Kurata K - Search Results

1

Clinical and genetic findings of a Japanese patient with RP1-related autosomal recessive retinitis pigmentosa.

Kurata K, Hosono K, Hotta Y. Kurata K, et al. Doc Ophthalmol. 2018 Aug;137(1):47-56. doi: 10.1007/s10633-018-9649-7. Epub 2018 Jul 19. Doc Ophthalmol. 2018. PMID: 30027431

2

Novel GUCY2D Gene Mutations in Japanese Male Twins with Leber Congenital Amaurosis.

Hosono K, Harada Y, Kurata K, Hikoya A, Sato M, Minoshima S, Hotta Y. Hosono K, et al. Among authors: kurata k. J Ophthalmol. 2015;2015:693468. doi: 10.1155/2015/693468. Epub 2015 May 13. J Ophthalmol. 2015. PMID: 26097748 Free PMC article.

3

Long-Term Clinical Course in a Patient with Complete Congenital Stationary Night Blindness.

Kurata K, Hosono K, Hotta Y. Kurata K, et al. Case Rep Ophthalmol. 2017 Apr 10;8(1):237-244. doi: 10.1159/000462961. eCollection 2017 Jan-Apr. Case Rep Ophthalmol. 2017. PMID: 28512427 Free PMC article.

4

Visual Outcomes in Japanese Patients with Retinitis Pigmentosa and Usher Syndrome Caused by USH2A Mutations.

Nagase Y, Kurata K, Hosono K, Suto K, Hikoya A, Nakanishi H, Mizuta K, Mineta H, Minoshima S, Hotta Y. Nagase Y, et al. Among authors: kurata k. Semin Ophthalmol. 2018;33(4):560-565. doi: 10.1080/08820538.2017.1340487. Epub 2017 Jul 5. Semin Ophthalmol. 2018. PMID: 28678594

5

Long-term clinical course of 2 Japanese patients with PRPF31-related retinitis pigmentosa.

Kurata K, Hosono K, Hotta Y. Kurata K, et al. Jpn J Ophthalmol. 2018 Mar;62(2):186-193. doi: 10.1007/s10384-017-0560-7. Epub 2018 Jan 5. Jpn J Ophthalmol. 2018. PMID: 29305715

6

Clinical characteristics of a Japanese patient with Bardet-Biedl syndrome caused by BBS10 mutations.

Kurata K, Hosono K, Hikoya A, Kato A, Saitsu H, Minoshima S, Ogata T, Hotta Y. Kurata K, et al. Jpn J Ophthalmol. 2018 Jul;62(4):458-466. doi: 10.1007/s10384-018-0591-8. Epub 2018 Apr 17. Jpn J Ophthalmol. 2018. PMID: 29666954

7

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: kurata k. Mol Vis. 2018 Apr 9;24:286-296. eCollection 2018. Mol Vis. 2018. PMID: 29681726 Free PMC article.

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

9

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. Kurata K, et al. Int J Mol Sci. 2019 Mar 26;20(6):1518. doi: 10.3390/ijms20061518. Int J Mol Sci. 2019. PMID: 30917587 Free PMC article.

10

A Japanese family with cone-rod dystrophy of delayed onset caused by a compound heterozygous combination of novel CDHR1 frameshift and known missense variants.

Haque MN, Kurata K, Hosono K, Ohtsubo M, Ohishi K, Sato M, Minoshima S, Hotta Y. Haque MN, et al. Among authors: kurata k. Hum Genome Var. 2019 Apr 12;6:18. doi: 10.1038/s41439-019-0048-8. eCollection 2019. Hum Genome Var. 2019. PMID: 30992995 Free PMC article.

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