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Items: 1 to 20 of 71

1.

Retinal structure in Leber's congenital amaurosis caused by RPGRIP1 mutations.

Miyamichi D, Nishina S, Hosono K, Yokoi T, Kurata K, Sato M, Hotta Y, Azuma N.

Hum Genome Var. 2019 Jun 27;6:32. doi: 10.1038/s41439-019-0064-8. eCollection 2019.

2.

SEVERE RECURRENT FIBROVASCULAR PROLIFERATION AFTER COMBINED INTRAVITREAL BEVACIZUMAB INJECTION AND LASER PHOTOCOAGULATION FOR AGGRESSIVE POSTERIOR RETINOPATHY OF PREMATURITY.

Tanaka S, Yokoi T, Katagiri S, Yoshida T, Nishina S, Azuma N.

Retin Cases Brief Rep. 2019 Jul 17. doi: 10.1097/ICB.0000000000000887. [Epub ahead of print]

PMID:
31339872
3.

Characteristics of Retinal Breaks and Surgical Outcomes in Rhegmatogenous Retinal Detachment in Familial Exudative Vitreoretinopathy.

Katagiri S, Yokoi T, Yoshida-Uemura T, Nishina S, Azuma N.

Ophthalmol Retina. 2018 Jul;2(7):720-725. doi: 10.1016/j.oret.2017.11.003. Epub 2017 Dec 29.

PMID:
31047381
4.

X-linked Retinitis Pigmentosa in Japan: Clinical and Genetic Findings in Male Patients and Female Carriers.

Kurata K, Hosono K, Hayashi T, Mizobuchi K, Katagiri S, Miyamichi D, Nishina S, Sato M, Azuma N, Nakano T, Hotta Y.

Int J Mol Sci. 2019 Mar 26;20(6). pii: E1518. doi: 10.3390/ijms20061518.

5.

The clock components Period2, Cryptochrome1a, and Cryptochrome2a function in establishing light-dependent behavioral rhythms and/or total activity levels in zebrafish.

Hirayama J, Alifu Y, Hamabe R, Yamaguchi S, Tomita J, Maruyama Y, Asaoka Y, Nakahama KI, Tamaru T, Takamatsu K, Takamatsu N, Hattori A, Nishina S, Azuma N, Kawahara A, Kume K, Nishina H.

Sci Rep. 2019 Jan 17;9(1):196. doi: 10.1038/s41598-018-37879-8.

6.

Optical coherence tomography and video recording of a case of bilateral contractile peripapillary staphyloma.

Yoshida T, Katagiri S, Yokoi T, Nishina S, Azuma N.

Am J Ophthalmol Case Rep. 2018 Dec 5;13:66-69. doi: 10.1016/j.ajoc.2018.12.002. eCollection 2019 Mar.

7.

Incidence of side effects of topical atropine sulfate and cyclopentolate hydrochloride for cycloplegia in Japanese children: a multicenter study.

Wakayama A, Nishina S, Miki A, Utsumi T, Sugasawa J, Hayashi T, Sato M, Kimura A, Fujikado T.

Jpn J Ophthalmol. 2018 Sep;62(5):531-536. doi: 10.1007/s10384-018-0612-7. Epub 2018 Jul 25.

PMID:
30046935
8.

Molecular Diagnosis of 34 Japanese Families with Leber Congenital Amaurosis Using Targeted Next Generation Sequencing.

Hosono K, Nishina S, Yokoi T, Katagiri S, Saitsu H, Kurata K, Miyamichi D, Hikoya A, Mizobuchi K, Nakano T, Minoshima S, Fukami M, Kondo H, Sato M, Hayashi T, Azuma N, Hotta Y.

Sci Rep. 2018 May 29;8(1):8279. doi: 10.1038/s41598-018-26524-z.

9.

Atypical intravitreal growth of retinoblastoma with a multi-branching configuration.

Nishina S, Katagiri S, Nakazawa A, Kiyotani C, Yokoi T, Azuma N.

Am J Ophthalmol Case Rep. 2017 Apr 12;7:4-8. doi: 10.1016/j.ajoc.2017.04.003. eCollection 2017 Sep.

10.

[Prolonged optic disc swelling in Kawasaki disease - A case report and literature review].

Tsumura Y, Masuda H, Nishina S, Kobayashi T, Ono H, Kato H, Abe J, Ishiguro A.

Nihon Rinsho Meneki Gakkai Kaishi. 2017;40(5):377-381. doi: 10.2177/jsci.40.377. Review. Japanese.

11.

Effects of neuroactive agents on axonal growth and pathfinding of retinal ganglion cells generated from human stem cells.

Yokoi T, Tanaka T, Matsuzaka E, Tamalu F, Watanabe SI, Nishina S, Azuma N.

Sci Rep. 2017 Dec 1;7(1):16757. doi: 10.1038/s41598-017-16727-1.

12.

Surgical treatments for fibrous tissue extending to the posterior retina in eyes with familial exudative vitreoretinopathy.

Takahashi M, Yokoi T, Katagiri S, Yoshida-Uemura T, Nishina S, Azuma N.

Jpn J Ophthalmol. 2018 Jan;62(1):63-67. doi: 10.1007/s10384-017-0547-4. Epub 2017 Nov 3.

PMID:
29101498
13.

ATYPICAL FORM OF RETINOPATHY OF PREMATURITY WITH SEVERE FIBROVASCULAR PROLIFERATION IN THE OPTIC DISK REGION.

Yokoi T, Katagiri S, Hiraoka M, Nakayama Y, Hosono K, Hotta Y, Nishina S, Azuma N.

Retina. 2018 Aug;38(8):1605-1612. doi: 10.1097/IAE.0000000000001779.

PMID:
28800017
14.

Long-term surgical outcome of conventional trabeculotomy for childhood glaucoma.

Ozawa H, Yamane M, Inoue E, Yoshida-Uemura T, Katagiri S, Yokoi T, Nishina S, Azuma N.

Jpn J Ophthalmol. 2017 May;61(3):237-244. doi: 10.1007/s10384-017-0506-0. Epub 2017 Mar 16.

PMID:
28303357
15.

Retinal Structure and Function in Eyes with Optic Nerve Hypoplasia.

Katagiri S, Nishina S, Yokoi T, Mikami M, Nakayama Y, Tanaka M, Azuma N.

Sci Rep. 2017 Feb 16;7:42480. doi: 10.1038/srep42480.

16.

Clinical features of a toddler with bilateral bullous retinoschisis with a novel RS1 mutation.

Katagiri S, Tanaka S, Yokoi T, Hayashi T, Matsuzaka E, Ueda K, Yoshida-Uemura T, Arakawa A, Nishina S, Kadonosono K, Azuma N.

Am J Ophthalmol Case Rep. 2016 Dec 14;5:76-80. doi: 10.1016/j.ajoc.2016.12.009. eCollection 2017 Apr.

17.

The mevalonate pathway regulates primitive streak formation via protein farnesylation.

Okamoto-Uchida Y, Yu R, Miyamura N, Arima N, Ishigami-Yuasa M, Kagechika H, Yoshida S, Hosoya T, Nawa M, Kasama T, Asaoka Y, Alois RW, Elling U, Penninger JM, Nishina S, Azuma N, Nishina H.

Sci Rep. 2016 Nov 24;6:37697. doi: 10.1038/srep37697.

18.

Different foveal schisis patterns in each retinal layer in eyes with hereditary juvenile retinoschisis evaluated by en-face optical coherence tomography.

Yoshida-Uemura T, Katagiri S, Yokoi T, Nishina S, Azuma N.

Graefes Arch Clin Exp Ophthalmol. 2017 Apr;255(4):719-723. doi: 10.1007/s00417-016-3552-2. Epub 2016 Nov 16.

PMID:
27853955
19.

Outer retinal deformity detected by optical coherence tomography in eyes with foveal hypoplasia.

Katagiri S, Yokoi T, Mikami M, Nishina S, Azuma N.

Graefes Arch Clin Exp Ophthalmol. 2016 Nov;254(11):2197-2201. Epub 2016 May 23.

PMID:
27216762
20.

Successful scleral buckling of late-onset visual decrease in eye with retinal folds.

Nakayama Y, Katagiri S, Yokoi T, Ui M, Nishina S, Azuma N.

Doc Ophthalmol. 2016 Oct;133(2):145-149. Epub 2016 Aug 23.

PMID:
27553815

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