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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.
American Journal of Human Genetics|December 10, 2002
Identification of CRYM as a candidate responsible for nonsyndromic deafness, through cDNA microarray analysis of human cochlear and vestibular tissuesSatoko Abe, Toyomasa Katagiri, Akihiko Saito-Hisaminato, 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.
Experimental Brain Research|October 10, 2002
Role of visual input in nonlinear postural control systemOsamu Sasaki, Shin-ichi Usami, Pierre-Marie Gagey, 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.
Acta Oto-Laryngologica|March 28, 2008
The responsible genes in Japanese deafness patients and clinical application using Invader assayShin-Ichi Usami, Michio Wagatsuma, Hisakuni Fukuoka, 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.
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