Cargando…

Achievement of hearing preservation in the presence of an electrode covering the residual hearing region

CONCLUSIONS: With full insertion with a long electrode, hearing preservation can be achieved even in the presence of a long electrode covering the residual hearing region. OBJECTIVES: Advances in developing new atraumatic concepts of electrode design as well as surgical technique have enabled hearin...

Descripción completa

Detalles Bibliográficos
Autores principales:	Usami, Shin-Ichi, Moteki, Hideaki, Suzuki, Nobuyoshi, Fukuoka, Hisakuni, Miyagawa, Maiko, Nishio, Shin-Ya, Takumi, Yutaka, Iwasaki, Satoshi, Jolly, Claude
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Informa Healthcare 2011
Materias:	Original Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3490476/ https://www.ncbi.nlm.nih.gov/pubmed/21208024 http://dx.doi.org/10.3109/00016489.2010.539266

Ejemplares similares

Hearing preservation and clinical outcome of 32 consecutive electric acoustic stimulation (EAS) surgeries
por: Usami, Shin-Ichi, et al.
Publicado: (2014)

Social Health Insurance-Based Simultaneous Screening for 154 Mutations in 19 Deafness Genes Efficiently Identified Causative Mutations in Japanese Hearing Loss Patients
por: Mori, Kentaro, et al.
Publicado: (2016)

Variants in CDH23 cause a broad spectrum of hearing loss: from non-syndromic to syndromic hearing loss as well as from congenital to age-related hearing loss
por: Usami, Shin-ichi, et al.
Publicado: (2022)

Clinical profile of hearing loss in children with congenital cytomegalovirus (CMV) infection: CMV DNA diagnosis using preserved umbilical cord
por: Furutate, Sakiko, et al.
Publicado: (2011)

Effects of EAS cochlear implantation surgery on vestibular function
por: Tsukada, Keita, et al.
Publicado: (2013)

Diagnostic pitfalls for GJB2‐related hearing loss: A novel deletion detected by Array‐CGH analysis in a Japanese patient with congenital profound hearing loss
por: Abe, Satoko, et al.
Publicado: (2018)

Patients with CDH23 mutations and the 1555A>G mitochondrial mutation are good candidates for electric acoustic stimulation (EAS)
por: Usami, Shin-Ichi, et al.
Publicado: (2012)

Prevalence and Clinical Characteristics of Hearing Loss Caused by MYH14 Variants
por: Hiramatsu, Ken, et al.
Publicado: (2021)

Experience with the Vibrant Soundbridge RW-Coupler for round window Vibroplasty with tympanosclerosis
por: Iwasaki, Satoshi, et al.
Publicado: (2012)

Prevalence and Clinical Features of Hearing Loss Patients with CDH23 Mutations: A Large Cohort Study
por: Miyagawa, Maiko, et al.
Publicado: (2012)

Different cortical metabolic activation by visual stimuli possibly due to different time courses of hearing loss in patients with GJB2 and SLC26A4 mutations
por: Moteki, Hideaki, et al.
Publicado: (2011)

Mutation spectrum and genotype–phenotype correlation of hearing loss patients caused by SLC26A4 mutations in the Japanese: a large cohort study
por: Miyagawa, Maiko, et al.
Publicado: (2014)

Cochlear Implantation From the Perspective of Genetic Background
por: Usami, Shin‐ichi, et al.
Publicado: (2020)

Gene Expression Pattern after Insertion of Dexamethasone-Eluting Electrode into the Guinea Pig Cochlea
por: Takumi, Yutaka, et al.
Publicado: (2014)

Comparison of the diagnostic value of 3 T MRI after intratympanic injection of GBCA, electrocochleography, and the glycerol test in patients with Meniere's disease
por: Fukuoka, Hisakuni, et al.
Publicado: (2012)

Mid-Frequency Hearing Loss Is Characteristic Clinical Feature of OTOA-Associated Hearing Loss
por: Sugiyama, Kenjiro, et al.
Publicado: (2019)

POU4F3 mutation screening in Japanese hearing loss patients: Massively parallel DNA sequencing-based analysis identified novel variants associated with autosomal dominant hearing loss
por: Kitano, Tomohiro, et al.
Publicado: (2017)

Clinical Characteristics and In Vitro Analysis of MYO6 Variants Causing Late-onset Progressive Hearing Loss
por: Oka, Shin-ichiro, et al.
Publicado: (2020)

Prevalence and clinical features of hearing loss caused by EYA4 variants
por: Shinagawa, Jun, et al.
Publicado: (2020)

Frequency of the STRC-CATSPER2 deletion in STRC-associated hearing loss patients
por: Nishio, Shin-ya, et al.
Publicado: (2022)

Prevalence and clinical features of autosomal dominant and recessive TMC1-associated hearing loss
por: Nishio, Shin-ya, et al.
Publicado: (2021)

Novel ACTG1 mutations in patients identified by massively parallel DNA sequencing cause progressive hearing loss
por: Miyajima, Hiroki, et al.
Publicado: (2020)

Milestones toward cochlear gene therapy for patients with hereditary hearing loss
por: Yoshimura, Hidekane, et al.
Publicado: (2021)

Simple and efficient germline copy number variant visualization method for the Ion AmpliSeq™ custom panel
por: Nishio, Shin‐ya, et al.
Publicado: (2018)

Comprehensive Genetic Analysis of Japanese Autosomal Dominant Sensorineural Hearing Loss Patients
por: Iwasa, Yoh-ichiro, et al.
Publicado: (2016)

The genetic etiology of hearing loss in Japan revealed by the social health insurance-based genetic testing of 10K patients
por: Usami, Shin-ichi, et al.
Publicado: (2021)

Frequency and clinical features of hearing loss caused by STRC deletions
por: Yokota, Yoh, et al.
Publicado: (2019)

WFS1 mutation screening in a large series of Japanese hearing loss patients: Massively parallel DNA sequencing-based analysis
por: Kobayashi, Masafumi, et al.
Publicado: (2018)

Sensorineural hearing loss and mild cardiac phenotype caused by an EYA4 mutation
por: Abe, Satoko, et al.
Publicado: (2018)

The advantages of sound localization and speech perception of bilateral electric acoustic stimulation
por: Moteki, Hideaki, et al.
Publicado: (2015)

Otological Features of Patients with Musculocontractural Ehlers–Danlos Syndrome Caused by Pathogenic Variants in CHST14 (mcEDS-CHST14)
por: Kawakita, Masayuki, et al.
Publicado: (2023)

Comprehensive analysis of syndromic hearing loss patients in Japan
por: Ideura, Michie, et al.
Publicado: (2019)

The Prevalence and Clinical Characteristics of TECTA-Associated Autosomal Dominant Hearing Loss
por: Yasukawa, Rika, et al.
Publicado: (2019)

Frequency of mitochondrial mutations in non-syndromic hearing loss as well as possibly responsible variants found by whole mitochondrial genome screening
por: Yano, Takuya, et al.
Publicado: (2014)

Haplotype Analysis of GJB2 Mutations: Founder Effect or Mutational Hot Spot?
por: Shinagawa, Jun, et al.
Publicado: (2020)

Genetic background in late-onset sensorineural hearing loss patients
por: Uehara, Natsumi, et al.
Publicado: (2021)

A Comprehensive Study on the Etiology of Patients Receiving Cochlear Implantation With Special Emphasis on Genetic Epidemiology
por: Miyagawa, Maiko, et al.
Publicado: (2016)

Simultaneous Screening of Multiple Mutations by Invader Assay Improves Molecular Diagnosis of Hereditary Hearing Loss: A Multicenter Study
por: Usami, Shin-ichi, et al.
Publicado: (2012)

Deafness Gene Expression Patterns in the Mouse Cochlea Found by Microarray Analysis
por: Yoshimura, Hidekane, et al.
Publicado: (2014)

OTOF mutation screening in Japanese severe to profound recessive hearing loss patients
por: Iwasa, Yoh-ichiro, et al.
Publicado: (2013)

Cannot write session to /tmp/vufind_sessions/sess_of8gp5tk8calg5ujtjnkccdumi