Zobrazeno 1 - 10
of 77
pro vyhledávání: '"Nobuhisa Nao-i"'
Publikováno v:
Case Reports in Ophthalmology, Vol 9, Iss 2, Pp 401-404 (2018)
A 79-year-old man who had been diagnosed with small cell lung carcinoma (SCLC) complained of right ocular pain and blurred vision. His right intraocular pressure (IOP) was 30 mm Hg, and anterior chamber cells and multiple grayish white iris masses as
Externí odkaz:
https://doaj.org/article/8584a1f86f8e4d4e8905d426ba8df52b
Publikováno v:
Case Reports in Ophthalmology, Vol 7, Iss 2, Pp 315-319 (2016)
Herein, we report a case of nontraumatic bilateral rhegmatogenous retinal detachment (RRD) during external beam radiotherapy for nonocular tumor, presented as an observational case study in conjunction with a review of the relevant literature. A 65-y
Externí odkaz:
https://doaj.org/article/13da9180903e412aa79124bec215414b
Autor:
Akiko Suga, Kazutoshi Yoshitake, Naoko Minematsu, Kazushige Tsunoda, Kaoru Fujinami, Yozo Miyake, Kazuki Kuniyoshi, Takaaki Hayashi, Kei Mizobuchi, Shinji Ueno, Hiroko Terasaki, Taro Kominami, Nobuhisa Nao‐I, Go Mawatari, Atsushi Mizota, Kei Shinoda, Mineo Kondo, Kumiko Kato, Tetsuju Sekiryu, Makoto Nakamura, Sentaro Kusuhara, Hiroyuki Yamamoto, Shuji Yamamoto, Kiyofumi Mochizuki, Hiroyuki Kondo, Itsuka Matsushita, Shuhei Kameya, Takeo Fukuchi, Tetsuhisa Hatase, Masayuki Horiguchi, Yoshiaki Shimada, Atsuhiro Tanikawa, Shuichi Yamamoto, Gen Miura, Nana Ito, Akira Murakami, Takuro Fujimaki, Yoshihiro Hotta, Koji Tanaka, Takeshi Iwata
Publikováno v:
Human Mutation. 43:2251-2264
Inherited retinal diseases (IRDs) comprise a phenotypically and genetically heterogeneous group of ocular disorders that cause visual loss via progressive retinal degeneration. Here, we report the genetic characterization of 1210 IRD pedigrees enroll
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bfcc4004071a45d33b0e85a7b3639efd
https://doi.org/10.1002/humu.24492
https://doi.org/10.1002/humu.24492
Autor:
Etsuko Shibuya, Yoshihiko Usui, Takashi Ono, Makoto Tomita, Tsutomu Sakai, Kazurori Miyata, Ayaka Takeda, Yuko Iwasaki, Yasutsugu Ida, Nobuhisa Mizuki, Mitsunao Ide, Ranko Aoyagi, Shintaro Horie, Hiroshi Takase, Nobuhisa Nao-i, Takashi Komizo, Akihiko Umazume, Junko Hori, Nobuyuki Ohguro, Kazuichi Maruyama, Koju Kamoi, Fumihiko Nitta, Satoko Nakano, Yutaka Kaneko, Yukiko Terada, Tomoko Yui, Hiroshi Goto, Kazunori Miyata, Manabu Mochizuki, Hideo Kohno
Publikováno v:
Japanese Journal of Ophthalmology. 66:119-129
PURPOSE To compare the efficacy and safety of a combination therapy of prednisolone and cyclosporine and corticosteroid pulse therapy in Vogt-Koyanagi-Harada (VKH) disease. STUDY DESIGN A prospective, multicenter, randomized, non-inferiority trial. M
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::848538358ea97133306e8c0cc1c62ac2
https://doi.org/10.1007/s10384-021-00878-w
https://doi.org/10.1007/s10384-021-00878-w
Publikováno v:
Clinical Optometry. 12:223-230
Purpose Progressive addition lenses (PAL) are effective, particularly for middle-aged and elderly people who require reading spectacles. However, with PALs, peripheral vision may be distorted and blurred because of both the lateral bending of the sur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::efb15e4b8c00337a8e8ecd34b3a990a9
https://doi.org/10.2147/opto.s282326
https://doi.org/10.2147/opto.s282326
Autor:
Kaoru Fujinami, Kei Shinoda, Yasuhiro Ikeda, Takeshi Iwata, Sentaro Kusuhara, Hiroyuki Kondo, Takaaki Hayashi, Nobuhisa Nao-i, Makoto Nakamura, Akitaka Tsujikawa, Kazuki Kuniyoshi, Akio Oishi, Shinji Ueno, Go Mawatari, Atsushi Mizota, Kazushige Tsunoda
Publikováno v:
Genes
Volume 12
Issue 11
Genes, Vol 12, Iss 1817, p 1817 (2021)
Volume 12
Issue 11
Genes, Vol 12, Iss 1817, p 1817 (2021)
Peripherin-2 (PRPH2) is one of the causative genes of inherited retinal dystrophy. While the gene is relatively common in Caucasians, reports from Asian ethnicities are limited. In the present study, we report 40 Japanese patients from 30 families wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8935f7a3c4ba9f03e80917e676616344
Autor:
Rong Zhou, Go Mawatari, Xue-Bi Cai, Ren-Juan Shen, Ya-Han Wang, Ya-Ting Wang, Yi-Ming Guo, Fei-Yang Guo, Jing Yuan, Deng Pan, Nobuhisa Nao-i, Zi-Bing Jin
Publikováno v:
Genetics in medicine : official journal of the American College of Medical Genetics. 24(6)
Macular degeneration is the leading cause of blindness worldwide. In this study, we aimed to define a new subtype of macular-retinal dystrophy and its genetic predisposition in 5 families.Exome sequencing was performed to determine the putative disea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::79f745677615767c55a9fc46679ce324
https://pubmed.ncbi.nlm.nih.gov/35331648
https://pubmed.ncbi.nlm.nih.gov/35331648
Autor:
Go Mawatari, Kaoru Fujinami, Xiao Liu, Lizhu Yang, Yu Fujinami-Yokokawa, Shiori Komori, Shinji Ueno, Hiroko Terasaki, Satoshi Katagiri, Takaaki Hayashi, Kazuki Kuniyoshi, Yozo Miyake, Kazushige Tsunoda, Kazutoshi Yoshitake, Takeshi Iwata, Nobuhisa Nao-i, on behalf of the JEGC study group
Publikováno v:
Human Genome Variation, Vol 7, Iss 1, Pp 1-3 (2020)
Variants in the retinitis pigmentosa GTPase regulator (RPGR) gene are a major cause of X-linked inherited retinal disorder (IRD). We herein describe the clinical and genetic features of 14 patients from 13 Japanese families harboring RPGR variants in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c64224a7059ae1bb83b222bd59b8bf35
http://link.springer.com/article/10.1038/s41439-019-0086-2
http://link.springer.com/article/10.1038/s41439-019-0086-2
Publikováno v:
Clinical Optometry
Purpose Progressive addition lenses (PAL) are effective, particularly for middle-aged and elderly people who require reading spectacles. However, with PALs, peripheral vision may be distorted and blurred because of both the lateral bending of the sur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d37ee7283723e6c2d8625ecce1d8f84b
https://pubmed.ncbi.nlm.nih.gov/33364869
https://pubmed.ncbi.nlm.nih.gov/33364869
Publikováno v:
Case Reports in Ophthalmology, Vol 9, Iss 2, Pp 401-404 (2018)
Case Reports in Ophthalmology
Case Reports in Ophthalmology
A 79-year-old man who had been diagnosed with small cell lung carcinoma (SCLC) complained of right ocular pain and blurred vision. His right intraocular pressure (IOP) was 30 mm Hg, and anterior chamber cells and multiple grayish white iris masses as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6f4a47649066704849be23fe58d0d2b3
https://doi.org/10.1159/000492713
https://doi.org/10.1159/000492713