Kameya S - Search Results

1

A new PDE6A missense variant p.Arg544Gln in rod-cone dystrophy.

Hayashi T, Mizobuchi K, Kameya S, Yoshitake K, Iwata T, Nakano T. Hayashi T, et al. Among authors: kameya s. Doc Ophthalmol. 2021 Aug;143(1):107-114. doi: 10.1007/s10633-021-09826-y. Epub 2021 Feb 21. Doc Ophthalmol. 2021. PMID: 33611760

2

A new mutation in the RP1L1 gene in a patient with occult macular dystrophy associated with a depolarizing pattern of focal macular electroretinograms.

Kabuto T, Takahashi H, Goto-Fukuura Y, Igarashi T, Akahori M, Kameya S, Iwata T, Mizota A, Yamaki K, Miyake Y, Takahashi H. Kabuto T, et al. Among authors: kameya s. Mol Vis. 2012;18:1031-9. Epub 2012 Apr 24. Mol Vis. 2012. PMID: 22605915 Free PMC article.

3

High-Resolution Imaging of Patients with Bietti Crystalline Dystrophy with CYP4V2 Mutation.

Gocho K, Kameya S, Akeo K, Kikuchi S, Usui A, Yamaki K, Hayashi T, Tsuneoka H, Mizota A, Takahashi H. Gocho K, et al. Among authors: kameya s. J Ophthalmol. 2014;2014:283603. doi: 10.1155/2014/283603. Epub 2014 Sep 3. J Ophthalmol. 2014. PMID: 25276414 Free PMC article.

4

Cone dystrophy in patient with homozygous RP1L1 mutation.

Kikuchi S, Kameya S, Gocho K, El Shamieh S, Akeo K, Sugawara Y, Yamaki K, Zeitz C, Audo I, Takahashi H. Kikuchi S, et al. Among authors: kameya s. Biomed Res Int. 2015;2015:545243. doi: 10.1155/2015/545243. Epub 2015 Jan 29. Biomed Res Int. 2015. PMID: 25692141 Free PMC article. Clinical Trial.

5

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: kameya s. 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.

6

Detailed analysis of family with autosomal recessive bestrophinopathy associated with new BEST1 mutation.

Kubota D, Gocho K, Akeo K, Kikuchi S, Sugahara M, Matsumoto CS, Shinoda K, Mizota A, Yamaki K, Takahashi H, Kameya S. Kubota D, et al. Among authors: kameya s. Doc Ophthalmol. 2016 Jun;132(3):233-43. doi: 10.1007/s10633-016-9540-3. Epub 2016 Apr 12. Doc Ophthalmol. 2016. PMID: 27071392 Free PMC article.

7

Novel RP1L1 Variants and Genotype-Photoreceptor Microstructural Phenotype Associations in Cohort of Japanese Patients With Occult Macular Dystrophy.

Fujinami K, Kameya S, Kikuchi S, Ueno S, Kondo M, Hayashi T, Shinoda K, Machida S, Kuniyoshi K, Kawamura Y, Akahori M, Yoshitake K, Katagiri S, Nakanishi A, Sakuramoto H, Ozawa Y, Tsubota K, Yamaki K, Mizota A, Terasaki H, Miyake Y, Iwata T, Tsunoda K. Fujinami K, et al. Among authors: kameya s. Invest Ophthalmol Vis Sci. 2016 Sep 1;57(11):4837-46. doi: 10.1167/iovs.16-19670. Invest Ophthalmol Vis Sci. 2016. PMID: 27623337

8

Closure of a full-thickness macular hole without vitrectomy in choroideraemia.

Ishikawa K, Gekka T, Hayashi T, Kikuchi S, Kameya S, Tsuneoka H. Ishikawa K, et al. Among authors: kameya s. Clin Exp Optom. 2017 May;100(3):294-295. doi: 10.1111/cxo.12467. Epub 2016 Sep 14. Clin Exp Optom. 2017. PMID: 27628750 Free article. No abstract available.

9

High-Resolution Adaptive Optics Retinal Image Analysis at Early Stage Central Areolar Choroidal Dystrophy With PRPH2 Mutation.

Gocho K, Akeo K, Itoh N, Kameya S, Hayashi T, Katagiri S, Gekka T, Ohkuma Y, Tsuneoka H, Takahashi H. Gocho K, et al. Among authors: kameya s. Ophthalmic Surg Lasers Imaging Retina. 2016 Dec 1;47(12):1115-1126. doi: 10.3928/23258160-20161130-05. Ophthalmic Surg Lasers Imaging Retina. 2016. PMID: 27977834

10

Heterozygous deletion of the OPA1 gene in patients with dominant optic atrophy.

Hayashi T, Sasano H, Katagiri S, Tsunoda K, Kameya S, Nakazawa M, Iwata T, Tsuneoka H. Hayashi T, et al. Among authors: kameya s. Jpn J Ophthalmol. 2017 Sep;61(5):395-401. doi: 10.1007/s10384-017-0522-0. Epub 2017 Jul 1. Jpn J Ophthalmol. 2017. PMID: 28668999

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