Hasil Pencarian - Shin‐ichi Usami

Perbaiki Hasil
  1. 1
    Vestibular Preservation After Cochlear Implantation Using the Round Window Approach

    Vestibular Preservation After Cochlear Implantation Using the Round Window Approach oleh Keita Tsukada, Shin-ichi Usami, Shin-ichi Usami

    Diterbitkan 2021-04-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  2. 2
    Frequency of the STRC-CATSPER2 deletion in STRC-associated hearing loss patients

    Frequency of the STRC-CATSPER2 deletion in STRC-associated hearing loss patients oleh Shin-ya Nishio, Shin-ichi Usami

    Diterbitkan 2022-01-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  3. 3
    Prevalence and clinical features of hearing loss patients with CDH23 mutations: a large cohort study.

    Prevalence and clinical features of hearing loss patients with CDH23 mutations: a large cohort study. oleh Maiko Miyagawa, Shin-ya Nishio, Shin-ichi Usami

    Diterbitkan 2012-01-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  4. 4
    Milestones toward cochlear gene therapy for patients with hereditary hearing loss

    Milestones toward cochlear gene therapy for patients with hereditary hearing loss oleh Hidekane Yoshimura, Shin‐Ya Nishio, Shin‐Ichi Usami

    Diterbitkan 2021-10-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  5. 5
    Comprehensive Genetic Analysis of Japanese Autosomal Dominant Sensorineural Hearing Loss Patients.

    Comprehensive Genetic Analysis of Japanese Autosomal Dominant Sensorineural Hearing Loss Patients. oleh Yoh-Ichiro Iwasa, Shin-Ya Nishio, Shin-Ichi Usami

    Diterbitkan 2016-01-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  6. 6
    Comparison of vestibular function in hereditary hearing loss patients with GJB2, CDH23, and SLC26A4 variants

    Comparison of vestibular function in hereditary hearing loss patients with GJB2, CDH23, and SLC26A4 variants oleh Keita Tsukada, Shin-ya Nishio, Yutaka Takumi, Shin-ichi Usami

    Diterbitkan 2024-05-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  7. 7
    Detailed Clinical Features of Deafness Caused by a Claudin-14 Variant

    Detailed Clinical Features of Deafness Caused by a Claudin-14 Variant oleh Tomohiro Kitano, Shin-ichiro Kitajiri, Shin-ya Nishio, Shin-ichi Usami

    Diterbitkan 2019-09-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  8. 8
    The prevalence and clinical features of MYO7A-related hearing loss including DFNA11, DFNB2 and USH1B

    The prevalence and clinical features of MYO7A-related hearing loss including DFNA11, DFNB2 and USH1B oleh Kizuki Watanabe, Shin-ya Nishio, Shin-ichi Usami, the Deafness Gene Study Consortium

    Diterbitkan 2024-04-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  9. 9
    Massively parallel DNA sequencing successfully identifies new causative mutations in deafness genes in patients with cochlear implantation and EAS.

    Massively parallel DNA sequencing successfully identifies new causative mutations in deafness genes in patients with cochlear implantation and EAS. oleh Maiko Miyagawa, Shin-ya Nishio, Takuo Ikeda, Kunihiro Fukushima, Shin-ichi Usami

    Diterbitkan 2013-01-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  10. 10
    Targeted exon sequencing successfully discovers rare causative genes and clarifies the molecular epidemiology of Japanese deafness patients.

    Targeted exon sequencing successfully discovers rare causative genes and clarifies the molecular epidemiology of Japanese deafness patients. oleh Maiko Miyagawa, Takehiko Naito, Shin-ya Nishio, Naoyuki Kamatani, Shin-ichi Usami

    Diterbitkan 2013-01-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  11. 11
    Social Health Insurance-Based Simultaneous Screening for 154 Mutations in 19 Deafness Genes Efficiently Identified Causative Mutations in Japanese Hearing Loss Patients.

    Social Health Insurance-Based Simultaneous Screening for 154 Mutations in 19 Deafness Genes Efficiently Identified Causative Mutations in Japanese Hearing Loss Patients. oleh Kentaro Mori, Hideaki Moteki, Maiko Miyagawa, Shin-Ya Nishio, Shin-Ichi Usami

    Diterbitkan 2016-01-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  12. 12
    Compound heterozygous dominant and recessive GJB2 mutations cause deafness with palmoplantar keratoderma

    Compound heterozygous dominant and recessive GJB2 mutations cause deafness with palmoplantar keratoderma oleh Yasuhiro Arai, Masahiro Takahashi, Naoko Sakuma, Shin-Ya Nisio, Nobuhiko Oridate, Shin-Ichi Usami

    Diterbitkan 2017-01-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  13. 13
    A novel case of concurrent occurrence of demyelinating-polyneuropathy-causing PMP22 duplication and SOX10 gene mutation producing severe hypertrophic neuropathy

    A novel case of concurrent occurrence of demyelinating-polyneuropathy-causing PMP22 duplication and SOX10 gene mutation producing severe hypertrophic neuropathy oleh Nozomu Matsuda, Koushi Ootsuki, Shunsuke Kobayashi, Ayaka Nemoto, Hitoshi Kubo, Shin-ichi Usami, Kazuaki Kanani

    Diterbitkan 2021-06-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  14. 14
    Deafness gene expression patterns in the mouse cochlea found by microarray analysis.

    Deafness gene expression patterns in the mouse cochlea found by microarray analysis. oleh Hidekane Yoshimura, Yutaka Takumi, Shin-ya Nishio, Nobuyoshi Suzuki, Yoh-ichiro Iwasa, Shin-ichi Usami

    Diterbitkan 2014-01-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  15. 15
    Simultaneous screening of multiple mutations by invader assay improves molecular diagnosis of hereditary hearing loss: a multicenter study.

    Simultaneous screening of multiple mutations by invader assay improves molecular diagnosis of hereditary hearing loss: a multicenter study. oleh Shin-ichi Usami, Shin-ya Nishio, Makoto Nagano, Satoko Abe, Toshikazu Yamaguchi, Deafness Gene Study Consortium

    Diterbitkan 2012-01-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  16. 16
    Vibrant soundbridge implantation prior to auricular reconstruction with unilateral microtia‐atresia

    Vibrant soundbridge implantation prior to auricular reconstruction with unilateral microtia‐atresia oleh Hidekane Yoshimura, Masahiro Takahashi, Satoshi Iwasaki, Jun Shinagawa, Ikkei Takashimizu, Fumio Nagai, Takatoshi Yotsuyanagi, Shin‐ichi Usami

    Diterbitkan 2021-08-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  17. 17
    Bilateral delayed endolymphatic hydrops evaluated by bilateral intratympanic injection of gadodiamide with 3T-MRI.

    Bilateral delayed endolymphatic hydrops evaluated by bilateral intratympanic injection of gadodiamide with 3T-MRI. oleh Yoh-Ichiro Iwasa, Keita Tsukada, Masafumi Kobayashi, Tomohiro Kitano, Kentaro Mori, Hidekane Yoshimura, Hisakuni Fukuoka, Shin-Ichi Usami

    Diterbitkan 2018-01-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  18. 18
    Cochlear implantation in a patient with a POU4F3 mutation

    Cochlear implantation in a patient with a POU4F3 mutation oleh Keitaro Miyake, Kyoko Shirai, Nobuhiro Nishiyama, Sachie Kawaguchi, Yoko Ohta, Atsushi Kawano, Shin‐ichi Usami, Tomohiro Kitano, Kiyoaki Tsukahara

    Diterbitkan 2021-01-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  19. 19
    Gene expression pattern after insertion of dexamethasone-eluting electrode into the guinea pig cochlea.

    Gene expression pattern after insertion of dexamethasone-eluting electrode into the guinea pig cochlea. oleh Yutaka Takumi, Shin-ya Nishio, Kenneth Mugridge, Tomohiro Oguchi, Shigenari Hashimoto, Nobuyoshi Suzuki, Satoshi Iwasaki, Claude Jolly, Shin-ichi Usami

    Diterbitkan 2014-01-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  20. 20
    Congenital Membranous Stapes Footplate Producing Episodic Pressure-Induced Perilymphatic Fistula Symptoms

    Congenital Membranous Stapes Footplate Producing Episodic Pressure-Induced Perilymphatic Fistula Symptoms oleh Han Matsuda, Yasuhiko Tanzawa, Tatsuro Sekine, Tomohiro Matsumura, Shiho Saito, Susumu Shindo, Shin-ichi Usami, Yasuhiro Kase, Akinori Itoh, Tetsuo Ikezono

    Diterbitkan 2020-11-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:

Alat Pencarian: