Suzuki M - Search Results

1

The clinical features and prognosis of mumps-associated hearing loss: a retrospective, multi-institutional investigation in Japan.

Morita S, Fujiwara K, Fukuda A, Fukuda S, Nishio SY, Kitoh R, Hato N, Ikezono T, Ishikawa K, Kaga K, Matsubara A, Matsunaga T, Murata T, Naito Y, Nishizaki K, Ogawa K, Sano H, Sato H, Sone M, Suzuki M, Takahashi H, Tono T, Yamashita H, Yamasoba T, Usami SI. Morita S, et al. Among authors: suzuki m. Acta Otolaryngol. 2017;137(sup565):S44-S47. doi: 10.1080/00016489.2017.1290826. Epub 2017 Mar 24. Acta Otolaryngol. 2017. PMID: 28338374

2

Autoantibodies against inner ear proteins in patients with delayed endolymphatic hydrops and unilateral juvenile deafness.

Suzuki M, Hanamitsu M, Kitanishi T, Kohzaki H, Kitano H. Suzuki M, et al. Acta Otolaryngol. 2006 Feb;126(2):117-21. doi: 10.1080/00016480500266008. Acta Otolaryngol. 2006. PMID: 16428186

3

Involvement of Epstein-Barr virus (EBV)-encoded latent membrane protein (LMP)-1 in the potentiation of C epsilon mRNA expression in human tonsil-derived cells.

Ohta S, Hanashiro K, Sunagawa M, Tono T, Suzuki M, Kosugi T. Ohta S, et al. Among authors: suzuki m. Eur Arch Otorhinolaryngol. 2007 Mar;264(3):245-50. doi: 10.1007/s00405-006-0191-y. Epub 2006 Nov 7. Eur Arch Otorhinolaryngol. 2007. PMID: 17089136

4

A large cohort study of GJB2 mutations in Japanese hearing loss patients.

Tsukada K, Nishio S, Usami S; Deafness Gene Study Consortium. Tsukada K, et al. Clin Genet. 2010 Nov;78(5):464-70. doi: 10.1111/j.1399-0004.2010.01407.x. Clin Genet. 2010. PMID: 20497192

5

Efficacy of diffusion-weighted magnetic resonance imaging in the diagnosis of middle ear cholesteatoma.

Ganaha A, Outa S, Kyuuna A, Matayoshi S, Yonaha A, Oyadomari M, Miyara T, Tono T, Suzuki M. Ganaha A, et al. Among authors: suzuki m. Auris Nasus Larynx. 2011 Jun;38(3):329-34. doi: 10.1016/j.anl.2010.11.004. Epub 2011 Jan 7. Auris Nasus Larynx. 2011. PMID: 21216121

6

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.

7

Pathogenic substitution of IVS15 + 5G > A in SLC26A4 in patients of Okinawa Islands with enlarged vestibular aqueduct syndrome or Pendred syndrome.

Ganaha A, Kaname T, Yanagi K, Naritomi K, Tono T, Usami S, Suzuki M. Ganaha A, et al. Among authors: suzuki m. BMC Med Genet. 2013 May 24;14:56. doi: 10.1186/1471-2350-14-56. BMC Med Genet. 2013. PMID: 23705809 Free PMC article.

8

[Three cases of external auditory exostoses in a habitual sauna user].

Goto T, Tono T, Nakanishi H, Matsuda K, Ganaha A, Suzuki M. Goto T, et al. Among authors: suzuki m. Nihon Jibiinkoka Gakkai Kaiho. 2013 Nov;116(11):1214-9. doi: 10.3950/jibiinkoka.116.1214. Nihon Jibiinkoka Gakkai Kaiho. 2013. PMID: 24397119 Japanese.

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

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.

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