Yamashita H - 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: yamashita h. Acta Otolaryngol. 2017;137(sup565):S44-S47. doi: 10.1080/00016489.2017.1290826. Epub 2017 Mar 24. Acta Otolaryngol. 2017. PMID: 28338374

2

Microtubule associated protein (MAP1A) mRNA was up-regulated by hypergravity in the rat inner ear.

Takumi Y, Iijima N, Suzuki N, Oguchi T, Ando N, Hashimoto M, Hara H, Yamashita H, Usami S. Takumi Y, et al. Among authors: yamashita h. Brain Res Mol Brain Res. 2002 Dec;108(1-2):139-42. doi: 10.1016/s0169-328x(02)00517-x. Brain Res Mol Brain Res. 2002. PMID: 12480186

3

The effect of hypergravity on the inner ear: CREB and syntaxin are up-regulated.

Iijima N, Suzuki N, Oguchi T, Hashimoto S, Takumi Y, Sugahara K, Okuda T, Yamashita H, Usami S. Iijima N, et al. Among authors: yamashita h. Neuroreport. 2004 Apr 29;15(6):965-9. doi: 10.1097/00001756-200404290-00007. Neuroreport. 2004. PMID: 15076716

4

Changes in the characteristics of definite Meniere's disease over time in Japan: a long-term survey by the Peripheral Vestibular Disorder Research Committee of Japan, formerly the Meniere's Disease Research Committee of Japan.

Shojaku H, Watanabe Y, Yagi T, Takahashi M, Takeda T, Ikezono T, Ito J, Kubo T, Suzuki M, Takumida M, Takeda N, Furuya N, Yamashita H; Peripheral Vestibular Disorder Research Committee of Japan. Shojaku H, et al. Among authors: yamashita h. Acta Otolaryngol. 2009 Feb;129(2):155-60. doi: 10.1080/00016480802112587. Acta Otolaryngol. 2009. PMID: 18607900

5

Effect of water-soluble coenzyme Q10 on noise-induced hearing loss in guinea pigs.

Hirose Y, Sugahara K, Mikuriya T, Hashimoto M, Shimogori H, Yamashita H. Hirose Y, et al. Among authors: yamashita h. Acta Otolaryngol. 2008 Oct;128(10):1071-6. doi: 10.1080/00016480801891694. Acta Otolaryngol. 2008. PMID: 18607964

6

Clinical characteristics of delayed endolymphatic hydrops in Japan: A nationwide survey by the Peripheral Vestibular Disorder Research Committee of Japan.

Shojaku H, Watanabe Y, Takeda N, Ikezono T, Takahashi M, Kakigi A, Ito J, Doi K, Suzuki M, Takumida M, Takahashi K, Yamashita H, Koizuka I, Usami S, Aoki M, Naganuma H. Shojaku H, et al. Among authors: yamashita h. Acta Otolaryngol. 2010 Oct;130(10):1135-40. doi: 10.3109/00016481003745543. Acta Otolaryngol. 2010. PMID: 20441535

7

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.

8

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.

9

Effectiveness of the leukotriene receptor antagonist pranlukast hydrate for the treatment of sleep disorder in patients with perennial allergic rhinitis.

Hara H, Sugahara K, Hashimoto M, Mikuriya T, Tahara S, Yamashita H. Hara H, et al. Among authors: yamashita h. Acta Otolaryngol. 2014 Mar;134(3):307-13. doi: 10.3109/00016489.2013.861926. Epub 2014 Jan 27. Acta Otolaryngol. 2014. PMID: 24460152

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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