原著論文1
Iejima D, Itabashi T, Kawamura Y, etal.
High-Temperature Requirement A Serine Peptidase 1 Gene is Transcriptionally Regulated by Insertion/Deletion Nucleotides Located at the 3 Prime End of Age-Related Maculopathy Susceptibility 2 Gene in Patients with Age-Related Macular Degeneration.
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原著論文2
Kuniyoshi K, Ikeo K, Sakuramoto H, et al.
Novel nonsense and splice site mutations in CRB1 gene in two Japanese patients with early-onset retinal dystrophy Documenta Ophthalmologica.
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原著論文3
Tanito M, Hara K, Akahori M, et al.
Lack of association of LOXL1 gene variants in Japanese patients with central retinal vein occlusion without clinically detectable pseudoexfoliation material deposits.
Acta Ophthalmologica
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原著論文4
Katagiri S, Hayashi T, Yoshitake K, et al.
Congenital Achromatopsia and Macular Atrophy Caused by a Novel Recessive PDE6C Mutation (p.E591K).
Ophthalmic Genetics
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原著論文5
Kuniyoshi K, Sakuramoto H, Yoshitake K, et al.
Reduced rod electroretinograms in carrier parents of two Japanese siblings with autosomal recessive retinitis pigmentosa associated with PDE6B gene mutations.
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原著論文6
Kato Y, Tsunoda K, Fujinami K, et al.
Association of retinal artery and other inner retinal structures with distribution of tapetal-like reflex in Oguchi's disease.
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原著論文7
Katagiri S, Hayashi T, Akahori M, et al.
RHO mutations (p.W126L and p.A346P) in two Japanese families with autosomal dominant retinitis pigmentosa.
Journal of Ophthalmology
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原著論文8
Katagiri S, Hayashi T, Yoshitake K, et al.
RPE65 mutations in two Japanese families with Leber congenital amaurosis.
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なし
原著論文9
Gallenberger M, Kroeber M, Koch M, et al.
Heterozygote Wdr36-deficient mice do not develop glaucoma.
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原著論文10
Nakayama M, Iejima D, Akahori M, et al.
Overexpression of Htra1 and exposure to mainstream cigarette smoke leads to choroidal neovascularization and subretinal deposits in aged mice.
Investigative Ophthalmology and Visual Science
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原著論文11
Katagiri S, Akahori M, Sergeev Y, et al.
Whole exome analysis identifies frequent CNGA1mutations in Japanese population with autosomal recessive retinitis pigmentosa.
PLoS One
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原著論文12
Katagiri S, Hayashi T, Yoshitake K, et al.
Novel C8orf37 mutations in patients with early-onset retinal dystrophy, macular atrophy, cataracts, and high myopia.
Ophthalmic Genetics
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原著論文13
Matsumoto CS, Shinoda K, Matsumoto H, et al.
Pattern visually evoked potentials elicited by organic electro-luminescence screen.
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原著論文14
Matsumoto CS, Nakagomi R, Matsumoto H, et al.
Binocular interaction of visually evoked cortical potentials elicited by dichoptic binocular stimulation.
Journal of Vision
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原著論文15
Katagiri S, Akahori M, Hayashi T, et al.
Autosomal recessive cone-rod dystrophy associated with compound heterozygous mutations in the EYS gene.
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原著論文16
Kuniyoshi K, Sakuramoto H, Yoshitake K, et al.
Longitudinal clinical course of three Japanese patients with Leber congenital amaurosis/severe early childhood onset retinal dystrophy with RDH12 mutation.
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原著論文17
Kobayashi H, Okamoto H, Murakami A, et al.
Plasma Proteome Analysis On Cynomolgus Monkey (Macaca fascicularis) Pedigrees With Early Onset Drusen Formation.
Journal of Experimental Animals
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原著論文18
Matsumoto CS, Shinoda K, Matsumoto H, et al.
What monitor can replace cathode ray tube for visual stimulation to elicit multifocal electroretinograms?
Journal of Vision
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