Vestibular Preservation After Cochlear Implantation Using the Round Window Approach

by Keita Tsukada, Shin-ichi Usami, Shin-ichi Usami
Published 2021-04-01

Prevalence and clinical features of hearing loss patients with CDH23 mutations: a large cohort study.

by Maiko Miyagawa, Shin-ya Nishio, Shin-ichi Usami
Published 2012-01-01

Comprehensive Genetic Analysis of Japanese Autosomal Dominant Sensorineural Hearing Loss Patients.

by Yoh-Ichiro Iwasa, Shin-Ya Nishio, Shin-Ichi Usami
Published 2016-01-01

Detailed Clinical Features of Deafness Caused by a Claudin-14 Variant

by Tomohiro Kitano, Shin-ichiro Kitajiri, Shin-ya Nishio, Shin-ichi Usami
Published 2019-09-01

Targeted exon sequencing successfully discovers rare causative genes and clarifies the molecular epidemiology of Japanese deafness patients.

by Maiko Miyagawa, Takehiko Naito, Shin-ya Nishio, Naoyuki Kamatani, Shin-ichi Usami
Published 2013-01-01

Haplotype Analysis of <i>GJB2</i> Mutations: Founder Effect or Mutational Hot Spot?

by Jun Shinagawa, Hideaki Moteki, Shin-ya Nishio, Yoshihiro Noguchi, Shin-ichi Usami
Published 2020-02-01

Social Health Insurance-Based Simultaneous Screening for 154 Mutations in 19 Deafness Genes Efficiently Identified Causative Mutations in Japanese Hearing Loss Patients.

by Kentaro Mori, Hideaki Moteki, Maiko Miyagawa, Shin-Ya Nishio, Shin-Ichi Usami
Published 2016-01-01

Massively parallel DNA sequencing successfully identifies new causative mutations in deafness genes in patients with cochlear implantation and EAS.

by Maiko Miyagawa, Shin-ya Nishio, Takuo Ikeda, Kunihiro Fukushima, Shin-ichi Usami
Published 2013-01-01

Compound heterozygous dominant and recessive GJB2 mutations cause deafness with palmoplantar keratoderma

by Yasuhiro Arai, Masahiro Takahashi, Naoko Sakuma, Shin-Ya Nisio, Nobuhiko Oridate, Shin-Ichi Usami
Published 2017-01-01

Deafness gene expression patterns in the mouse cochlea found by microarray analysis.

by Hidekane Yoshimura, Yutaka Takumi, Shin-ya Nishio, Nobuyoshi Suzuki, Yoh-ichiro Iwasa, Shin-ichi Usami
Published 2014-01-01

A novel case of concurrent occurrence of demyelinating-polyneuropathy-causing PMP22 duplication and SOX10 gene mutation producing severe hypertrophic neuropathy

by Nozomu Matsuda, Koushi Ootsuki, Shunsuke Kobayashi, Ayaka Nemoto, Hitoshi Kubo, Shin-ichi Usami, Kazuaki Kanani
Published 2021-06-01

Simultaneous screening of multiple mutations by invader assay improves molecular diagnosis of hereditary hearing loss: a multicenter study.

by Shin-ichi Usami, Shin-ya Nishio, Makoto Nagano, Satoko Abe, Toshikazu Yamaguchi, Deafness Gene Study Consortium
Published 2012-01-01

Bilateral delayed endolymphatic hydrops evaluated by bilateral intratympanic injection of gadodiamide with 3T-MRI.

by Yoh-Ichiro Iwasa, Keita Tsukada, Masafumi Kobayashi, Tomohiro Kitano, Kentaro Mori, Hidekane Yoshimura, Hisakuni Fukuoka, Shin-Ichi Usami
Published 2018-01-01

Cochlear implantation in a patient with a POU4F3 mutation

by Keitaro Miyake, Kyoko Shirai, Nobuhiro Nishiyama, Sachie Kawaguchi, Yoko Ohta, Atsushi Kawano, Shin‐ichi Usami, Tomohiro Kitano, Kiyoaki Tsukahara
Published 2021-01-01

Gene expression pattern after insertion of dexamethasone-eluting electrode into the guinea pig cochlea.

by Yutaka Takumi, Shin-ya Nishio, Kenneth Mugridge, Tomohiro Oguchi, Shigenari Hashimoto, Nobuyoshi Suzuki, Satoshi Iwasaki, Claude Jolly, Shin-ichi Usami
Published 2014-01-01

Congenital Membranous Stapes Footplate Producing Episodic Pressure-Induced Perilymphatic Fistula Symptoms

by Han Matsuda, Yasuhiko Tanzawa, Tatsuro Sekine, Tomohiro Matsumura, Shiho Saito, Susumu Shindo, Shin-ichi Usami, Yasuhiro Kase, Akinori Itoh, Tetsuo Ikezono
Published 2020-11-01

Comprehensive genetic screening of KCNQ4 in a large autosomal dominant nonsyndromic hearing loss cohort: genotype-phenotype correlations and a founder mutation.

by Takehiko Naito, Shin-ya Nishio, Yoh-ichiro Iwasa, Takuya Yano, Kozo Kumakawa, Satoko Abe, Kotaro Ishikawa, Hiromi Kojima, Atsushi Namba, Chie Oshikawa, Shin-ichi Usami
Published 2013-01-01

Mid-Frequency Hearing Loss Is Characteristic Clinical Feature of <i>OTOA</i>-Associated Hearing Loss

by Kenjiro Sugiyama, Hideaki Moteki, Shin-ichiro Kitajiri, Tomohiro Kitano, Shin-ya Nishio, Tomomi Yamaguchi, Keiko Wakui, Satoko Abe, Akiko Ozaki, Remi Motegi, Hirooki Matsui, Masato Teraoka, Yumiko Kobayashi, Tomoki Kosho, Shin-ichi Usami
Published 2019-09-01

Massively parallel DNA sequencing facilitates diagnosis of patients with Usher syndrome type 1.

by Hidekane Yoshimura, Satoshi Iwasaki, Shin-Ya Nishio, Kozo Kumakawa, Tetsuya Tono, Yumiko Kobayashi, Hiroaki Sato, Kyoko Nagai, Kotaro Ishikawa, Tetsuo Ikezono, Yasushi Naito, Kunihiro Fukushima, Chie Oshikawa, Takashi Kimitsuki, Hiroshi Nakanishi, Shin-Ichi Usami
Published 2014-01-01

The diagnostic performance of a novel ELISA for human CTP (Cochlin-tomoprotein) to detect perilymph leakage.

by Tetsuo Ikezono, Tomohiro Matsumura, Han Matsuda, Satomi Shikaze, Shiho Saitoh, Susumu Shindo, Setsuo Hasegawa, Seung Ha Oh, Yoshiaki Hagiwara, Yasuo Ogawa, Hiroshi Ogawa, Hiroaki Sato, Tetsuya Tono, Ryuichiro Araki, Yukihide Maeda, Shin-Ichi Usami, Yasuhiro Kase
Published 2018-01-01