Showing results (231-240 of 255) with videos related to
Sort By:
Pageof 26
Genes|January 25, 2025
Novel OTOG Variants and Clinical Features of Hearing Loss in a Large Japanese CohortYasuhiro Arai, Shin-Ya Nishio, Shinichi Goto, et al.Plos One|March 13, 2018
WFS1 mutation screening in a large series of Japanese hearing loss patients: Massively parallel DNA sequencing-based analysisMasafumi Kobayashi, Maiko Miyagawa, Shin-Ya Nishio, et al.BMC Medicine|November 20, 2014
A randomized controlled clinical trial of topical insulin-like growth factor-1 therapy for sudden deafness refractory to systemic corticosteroid treatmentTakayuki Nakagawa, Kozo Kumakawa, Shin-ichi Usami, et al.Plos One|May 26, 2017
POU4F3 mutation screening in Japanese hearing loss patients: Massively parallel DNA sequencing-based analysis identified novel variants associated with autosomal dominant hearing lossTomohiro Kitano, Maiko Miyagawa, Shin-Ya Nishio, et al.Genes|February 27, 2026
The Clinical Details of MYH9-Related Disease and DFNA17 in a Large Japanese Hearing Loss CohortShinichi Goto, Akira Sasaki, Shin-Ya Nishio, et al.Journal of Personalized Medicine|October 27, 2022
Minimally Traumatic Cochlear Implant Surgery: Expert Opinion in 2010 and 2020Vedat Topsakal, Sumit Agrawal, Marcus Atlas, et al.Auris, Nasus, Larynx|May 20, 2003
Effect of single-drug treatment on idiopathic sudden sensorineural hearing lossJin Kanzaki, Yasuhiro Inoue, Kaoru Ogawa, et al.Plos One|May 17, 2019
OTOF mutation analysis with massively parallel DNA sequencing in 2,265 Japanese sensorineural hearing loss patientsYoh-Ichiro Iwasa, Shin-Ya Nishio, Akiko Sugaya, et al.Cochlear Implants International|March 12, 2020
The reliability of hearing implants: report on the type and incidence of cochlear implant failuresPaul Van de Heyning, Marcus Atlas, Wolf-Dieter Baumgartner, et al.Nature Communications|March 14, 2020
Digenic inheritance of mutations in EPHA2 and SLC26A4 in Pendred syndromeMengnan Li, Shin-Ya Nishio, Chie Naruse, et al.Pageof 26