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List of works by Maiko Miyagawa

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

scientific article

Cochlear Implantation From the Perspective of Genetic Background

scientific article published on 06 February 2020

Comprehensive analysis of syndromic hearing loss patients in Japan

scientific article published on 19 August 2019

Detailed hearing and vestibular profiles in the patients with COCH mutations

scientific article published on 16 March 2015

Feasibility of hearing preservation for residual hearing with longer cochlear implant electrodes

scientific article published on 01 December 2018

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

scientific article published on 21 January 2016

Gene expression profiles of the cochlea and vestibular endorgans: localization and function of genes causing deafness

scientific article published on 26 March 2015

Germinal mosaicism in a family with BO syndrome.

scientific article published on 16 March 2015

Hearing preservation and clinical outcome of 32 consecutive electric acoustic stimulation (EAS) surgeries

scientific article

Long-term results of hearing preservation cochlear implant surgery in patients with residual low frequency hearing.

scientific article published on 17 November 2016

Massively parallel DNA sequencing successfully identified seven families with deafness-associated MYO6 mutations: the mutational spectrum and clinical characteristics

scientific article published in May 2015

Mutation spectrum and genotype-phenotype correlation of hearing loss patients caused by SLC26A4 mutations in the Japanese: a large cohort study.

scientific article published on 6 March 2014

Mutational spectrum and clinical features of patients with ACTG1 mutations identified by massively parallel DNA sequencing.

scientific article published on 19 March 2015

Mutations in the MYO15A gene are a significant cause of nonsyndromic hearing loss: massively parallel DNA sequencing-based analysis

scientific article published on 19 March 2015

POU4F3 mutation screening in Japanese hearing loss patients: Massively parallel DNA sequencing-based analysis identified novel variants associated with autosomal dominant hearing loss

scientific article

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

scientific article

The patients associated with TMPRSS3 mutations are good candidates for electric acoustic stimulation.

scientific article published on 13 March 2015

WFS1 mutation screening in a large series of Japanese hearing loss patients: Massively parallel DNA sequencing-based analysis.

scientific article published on 12 March 2018

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