Nishio SY - Search Results

1

Massively parallel DNA sequencing facilitates diagnosis of patients with Usher syndrome type 1.

Yoshimura H, Iwasaki S, Nishio SY, Kumakawa K, Tono T, Kobayashi Y, Sato H, Nagai K, Ishikawa K, Ikezono T, Naito Y, Fukushima K, Oshikawa C, Kimitsuki T, Nakanishi H, Usami S. Yoshimura H, et al. Among authors: nishio sy. PLoS One. 2014 Mar 11;9(3):e90688. doi: 10.1371/journal.pone.0090688. eCollection 2014. PLoS One. 2014. PMID: 24618850 Free PMC article.

2

The responsible genes in Japanese deafness patients and clinical application using Invader assay.

Usami S, Wagatsuma M, Fukuoka H, Suzuki H, Tsukada K, Nishio S, Takumi Y, Abe S. Usami S, et al. Acta Otolaryngol. 2008 Apr;128(4):446-54. doi: 10.1080/00016480701785046. Acta Otolaryngol. 2008. PMID: 18368581 Review.

3

Factors that affect hearing level in individuals with the mitochondrial 1555A.G mutation.

Lu SY, Nishio S, Tsukada K, Oguchi T, Kobayashi K, Abe S, Usami S. Lu SY, et al. Among authors: nishio s. Clin Genet. 2009 May;75(5):480-4. doi: 10.1111/j.1399-0004.2008.01138.x. Clin Genet. 2009. PMID: 19475720

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

Achievement of hearing preservation in the presence of an electrode covering the residual hearing region.

Usami S, Moteki H, Suzuki N, Fukuoka H, Miyagawa M, Nishio SY, Takumi Y, Iwasaki S, Jolly C. Usami S, et al. Among authors: nishio sy. Acta Otolaryngol. 2011 Apr;131(4):405-12. doi: 10.3109/00016489.2010.539266. Epub 2011 Jan 5. Acta Otolaryngol. 2011. PMID: 21208024 Free PMC article.

6

Clinical profile of hearing loss in children with congenital cytomegalovirus (CMV) infection: CMV DNA diagnosis using preserved umbilical cord.

Furutate S, Iwasaki S, Nishio SY, Moteki H, Usami S. Furutate S, et al. Among authors: nishio sy. Acta Otolaryngol. 2011 Sep;131(9):976-82. doi: 10.3109/00016489.2011.583268. Epub 2011 May 26. Acta Otolaryngol. 2011. PMID: 21612560 Free PMC article.

7

Different cortical metabolic activation by visual stimuli possibly due to different time courses of hearing loss in patients with GJB2 and SLC26A4 mutations.

Moteki H, Naito Y, Fujiwara K, Kitoh R, Nishio SY, Oguchi K, Takumi Y, Usami S. Moteki H, et al. Among authors: nishio sy. Acta Otolaryngol. 2011 Nov;131(11):1232-6. doi: 10.3109/00016489.2011.593719. Epub 2011 Jul 5. Acta Otolaryngol. 2011. PMID: 21728752 Free PMC article.

8

Language development in Japanese children who receive cochlear implant and/or hearing aid.

Iwasaki S, Nishio S, Moteki H, Takumi Y, Fukushima K, Kasai N, Usami S. Iwasaki S, et al. Int J Pediatr Otorhinolaryngol. 2012 Mar;76(3):433-8. doi: 10.1016/j.ijporl.2011.12.027. Epub 2012 Jan 26. Int J Pediatr Otorhinolaryngol. 2012. PMID: 22281374 Free article.

9

Mutations in the NOG gene are commonly found in congenital stapes ankylosis with symphalangism, but not in otosclerosis.

Usami S, Abe S, Nishio S, Sakurai Y, Kojima H, Tono T, Suzuki N. Usami S, et al. Clin Genet. 2012 Dec;82(6):514-20. doi: 10.1111/j.1399-0004.2011.01831.x. Epub 2012 Jan 30. Clin Genet. 2012. PMID: 22288654 Free PMC article.

10

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. Among authors: nishio sy. PLoS One. 2012;7(2):e31276. doi: 10.1371/journal.pone.0031276. Epub 2012 Feb 24. PLoS One. 2012. PMID: 22384008 Free PMC article.

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