産業医科大学
過去5年間（2018年〜2022年）の研究業績
| 著者 | タイトル | 雑誌 | 年 | doi | 分野 |
|---|---|---|---|---|---|
| Y. Sano; Y. Matsukane; A. Watanabe; K. Sonoda; H. Kondo | Lack of FOXE3 coding mutation in a case of congenital aphakia | Ophthalmic Genetics | 2018 | 10.1080/13816810.2017.1350722 | 白内障・屈折異常 |
| H. Kondo | Foveal hypoplasia and optical coherence tomographic imaging | Taiwan Journal of Ophthalmology | 2018 | 10.4103/tjo.tjo_101_18 | 網膜 |
| H. Kondo; E. Uchio; S. Kusaka; K. Higasa | Risk allele of the FZD4 gene for familial exudative vitreoretinopathy | Ophthalmic Genetics | 2018 | 10.1080/13816810.2017.1401090 | 網膜 |
| I. Matsushita; H. Morita; H. Kondo | Autosomal dominant foveal hypoplasia without visible macular abnormalities andPAX6mutations | Japanese Journal of Ophthalmology | 2020 | 10.1007/s10384-020-00766-9 | 網膜 |
| H. Kondo; K. Fujimoto; M. Imagawa; K. Oku; I. Matsushita; T. Hayashi; T. Nagata | Electroretinograms of eyes with Stickler syndrome | Documenta Ophthalmologica | 2020 | 10.1007/s10633-019-09739-x | 網膜 |
| S. Katagiri; T. Hayashi; M. Nakamura; K. Mizobuchi; T. Gekka; S. Komori; S. Ueno; H. Terasaki; H. Sakuramoto; K. Kuniyoshi; S. Kusaka; R. Nagashima; M. Kondo; K. Fujinami; K. Tsunoda; T. Matsuura; H. Kondo; K. Yoshitake; T. Iwata; T. Nakano | RDH5-Related Fundus Albipunctatus in a Large Japanese Cohort | Investigative Ophthalmology & Visual Science | 2020 | 10.1167/iovs.61.3.53 | 網膜 |
| T. Nagata; Y. Harada; M. Arai; T. Hirose; H. Kondo | Polyethylene Glycol-Based Synthetic Hydrogel Sealant for Filtration Bleb Leaks: An In Vivo and Histologic Study | Translational Vision Science & Technology | 2020 | 10.1167/tvst.9.6.24 | 緑内障 |
| Y. Oshima; Y. Ishibashi; N. Umeda; T. Nagata; S. Yoshida; E. Uchio; H. Kondo; K. H. Sonoda; T. Ishibashi | Correlation between improvement in visual acuity and QOL after Ranibizumab treatment for age-related macular degeneration patients: QUATRO study | Bmc Ophthalmology | 2021 | 10.1186/s12886-021-01816-7 | 網膜 |
| K. Oku; K. Tokutsu; S. Matsuda; H. Kondo | Epidemiologic study of rhegmatogenous retinal detachment in Japan from the Diagnosis Procedure Combination database over a 2-year period (2014-2015) | Japanese Journal of Ophthalmology | 2021 | 10.1007/s10384-021-00867-z | 網膜 |
| T. Asano; K. Oku; H. Kondo | Familial exudative vitreoretinopathy with TGFBR2 mutation without signs of Loeys-Dietz syndrome | Ophthalmic Genetics | 2021 | 10.1080/13816810.2021.1938137 | 網膜 |
| T. Hayashi; H. Kondo; I. Matsushita; K. Mizobuchi; A. Baba; K. Iida; H. Kubo; T. Nakano | Homozygous single nucleotide duplication of SLC38A8 in autosomal recessive foveal hypoplasia: The first Japanese case report | Documenta Ophthalmologica | 2021 | 10.1007/s10633-021-09842-y | 網膜 |
| H. Kondo; I. Matsushita; T. Nagata; E. Fujihara; K. Hosono; E. Uchio; Y. Hotta; S. Kusaka | Retinal Features of Family MembersWith Familial Exudative Vitreoretinopathy Caused By Mutations in KIF11 Gene | Translational Vision Science & Technology | 2021 | 10.1167/tvst.10.7.18 | 網膜 |
| K. Fujimoto; T. Nagata; I. Matsushita; K. Oku; M. Imagawa; K. Kuniyoshi; T. Hayashi; K. Kimoto; M. Ohji; S. Kusaka; H. Kondo | ULTRA-WIDE FIELD FUNDUS AUTOFLUORESCENCE IMAGING OF EYES WITH STICKLER SYNDROME | Retina-the Journal of Retinal and Vitreous Diseases | 2021 | 10.1097/iae.0000000000002879 | 網膜 |
| F. Mano; K. Sugioka; K. Kuniyoshi; H. Kondo; S. Kusaka | Identification of Interphotoreceptor retinoid-binding protein in the Schisis cavity fluid of a patient with congenital X-linked Retinoschisis | Bmc Ophthalmology | 2022 | 10.1186/s12886-021-02234-5 | 網膜 |
| M. Asano; K. Yokoyama; K. Oku; I. Matsushita; K. Kimoto; T. Kubota; H. Kondo | Severe foveal hypoplasia and macular degeneration in Stickler syndrome caused by missense mutation in COL2A1 gene | Ophthalmic Genetics | 2022 | 10.1080/13816810.2022.2068044 | 網膜 |
