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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 hearing
Hideaki 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 stimulation
Hideaki Moteki, Ryosuke Kitoh, Keita Tsukada, et al.
Acta Oto-Laryngologica
|
November 26, 2021
Frequency and natural course of congenital cytomegalovirus-associated hearing loss in children
Mariko Kasuga, Hidekane Yoshimura, Jun Shinagawa, et al.
Plos One
|
March 29, 2014
Deafness gene expression patterns in the mouse cochlea found by microarray analysis
Hidekane 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 survey
Shinsuke 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 Marmoset
Shu 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-blindness
Hidekane 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 loss
Ryosuke 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 patients
Yoh-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 sequencing
Maiko Miyagawa, Shin-Ya Nishio, Aya Ichinose, et al.
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Search research articles
Search
Showing results (61-70 of 142) with videos related to
Sort By:
Page
of 15
Acta Oto-Laryngologica
|
November 18, 2016
Long-term results of hearing preservation cochlear implant surgery in patients with residual low frequency hearing
Hideaki 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 stimulation
Hideaki Moteki, Ryosuke Kitoh, Keita Tsukada, et al.
Acta Oto-Laryngologica
|
November 26, 2021
Frequency and natural course of congenital cytomegalovirus-associated hearing loss in children
Mariko Kasuga, Hidekane Yoshimura, Jun Shinagawa, et al.
Plos One
|
March 29, 2014
Deafness gene expression patterns in the mouse cochlea found by microarray analysis
Hidekane 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 survey
Shinsuke 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 Marmoset
Shu 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-blindness
Hidekane 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 loss
Ryosuke 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 patients
Yoh-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 sequencing
Maiko Miyagawa, Shin-Ya Nishio, Aya Ichinose, et al.
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of 15