Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Masako Sugahara"'
Autor:
Kyoko Kawashima-Kumagai, Kenji Yamashiro, Munemitsu Yoshikawa, Masahiro Miyake, Gemmy Cheung Chui Ming, Qiao Fan, Jia Yu Koh, Masaaki Saito, Masako Sugahara-Kuroda, Maho Oishi, Yumiko Akagi-Kurashige, Isao Nakata, Hideo Nakanishi, Norimoto Gotoh, Akio Oishi, Hiroshi Tamura, Sotaro Ooto, Akitaka Tsujikawa, Yasuo Kurimoto, Tetsuju Sekiryu, Fumihiko Matsuda, Chiea-Chuen Khor, Ching-Yu Cheng, Tien Yin Wong, Nagahisa Yoshimura
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-8 (2017)
Abstract Bilateral neovascular age-related macular degeneration (AMD) causes much more handicaps for patients than unilateral neovascular AMD. Although several AMD-susceptibility genes have been evaluated for their associations to bilaterality, genom
Externí odkaz:
https://doaj.org/article/51f45ede27f14284a3b7850c22ea583a
Autor:
Kayo Shimizu, Akio Oishi, Maho Oishi, Ken Ogino, Satoshi Morooka, Masako Sugahara, Norimoto Gotoh, Nagahisa Yoshimura
Publikováno v:
Case Reports in Ophthalmology, Vol 6, Iss 2, Pp 246-250 (2015)
We screened patients with choroideremia using next-generation sequencing (NGS) and identified a novel mutation and a known mutation in the CHM gene. One patient presented an atypical fundus appearance for choroideremia. Another patient presented macu
Externí odkaz:
https://doaj.org/article/0399c1e7c09e4d7085a32488cdda0b30
Autor:
Masako Sugahara, Akio Oishi, Nagahisa Yoshimura, Satoshi Morooka, Satoko Nakagawa, Maho Oishi, Ken Ogino
Publikováno v:
Retina. 36:1340-1344
Purpose To report the characteristic changes of fundus autofluorescence in the nasal retina of patients with retinitis pigmentosa. Methods We investigated 113 eyes of 113 patients with retinitis pigmentosa. We obtained wide-field fundus autofluoresce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::de150454d99e180a7133984d5d28392b
https://doi.org/10.1097/iae.0000000000000904
https://doi.org/10.1097/iae.0000000000000904
Autor:
Satoshi Morooka, Norimoto Gotoh, Masako Sugahara, Nagahisa Yoshimura, Inyeop Kang, Ken Ogino, Akio Oishi, Maho Oishi
Publikováno v:
Ophthalmic Genetics. 38:70-73
Purpose: In this study, we aimed to detect mutations in the SLC7A14 cationic transporter gene, which has recently been reported as a causative gene for retinitis pigmentosa (RP), in Japanese patients with autosomal recessive (AR) or sporadic RP. Mate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b8579b8a39b63c327774513e3b4140d6
https://doi.org/10.3109/13816810.2015.1136336
https://doi.org/10.3109/13816810.2015.1136336
Autor:
Satoshi Morooka, Masako Sugahara, Nagahisa Yoshimura, Norimoto Gotoh, Ken Ogino, Maho Oishi, Akio Oishi, Masafumi Kurimoto
Publikováno v:
Clinical Ophthalmology (Auckland, N.Z.)
Ken Ogino,1 Maho Oishi,1 Akio Oishi,1 Satoshi Morooka,1 Masako Sugahara,1 Norimoto Gotoh,1,2 Masafumi Kurimoto,3 Nagahisa Yoshimura1 1Department of Ophthalmology and Visual Sciences, Kyoto University Graduate School of Medicine, 2Center for Genomic M
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9bb8c7f0085d46e3e7a5646971e37336
http://hdl.handle.net/2433/215066
http://hdl.handle.net/2433/215066
Autor:
Masako Sugahara, Satoshi Morooka, Norimoto Gotoh, Akio Oishi, Ken Ogino, Maho Oishi, Kayo Shimizu, Nagahisa Yoshimura
Publikováno v:
Case Reports in Ophthalmology, Vol 6, Iss 2, Pp 246-250 (2015)
Case Reports in Ophthalmology
Case Reports in Ophthalmology
We screened patients with choroideremia using next-generation sequencing (NGS) and identified a novel mutation and a known mutation in the CHM gene. One patient presented an atypical fundus appearance for choroideremia. Another patient presented macu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bb2c801cb1a30fcc94b0650de117344f
https://doi.org/10.1159/000437348
https://doi.org/10.1159/000437348
Autor:
Tomoko Hasegawa, Masako Sugahara, Munemitsu Yoshikawa, Maho Oishi, Ken Ogino, Akitaka Tsujikawa, Masayuki Hata, Manabu Miyata, Kenji Ishihara, Akio Oishi, Takako Hirashima
Publikováno v:
The British journal of ophthalmology. 102(9)
Background/AimsThis study aimed to evaluate blood flow in the choriocapillaris in patients with Bietti crystalline dystrophy (BCD) with CYP4V2 mutations using optical coherence tomography angiography (OCTA), and to explore the parameters associated w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c13d4978215fedf3bc471dc5d57ac827
https://pubmed.ncbi.nlm.nih.gov/29197825
https://pubmed.ncbi.nlm.nih.gov/29197825
Autor:
Munemitsu Yoshikawa, Gemmy Cheung Chui Ming, Maho Oishi, Nagahisa Yoshimura, Masako Sugahara-Kuroda, Hideo Nakanishi, Kenji Yamashiro, Akio Oishi, Tien Yin Wong, Hiroshi Tamura, Kyoko Kawashima-Kumagai, Yasuo Kurimoto, Tetsuju Sekiryu, Yumiko Akagi-Kurashige, Norimoto Gotoh, Masaaki Saito, Qiao Fan, Ching-Yu Cheng, Fumihiko Matsuda, Sotaro Ooto, Akitaka Tsujikawa, Chiea Chuen Khor, Isao Nakata, Jia Yu Koh, Masahiro Miyake
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-8 (2017)
Scientific Reports
Scientific Reports
Bilateral neovascular age-related macular degeneration (AMD) causes much more handicaps for patients than unilateral neovascular AMD. Although several AMD-susceptibility genes have been evaluated for their associations to bilaterality, genome-wide as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2674d0d65d9a8d790b3e2f83497c4d61
https://doi.org/10.1038/s41598-017-07526-9
https://doi.org/10.1038/s41598-017-07526-9
Autor:
Nagahisa Yoshimura, Manabu Miyata, Kenji Ishihara, Masako Sugahara, Takako Hirashima, Munemitsu Yoshikawa, Yuki Muraoka, Sotaro Ooto, Ken Ogino, Tomoko Hasegawa, Masayuki Hata, Norimoto Gotoh, Satoshi Morooka, Kenji Yamashiro
Publikováno v:
Scientific Reports
Ophthalmologists sometimes face difficulties in identifying the origin of visual acuity (VA) loss in a retinitis pigmentosa (RP) patient, particularly before cataract surgery: cataract or the retinal disease state. Therefore, it is important to ident
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5a21bfc9239dc9f2f58cac7e1fef2607
https://doi.org/10.1038/srep46396
https://doi.org/10.1038/srep46396
Autor:
Masako Sugahara, Yoshimasa Kuroda, Takako Hirashima, Manabu Miyata, Sotaro Ooto, Tomoko Hasegawa, Norimoto Gotoh, Satoshi Morooka, Nagahisa Yoshimura, Masayuki Hata, Ken Ogino, Kenji Yamashiro
Publikováno v:
Retina (Philadelphia, Pa.). 37(6)
PURPOSE:: To compare atrophy of the choroid and retina between Bietti crystalline dystrophy (BCD) patients and EYS-related retinitis pigmentosa (RP) patients with a similar degree of central visual field defects, age, and axial length (AL). METHODS::
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::04fd6b33aad4aada29da3d81796991b6
https://pubmed.ncbi.nlm.nih.gov/27658286
https://pubmed.ncbi.nlm.nih.gov/27658286