Usami SI - Search Results

1

Development and validation of an iPad-based Japanese language monosyllable speech perception test (iCI2004 monosyllable).

Nishio SY, Tono T, Iwaki T, Moteki H, Suzuki K, Tsushima Y, Kashio A, Akamatsu Y, Sato H, Yaegashi K, Takeda H, Kumagai F, Nakashima T, Matsuda Y, Hato N, Dairoku T, Shiroma M, Kawai R, Usami SI. Nishio SY, et al. Among authors: usami si. Acta Otolaryngol. 2021 Mar;141(3):267-272. doi: 10.1080/00016489.2020.1853229. Epub 2020 Dec 15. Acta Otolaryngol. 2021. PMID: 33320029 Free article.

2

Isepamicin sulfate-induced sensorineural hearing loss in patients with the 1555 A-->G mitochondrial mutation.

Usami S, Abe S, Tono T, Komune S, Kimberling WJ, Shinkawa H. Usami S, et al. ORL J Otorhinolaryngol Relat Spec. 1998 May-Jun;60(3):164-9. doi: 10.1159/000027590. ORL J Otorhinolaryngol Relat Spec. 1998. PMID: 9579362

3

Cochlear implantation in a patient with profound hearing loss with the A1555G mitochondrial mutation.

Tono T, Ushisako Y, Kiyomizu K, Usami S, Abe S, Shinkawa H, Komune S. Tono T, et al. Am J Otol. 1998 Nov;19(6):754-7. Am J Otol. 1998. PMID: 9831149

4

Changes of perilymphatic glutamate and cochlear blood flow following ischemia.

Haruta A, Matsuda K, Tono T, Komune S, Matsubara A, Usami S. Haruta A, et al. Acta Otolaryngol Suppl. 1998;539:44-7. doi: 10.1080/00016489850182116. Acta Otolaryngol Suppl. 1998. PMID: 10095860

5

Quantitative immunogold cytochemistry reveals sources of glutamate release in inner ear ischemia.

Matsubara A, Kawabata Y, Takumi Y, Usami S, Shinkawa H, Haruta A, Matsuda K, Tono T. Matsubara A, et al. Acta Otolaryngol Suppl. 1998;539:48-51. Acta Otolaryngol Suppl. 1998. PMID: 10095861

6

Prevalence of mitochondrial gene mutations among hearing impaired patients.

Usami S, Abe S, Akita J, Namba A, Shinkawa H, Ishii M, Iwasaki S, Hoshino T, Ito J, Doi K, Kubo T, Nakagawa T, Komiyama S, Tono T, Komune S. Usami S, et al. J Med Genet. 2000 Jan;37(1):38-40. doi: 10.1136/jmg.37.1.38. J Med Genet. 2000. PMID: 10633132 Free PMC article.

7

Different clinical characteristics of aminoglycoside-induced profound deafness with and without the 1555 A-->G mitochondrial mutation.

Tono T, Kiyomizu K, Matsuda K, Komune S, Usami S, Abe S, Shinkawa H. Tono T, et al. ORL J Otorhinolaryngol Relat Spec. 2001 Jan-Feb;63(1):25-30. doi: 10.1159/000055702. ORL J Otorhinolaryngol Relat Spec. 2001. PMID: 11174059

8

[A case of enlarged vestibular aqueduct syndrome with PDS gene mutations].

Kiyomizu K, Tsuboi Y, Tono T, Komune S, Abe S, Shinkawa H, Tsukamoto K, Usami S. Kiyomizu K, et al. Nihon Jibiinkoka Gakkai Kaiho. 2002 Feb;105(2):174-7. doi: 10.3950/jibiinkoka.105.174. Nihon Jibiinkoka Gakkai Kaiho. 2002. PMID: 11905055 Japanese.

9

Deafness due to A1555G mitochondrial mutation without use of aminoglycoside.

Matsunaga T, Kumanomido H, Shiroma M, Ohtsuka A, Asamura K, Usami S. Matsunaga T, et al. Laryngoscope. 2004 Jun;114(6):1085-91. doi: 10.1097/00005537-200406000-00024. Laryngoscope. 2004. PMID: 15179218

10

Audiological features and mitochondrial DNA sequence in a large family carrying mitochondrial A1555G mutation without use of aminoglycoside.

Matsunaga T, Kumanomido H, Shiroma M, Goto Y, Usami S. Matsunaga T, et al. Ann Otol Rhinol Laryngol. 2005 Feb;114(2):153-60. doi: 10.1177/000348940511400213. Ann Otol Rhinol Laryngol. 2005. PMID: 15757197

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