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Acta Oto-Laryngologica|May 13, 2017
Outcomes of cochlear implantation for the patients with specific genetic etiologies: a systematic literature reviewShin-Ya Nishio, Shin-Ichi UsamiScientific Reports|January 13, 2022
Frequency of the STRC-CATSPER2 deletion in STRC-associated hearing loss patientsShin-Ya Nishio, Shin-Ichi UsamiHuman Mutation|December 24, 2016
The Clinical Next-Generation Sequencing Database: A Tool for the Unified Management of Clinical Information and Genetic Variants to Accelerate Variant Pathogenicity ClassificationShin-Ya Nishio, Shin-Ichi UsamiThe Annals of Otology, Rhinology, and Laryngology|March 20, 2015
Deafness gene variations in a 1120 nonsyndromic hearing loss cohort: molecular epidemiology and deafness mutation spectrum of patients in JapanShin-Ya Nishio, Shin-Ichi UsamiHuman Genetics|October 2, 2021
The genetic etiology of hearing loss in Japan revealed by the social health insurance-based genetic testing of 10K patientsShin-Ichi Usami, Shin-Ya NishioHuman Genetics|September 15, 2021
Prevalence and clinical features of autosomal dominant and recessive TMC1-associated hearing lossShin-Ya Nishio, Shin-Ichi UsamiGenetic Testing|October 24, 2007
Application of deafness diagnostic screening panel based on deafness mutation/gene database using invader assaySatoko Abe, Toshikazu Yamaguchi, Shin-Ichi UsamiAudiology & Neuro-Otology|April 1, 2015
Vestibular functions of hereditary hearing loss patients with GJB2 mutationsKeita Tsukada, Hisakuni Fukuoka, Shin-Ichi UsamiJournal of Human Genetics|October 25, 2003
Mutations in the gene encoding KIAA1199 protein, an inner-ear protein expressed in Deiters' cells and the fibrocytes, as the cause of nonsyndromic hearing lossSatoko Abe, Shin-ichi Usami, Yusuke NakamuraActa Oto-Laryngologica|February 17, 2016
SOD1 gene polymorphisms in sudden sensorineural hearing lossRyosuke Kitoh, Shin-Ya Nishio, Kaoru Ogawa, et al.Pageof 26