Nakanishi H - 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: nakanishi h. 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

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

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

10

[Problem and assignment for distinguishing the Usher syndrome type].

Iwasaki S, Yoshimura H, Takeichi N, Satou H, Ishikawa K, Kaga K, Kumakawa K, Nagai K, Furuya N, Ikezono T, Nakanishi H, Naitou Y, Fukushima K, Tono T, Kimitsuki T, Nishio S, Takumi Y, Usami S. Iwasaki S, et al. Among authors: nakanishi h. Nihon Jibiinkoka Gakkai Kaiho. 2012 Oct;115(10):894-901. doi: 10.3950/jibiinkoka.115.894. Nihon Jibiinkoka Gakkai Kaiho. 2012. PMID: 23214047 Japanese.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

2,104 results

Search Page

Filters