Zobrazeno 1 - 10
of 69
pro vyhledávání: '"Kei Mizobuchi"'
Autor:
Natsuki Higa, Takaaki Hayashi, Kei Mizobuchi, Maki Iwasa, Shingo Kubota, Kazuki Kuniyoshi, Shuhei Kameya, Hiroyuki Kondo, Mineo Kondo, Tadashi Nakano
Publikováno v:
Frontiers in Medicine, Vol 11 (2024)
IntroductionIn Japan, inherited retinal dystrophy caused by biallelic variants of the RPE65 gene is exceedingly rare. The purpose of this study was to describe a Japanese male patient with a novel variant in RPE65 associated with Leber congenital ama
Externí odkaz:
https://doaj.org/article/0140d53651fb47e9808b8b5d93959952
Autor:
Kyohei Sugawara, Ryosuke Ito, Hiroshi Horiguchi, Kei Mizobuchi, Satoshi Katagiri, Hisato Gunji, Tadashi Nakano
Publikováno v:
International Journal of Ophthalmology, Vol 16, Iss 12, Pp 2004-2010 (2023)
AIM: To compare the surgical outcomes of a multifocal intraocular lens (IOL; Lentis Comfort LS-313 MF15) with those of an enhanced monofocal IOL (Tecnis Eyhance DIB00V). METHODS: This retrospective study included patients who underwent cataract surge
Externí odkaz:
https://doaj.org/article/7ced1ad17c1145869ac889fc3e5c6c25
Autor:
Akiko Suga, Kei Mizobuchi, Taiga Inooka, Kazutoshi Yoshitake, Naoko Minematsu, Kazushige Tsunoda, Kazuki Kuniyoshi, Yosuke Kawai, Yosuke Omae, Katsushi Tokunaga, Takaaki Hayashi, Shinji Ueno, Takeshi Iwata, Hatsue Ishibashi-Ueda, Tsutomu Tomita, Michio Noguchi, Ayako Takahashi, Yu-ichi Goto, Sumiko Yoshida, Kotaro Hattori, Ryo Matsumura, Aritoshi Iida, Yutaka Maruoka, Hiroyuki Gatanaga, Masaya Sugiyama, Satoshi Suzuki, Kengo Miyo, Yoichi Matsubara, Akihiro Umezawa, Kenichiro Hata, Tadashi Kaname, Kouichi Ozaki, Haruhiko Tokuda, Hiroshi Watanabe, Shumpei Niida, Eisei Noiri, Koji Kitajima, Reiko Miyahara, Hideyuki Shimanuki
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 101843- (2024)
Purpose: Achromatopsia (ACHM) is an early-onset cone dysfunction caused by 5 genes with cone-specific functions (CNGA3, CNGB3, GNAT2, PDE6C, and PDE6H) and by ATF6, a transcription factor with ubiquitous expression. To improve the relatively low vari
Externí odkaz:
https://doaj.org/article/a0a40200ace245f49c062e5cf42c6c3b
Autor:
Ayaka Nakajima, Kazuki Kuniyoshi, Chiharu Iwahashi, Fukutaro Mano, Takaaki Hayashi, Hiroyuki Kondo, Kei Mizobuchi, Itsuka Matsushita, Akiko Suga, Kazutoshi Yoshitake, Tadashi Nakano, Takeshi Iwata, Chota Matsumoto, Shunji Kusaka
Publikováno v:
Frontiers in Medicine, Vol 10 (2023)
IntroductionCongenital X-linked retinoschisis (XLRS) presents as macular retinoschisis/degeneration in almost all patients and as peripheral retinoschisis in half the patients. Although the optical coherence tomography (OCT) findings of macular retin
Externí odkaz:
https://doaj.org/article/5cc438d37d1e4519a8275761f4cfe3bc
Publikováno v:
Case Reports in Ophthalmology, Vol 13, Iss 3, Pp 862-867 (2022)
A 36-year-old primigravid woman with suspected gestational hypertension was referred to our hospital for further examination and treatment of bilateral serous retinal detachment (SRD). At the previous hospital immediately after the onset of visual sy
Externí odkaz:
https://doaj.org/article/812fa3df49e54a64aeb071da40fed0d3
Autor:
Kaoruko Torii, Sachiko Nishina, Hazuki Morikawa, Kei Mizobuchi, Masakazu Takayama, Nobutaka Tachibana, Kentaro Kurata, Akiko Hikoya, Miho Sato, Tadashi Nakano, Maki Fukami, Noriyuki Azuma, Takaaki Hayashi, Hirotomo Saitsu, Yoshihiro Hotta
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 18, p 13678 (2023)
Leber congenital amaurosis (LCA) is the most severe form of inherited retinal dystrophy. RPGRIP1-related LCA accounts for 5–6% of LCA. We performed whole-exome sequencing and whole-genome sequencing (WGS) on 29 patients with clinically suspected LC
Externí odkaz:
https://doaj.org/article/fd1ddcea7e474033ac490adbafb3f5fd
Publikováno v:
Case Reports in Ophthalmology, Vol 12, Iss 2, Pp 538-542 (2021)
A 88-year-old female who was being treated for end-stage pseudoexfoliation syndrome was referred to our hospital for treatment of dislocated intraocular lens (IOL) and the elevated intraocular pressure (IOP) and in the right eye (RE). At the first vi
Externí odkaz:
https://doaj.org/article/f1a49e9eeb49486a9d15669b27be8db8
Autor:
Akira Watanabe, MD, PhD, Wakana Ninomiya, PhD, Kei Mizobuchi, MD, PhD, Tomoyuki Watanabe, MD, Tadashi Nakano, MD, PhD, Rosa E. Alvarado-Villacorta.
Publikováno v:
Medicine, Vol 101, Iss 18, p e29205 (2022)
Abstract. To investigate changes in the corneal shape caused by fluid–gas exchange after vitrectomy. This retrospective case-control study included 43 eyes that underwent a combination of cataract surgery and vitrectomy. The corneal shape was measu
Externí odkaz:
https://doaj.org/article/980a256bec7044b2bd60deb3d2d65b82
Autor:
Naoko Ishiguro, Takaaki Hayashi, Yoshiko Yamawaki, Kei Mizobuchi, Tsutomu Yasukawa, Shigeru Honda, Tadashi Nakano
Publikováno v:
Case Reports in Ophthalmological Medicine, Vol 2022 (2022)
Individuals with pachydrusen, larger than 125 μm, have a significantly thicker choroid than do those with soft drusen or reticular pseudodrusen. Little is known about cases of abnormal blood flow within pachydrusen. The purpose of this report was to
Externí odkaz:
https://doaj.org/article/aea8c8eda33d46cd8fade42483da4792
Autor:
Takaaki Hayashi, Satoshi Katagiri, Daiki Kubota, Kei Mizobuchi, Yozo Ishiuji, Akihiko Asahina, Shuhei Kameya, Tadashi Nakano
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 9, Iss 6, Pp n/a-n/a (2021)
Abstract Background Hypotrichosis with juvenile macular dystrophy (HJMD) is a rare autosomal recessive inherited disorder caused by biallelic variants in the CDH3 gene encoding P‐cadherin. Here, we report two Japanese sibling patients with HJMD. Me
Externí odkaz:
https://doaj.org/article/c874c589ce4c41a7b8e99730ab3be08d