Kameya S - Search Results

1

High-resolution en face images of microcystic macular edema in patients with autosomal dominant optic atrophy.

Gocho K, Kikuchi S, Kabuto T, Kameya S, Shinoda K, Mizota A, Yamaki K, Takahashi H. Gocho K, et al. Among authors: kameya s. Biomed Res Int. 2013;2013:676803. doi: 10.1155/2013/676803. Epub 2013 Nov 28. Biomed Res Int. 2013. PMID: 24369534 Free PMC article.

2

Identification of the hexon region of an adenovirus involved in a new outbreak of keratoconjunctivitis.

Imai Y, Kameya S, Ohkoshi M, Yamaki K, Sakuragi S. Imai Y, et al. Among authors: kameya s. J Clin Microbiol. 2001 Aug;39(8):2975-7. doi: 10.1128/JCM.39.8.2975-2977.2001. J Clin Microbiol. 2001. PMID: 11474026 Free PMC article.

3

Neuromyelitis optica preceded by hyperCKemia episode.

Suzuki N, Takahashi T, Aoki M, Misu T, Konohana S, Okumura T, Takahashi H, Kameya S, Yamaki K, Kumagai T, Fujihara K, Itoyama Y. Suzuki N, et al. Among authors: kameya s. Neurology. 2010 May 11;74(19):1543-5. doi: 10.1212/WNL.0b013e3181dd445b. Neurology. 2010. PMID: 20458072

4

Reactive gliosis of astrocytes and Müller glial cells in retina of POMGnT1-deficient mice.

Takahashi H, Kanesaki H, Igarashi T, Kameya S, Yamaki K, Mizota A, Kudo A, Miyagoe-Suzuki Y, Takeda S, Takahashi H. Takahashi H, et al. Among authors: kameya s. Mol Cell Neurosci. 2011 Jun;47(2):119-30. doi: 10.1016/j.mcn.2011.03.006. Epub 2011 Apr 8. Mol Cell Neurosci. 2011. PMID: 21447391

5

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.

6

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.

7

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.

8

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.

9

Detailed Morphological Changes of Foveoschisis in Patient with X-Linked Retinoschisis Detected by SD-OCT and Adaptive Optics Fundus Camera.

Akeo K, Kameya S, Gocho K, Kubota D, Yamaki K, Takahashi H. Akeo K, et al. Among authors: kameya s. Case Rep Ophthalmol Med. 2015;2015:432782. doi: 10.1155/2015/432782. Epub 2015 Aug 18. Case Rep Ophthalmol Med. 2015. PMID: 26356828 Free PMC article.

10

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.

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