Nakano T - Search Results

1

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. Hosono K, et al. Among authors: nakano t. Sci Rep. 2018 May 29;8(1):8279. doi: 10.1038/s41598-018-26524-z. Sci Rep. 2018. PMID: 29844330 Free PMC article.

2

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

3

Occult macular dystrophy with bilateral chronic subfoveal serous retinal detachment associated with a novel RP1L1 mutation (p.S1199P).

Takahashi H, Hayashi T, Tsuneoka H, Nakano T, Yamada H, Katagiri S, Fujino Y, Noda Y, Yoshimoto M, Kawashima H. Takahashi H, et al. Among authors: nakano t. Doc Ophthalmol. 2014 Aug;129(1):49-56. doi: 10.1007/s10633-014-9443-0. Epub 2014 May 17. Doc Ophthalmol. 2014. PMID: 24838559

4

ABCC6 Gene Analysis in 20 Japanese Patients with Angioid Streaks Revealing Four Frequent and Two Novel Variants and Pseudodominant Inheritance.

Katagiri S, Negishi Y, Mizobuchi K, Urashima M, Nakano T, Hayashi T. Katagiri S, et al. Among authors: nakano t. J Ophthalmol. 2017;2017:1079687. doi: 10.1155/2017/1079687. Epub 2017 Aug 20. J Ophthalmol. 2017. PMID: 28912966 Free PMC article.

5

Autosomal dominant retinitis pigmentosa with macular involvement associated with a disease haplotype that included a novel PRPH2 variant (p.Cys250Gly).

Katagiri S, Hayashi T, Mizobuchi K, Yoshitake K, Iwata T, Nakano T. Katagiri S, et al. Among authors: nakano t. Ophthalmic Genet. 2018 Jun;39(3):357-365. doi: 10.1080/13816810.2018.1459737. Epub 2018 Apr 9. Ophthalmic Genet. 2018. PMID: 29630435

6

Early onset flecked retinal dystrophy associated with new compound heterozygous RPE65 variants.

Katagiri S, Hosono K, Hayashi T, Kurata K, Mizobuchi K, Matsuura T, Yoshitake K, Iwata T, Nakano T, Hotta Y. Katagiri S, et al. Among authors: nakano t. Mol Vis. 2018 Apr 9;24:286-296. eCollection 2018. Mol Vis. 2018. PMID: 29681726 Free PMC article.

7

Reconstruction of Photoreceptor Outer Layers after Steroid Therapy in Solar Retinopathy.

Nakamura M, Komatsu K, Katagiri S, Hayashi T, Nakano T. Nakamura M, et al. Among authors: nakano t. Case Rep Ophthalmol Med. 2018 Jun 11;2018:7850467. doi: 10.1155/2018/7850467. eCollection 2018. Case Rep Ophthalmol Med. 2018. PMID: 29992070 Free PMC article.

8

PARACENTRAL ACUTE MIDDLE MACULOPATHY AFTER ENDOVASCULAR COIL EMBOLIZATION.

Nakamura M, Katagiri S, Hayashi T, Yoshioka M, Nakano T. Nakamura M, et al. Among authors: nakano t. Retin Cases Brief Rep. 2021 May 1;15(3):281-285. doi: 10.1097/ICB.0000000000000784. Retin Cases Brief Rep. 2021. PMID: 30015772

9

Genotype determination of the OPN1LW/OPN1MW genes: novel disease-causing mechanisms in Japanese patients with blue cone monochromacy.

Katagiri S, Iwasa M, Hayashi T, Hosono K, Yamashita T, Kuniyoshi K, Ueno S, Kondo M, Ueyama H, Ogita H, Shichida Y, Inagaki H, Kurahashi H, Kondo H, Ohji M, Hotta Y, Nakano T. Katagiri S, et al. Among authors: nakano t. Sci Rep. 2018 Jul 31;8(1):11507. doi: 10.1038/s41598-018-29891-9. Sci Rep. 2018. PMID: 30065301 Free PMC article.

10

Compound heterozygous splice site variants in the SCLT1 gene highlight an additional candidate locus for Senior-Løken syndrome.

Katagiri S, Hayashi T, Yoshitake K, Murai N, Matsui Z, Kubo H, Satoh H, Matsufuji S, Takamura T, Yokoo T, Omori Y, Furukawa T, Iwata T, Nakano T. Katagiri S, et al. Among authors: nakano t. Sci Rep. 2018 Nov 13;8(1):16733. doi: 10.1038/s41598-018-35152-6. Sci Rep. 2018. PMID: 30425282 Free PMC article.

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