Zobrazeno 1 - 10
of 46
pro vyhledávání: '"Akiko Hikoya"'
Autor:
Takeshi Morimoto, Sadao Suzuki, Osamu Hieda, Noriyuki Azuma, Sachiko Nishina, Noriko Nishikawa, Miho Sato, Yukiko Shimizu, Hirohito Iimori, Reiko Kinouchi, Tomoyo Yoshida, Akiko Hikoya, Miwa Komori, Toshiaki Goseki, Takafumi Mori, Takashi Negishi, Tamami Shimizu, Shion Hayashi, Yoshiko Sugiyama, Yoshimi Yokoyama, Akiko Kimura, Hiroko Suzuki
Publikováno v:
BMJ Open Ophthalmology, Vol 9, Iss 1 (2024)
Objective The objective of this study is to investigate factors associated with outcomes after 3 months of instructed usage of hand-held digital devices (DD) in patients with acquired comitant esotropia (ACE).Methods and analysis This prospective mul
Externí odkaz:
https://doaj.org/article/1b79e2e702b6493dadc30e1041caa0a0
Publikováno v:
American Journal of Ophthalmology Case Reports, Vol 32, Iss , Pp 101892- (2023)
Purpose: To report stereopsis after bilateral Yokoyama procedure in patients with highly myopic strabismus and good visual acuity. Observations: Five patients aged between 34 and 81 years with best-corrected visual acuity of 20/25 or better were oper
Externí odkaz:
https://doaj.org/article/be0aafba583c4a10a5f104f323bfda02
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:
American Journal of Ophthalmology Case Reports, Vol 21, Iss , Pp 101011- (2021)
Purpose: To report two cases of acquired bilateral trochlea nerve palsy with large torsional deviation successfully treated by simultaneous bilateral inferior rectus muscle (IR) nasal transposition and inferior oblique muscle (IO) myectomy. Observati
Externí odkaz:
https://doaj.org/article/e788e36c99c0450b8a8bbe3125fad40b
Publikováno v:
PLoS ONE, Vol 11, Iss 12, p e0168245 (2016)
To clarify the efficacy of a surgical strategy based on the superior oblique tendon traction test.A retrospective chart review was performed between January 2002 and June 2015. During that period, a single inferior oblique muscle (IO) myectomy and a
Externí odkaz:
https://doaj.org/article/7b26770005514950afe997df7975d4f0
Autor:
Katsuhiro Hosono, Yuko Harada, Kentaro Kurata, Akiko Hikoya, Miho Sato, Shinsei Minoshima, Yoshihiro Hotta
Publikováno v:
Journal of Ophthalmology, Vol 2015 (2015)
Purpose. Leber congenital amaurosis (LCA), a genetically and clinically heterogeneous disease, is the earliest onset retinitis pigmentosa (RP) and is the most severe of hereditary retinal dystrophies. This study was conducted to investigate genetic a
Externí odkaz:
https://doaj.org/article/df90e5caf7e84fc3a333128ae8fe3907
Autor:
Katsuhiro Hosono, Chie Ishigami, Masayo Takahashi, Dong Ho Park, Yasuhiko Hirami, Hiroshi Nakanishi, Shinji Ueno, Tadashi Yokoi, Akiko Hikoya, Taichi Fujita, Yang Zhao, Sachiko Nishina, Jae Pil Shin, In Taek Kim, Shuichi Yamamoto, Noriyuki Azuma, Hiroko Terasaki, Miho Sato, Mineo Kondo, Shinsei Minoshima, Yoshihiro Hotta
Publikováno v:
PLoS ONE, Vol 7, Iss 2, p e31036 (2012)
Retinitis pigmentosa (RP) is a highly heterogeneous genetic disease including autosomal recessive (ar), autosomal dominant (ad), and X-linked inheritance. Recently, arRP has been associated with mutations in EYS (Eyes shut homolog), which is a major
Externí odkaz:
https://doaj.org/article/169e92ad12be4338a0b4893c40a96637
Autor:
Akiko Hikoya, Katsuhiro Hosono, Kaoru Ono, Shinji Arai, Nobutaka Tachibana, Kentaro Kurata, Kaoruko Torii, Miho Sato, Hirotomo Saitsu, Tsutomu Ogata, Yoshihiro Hotta
Publikováno v:
Ophthalmic Genetics. :1-6
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b5a7118dd25ccd8c76d51633d65763c5
https://doi.org/10.1080/13816810.2022.2141788
https://doi.org/10.1080/13816810.2022.2141788
Autor:
Yu Takeda, Hiroko Suzuki, Katsuhiro Hosono, Akiko Hikoya, Miwa Komori, Risako Inagaki, Takashi Haseoka, Shinji Arai, Yuri Takagi, Yoshihiro Hotta, Miho Sato
Publikováno v:
Japanese Journal of Ophthalmology. 66:314-319
Chronic progressive external ophthalmoplegia (CPEO) is a mitochondrial disease characterized by slowly progressive ptosis and limitations in ocular motility. Although exophthalmos is not considered to be a common feature of CPEO, this study focused o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6cdfd6e7a3a29d2f178f136a1c1d161d
https://doi.org/10.1007/s10384-022-00920-5
https://doi.org/10.1007/s10384-022-00920-5
Publikováno v:
Japanese Journal of Ophthalmology. 66:87-93
This study aimed to identify the characteristics of acute acquired comitant esotropia (AACE) in young patients from a single institution; and clarify their relationship with the excess use of digital devices. Retrospective, observational. We extracte
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a0456abab1b97f4c0dc747b2ec924ed7
https://doi.org/10.1007/s10384-021-00879-9
https://doi.org/10.1007/s10384-021-00879-9