H. Kondo

发表

A homozygosity-based search for mutations in patients with autosomal recessive retinitis pigmentosa, using microsatellite markers.

T. Tahira, K. Hayashi, M. Kondo, 2004, Investigative ophthalmology & visual science.

Transcriptional regulation of activating transcription factor 4 under oxidative stress in retinal pigment epithelial ARPE-19/HPV-16 cells.

Y. Sasaguri, H. Izumi, K. Kohno, 2011, Investigative ophthalmology & visual science.

Epidemiologic study of rhegmatogenous retinal detachment in Japan from the Diagnosis Procedure Combination database over a 2-year period (2014–2015)

S. Matsuda, H. Kondo, Kazuma Oku, 2021, Japanese Journal of Ophthalmology.

Identification of causative pathogens in eyes with bacterial conjunctivitis by bacterial cell count and microbiota analysis.

Kazumasa Fukuda, H. Taniguchi, H. Kondo, 2013, Ophthalmology.

Genetic Spectrum of EYS-associated Retinal Disease in a Large Japanese Cohort: Identification of Disease-associated Variants with Relatively High Allele Frequency

Y. Hayashizaki, M. Itoh, H. Kawaji, 2020, Scientific Reports.

Color Functionality Used in Visual Display for Occupational and Environmental Safety and Managing Color Vision Deficiency.

H. Kondo, Nobuhisa Ochiai, 2017, Journal of UOEH.

Lens-sparing vitrectomy effective for reattachment of newly developed falciform retinal detachment in a patient with Norrie disease.

Y. Tano, T. Fujikado, S. Kusaka, 2009, Archives of ophthalmology.

Properties of new diffusion filters for treatment of amblyopia with accurate occlusive effects

H. Kondo, A. Tawara, T. Iwasaki, 2016, Graefe's Archive for Clinical and Experimental Ophthalmology.

Clinical and Genetic Characteristics of 18 Patients from 13 Japanese Families with CRX-associated retinal disorder: Identification of Genotype-phenotype Association

Y. Hayashizaki, H. Kawaji, K. Tsubota, 2020, Scientific Reports.

Late Vitreoretinal Complications of Regressed Retinopathy of Prematurity: Retinal Break, Vitreous Hemorrhage and Retinal Detachment.

M. K. Walsh, M. Trese, Samir N. Patel, 2022, Ophthalmology. Retina.

Novel OPA1 mutations identified in Japanese pedigrees with optic atrophy.

T. Tahira, K. Hayashi, Minghui Qin, 2006, Molecular Vision.

Electroretinograms of eyes with Stickler syndrome

Takaaki Hayashi, H. Kondo, Kazuma Oku, 2019, Documenta Ophthalmologica.

Risk allele of the FZD4 gene for familial exudative vitreoretinopathy

K. Higasa, S. Kusaka, H. Kondo, 2018, Ophthalmic genetics.

Revesz syndrome with bilateral retinal detachments successfully treated by pars plana vitrectomy

K. Sonoda, H. Kondo, Mamika Asano, 2021, American journal of ophthalmology case reports.

A Case of Incontinentia Pigmenti in Japan and Its Genetic Examination

H. Kondo, E. Uchio, Jane Y. Huang, 2007, Japanese Journal of Ophthalmology.

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

T. Tahira, Aki Yoshinaga, S. Kusaka, 2011, American journal of ophthalmology.

Familial exudative vitreoretinopathy with TGFBR2 mutation without signs of Loeys-Dietz syndrome

H. Kondo, Kazuma Oku, Toshiaki Asano, 2021, Ophthalmic genetics.

Vitrectomy and external drainage of subretinal fluid containing high concentration of vascular endothelial growth factor for advanced coats disease

S. Kusaka, H. Kondo, Fukutaro Mano, 2021, Scientific Reports.

Complex genetics of familial exudative vitreoretinopathy and related pediatric retinal detachments

H. Kondo, 2015, Taiwan journal of ophthalmology.

Correlation between improvement in visual acuity and QOL after Ranibizumab treatment for age-related macular degeneration patients: QUATRO study

S. Yoshida, K. Sonoda, Y. Oshima, 2020, BMC Ophthalmology.

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

M. Ohji, Takaaki Hayashi, S. Kusaka, 2020, Retina.

Genetic characterization of 1210 Japanese pedigrees with inherited retinal diseases by whole‐exome sequencing

K. Tsunoda, Makoto Nakamura, K. Yoshitake, 2022, Human mutation.

Survey of microphthalmia in Japan

Y. Nishida, D. Kurosaka, S. Nishina, 2012, Japanese Journal of Ophthalmology.

Reconstruction of a nonfunctional trabeculectomy bleb using an amniotic membrane-wrapped silicone sponge to treat refractory glaucoma

H. Kondo, N. Miyamoto, A. Tawara, 2013, Graefe's Archive for Clinical and Experimental Ophthalmology.

[Effect of Intravitreal Bevacizumab Injection on Iris and Iridocorneal Angle Neovascularization in Neovascular Glaucoma].

H. Kondo, S. Ishibashi, 2015, Journal of UOEH.

A Japanese Family With Autosomal Dominant Oculocutaneous Albinism Type 4.

T. Kubota, H. Kondo, K. Kimoto, 2017, Investigative ophthalmology & visual science.

Defects in the Cell Signaling Mediator β-Catenin Cause the Retinal Vascular Condition FEVR.

C. Inglehearn, B. Chung, C. Toomes, 2017, American journal of human genetics.

Severe foveal hypoplasia and macular degeneration in Stickler syndrome caused by missense mutation in COL2A1 gene

T. Kubota, H. Kondo, Katsuhiko Yokoyama, 2022, Ophthalmic genetics.

Clinical and Genetic Characteristics of 18 Patients from 13 Japanese Families with CRX-associated retinal disorder: Identification of Genotype-phenotype Association

Y. Hayashizaki, H. Kawaji, K. Tsubota, 2020, Scientific Reports.

Microsatellite genotyping of post-PCR fluorescently labeled markers.

H. Hayashi, T. Tahira, K. Hayashi, 2000, BioTechniques.

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

T. Tahira, Aki Yoshinaga, S. Kusaka, 2013, Molecular vision.

Autosomal dominant foveal hypoplasia without visible macular abnormalities and PAX6 mutations

H. Kondo, Itsuka Matsushita, H. Morita, 2020, Japanese Journal of Ophthalmology.

Genetic and Phenotypic Landscape of PRPH2-Associated Retinal Dystrophy in Japan

K. Tsunoda, A. Tsujikawa, Makoto Nakamura, 2021, Genes.

Novel mutations in the RS1 gene in Japanese patients with X-linked congenital retinoschisis

T. Morimoto, K. Tsunoda, K. Yoshitake, 2019, Human Genome Variation.

ZNF408 is mutated in familial exudative vitreoretinopathy and is crucial for the development of zebrafish retinal vasculature

Christian Gilissen, Alexander Hoischen, Tomoko Tahira, 2013, Proceedings of the National Academy of Sciences.

Late recurrence of retinal detachment following successful vitreous surgery for stages 4B and 5 retinopathy of prematurity.

H. Kondo, H. Hayashi, K. Oshima, 2009, American journal of ophthalmology.

Submicroscopic deletions at 13q32.1 cause congenital microcoria.

Yusuke Nakamura, Toshihiro Tanaka, A. Munnich, 2015, American journal of human genetics.

Complexity of the genotype–phenotype correlation in familial exudative vitreoretinopathy with mutations in the LRP5 and/or FZD4 genes

T. Tahira, K. Hayashi, Minghui Qin, 2005, Human mutation.

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

K. Kusuhara, S. Ohga, K. Sonoda, 2021, BMJ Open.

EFFICACY OF INNER WALL RETINECTOMY FOR BULLOUS SCHISIS CAVITY HANGING OVER OR THREATENING THE MACULA IN PATIENTS WITH CONGENITAL X-LINKED RETINOSCHISIS

S. Kusaka, H. Kondo, C. Iwahashi, 2022, Retina.

Identification of Interphotoreceptor retinoid-binding protein in the Schisis cavity fluid of a patient with congenital X-linked Retinoschisis

K. Sugioka, S. Kusaka, H. Kondo, 2022, BMC Ophthalmology.

Genotype-Phenotype Correlations in RP1-Associated Retinal Dystrophies: A Multi-Center Cohort Study in JAPAN

K. Higasa, T. Matsuura, K. Yoshitake, 2021, Journal of clinical medicine.

K. Tsunoda, T. Matsuura, K. Yoshitake, 2020, Investigative ophthalmology & visual science.

Novel mutation in PAX3 gene in Waardenburg syndrome accompanied by unilateral macular degeneration

T. Tahira, K. Hayashi, H. Kondo, 2009, Eye.

Serous supraciliochoroidal effusion after trabeculotomy ab externo

Peiquan Zhao, H. Kondo, H. Hayashi, 2002 .

Genotype determination of the OPN1LW/OPN1MW genes: novel disease-causing mechanisms in Japanese patients with blue cone monochromacy

H. Kurahashi, H. Ogita, M. Kondo, 2018, Scientific Reports.

Diagnosis of autosomal dominant retinitis pigmentosa by linkage-based exclusion screening with multiple locus-specific microsatellite markers.

T. Tahira, K. Hayashi, E. Adachi-Usami, 2003, Investigative ophthalmology & visual science.

Title Genotype determination of the OPN 1 LW / OPN 1 MW genes : novel disease-causing mechanisms in Japanese patients with blue cone monochromacy

H. Kurahashi, H. Ogita, M. Kondo, 2019 .

Genotype determination of the OPN1LW/OPN1MW genes: novel disease-causing mechanisms in Japanese patients with blue cone monochromacy

H. Kurahashi, H. Ogita, M. Kondo, 2018, Scientific Reports.

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

Takaaki Hayashi, T. Nakano, H. Kondo, 2021, Documenta Ophthalmologica.

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

S. Kusaka, H. Kondo, E. Uchio, 2021, Translational vision science & technology.

Familial acorea, microphthalmia and cataract syndrome

T. Tahira, H. Kondo, A. Tawara, 2013, British Journal of Ophthalmology.

Lack of FOXE3 coding mutation in a case of congenital aphakia

K. Sonoda, H. Kondo, Y. Sano, 2018, Ophthalmic genetics.

Iridocorneal apposition after vitrectomy and gas injection.

H. Kondo, K. Oshima, K. Konishi, 2000, Retina.

Foveal hypoplasia and optical coherence tomographic imaging

H. Kondo, 2018, Taiwan journal of ophthalmology.

Quercetin induces the expression of peroxiredoxins 3 and 5 via the Nrf2/NRF1 transcription pathway.

Y. Sasaguri, H. Izumi, K. Kohno, 2011, Investigative ophthalmology & visual science.

Severe Form of Familial Exudative Vitreoretinopathy Caused by Homozygous R417Q Mutation in Frizzled-4 Gene

T. Tahira, K. Hayashi, Minghui Qin, 2007, Ophthalmic genetics.

Frizzled 4 gene (FZD4) mutations in patients with familial exudative vitreoretinopathy with variable expressivity

K Oshima, T. Tahira, K. Hayashi, 2003, The British journal of ophthalmology.

Mutations in TSPAN12 cause autosomal-dominant familial exudative vitreoretinopathy.

D. Mackey, K. Hayashi, A. Markham, 2010, American journal of human genetics.

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

T. Tahira, K. Hayashi, Minghui Qin, 2007, Investigative ophthalmology & visual science.

Moderate reduction of Norrin signaling activity associated with the causative missense mutations identified in patients with familial exudative vitreoretinopathy

T. Tahira, K. Hayashi, Minghui Qin, 2007, Human Genetics.

Delineation of the critical interval for the familial exudative vitreoretinopathy gene by linkage and haplotype analysis

Kenshi Hayashi, Kenji Oshima, Tomoko Tahira, 2001, Human Genetics.

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

S. Kusaka, H. Kondo, K. Kuniyoshi, 2019, American journal of ophthalmology case reports.

Foveal Hypoplasia in Patients with Stickler Syndrome.

M. Ohji, Takaaki Hayashi, T. Kubota, 2017, Ophthalmology.

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

H. Kondo, A. Tawara, Itsuka Matsushita, 2012, Japanese Journal of Ophthalmology.

Molecular Diagnosis of 34 Japanese Families with Leber Congenital Amaurosis Using Targeted Next Generation Sequencing

S. Minoshima, H. Saitsu, Miho Sato, 2018, Scientific Reports.

A classic temporal optic disc pit showing progression in the corresponding optic nerve fiber and visual field defects

H. Kondo, R. Miyamoto, A. Tawara, 2013, Japanese Journal of Ophthalmology.

A case of Fukuyama congenital muscular dystrophy associated with negative electroretinograms

Kayoko Saito, M. Kondo, H. Kondo, 2010, Japanese Journal of Ophthalmology.

Non-Paralleled Increase of Hepatocyte Growth Factor and Vascular Endothelial Growth Factor in the Eyes with Angiogenic and Nonangiogenic Fibroproliferation

H. Kondo, H. Hayashi, K. Oshima, 2002, Ophthalmic Research.

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

M. Kondo, M. Ohji, Takaaki Hayashi, 2016, Human Genome Variation.

Functional Characteristics of Diverse PAX6 Mutations Associated with Isolated Foveal Hypoplasia

K. Tsunoda, Kaoru Fujinami, Takaaki Hayashi, 2023, Genes.

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

T. Tahira, S. Kusaka, H. Kondo, 2016, Ophthalmic genetics.

The effects of a convex rear-view mirror on ocular accommodative responses.

H. Kondo, A. Tawara, T. Iwasaki, 2013, Applied ergonomics.

Complex genetics of familial exudative vitreoretinopathy and related pediatric retinal detachments

H. Kondo, 2015, Taiwan journal of ophthalmology.

Genotype–Phenotype Correlation in Familial Exudative Vitreoretinopathy or Norrie Disease With Mutations in the Norrie Disease Gene

T. Tahira, K. Hayashi, Minghui Qin, 2006 .

The 7th Corneal Conference

C. Sotozono, D. Kurosaka, S. Gupta, 2002, Ophthalmic Research.