Kondo H
Genetic testing in pediatric retina
A quick quide to pediatric retina
edited by Wu WC, Lam WC
Springer Nature Singapore, 2021
Nudleman E, Nagata T, Mukai S
Retinal lesions presenting in childhood
Albert and Jakobiec’s Principles and Practices of Ophthalmology ver.6
edited by Albert D, Miller J, Azar D, Young LH
Springer, 2021
Kondo H, Matsushita I, Nagata T, Fujihara E, Hosono K, Uchio E, Hotta Y, Kusaka S: Retinal features of family members with familial exudative vitreoretinopathy caused by mutations in KIF11 gene.
Transl Vis Sci Technol 10: 18, 2021
Oku K, Tokutsu K, Matsuda S, Kondo H: Epidemiologic study of rhegmatogenous retinal detachment in Japan from the Diagnosis Procedure Combination database over a 2-year period (2014-2015).
Jpn J Ophthalmol 65: 797-802, 2021
Asano T, Oku K, Kondo H: Familial exudative vitreoretinopathy with TGFBR2 mutation without signs of Loeys-Dietz syndrome.
Ophthalmic Genet 42: 637-640, 2021
Asano M, Tsukamoto S, Sonoda KH, Kondo H: Revesz syndrome with bilateral retinal detachments successfully treated by pars plana vitrectomy.
Am J Ophthalmol Case Rep 23: 101137, 2021
Fujimoto K, Nagata T, Matsushita I, Oku K, Imagawa M, Kuniyoshi K, Hayashi T, Kimoto K, Ohji M, Kusaka S, Kondo H: Ultra-wide field fundus autofluorescence imaging of eyes with Stickler syndrome. Retina 41: 638-645, 2021
Hayashi T, Kondo H, Matsushita I, Mizobuchi K, Baba A, Iida K, Kubo H, Nakano T: Homozygous single nucleotide duplication of SLC38A8 in autosomal recessive foveal hypoplasia: The first Japanese case report.
Doc Ophthalmol 143: 323-330, 2021
Mano F, Matsushita I, Kondo H, Utamura S, Kondo C, Kusaka S: Vitrectomy and external drainage of subretinal fluid containing high concentration of vascular endothelial growth factor for advanced coats disease.
Sci Rep 11: 19333, 2021
Mizobuchi K, Hayashi T, Oishi N, Kubota D, Kameya S, Higasa K, Futami T, Kondo H, Hosono K, Kurata K, Hotta Y, Yoshitake K, Iwata T, Matsuura T, Nakano T: Genotype-Phenotype Correlations in RP1-Associated Retinal Dystrophies: A Multi-Center Cohort Study in JAPAN.
J Clin Med 10: 2265, 2021
Oishi A, Fujinami K, Mawatari G, Naoi N, Ikeda Y, Ueno S, Kuniyoshi K, Hayashi T, Kondo H, Mizota A, Shinoda K, Kusuhara S, Nakamura M, Iwata T, Tsujikawa A, Tsunoda K: Genetic and Phenotypic Landscape of PRPH2-Associated Retinal Dystrophy in Japan.
Genes (Basel) 12: 1817, 2021
Oshima Y, Ishibashi Y, Umeda N, Nagata T, Yoshida S, Uchio E, Kondo H, Sonoda KH, Ishibashi T: Correlation between improvement in visual acuity and QOL after Ranibizumab treatment for age-related macular degeneration patients: QUATRO study.
BMC Ophthalmol. 21:58, 2021
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: 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.
BMJ Open. 11: e047003. doi:10.1136/bmjopen-2020-047003,2021
岡本美里,松下五佳,永田竜朗,近藤寛之: Scoring System of Ultra-Wide Field Fluorescein Angiographic Imaging in Parents with Infantile Familial Exudative Vitreoretinopathy
第60回日本網膜硝子体学会総会,12月,東京
Oki R, Yamada K , Nakano S, Kimoto K, Yamamoto K, Kondo H, Kubota T:
A Japanese Family With Autosomal Dominant Oculocutaneous Albinism Type 4.
Investigative ophthalmology & visual science, 58:1008-1016,2017
Panagiotou ES, Sanjurjo Soriano C, Poulter JA, Lord EC, Dzulova D,
Kondo H, Hiyoshi A, Chung BH, Chu Yoyo YW, Lai CHY, Tafoya ME,
Karjosukarso D, Collin RWJ, Topping J, Downey LM, Ali M, Inglehearn CF, Toomes C:
Defects in the Cell Signaling Mediator β-Catenin Cause the Retinal Vascular Condition FEVR.
American journal of human genetics, 100:960-968,2017
Kondo H,Uchio E,Kusaka S & Higasa K:
Risk allele of the FZD4 gene for familial exudative vitreoretinopathy.
OphthalmicGenetics,39:1-2, 2017