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Detailed hearing and vestibular profiles in the patients with COCH mutations.
Tsukada K, Ichinose A, Miyagawa M, Mori K, Hattori M, Nishio SY, Naito Y, Kitajiri S, Usami S. Tsukada K, et al. Among authors: hattori m. Ann Otol Rhinol Laryngol. 2015 May;124 Suppl 1:100S-10S. doi: 10.1177/0003489415573074. Epub 2015 Mar 16. Ann Otol Rhinol Laryngol. 2015. PMID: 25780252
Germinal mosaicism in a family with BO syndrome.
Miyagawa M, Nishio SY, Hattori M, Takumi Y, Usami S. Miyagawa M, et al. Among authors: hattori m. Ann Otol Rhinol Laryngol. 2015 May;124 Suppl 1:118S-22S. doi: 10.1177/0003489415575062. Epub 2015 Mar 16. Ann Otol Rhinol Laryngol. 2015. PMID: 25780253
Hearing loss caused by a P2RX2 mutation identified in a MELAS family with a coexisting mitochondrial 3243AG mutation.
Moteki H, Azaiez H, Booth KT, Hattori M, Sato A, Sato Y, Motobayashi M, Sloan CM, Kolbe DL, Shearer AE, Smith RJ, Usami S. Moteki H, et al. Among authors: hattori m. Ann Otol Rhinol Laryngol. 2015 May;124 Suppl 1(1 0):177S-83S. doi: 10.1177/0003489415575045. Epub 2015 Mar 18. Ann Otol Rhinol Laryngol. 2015. PMID: 25788561 Free PMC article.
2,633 results