Matsushita I - Search Results

1

Novel mutations in the COL2A1 gene in Japanese patients with Stickler syndrome.

Kondo H, Matsushita I, Nagata T, Hayashi T, Kakinoki M, Uchio E, Kondo M, Ohji M, Kusaka S. Kondo H, et al. Among authors: matsushita i. Hum Genome Var. 2016 Jul 7;3:16018. doi: 10.1038/hgv.2016.18. eCollection 2016. Hum Genome Var. 2016. PMID: 27408751 Free PMC article.

2

Novel compound heterozygous mutations in the MFRP gene in a Japanese patient with posterior microphthalmos.

Matsushita I, Kondo H, Tawara A. Matsushita I, et al. Jpn J Ophthalmol. 2012 Jul;56(4):396-400. doi: 10.1007/s10384-012-0145-4. Epub 2012 May 9. Jpn J Ophthalmol. 2012. PMID: 22565643

3

Mutations in ATOH7 gene in patients with nonsyndromic congenital retinal nonattachment and familial exudative vitreoretinopathy.

Kondo H, Matsushita I, Tahira T, Uchio E, Kusaka S. Kondo H, et al. Among authors: matsushita i. Ophthalmic Genet. 2016 Dec;37(4):462-464. doi: 10.3109/13816810.2015.1120316. Epub 2016 Mar 2. Ophthalmic Genet. 2016. PMID: 26933893 No abstract available.

4

Foveal Hypoplasia in Patients with Stickler Syndrome.

Matsushita I, Nagata T, Hayashi T, Kimoto K, Kubota T, Ohji M, Kusaka S, Kondo H. Matsushita I, et al. Ophthalmology. 2017 Jun;124(6):896-902. doi: 10.1016/j.ophtha.2017.01.046. Epub 2017 Mar 7. Ophthalmology. 2017. PMID: 28283280

5

Electroretinograms of eyes with Stickler syndrome.

Kondo H, Fujimoto K, Imagawa M, Oku K, Matsushita I, Hayashi T, Nagata T. Kondo H, et al. Among authors: matsushita i. Doc Ophthalmol. 2020 Jun;140(3):233-243. doi: 10.1007/s10633-019-09739-x. Epub 2019 Nov 28. Doc Ophthalmol. 2020. PMID: 31781920

6

ULTRA-WIDE FIELD FUNDUS AUTOFLUORESCENCE IMAGING OF EYES WITH STICKLER SYNDROME.

Fujimoto K, Nagata T, Matsushita I, Oku K, Imagawa M, Kuniyoshi K, Hayashi T, Kimoto K, Ohji M, Kusaka S, Kondo H. Fujimoto K, et al. Among authors: matsushita i. Retina. 2021 Mar 1;41(3):638-645. doi: 10.1097/IAE.0000000000002879. Retina. 2021. PMID: 32639332 Free PMC article.

7

Autosomal dominant foveal hypoplasia without visible macular abnormalities and PAX6 mutations.

Matsushita I, Morita H, Kondo H. Matsushita I, et al. Jpn J Ophthalmol. 2020 Nov;64(6):635-641. doi: 10.1007/s10384-020-00766-9. Epub 2020 Aug 28. Jpn J Ophthalmol. 2020. PMID: 32857266 Review.

8

Homozygous single nucleotide duplication of SLC38A8 in autosomal recessive foveal hypoplasia: The first Japanese case report.

Hayashi T, Kondo H, Matsushita I, Mizobuchi K, Baba A, Iida K, Kubo H, Nakano T. Hayashi T, et al. Among authors: matsushita i. Doc Ophthalmol. 2021 Dec;143(3):323-330. doi: 10.1007/s10633-021-09842-y. Epub 2021 May 26. Doc Ophthalmol. 2021. PMID: 34037952

9

Retinal Features of Family Members With Familial Exudative Vitreoretinopathy Caused By Mutations in KIF11 Gene.

Kondo H, Matsushita I, Nagata T, Fujihara E, Hosono K, Uchio E, Hotta Y, Kusaka S. Kondo H, et al. Among authors: matsushita i. Transl Vis Sci Technol. 2021 Jun 1;10(7):18. doi: 10.1167/tvst.10.7.18. Transl Vis Sci Technol. 2021. PMID: 34128965 Free PMC article.

10

Study protocol for a multicentre, open-label, single-arm phase I/II trial to evaluate the safety and efficacy of ripasudil 0.4% eye drops for retinopathy of prematurity.

Arima M, Inoue H, Nakao S, Misumi A, Suzuki M, Matsushita I, Araki S, Yamashiro C, Takahashi K, Ochiai M, Yoshida N, Hirose M, Kishimoto J, Todaka K, Hasegawa S, Kimura K, Kusuhara K, Kondo H, Ohga S, Sonoda KH. Arima M, et al. Among authors: matsushita i. BMJ Open. 2021 Jul 27;11(7):e047003. doi: 10.1136/bmjopen-2020-047003. BMJ Open. 2021. PMID: 34315793 Free PMC article.

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