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Case Reports in Ophthalmology|December 5, 2022
Clinical Course of OCTA en face Imaging Findings in a Patient with HELLP SyndromeKokoro Konuma, Kei Mizobuchi, Akira Watanabe, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|October 17, 2020
Novel biallelic TRPM1 variants in an elderly patient with complete congenital stationary night blindnessTakaaki Hayashi, Kei Mizobuchi, Shinsuke Kikuchi, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|May 10, 2023
Electroretinographic abnormalities in Alport syndrome with a novel COL4A5 truncated variant (p.Try20GlyfsTer19)Kei Mizobuchi, Takaaki Hayashi, Ryo Ohira, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|June 2, 2022
Clinical characterization of autosomal dominant retinitis pigmentosa with NRL mutation in a three-generation Japanese familyKei Mizobuchi, Takaaki Hayashi, Tomokazu Matsuura, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|October 6, 2025
Best vitelliform macular dystrophy caused by a BEST1 p.(Ser246Asn) variant coexisting with diabetic retinopathyYusuke Tatemoto, Takaaki Hayashi, Kei Mizobuchi, et al.
Case Reports in Ophthalmology|July 12, 2021
Minimally Invasive Surgery for Intraocular Lens Removal and Intrascleral Intraocular Lens Fixation with Trabeculectomy in a Patient with Dislocated Intraocular Lens and Elevated Intraocular PressureYuko Mano, Kei Mizobuchi, Tomoyuki Watanabe, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|February 5, 2021
Vitamin A deficiency after prolonged intake of an unbalanced diet in a Japanese hemodialysis patientNanami Kishimoto, Takaaki Hayashi, Kei Mizobuchi, et al.
Case Reports in Ophthalmological Medicine|May 1, 2026
Gyrate Atrophy of the Choroid and Retina Diagnosed in Adulthood With a Homozygous <i>OAT</i> Variant: A Case Report Highlighting the Need for Long-Term CareHitomi Taniai, Kei Mizobuchi, Takaaki Hara, et al.
Optometry and Vision Science : Official Publication of the American Academy of Optometry|August 1, 2022
Case Report: Improved Choroidal Circulation in a Patient with Unilateral Acute Idiopathic MaculopathyAkiko Sotozono, Kei Mizobuchi, Takaaki Hayashi, et al.
Ophthalmic Genetics|June 26, 2025
A novel <i>NR2F1</i>-associated microdeletion underlying Bosch-Boonstra-Schaaf optic atrophy syndromeTakaaki Hayashi, Kei Mizobuchi, Akiko Suga, et al.
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