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Shin-Ichi Usami

Showing results (81-90 of 241) with videos related to

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Head & Neck|July 12, 2002
Pendred's syndrome with goiter and enlarged vestibular aqueducts diagnosed by PDS gene mutationHajime Ishinaga, Takeshi Shimizu, Atsushi Yuta, et al.
Acta Oto-Laryngologica|March 6, 2012
Experience with the Vibrant Soundbridge RW-Coupler for round window Vibroplasty with tympanosclerosisSatoshi Iwasaki, Hiroaki Suzuki, Hideaki Moteki, et al.
Acta Oto-Laryngologica|February 1, 2019
Feasibility of hearing preservation for residual hearing with longer cochlear implant electrodesHideaki Moteki, Shin-Ya Nishio, Maiko Miyagawa, et al.
Acta Oto-Laryngologica|March 6, 2020
Genetic testing has the potential to impact hearing preservation following cochlear implantationHidekane Yoshimura, Hideaki Moteki, Shin-Ya Nishio, et al.
The Annals of Otology, Rhinology, and Laryngology|March 25, 2015
Novel mutation in GRXCR1 at DFNB25 lead to progressive hearing loss and dizzinessKentaro Mori, Ikuyo Miyanohara, Hideaki Moteki, et al.
International Journal of Epidemiology|April 12, 2024
Epidemiology, aetiology and diagnosis of congenital hearing loss via hearing screening of 153 913 newbornsHidekane Yoshimura, Takuya Okubo, Jun Shinagawa, et al.
Clinical Case Reports|November 21, 2018
Diagnostic pitfalls for <i>GJB2</i>-related hearing loss: A novel deletion detected by Array-CGH analysis in a Japanese patient with congenital profound hearing lossSatoko Abe, Shin-Ya Nishio, Yoh Yokota, et al.
Genes|May 25, 2024
Comprehensive Genetic Evaluation in Patients with Special Reference to Late-Onset Sensorineural Hearing LossIkuyo Miyanohara, Junichiro Ohori, Minako Tabuchi, et al.
Genes|July 29, 2023
Otological Features of Patients with Musculocontractural Ehlers-Danlos Syndrome Caused by Pathogenic Variants in <i>CHST14</i> (mcEDS-<i>CHST14</i>)Masayuki Kawakita, Satoshi Iwasaki, Hideaki Moteki, et al.
Mitochondrion|October 9, 2020
The use of a MITO-Porter to deliver exogenous therapeutic RNA to a mitochondrial disease's cell with a A1555G mutation in the mitochondrial 12S rRNA gene results in an increase in mitochondrial respiratory activityYuma Yamada, Minako Maruyama, Tomoko Kita, et al.
Pageof 25

Showing results (81-90 of 241) with videos related to

Sort By:
Pageof 25
Head & Neck|July 12, 2002
Pendred's syndrome with goiter and enlarged vestibular aqueducts diagnosed by PDS gene mutationHajime Ishinaga, Takeshi Shimizu, Atsushi Yuta, et al.
Acta Oto-Laryngologica|March 6, 2012
Experience with the Vibrant Soundbridge RW-Coupler for round window Vibroplasty with tympanosclerosisSatoshi Iwasaki, Hiroaki Suzuki, Hideaki Moteki, et al.
Acta Oto-Laryngologica|February 1, 2019
Feasibility of hearing preservation for residual hearing with longer cochlear implant electrodesHideaki Moteki, Shin-Ya Nishio, Maiko Miyagawa, et al.
Acta Oto-Laryngologica|March 6, 2020
Genetic testing has the potential to impact hearing preservation following cochlear implantationHidekane Yoshimura, Hideaki Moteki, Shin-Ya Nishio, et al.
The Annals of Otology, Rhinology, and Laryngology|March 25, 2015
Novel mutation in GRXCR1 at DFNB25 lead to progressive hearing loss and dizzinessKentaro Mori, Ikuyo Miyanohara, Hideaki Moteki, et al.
International Journal of Epidemiology|April 12, 2024
Epidemiology, aetiology and diagnosis of congenital hearing loss via hearing screening of 153 913 newbornsHidekane Yoshimura, Takuya Okubo, Jun Shinagawa, et al.
Clinical Case Reports|November 21, 2018
Diagnostic pitfalls for <i>GJB2</i>-related hearing loss: A novel deletion detected by Array-CGH analysis in a Japanese patient with congenital profound hearing lossSatoko Abe, Shin-Ya Nishio, Yoh Yokota, et al.
Genes|May 25, 2024
Comprehensive Genetic Evaluation in Patients with Special Reference to Late-Onset Sensorineural Hearing LossIkuyo Miyanohara, Junichiro Ohori, Minako Tabuchi, et al.
Genes|July 29, 2023
Otological Features of Patients with Musculocontractural Ehlers-Danlos Syndrome Caused by Pathogenic Variants in <i>CHST14</i> (mcEDS-<i>CHST14</i>)Masayuki Kawakita, Satoshi Iwasaki, Hideaki Moteki, et al.
Mitochondrion|October 9, 2020
The use of a MITO-Porter to deliver exogenous therapeutic RNA to a mitochondrial disease's cell with a A1555G mutation in the mitochondrial 12S rRNA gene results in an increase in mitochondrial respiratory activityYuma Yamada, Minako Maruyama, Tomoko Kita, et al.
Pageof 25