Milestones toward cochlear gene therapy for patients with hereditary hearing loss

por Yoshimura, Hidekane, Nishio, Shin‐Ya, Usami, Shin‐Ichi
Publicado 2021

A case of hematohidrosis successfully treated with a beta‐blocker

por Sha, Yoshikazu, Yoshimura, Hidekane, Saito, Shoji, Kitoh, Ryosuke, Takumi, Yutaka
Publicado 2023

Enhanced viral-mediated cochlear gene delivery in adult mice by combining canal fenestration with round window membrane inoculation

por Yoshimura, Hidekane, Shibata, Seiji B., Ranum, Paul T., Smith, Richard J. H.
Publicado 2018

Frequency of Usher syndrome type 1 in deaf children by massively parallel DNA sequencing

por Yoshimura, Hidekane, Miyagawa, Maiko, Kumakawa, Kozo, Nishio, Shin-ya, Usami, Shin-ichi
Publicado 2016

Cochlear Implantation From the Perspective of Genetic Background

por Usami, Shin‐ichi, Nishio, Shin‐ya, Moteki, Hideaki, Miyagawa, Maiko, Yoshimura, Hidekane
Publicado 2020

Intravenous rAAV2/9 injection for murine cochlear gene delivery

por Shibata, Seiji B., Yoshimura, Hidekane, Ranum, Paul T., Goodwin, Alexander T., Smith, Richard J. H.
Publicado 2017

Hair Cell Transduction Efficiency of Single- and Dual-AAV Serotypes in Adult Murine Cochleae

por Omichi, Ryotaro, Yoshimura, Hidekane, Shibata, Seiji B., Vandenberghe, Luk H., Smith, Richard J.H.
Publicado 2020

Deafness Gene Expression Patterns in the Mouse Cochlea Found by Microarray Analysis

por Yoshimura, Hidekane, Takumi, Yutaka, Nishio, Shin-ya, Suzuki, Nobuyoshi, Iwasa, Yoh-ichiro, Usami, Shin-ichi
Publicado 2014

Vibrant soundbridge implantation prior to auricular reconstruction with unilateral microtia‐atresia

por Yoshimura, Hidekane, Takahashi, Masahiro, Iwasaki, Satoshi, Shinagawa, Jun, Takashimizu, Ikkei, Nagai, Fumio, Yotsuyanagi, Takatoshi, Usami, Shin‐ichi
Publicado 2021

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

por Iwasa, Yoh-ichiro, Tsukada, Keita, Kobayashi, Masafumi, Kitano, Tomohiro, Mori, Kentaro, Yoshimura, Hidekane, Fukuoka, Hisakuni, Usami, Shin-ichi
Publicado 2018

Clinical and molecular features of patients with COL1 ‐related disorders: Implications for the wider spectrum and the risk of vascular complications

por Takeda, Ryojun, Yamaguchi, Tomomi, Hayashi, Shujiro, Sano, Shinichirou, Kawame, Hiroshi, Kanki, Sachiko, Taketani, Takeshi, Yoshimura, Hidekane, Nakamura, Yukio, Kosho, Tomoki
Publicado 2022

OTOF mutation screening in Japanese severe to profound recessive hearing loss patients

por Iwasa, Yoh-ichiro, Nishio, Shin-ya, Yoshimura, Hidekane, Kanda, Yukihiko, Kumakawa, Kozo, Abe, Satoko, Naito, Yasushi, Nagai, Kyoko, Usami, Shin-ichi
Publicado 2013

Single-cell RNA-sequencing of stria vascularis cells in the adult Slc26a4(-/-) mouse

por Koh, Jin-Young, Affortit, Corentin, Ranum, Paul T., West, Cody, Walls, William D., Yoshimura, Hidekane, Shao, Jian Q., Mostaert, Brian, Smith, Richard J.H.
Publicado 2023

A clinical experience of ‘STAMP’ plate-guided Bonebridge implantation

por Takumi, Yutaka, Matsumoto, Nozomu, Cho, Byunghyun, Ono, Hidenori, Mori, Kentaro, Tsukada, Keita, Ichinose, Aya, Yoshimura, Hidekane, Iwasaki, Satoshi, Komune, Shizuo, Usami, Shin-ichi
Publicado 2014

Insights into the Biology of Hearing and Deafness Revealed by Single-Cell RNA Sequencing

por Ranum, Paul T., Goodwin, Alexander T., Yoshimura, Hidekane, Kolbe, Diana L., Walls, William D., Koh, Jin-Young, He, David Z.Z., Smith, Richard J.H.
Publicado 2019

Mutation-agnostic RNA interference with engineered replacement rescues Tmc1-related hearing loss

por Iwasa, Yoichiro, Klimara, Miles J, Yoshimura, Hidekane, Walls, William D, Omichi, Ryotaro, West, Cody A, Shibata, Seiji B, Ranum, Paul T, Smith, Richard JH
Publicado 2022

Massively Parallel DNA Sequencing Facilitates Diagnosis of Patients with Usher Syndrome Type 1

por Yoshimura, Hidekane, Iwasaki, Satoshi, Nishio, Shin-ya, Kumakawa, Kozo, Tono, Tetsuya, Kobayashi, Yumiko, Sato, Hiroaki, Nagai, Kyoko, Ishikawa, Kotaro, Ikezono, Tetsuo, Naito, Yasushi, Fukushima, Kunihiro, Oshikawa, Chie, Kimitsuki, Takashi, Nakanishi, Hiroshi, Usami, Shin-ichi
Publicado 2014

Correction to: Detailed clinical features and genotype–phenotype correlation in an OTOF-related hearing loss cohort in Japan

por Iwasa, Yoh-ichiro, Nishio, Shin-ya, Yoshimura, Hidekane, Sugaya, Akiko, Kataoka, Yuko, Maeda, Yukihide, Kanda, Yukihiko, Nagai, Kyoko, Naito, Yasushi, Yamazaki, Hiroshi, Ikezono, Tetsuo, Matsuda, Han, Nakai, Masako, Tona, Risa, Sakurai, Yuika, Motegi, Remi, Takeda, Hidehiko, Kobayashi, Marina, Kihara, Chiharu, Ishino, Takashi, Morita, Shin-ya, Iwasaki, Satoshi, Takahashi, Masahiro, Furutate, Sakiko, Oka, Shin-ichiro, Kubota, Toshinori, Arai, Yasuhiro, Kobayashi, Yumiko, Kikuchi, Daisuke, Shintani, Tomoko, Ogasawara, Noriko, Honkura, Yohei, Izumi, Shuji, Hyogo, Misako, Ninoyu, Yuzuru, Suematsu, Mayumi, Nakayama, Jun, Tsuchihashi, Nana, Okami, Mayuri, Sakata, Hideaki, Yoshihashi, Hiroshi, Kobayashi, Taisuke, Kumakawa, Kozo, Yoshida, Tadao, Esaki, Tomoko, Usami, Shin-ichi
Publicado 2021

Detailed clinical features and genotype–phenotype correlation in an OTOF-related hearing loss cohort in Japan

por Iwasa, Yoh-ichiro, Nishio, Shin-ya, Yoshimura, Hidekane, Sugaya, Akiko, Kataoka, Yuko, Maeda, Yukihide, Kanda, Yukihiko, Nagai, Kyoko, Naito, Yasushi, Yamazaki, Hiroshi, Ikezono, Tetsuo, Matsuda, Han, Nakai, Masako, Tona, Risa, Sakurai, Yuika, Motegi, Remi, Takeda, Hidehiko, Kobayashi, Marina, Kihara, Chiharu, Ishino, Takashi, Morita, Shin-ya, Iwasaki, Satoshi, Takahashi, Masahiro, Furutate, Sakiko, Oka, Shin-ichiro, Kubota, Toshinori, Arai, Yasuhiro, Kobayashi, Yumiko, Kikuchi, Daisuke, Shintani, Tomoko, Ogasawara, Noriko, Honkura, Yohei, Izumi, Shuji, Hyogo, Misako, Ninoyu, Yuzuru, Suematsu, Mayumi, Nakayama, Jun, Tsuchihashi, Nana, Okami, Mayuri, Sakata, Hideaki, Yoshihashi, Hiroshi, Kobayashi, Taisuke, Kumakawa, Kozo, Yoshida, Tadao, Esaki, Tomoko, Usami, Shin-ichi
Publicado 2021