Search Results1-12 of  12

  • Miyagawa Maiko ID: 9000248198824

    Articles in CiNii:1

    • Mutation spectrum and genotype-phenotype correlation of hearing loss patients caused by SLC26A4 mutations in the Japanese : a large cohort study (2014)
  • Miyagawa Maiko ID: 9000324663061

    Articles in CiNii:1

    • Frequency of Usher syndrome type 1 in deaf children by massively parallel DNA sequencing (2016)
  • MIYAGAWA Maiko ID: 9000002141116

    信州大学 医学部 耳鼻咽喉科 (2013 from CiNii)

    Articles in CiNii:19

    • 伝音難聴治療前後での気導/骨導ASSR閾値の検討 (2007)
    • 高音急墜型/高音漸傾型感音難聴症例の臨床像と遺伝的背景 (2009)
    • GJB2遺伝子変異症例におけるASSRでの推定聴力閾値と成長後の純音聴力検査閾値比較 (2010)
  • Miyagawa Maiko ID: 9000252749926

    Articles in CiNii:1

    • Patients with CDH23 mutations and the 1555A > G mitochondrial mutation are good candidates for electric acoustic stimulation (EAS) (2012)
  • Miyagawa Maiko ID: 9000252749936

    Articles in CiNii:1

    • Experience with the Vibrant Soundbridge RW-Coupler for round window Vibroplasty with tympanosclerosis (2012)
  • Miyagawa Maiko ID: 9000252749942

    Articles in CiNii:1

    • 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 (2012)
  • Miyagawa Maiko ID: 9000252749959

    Articles in CiNii:1

    • Achievement of hearing preservation in the presence of an electrode covering the residual hearing region (2011)
  • Miyagawa Maiko ID: 9000258221328

    Department of Otorhinolaryngology, Shinshu University School of Medicine (2011 from CiNii)

    Articles in CiNii:1

    • Results of electric acoustic stimulation for partial deafness in japan: three case reports (2011)
  • Miyagawa Maiko ID: 9000303165295

    Articles in CiNii:1

    • Prevalence and Clinical Features of Hearing Loss Patients with CDH23 Mutations: A Large Cohort Study (2012)
  • Miyagawa Maiko ID: 9000318587168

    Department of Otorhinolaryngology, Shinshu University School of Medicine|Department of Hearing Implant Sciences, Shinshu University School of Medicine (2015 from CiNii)

    Articles in CiNii:1

    • Clinical Impact of genetic testing (2015)
  • Miyagawa Maiko ID: 9000399009219

    Articles in CiNii:1

    • POU4F3 mutation screening in Japanese hearing loss patients: Massively parallel DNA sequencing-based analysis identified novel variants associated with autosomal dominant hearing loss (2017)
  • Miyagawa Maiko ID: 9000403316576

    Articles in CiNii:1

    • Gene Expression Profiles of the Cochlea and Vestibular Endorgans: Localization and Function of Genes Causing Deafness (2015)
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