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Shin-Ichi Usami

Showing results (71-80 of 256) with videos related to

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Acta Oto-Laryngologica|April 21, 2023
The relationship between preoperative factors and the pattern of longitudinal improvement in speech perception following cochlear implantationJun Shinagawa, Hidekane Yoshimura, Shin-Ya Nishio, et al.
The Annals of Otology, Rhinology, and Laryngology|March 18, 2015
Germinal mosaicism in a family with BO syndromeMaiko Miyagawa, Shin-Ya Nishio, Mitsuru Hattori, et al.
The Annals of Otology, Rhinology, and Laryngology|March 20, 2015
Novel mutations in LRTOMT associated with moderate progressive hearing loss in autosomal recessive inheritanceAya Ichinose, Hideaki Moteki, Mitsuru Hattori, et al.
Plos One|March 3, 2012
Simultaneous screening of multiple mutations by invader assay improves molecular diagnosis of hereditary hearing loss: a multicenter studyShin-ichi Usami, Shin-ya Nishio, Makoto Nagano, et al.
Acta Oto-Laryngologica|August 28, 2021
A nationwide epidemiologic, clinical, genetic study of Usher syndrome in JapanHidekane Yoshimura, Shin-Ya Nishio, Yuichi Isaka, et al.
Plos One|October 17, 2013
Massively parallel DNA sequencing successfully identifies new causative mutations in deafness genes in patients with cochlear implantation and EASMaiko Miyagawa, Shin-ya Nishio, Takuo Ikeda, et al.
The Annals of Otology, Rhinology, and Laryngology|March 11, 2005
Audiological features and mitochondrial DNA sequence in a large family carrying mitochondrial A1555G mutation without use of aminoglycosideTatsuo Matsunaga, Hiroshi Kumanomido, Masae Shiroma, et al.
Plos One|September 15, 2016
Social Health Insurance-Based Simultaneous Screening for 154 Mutations in 19 Deafness Genes Efficiently Identified Causative Mutations in Japanese Hearing Loss PatientsKentaro Mori, Hideaki Moteki, Maiko Miyagawa, et al.
Genes|February 26, 2025
Auditory Neuropathy Caused by a Structural Variation in the <i>OTOF</i> Gene, Identified Using Oxford Nanopore Adaptive SamplingTakumi Kumai, Shin-Ya Nishio, Hideaki Moteki, et al.
Acta Oto-Laryngologica|May 27, 2011
Clinical profile of hearing loss in children with congenital cytomegalovirus (CMV) infection: CMV DNA diagnosis using preserved umbilical cordSakiko Furutate, Satoshi Iwasaki, Shin-ya Nishio, et al.
Pageof 26

Showing results (71-80 of 256) with videos related to

Sort By:
Pageof 26
Acta Oto-Laryngologica|April 21, 2023
The relationship between preoperative factors and the pattern of longitudinal improvement in speech perception following cochlear implantationJun Shinagawa, Hidekane Yoshimura, Shin-Ya Nishio, et al.
The Annals of Otology, Rhinology, and Laryngology|March 18, 2015
Germinal mosaicism in a family with BO syndromeMaiko Miyagawa, Shin-Ya Nishio, Mitsuru Hattori, et al.
The Annals of Otology, Rhinology, and Laryngology|March 20, 2015
Novel mutations in LRTOMT associated with moderate progressive hearing loss in autosomal recessive inheritanceAya Ichinose, Hideaki Moteki, Mitsuru Hattori, et al.
Plos One|March 3, 2012
Simultaneous screening of multiple mutations by invader assay improves molecular diagnosis of hereditary hearing loss: a multicenter studyShin-ichi Usami, Shin-ya Nishio, Makoto Nagano, et al.
Acta Oto-Laryngologica|August 28, 2021
A nationwide epidemiologic, clinical, genetic study of Usher syndrome in JapanHidekane Yoshimura, Shin-Ya Nishio, Yuichi Isaka, et al.
Plos One|October 17, 2013
Massively parallel DNA sequencing successfully identifies new causative mutations in deafness genes in patients with cochlear implantation and EASMaiko Miyagawa, Shin-ya Nishio, Takuo Ikeda, et al.
The Annals of Otology, Rhinology, and Laryngology|March 11, 2005
Audiological features and mitochondrial DNA sequence in a large family carrying mitochondrial A1555G mutation without use of aminoglycosideTatsuo Matsunaga, Hiroshi Kumanomido, Masae Shiroma, et al.
Plos One|September 15, 2016
Social Health Insurance-Based Simultaneous Screening for 154 Mutations in 19 Deafness Genes Efficiently Identified Causative Mutations in Japanese Hearing Loss PatientsKentaro Mori, Hideaki Moteki, Maiko Miyagawa, et al.
Genes|February 26, 2025
Auditory Neuropathy Caused by a Structural Variation in the <i>OTOF</i> Gene, Identified Using Oxford Nanopore Adaptive SamplingTakumi Kumai, Shin-Ya Nishio, Hideaki Moteki, et al.
Acta Oto-Laryngologica|May 27, 2011
Clinical profile of hearing loss in children with congenital cytomegalovirus (CMV) infection: CMV DNA diagnosis using preserved umbilical cordSakiko Furutate, Satoshi Iwasaki, Shin-ya Nishio, et al.
Pageof 26