the pathogenesis of HELLP syndromeFrancesca Crovetto, Nicolò Borsa, Barbara Acaia, et al.
American Journal of Medical Genetics. Part A|January 25, 2005
GJB2 mutations: passage through IranHossein Najmabadi, Carla Nishimura, Kimia Kahrizi, et al.
American Journal of Medical Genetics. Part A|October 16, 2007
Molecular characterization of a novel X-linked syndrome involving developmental delay and deafnessMichael S Hildebrand, Michelle G de Silva, Tiong Yang Tan, et al.
American Journal of Medical Genetics. Part A|April 13, 2011
Two Iranian families with a novel mutation in GJB2 causing autosomal dominant nonsyndromic hearing lossNiloofar Bazazzadegan, Abraham M Sheffield, Masoomeh Sobhani, et al.
American Journal of Human Genetics|September 25, 2018
Genomic Landscape and Mutational Signatures of Deafness-Associated GenesHela Azaiez, Kevin T Booth, Sean S Ephraim, et al.
Pageof 3