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Facial nerve stimulation following cochlear implantation for X-linked stapes gusher syndrome leading to identification of a novel POU3F4 mutation.
Wester, Jacob L; Merna, Catherine; Peng, Kevin A; Lewis, Rebecca; Sepahdari, Ali R; Ishiyama, Gail; Hosokawa, Kumiko; Kumakawa, Kozo; Ishiyama, Akira.
Afiliação
  • Wester JL; Department of Head and Neck Surgery, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA, USA.
  • Merna C; Department of Head and Neck Surgery, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA, USA.
  • Peng KA; Department of Head and Neck Surgery, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA, USA.
  • Lewis R; Department of Audiology and Speech Pathology, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA, USA.
  • Sepahdari AR; Department of Radiological Sciences, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA, USA.
  • Ishiyama G; Department of Neurology, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA, USA.
  • Hosokawa K; Department of Otolaryngology, Hamamatsu University School of Medicine, Hamamatsu, Shizuoka, Japan.
  • Kumakawa K; Department of Otolaryngology, Toranomon Hospital, Minato-ku, Tokyo, Japan.
  • Ishiyama A; Department of Head and Neck Surgery, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA, USA. Electronic address: ishiyama@ucla.edu.
Int J Pediatr Otorhinolaryngol ; 91: 121-123, 2016 Dec.
Article em En | MEDLINE | ID: mdl-27863625
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Implantes Cocleares / Doenças Genéticas Ligadas ao Cromossomo X / Estimulação Elétrica / Fator de Transcrição Brn-3A / Nervo Facial / Perda Auditiva Condutiva / Perda Auditiva Neurossensorial Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Child / Humans / Male Idioma: En Revista: Int J Pediatr Otorhinolaryngol Ano de publicação: 2016 Tipo de documento: Article
Texto completo
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Implantes Cocleares / Doenças Genéticas Ligadas ao Cromossomo X / Estimulação Elétrica / Fator de Transcrição Brn-3A / Nervo Facial / Perda Auditiva Condutiva / Perda Auditiva Neurossensorial Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Child / Humans / Male Idioma: En Revista: Int J Pediatr Otorhinolaryngol Ano de publicação: 2016 Tipo de documento: Article