Nakanishi H - Search Results

1

Yamatodani T, Misawa K, Endo S, Nakanishi H, Hosokawa S, Mineta H. Yamatodani T, et al. Among authors: nakanishi h. J Int Adv Otol. 2019 Apr;15(1):173-176. doi: 10.5152/iao.2019.5433. J Int Adv Otol. 2019. PMID: 30924778 Free PMC article.

2

Cochlear implant in children with asymptomatic congenital cytomegalovirus infection.

Iwasaki S, Nakanishi H, Misawa K, Tanigawa T, Mizuta K. Iwasaki S, et al. Among authors: nakanishi h. Audiol Neurootol. 2009;14(3):146-52. doi: 10.1159/000171476. Epub 2008 Nov 13. Audiol Neurootol. 2009. PMID: 19005248

3

Diaphragmatic rupture due to violent cough during tracheostomy.

Nakanishi H, Iwasaki S, Ohkawa Y, Nakazawa H, Mineta H. Nakanishi H, et al. Auris Nasus Larynx. 2010 Feb;37(1):121-4. doi: 10.1016/j.anl.2009.01.015. Epub 2009 May 6. Auris Nasus Larynx. 2010. PMID: 19423248

4

Identification of 11 novel mutations in USH2A among Japanese patients with Usher syndrome type 2.

Nakanishi H, Ohtsubo M, Iwasaki S, Hotta Y, Mizuta K, Mineta H, Minoshima S. Nakanishi H, et al. Clin Genet. 2009 Oct;76(4):383-91. doi: 10.1111/j.1399-0004.2009.01257.x. Epub 2009 Sep 8. Clin Genet. 2009. PMID: 19737284

5

Ultrastructural localization of cochlin in the rat cochlear duct.

Hosokawa S, Mizuta K, Nakanishi H, Hashimoto Y, Arai M, Mineta H, Shindo S, Ikezono T. Hosokawa S, et al. Among authors: nakanishi h. Audiol Neurootol. 2010;15(4):247-53. doi: 10.1159/000256664. Epub 2009 Nov 10. Audiol Neurootol. 2010. PMID: 19907161

6

Hair roots as an mRNA source for mutation analysis of Usher syndrome-causing genes.

Nakanishi H, Ohtsubo M, Iwasaki S, Hotta Y, Mizuta K, Mineta H, Minoshima S. Nakanishi H, et al. J Hum Genet. 2010 Oct;55(10):701-3. doi: 10.1038/jhg.2010.83. Epub 2010 Jul 1. J Hum Genet. 2010. PMID: 20596040

7

Hereditary isolated ossicular anomalies in two generations of patients.

Nakanishi H, Mizuta K, Hamada N, Iwasaki S, Mineta H. Nakanishi H, et al. Auris Nasus Larynx. 2011 Feb;38(1):114-8. doi: 10.1016/j.anl.2010.06.003. Epub 2010 Aug 19. Auris Nasus Larynx. 2011. PMID: 20727699

8

Mutation analysis of the MYO7A and CDH23 genes in Japanese patients with Usher syndrome type 1.

Nakanishi H, Ohtsubo M, Iwasaki S, Hotta Y, Takizawa Y, Hosono K, Mizuta K, Mineta H, Minoshima S. Nakanishi H, et al. J Hum Genet. 2010 Dec;55(12):796-800. doi: 10.1038/jhg.2010.115. Epub 2010 Sep 16. J Hum Genet. 2010. PMID: 20844544

9

Specific localization of five phosphatidylcholine species in the cochlea by mass microscopy.

Takizawa Y, Mizuta K, Hayasaka T, Nakanishi H, Okamura J, Mineta H, Setou M. Takizawa Y, et al. Among authors: nakanishi h. Audiol Neurootol. 2011;16(5):315-22. doi: 10.1159/000322308. Epub 2010 Dec 15. Audiol Neurootol. 2011. PMID: 21160178

10

Novel USH2A mutations in Japanese Usher syndrome type 2 patients: marked differences in the mutation spectrum between the Japanese and other populations.

Nakanishi H, Ohtsubo M, Iwasaki S, Hotta Y, Usami S, Mizuta K, Mineta H, Minoshima S. Nakanishi H, et al. J Hum Genet. 2011 Jul;56(7):484-90. doi: 10.1038/jhg.2011.45. Epub 2011 May 19. J Hum Genet. 2011. PMID: 21593743

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