Kondo H - Search Results

1

Familial Exudative Vitreoretinopathy With and Without Pathogenic Variants of Norrin/β-Catenin Signaling Genes.

Kondo H, Tsukahara-Kawamura T, Matsushita I, Nagata T, Hayashi T, Nishina S, Higasa K, Uchio E, Kondo M, Sakamoto T, Kusaka S. Kondo H, et al. Among authors: kondo m. Ophthalmol Sci. 2024 Mar 15;4(5):100514. doi: 10.1016/j.xops.2024.100514. eCollection 2024 Sep-Oct. Ophthalmol Sci. 2024. PMID: 38881609 Free PMC article.

2

Novel mutations in Norrie disease gene in Japanese patients with Norrie disease and familial exudative vitreoretinopathy.

Kondo H, Qin M, Kusaka S, Tahira T, Hasebe H, Hayashi H, Uchio E, Hayashi K. Kondo H, et al. Invest Ophthalmol Vis Sci. 2007 Mar;48(3):1276-82. doi: 10.1167/iovs.06-1042. Invest Ophthalmol Vis Sci. 2007. PMID: 17325173

3

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. 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.

4

Mutations in the TSPAN12 gene in Japanese patients with familial exudative vitreoretinopathy.

Kondo H, Kusaka S, Yoshinaga A, Uchio E, Tawara A, Hayashi K, Tahira T. Kondo H, et al. Am J Ophthalmol. 2011 Jun;151(6):1095-1100.e1. doi: 10.1016/j.ajo.2010.11.026. Epub 2011 Feb 19. Am J Ophthalmol. 2011. PMID: 21334594

5

Genetic variants of FZD4 and LRP5 genes in patients with advanced retinopathy of prematurity.

Kondo H, Kusaka S, Yoshinaga A, Uchio E, Tawara A, Tahira T. Kondo H, et al. Mol Vis. 2013;19:476-85. Epub 2013 Feb 25. Mol Vis. 2013. PMID: 23441120 Free PMC article.

6

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. 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.

7

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. Among authors: kondo h. Ophthalmology. 2017 Jun;124(6):896-902. doi: 10.1016/j.ophtha.2017.01.046. Epub 2017 Mar 7. Ophthalmology. 2017. PMID: 28283280

8

Risk allele of the FZD4 gene for familial exudative vitreoretinopathy.

Kondo H, Uchio E, Kusaka S, Higasa K. Kondo H, et al. Ophthalmic Genet. 2018 Jun;39(3):405-406. doi: 10.1080/13816810.2017.1401090. Epub 2017 Nov 14. Ophthalmic Genet. 2018. PMID: 29135315 No abstract available.

9

Early vitrectomy to reverse macular dragging in a one-month-old boy with familial exudative vitreoretinopathy.

Iwata A, Kusaka S, Ishimaru M, Kondo H, Kuniyoshi K. Iwata A, et al. Among authors: kondo h. Am J Ophthalmol Case Rep. 2019 Jun 11;15:100493. doi: 10.1016/j.ajoc.2019.100493. eCollection 2019 Sep. Am J Ophthalmol Case Rep. 2019. PMID: 31294129 Free PMC article.

10

Electroretinograms of eyes with Stickler syndrome.

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

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