Gekka T - Search Results

1

Multimodal imaging of a case of peripheral cone dystrophy.

Ito N, Kameya S, Gocho K, Hayashi T, Kikuchi S, Katagiri S, Gekka T, Yamaki K, Takahashi H, Tsuneoka H. Ito N, et al. Among authors: gekka t. Doc Ophthalmol. 2015 Jun;130(3):241-51. doi: 10.1007/s10633-015-9490-1. Epub 2015 Feb 24. Doc Ophthalmol. 2015. PMID: 25708979 Free PMC article.

2

A novel homozygous GRK1 mutation (P391H) in 2 siblings with Oguchi disease with markedly reduced cone responses.

Hayashi T, Gekka T, Takeuchi T, Goto-Omoto S, Kitahara K. Hayashi T, et al. Among authors: gekka t. Ophthalmology. 2007 Jan;114(1):134-41. doi: 10.1016/j.ophtha.2006.05.069. Epub 2006 Oct 27. Ophthalmology. 2007. PMID: 17070587

3

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. Among authors: gekka t. Eur J Ophthalmol. 2011 Sep-Oct;21(5):657-60. doi: 10.5301/EJO.2011.6337. Eur J Ophthalmol. 2011. PMID: 21319138

4

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: gekka 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

5

Multifocal electroretinographic evaluation of macular function in acute posterior multifocal placoid pigment epitheliopathy.

Aoyagi R, Hayashi T, Gekka T, Kozaki K, Tsuneoka H. Aoyagi R, et al. Among authors: gekka t. Doc Ophthalmol. 2013 Jun;126(3):253-8. doi: 10.1007/s10633-013-9378-x. Epub 2013 Mar 8. Doc Ophthalmol. 2013. PMID: 23471725

6

OAT mutations and clinical features in two Japanese brothers with gyrate atrophy of the choroid and retina.

Katagiri S, Gekka T, Hayashi T, Ida H, Ohashi T, Eto Y, Tsuneoka H. Katagiri S, et al. Among authors: gekka t. Doc Ophthalmol. 2014 Apr;128(2):137-48. doi: 10.1007/s10633-014-9426-1. Epub 2014 Jan 16. Doc Ophthalmol. 2014. PMID: 24429551

7

Autosomal recessive cone-rod dystrophy associated with compound heterozygous mutations in the EYS gene.

Katagiri S, Akahori M, Hayashi T, Yoshitake K, Gekka T, Ikeo K, Tsuneoka H, Iwata T. Katagiri S, et al. Among authors: gekka t. Doc Ophthalmol. 2014 Jun;128(3):211-7. doi: 10.1007/s10633-014-9435-0. Epub 2014 Mar 21. Doc Ophthalmol. 2014. PMID: 24652164

8

Novel C8orf37 Mutations in Patients with Early-onset Retinal Dystrophy, Macular Atrophy, Cataracts, and High Myopia.

Katagiri S, Hayashi T, Yoshitake K, Akahori M, Ikeo K, Gekka T, Tsuneoka H, Iwata T. Katagiri S, et al. Among authors: gekka t. Ophthalmic Genet. 2016;37(1):68-75. doi: 10.3109/13816810.2014.949380. Epub 2014 Aug 12. Ophthalmic Genet. 2016. PMID: 25113443

9

Somatic instability of expanded CAG repeats of ATXN7 in Japanese patients with spinocerebellar ataxia type 7.

Katagiri S, Hayashi T, Takeuchi T, Yamada H, Gekka T, Kawabe K, Kurita A, Tsuneoka H. Katagiri S, et al. Among authors: gekka t. Doc Ophthalmol. 2015 Jun;130(3):189-95. doi: 10.1007/s10633-015-9488-8. Epub 2015 Feb 3. Doc Ophthalmol. 2015. PMID: 25643591

10

Early postoperative evaluation of retinal function by electroretinography after vitreous surgery for idiopathic epimacular membrane.

Watanabe A, Gekka T, Arai K, Kohzaki K, Tsuneoka H. Watanabe A, et al. Among authors: gekka t. Doc Ophthalmol. 2017 Jun;134(3):167-173. doi: 10.1007/s10633-017-9583-0. Epub 2017 Mar 18. Doc Ophthalmol. 2017. PMID: 28315987

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