Okamoto M - Search Results

1

SOD1 gene polymorphisms in sudden sensorineural hearing loss.

Kitoh R, Nishio SY, Ogawa K, Okamoto M, Kitamura K, Gyo K, Sato H, Nakashima T, Fukuda S, Fukushima K, Hara A, Yamasoba T, Usami S. Kitoh R, et al. Among authors: okamoto m. Acta Otolaryngol. 2016;136(5):465-9. doi: 10.3109/00016489.2015.1116047. Epub 2016 Feb 16. Acta Otolaryngol. 2016. PMID: 26882452

2

Effect of single-drug treatment on idiopathic sudden sensorineural hearing loss.

Kanzaki J, Inoue Y, Ogawa K, Fukuda S, Fukushima K, Gyo K, Yanagihara N, Hoshino T, Ishitoya J, Toriyama M, Kitamura K, Murai K, Nakashima T, Niwa H, Nomura Y, Kobayashi H, Oda M, Okamoto M, Shitara T, Sakagami M, Tono T, Usami S. Kanzaki J, et al. Among authors: okamoto m. Auris Nasus Larynx. 2003 May;30(2):123-7. doi: 10.1016/s0385-8146(03)00009-9. Auris Nasus Larynx. 2003. PMID: 12753981

3

Simultaneous screening of multiple mutations by invader assay improves molecular diagnosis of hereditary hearing loss: a multicenter study.

Usami S, Nishio SY, Nagano M, Abe S, Yamaguchi T; Deafness Gene Study Consortium. Usami S, et al. PLoS One. 2012;7(2):e31276. doi: 10.1371/journal.pone.0031276. Epub 2012 Feb 24. PLoS One. 2012. PMID: 22384008 Free PMC article.

4

Quality of life reported by patients with idiopathic sudden sensorineural hearing loss.

Sano H, Okamoto M, Ohhashi K, Iwasaki S, Ogawa K. Sano H, et al. Among authors: okamoto m. Otol Neurotol. 2013 Jan;34(1):36-40. doi: 10.1097/MAO.0b013e318278540e. Otol Neurotol. 2013. PMID: 23232830

5

Hearing handicap in adults with unilateral deafness and bilateral hearing loss.

Iwasaki S, Sano H, Nishio S, Takumi Y, Okamoto M, Usami S, Ogawa K. Iwasaki S, et al. Among authors: okamoto m. Otol Neurotol. 2013 Jun;34(4):644-9. doi: 10.1097/MAO.0b013e318287f1fe. Otol Neurotol. 2013. PMID: 23657210

6

Self-reported symptoms in patients with idiopathic sudden sensorineural hearing loss.

Sano H, Okamoto M, Ohhashi K, Ino T, Iwasaki S, Ogawa K. Sano H, et al. Among authors: okamoto m. Otol Neurotol. 2013 Oct;34(8):1405-10. doi: 10.1097/MAO.0b013e3182a03705. Otol Neurotol. 2013. PMID: 24026023

7

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

Miyagawa M, Nishio SY, Usami S; Deafness Gene Study Consortium. Miyagawa M, et al. J Hum Genet. 2014 May;59(5):262-8. doi: 10.1038/jhg.2014.12. Epub 2014 Mar 6. J Hum Genet. 2014. PMID: 24599119 Free PMC article.

8

A nationwide study on enlargement of the vestibular aqueduct in Japan.

Noguchi Y, Fukuda S, Fukushima K, Gyo K, Hara A, Nakashima T, Ogawa K, Okamoto M, Sato H, Usami SI, Yamasoba T, Yokoyama T, Kitamura K. Noguchi Y, et al. Among authors: okamoto m. Auris Nasus Larynx. 2017 Feb;44(1):33-39. doi: 10.1016/j.anl.2016.04.012. Epub 2016 May 6. Auris Nasus Larynx. 2017. PMID: 27160786

9

Frequency of mitochondrial mutations in non-syndromic hearing loss as well as possibly responsible variants found by whole mitochondrial genome screening.

Yano T, Nishio SY, Usami S; Deafness Gene Study Consortium. Yano T, et al. J Hum Genet. 2014 Feb;59(2):100-6. doi: 10.1038/jhg.2013.128. Epub 2014 Jan 9. J Hum Genet. 2014. PMID: 24401907 Free PMC article. Clinical Trial.

10

Investigation of Stress Levels before the Onset of Idiopathic Sudden Sensorineural Hearing Loss.

Watanabe H, Sano H, Maki A, Ino T, Nakagawa T, Okamoto M, Yamashita T. Watanabe H, et al. Among authors: okamoto m. J Int Adv Otol. 2019 Apr;15(1):51-55. doi: 10.5152/iao.2019.6197. J Int Adv Otol. 2019. PMID: 31058595 Free PMC article.

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