Hayashi T - Search Results

1

Retinal angiomatous proliferation associated with risk alleles of ARMS2/HTRA1 gene polymorphisms in Japanese patients.

Ohkuma Y, Hayashi T, Sakai T, Watanabe A, Yamada H, Akahori M, Itabashi T, Iwata T, Noda T, Tsuneoka H. Ohkuma Y, et al. Among authors: hayashi t. Clin Ophthalmol. 2014;8:143-8. doi: 10.2147/OPTH.S56483. Epub 2013 Dec 27. Clin Ophthalmol. 2014. PMID: 24403817 Free PMC article.

2

Enhanced S-cone syndrome in a Japanese family with a nonsense NR2E3 mutation (Q350X).

Nakamura Y, Hayashi T, Kozaki K, Kubo A, Omoto S, Watanabe A, Toda K, Takeuchi T, Gekka T, Kitahara K. Nakamura Y, et al. Among authors: hayashi t. Acta Ophthalmol Scand. 2004 Oct;82(5):616-22. doi: 10.1111/j.1600-0420.2004.00328.x. Acta Ophthalmol Scand. 2004. PMID: 15453866 Free article.

3

Clinical heterogeneity between two Japanese siblings with congenital achromatopsia.

Hayashi T, Kozaki K, Kitahara K, Kubo A, Nishio Y, Omoto S, Nakamura Y, Watanabe A, Toda K, Ueoka Y. Hayashi T, et al. Vis Neurosci. 2004 May-Jun;21(3):413-20. doi: 10.1017/s0952523804213396. Vis Neurosci. 2004. PMID: 15518223

4

A novel haplotype with the R345W mutation in the EFEMP1 gene associated with autosomal dominant drusen in a Japanese family.

Takeuchi T, Hayashi T, Bedell M, Zhang K, Yamada H, Tsuneoka H. Takeuchi T, et al. Among authors: hayashi t. Invest Ophthalmol Vis Sci. 2010 Mar;51(3):1643-50. doi: 10.1167/iovs.09-4497. Epub 2009 Oct 22. Invest Ophthalmol Vis Sci. 2010. PMID: 19850834 Free PMC article.

5

A novel mutation (Cys83Tyr) in the second zinc finger of NR2E3 in enhanced S-cone syndrome.

Rocha-Sousa A, Hayashi T, Gomes NL, Penas S, Brandão E, Rocha P, Urashima M, Yamada H, Tsuneoka H, Falcão-Reis F. Rocha-Sousa A, et al. Among authors: hayashi t. Graefes Arch Clin Exp Ophthalmol. 2011 Feb;249(2):201-8. doi: 10.1007/s00417-010-1482-y. Epub 2010 Aug 20. Graefes Arch Clin Exp Ophthalmol. 2011. PMID: 20725840

6

Improvement in S-cone-mediated visual fields and rod function after correction of vitamin A deficiency.

Hayashi T, Gekka T, Nakano T, Tsuneoka H. Hayashi T, et al. Eur J Ophthalmol. 2011 Sep-Oct;21(5):657-60. doi: 10.5301/EJO.2011.6337. Eur J Ophthalmol. 2011. PMID: 21319138

7

Macular Dysfunction in Oguchi Disease with the Frequent Mutation 1147delA in the SAG Gene.

Hayashi T, Tsuzuranuki S, Kozaki K, Urashima M, Tsuneoka H. Hayashi T, et al. Ophthalmic Res. 2011 Oct;46(4):175-80. doi: 10.1159/000325024. Epub 2011 Mar 29. Ophthalmic Res. 2011. PMID: 21447990

8

Subfoveal choroidal thickness in multiple evanescent white dot syndrome.

Aoyagi R, Hayashi T, Masai A, Mitooka K, Gekka T, Kozaki K, Tsuneoka H. Aoyagi R, et al. Among authors: hayashi t. Clin Exp Optom. 2012 Mar;95(2):212-7. doi: 10.1111/j.1444-0938.2011.00668.x. Epub 2011 Oct 24. Clin Exp Optom. 2012. PMID: 22023216 Free article.

9

Color vision in an elderly patient with protanopic genotype and successfully treated unilateral age-related macular degeneration.

Kitakawa T, Hayashi T, Tsuzuranuki S, Kubo A, Tsuneoka H. Kitakawa T, et al. Among authors: hayashi t. Int Ophthalmol. 2011 Dec;31(6):471-5. doi: 10.1007/s10792-011-9479-z. Epub 2011 Nov 11. Int Ophthalmol. 2011. PMID: 22076412

10

Improvement of central visual function following steroid pulse therapy in acute zonal occult outer retinopathy.

Kitakawa T, Hayashi T, Takashina H, Mitooka K, Gekka T, Tsuneoka H. Kitakawa T, et al. Among authors: hayashi t. Doc Ophthalmol. 2012 Jun;124(3):249-54. doi: 10.1007/s10633-012-9318-1. Epub 2012 Mar 9. Doc Ophthalmol. 2012. PMID: 22402912

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