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Shin-Ya Nishio

Showing results (61-70 of 142) with videos related to

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Acta Oto-Laryngologica|November 18, 2016
Long-term results of hearing preservation cochlear implant surgery in patients with residual low frequency hearingHideaki Moteki, Shin-Ya Nishio, Maiko Miyagawa, et al.
Acta Oto-Laryngologica|November 26, 2014
The advantages of sound localization and speech perception of bilateral electric acoustic stimulationHideaki Moteki, Ryosuke Kitoh, Keita Tsukada, et al.
Acta Oto-Laryngologica|November 26, 2021
Frequency and natural course of congenital cytomegalovirus-associated hearing loss in childrenMariko Kasuga, Hidekane Yoshimura, Jun Shinagawa, et al.
Plos One|March 29, 2014
Deafness gene expression patterns in the mouse cochlea found by microarray analysisHidekane Yoshimura, Yutaka Takumi, Shin-ya Nishio, et al.
Acta Oto-Laryngologica|December 15, 2022
Estimated number and prevalence of patients with delayed endolymphatic hydrops in Japan: a nationwide surveyShinsuke Ito, Hiromasa Takakura, Katsuichi Akaogi, et al.
HGG Advances|February 8, 2026
Identification of Alternative Splicing in WFS1 Associated with Low-Frequency Hearing Loss in Common MarmosetShu Yokota, Hidekane Yoshimura, Shin-Ya Nishio, et al.
The Annals of Otology, Rhinology, and Laryngology|March 7, 2015
Novel ABHD12 mutations in PHARC patients: the differential diagnosis of deaf-blindnessHidekane Yoshimura, Takao Hashimoto, Toshinori Murata, et al.
Auris, Nasus, Larynx|July 5, 2024
Clinical practice guidelines for the diagnosis and management of acute sensorineural hearing lossRyosuke Kitoh, Shin-Ya Nishio, Hiroaki Sato, et al.
The Annals of Otology, Rhinology, and Laryngology|March 18, 2015
Non-ocular Stickler syndrome with a novel mutation in COL11A2 diagnosed by massively parallel sequencing in Japanese hearing loss patientsYoh-Ichiro Iwasa, Hideaki Moteki, Mitsuru Hattori, et al.
The Annals of Otology, Rhinology, and Laryngology|March 21, 2015
Mutational spectrum and clinical features of patients with ACTG1 mutations identified by massively parallel DNA sequencingMaiko Miyagawa, Shin-Ya Nishio, Aya Ichinose, et al.
Pageof 15

Showing results (61-70 of 142) with videos related to

Sort By:
Pageof 15
Acta Oto-Laryngologica|November 18, 2016
Long-term results of hearing preservation cochlear implant surgery in patients with residual low frequency hearingHideaki Moteki, Shin-Ya Nishio, Maiko Miyagawa, et al.
Acta Oto-Laryngologica|November 26, 2014
The advantages of sound localization and speech perception of bilateral electric acoustic stimulationHideaki Moteki, Ryosuke Kitoh, Keita Tsukada, et al.
Acta Oto-Laryngologica|November 26, 2021
Frequency and natural course of congenital cytomegalovirus-associated hearing loss in childrenMariko Kasuga, Hidekane Yoshimura, Jun Shinagawa, et al.
Plos One|March 29, 2014
Deafness gene expression patterns in the mouse cochlea found by microarray analysisHidekane Yoshimura, Yutaka Takumi, Shin-ya Nishio, et al.
Acta Oto-Laryngologica|December 15, 2022
Estimated number and prevalence of patients with delayed endolymphatic hydrops in Japan: a nationwide surveyShinsuke Ito, Hiromasa Takakura, Katsuichi Akaogi, et al.
HGG Advances|February 8, 2026
Identification of Alternative Splicing in WFS1 Associated with Low-Frequency Hearing Loss in Common MarmosetShu Yokota, Hidekane Yoshimura, Shin-Ya Nishio, et al.
The Annals of Otology, Rhinology, and Laryngology|March 7, 2015
Novel ABHD12 mutations in PHARC patients: the differential diagnosis of deaf-blindnessHidekane Yoshimura, Takao Hashimoto, Toshinori Murata, et al.
Auris, Nasus, Larynx|July 5, 2024
Clinical practice guidelines for the diagnosis and management of acute sensorineural hearing lossRyosuke Kitoh, Shin-Ya Nishio, Hiroaki Sato, et al.
The Annals of Otology, Rhinology, and Laryngology|March 18, 2015
Non-ocular Stickler syndrome with a novel mutation in COL11A2 diagnosed by massively parallel sequencing in Japanese hearing loss patientsYoh-Ichiro Iwasa, Hideaki Moteki, Mitsuru Hattori, et al.
The Annals of Otology, Rhinology, and Laryngology|March 21, 2015
Mutational spectrum and clinical features of patients with ACTG1 mutations identified by massively parallel DNA sequencingMaiko Miyagawa, Shin-Ya Nishio, Aya Ichinose, et al.
Pageof 15