Hirami Y - Search Results

1

Retinal pigment epithelium melanin imaging using polarization-sensitive optical coherence tomography for patients with retinitis pigmentosa.

Sakai D, Takagi S, Totani K, Yamamoto M, Matsuzaki M, Yamanari M, Sugiyama S, Yokota S, Maeda A, Hirami Y, Mandai M, Takahashi M, Nakamura M, Kurimoto Y. Sakai D, et al. Among authors: hirami y. Sci Rep. 2022 May 3;12(1):7115. doi: 10.1038/s41598-022-11192-x. Sci Rep. 2022. PMID: 35504937 Free PMC article.

2

Otx2 homeobox gene induces photoreceptor-specific phenotypes in cells derived from adult iris and ciliary tissue.

Akagi T, Mandai M, Ooto S, Hirami Y, Osakada F, Kageyama R, Yoshimura N, Takahashi M. Akagi T, et al. Among authors: hirami y. Invest Ophthalmol Vis Sci. 2004 Dec;45(12):4570-5. doi: 10.1167/iovs.04-0697. Invest Ophthalmol Vis Sci. 2004. PMID: 15557469

3

Alterations of retinal pigment epithelium in central serous chorioretinopathy.

Hirami Y, Tsujikawa A, Sasahara M, Gotoh N, Tamura H, Otani A, Mandai M, Yoshimura N. Hirami Y, et al. Clin Exp Ophthalmol. 2007 Apr;35(3):225-30. doi: 10.1111/j.1442-9071.2006.01447.x. Clin Exp Ophthalmol. 2007. PMID: 17430508

4

Microrips of the retinal pigment epithelium in polypoidal choroidal vasculopathy.

Musashi K, Tsujikawa A, Hirami Y, Otani A, Yodoi Y, Tamura H, Yoshimura N. Musashi K, et al. Among authors: hirami y. Am J Ophthalmol. 2007 May;143(5):883-885. doi: 10.1016/j.ajo.2006.12.024. Am J Ophthalmol. 2007. PMID: 17452180

5

Hemorrhagic complications after photodynamic therapy for polypoidal choroidal vasculopathy.

Hirami Y, Tsujikawa A, Otani A, Yodoi Y, Aikawa H, Mandai M, Yoshimura N. Hirami Y, et al. Retina. 2007 Mar;27(3):335-41. doi: 10.1097/01.iae.0000233647.78726.46. Retina. 2007. PMID: 17460589

6

[Peripherin/RDS gene mutation in a patient with choroidal neovascularization].

Kawagoe N, Takahashi M, Mandai M, Akimoto M, Suzuki T, Murakami T, Hirami Y, Ikeda H, Yoshimura N. Kawagoe N, et al. Among authors: hirami y. Nippon Ganka Gakkai Zasshi. 2007 Apr;111(4):336-42. Nippon Ganka Gakkai Zasshi. 2007. PMID: 17461040 Japanese.

7

Identifying pathogenic genetic background of simplex or multiplex retinitis pigmentosa patients: a large scale mutation screening study.

Jin ZB, Mandai M, Yokota T, Higuchi K, Ohmori K, Ohtsuki F, Takakura S, Itabashi T, Wada Y, Akimoto M, Ooto S, Suzuki T, Hirami Y, Ikeda H, Kawagoe N, Oishi A, Ichiyama S, Takahashi M, Yoshimura N, Kosugi S. Jin ZB, et al. Among authors: hirami y. J Med Genet. 2008 Jul;45(7):465-72. doi: 10.1136/jmg.2007.056416. Epub 2008 Feb 29. J Med Genet. 2008. PMID: 18310263

8

Allelic copy number variation in FSCN2 detected using allele-specific genotyping and multiplex real-time PCRs.

Jin ZB, Mandai M, Homma K, Ishigami C, Hirami Y, Nao-I N, Takahashi M. Jin ZB, et al. Among authors: hirami y. Invest Ophthalmol Vis Sci. 2008 Sep;49(9):3799-805. doi: 10.1167/iovs.07-1656. Epub 2008 Apr 30. Invest Ophthalmol Vis Sci. 2008. PMID: 18450588

9

Detection of localized retinal malfunction in retinal degeneration model using a multielectrode array system.

Homma K, Osakada F, Hirami Y, Jin ZB, Mandai M, Takahashi M. Homma K, et al. Among authors: hirami y. J Neurosci Res. 2009 Jul;87(9):2175-82. doi: 10.1002/jnr.22024. J Neurosci Res. 2009. PMID: 19224574

10

Generation of retinal cells from mouse and human induced pluripotent stem cells.

Hirami Y, Osakada F, Takahashi K, Okita K, Yamanaka S, Ikeda H, Yoshimura N, Takahashi M. Hirami Y, et al. Neurosci Lett. 2009 Jul 24;458(3):126-31. doi: 10.1016/j.neulet.2009.04.035. Epub 2009 Apr 18. Neurosci Lett. 2009. PMID: 19379795

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