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Shin-ichi Usami

Showing results (31-40 of 256) with videos related to

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Journal of Human Genetics|March 7, 2014
Mutation spectrum and genotype-phenotype correlation of hearing loss patients caused by SLC26A4 mutations in the Japanese: a large cohort studyMaiko Miyagawa, Shin-Ya Nishio, Shin-Ichi Usami, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|January 13, 2016
A Comprehensive Study on the Etiology of Patients Receiving Cochlear Implantation With Special Emphasis on Genetic EpidemiologyMaiko Miyagawa, Shin-Ya Nishio, Shin-ichi Usami
Laryngoscope Investigative Otolaryngology|October 25, 2021
Milestones toward cochlear gene therapy for patients with hereditary hearing lossHidekane Yoshimura, Shin-Ya Nishio, Shin-Ichi Usami
Journal of Human Genetics|January 10, 2014
Frequency of mitochondrial mutations in non-syndromic hearing loss as well as possibly responsible variants found by whole mitochondrial genome screeningTakuya Yano, Shin-ya Nishio, Shin-ichi Usami, et al.
Scientific Reports|December 22, 2025
Targeted long-read nanopore sequencing as a complementary approach for detecting STRC variants and distinguishing the STRCP1 pseudogeneHideaki Moteki, Shin-Ya Nishio, Shin-Ichi Usami
Auris, Nasus, Larynx|February 10, 2007
Meningioma of the paranasal sinus: a case reportKazuyuki Kainuma, Yutaka Takumi, Takeshi Uehara, et al.
Acta Oto-Laryngologica|November 3, 2010
Inverted papilloma of the middle ear: a case report and review of the literatureKazuyuki Kainuma, Ryosuke Kitoh, Sano Kenji, et al.
Acta Oto-Laryngologica|September 6, 2011
The first report of bilateral retropharyngeal lymph node metastasis from papillary thyroid carcinoma and review of the literatureKazuyuki Kainuma, Ryosuke Kitoh, Hidekane Yoshimura, et al.
Auris, Nasus, Larynx|March 13, 2013
Long term speech perception after cochlear implant in pediatric patients with GJB2 mutationsHaruo Yoshida, Haruo Takahashi, Yukihiko Kanda, et al.
Acta Oto-Laryngologica|March 17, 2007
Phenotypic consequences in a Japanese family having branchio-oto-renal syndrome with a novel frameshift mutation in the gene EYA1Tatsuo Matsunaga, Michiyo Okada, Shin-Ichi Usami, et al.
Pageof 26

Showing results (31-40 of 256) with videos related to

Sort By:
Pageof 26
Journal of Human Genetics|March 7, 2014
Mutation spectrum and genotype-phenotype correlation of hearing loss patients caused by SLC26A4 mutations in the Japanese: a large cohort studyMaiko Miyagawa, Shin-Ya Nishio, Shin-Ichi Usami, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|January 13, 2016
A Comprehensive Study on the Etiology of Patients Receiving Cochlear Implantation With Special Emphasis on Genetic EpidemiologyMaiko Miyagawa, Shin-Ya Nishio, Shin-ichi Usami
Laryngoscope Investigative Otolaryngology|October 25, 2021
Milestones toward cochlear gene therapy for patients with hereditary hearing lossHidekane Yoshimura, Shin-Ya Nishio, Shin-Ichi Usami
Journal of Human Genetics|January 10, 2014
Frequency of mitochondrial mutations in non-syndromic hearing loss as well as possibly responsible variants found by whole mitochondrial genome screeningTakuya Yano, Shin-ya Nishio, Shin-ichi Usami, et al.
Scientific Reports|December 22, 2025
Targeted long-read nanopore sequencing as a complementary approach for detecting STRC variants and distinguishing the STRCP1 pseudogeneHideaki Moteki, Shin-Ya Nishio, Shin-Ichi Usami
Auris, Nasus, Larynx|February 10, 2007
Meningioma of the paranasal sinus: a case reportKazuyuki Kainuma, Yutaka Takumi, Takeshi Uehara, et al.
Acta Oto-Laryngologica|November 3, 2010
Inverted papilloma of the middle ear: a case report and review of the literatureKazuyuki Kainuma, Ryosuke Kitoh, Sano Kenji, et al.
Acta Oto-Laryngologica|September 6, 2011
The first report of bilateral retropharyngeal lymph node metastasis from papillary thyroid carcinoma and review of the literatureKazuyuki Kainuma, Ryosuke Kitoh, Hidekane Yoshimura, et al.
Auris, Nasus, Larynx|March 13, 2013
Long term speech perception after cochlear implant in pediatric patients with GJB2 mutationsHaruo Yoshida, Haruo Takahashi, Yukihiko Kanda, et al.
Acta Oto-Laryngologica|March 17, 2007
Phenotypic consequences in a Japanese family having branchio-oto-renal syndrome with a novel frameshift mutation in the gene EYA1Tatsuo Matsunaga, Michiyo Okada, Shin-Ichi Usami, et al.
Pageof 26