Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Shoko Tsukamoto"'
Autor:
Hiroshi Ichise, Shoko Tsukamoto, Tsuyoshi Hirashima, Yoshinobu Konishi, Choji Oki, Shinya Tsukiji, Satoshi Iwano, Atsushi Miyawaki, Kenta Sumiyama, Kenta Terai, Michiyuki Matsuda
Publikováno v:
eLife, Vol 11 (2022)
Natural killer (NK) cells lyse invading tumor cells to limit metastatic growth in the lung, but how some cancers evade this host protective mechanism to establish a growing lesion is unknown. Here, we have combined ultra-sensitive bioluminescence ima
Externí odkaz:
https://doaj.org/article/0181e79d5876476faaf234e34d7941c6
Autor:
Kei Nishiyama, Mari Kurokawa, Michiko Torio, Yasunari Sakai, Mitsuru Arima, Shoko Tsukamoto, Satoshi Obata, Shogo Minamikawa, Kandai Nozu, Noriyuki Kaku, Yoshihiko Maehara, Koh-Hei Sonoda, Tomoaki Taguchi, Shouichi Ohga
Publikováno v:
BMC Medical Genetics, Vol 21, Iss 1, Pp 1-7 (2020)
Abstract Background Pierson syndrome (PS) is a rare autosomal recessive disorder, characterized by congenital nephrotic syndrome and microcoria. Advances in renal replacement therapies have extended the lifespan of patients, whereas the full clinical
Externí odkaz:
https://doaj.org/article/89410397a9ad484e82d6857e80d0f856
Publikováno v:
American Journal of Ophthalmology Case Reports, Vol 23, Iss , Pp 101137- (2021)
Background: Revesz syndrome is a rare type of the dyskeratosis congenita spectrum disorder that is characterized by nail dystrophy, oral leukoplakia, and abnormal skin pigmentation. The retinal features are similar to those of exudative retinopathy w
Externí odkaz:
https://doaj.org/article/750d21574b984ea3813bd91a1decd09c
Autor:
Mitsuru Arima, Masato Akiyama, Kohta Fujiwara, Yujiro Mori, Hirosuke Inoue, Eiko Seki, Takahito Nakama, Shoko Tsukamoto, Masayuki Ochiai, Shouichi Ohga, Koh-Hei Sonoda
Publikováno v:
PLoS ONE, Vol 15, Iss 3, p e0230678 (2020)
PURPOSE:The purpose of this study was to evaluate neurodevelopmental outcomes in 18-month old (corrected age) preterm infants who received an intravitreal bevacizumab (IVB) injection for the treatment of type 1 retinopathy of prematurity (ROP). METHO
Externí odkaz:
https://doaj.org/article/aa790ce01e4f408c9ef1ccdb0696ca30
Autor:
Mitsuru Arima, Shoko Tsukamoto, Kohta Fujiwara, Miwa Murayama, Kanako Fujikawa, Koh-Hei Sonoda
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-8 (2017)
Abstracts Visual loss caused by retinopathy of prematurity (ROP) will be prevented if treatment-requiring ROP (TR-ROP) can be predicted. In this retrospective study including 418 infants with ≤32 weeks of gestational age (GA) and/or ≤1500 grams o
Externí odkaz:
https://doaj.org/article/63b864e70c9548dabca74f4101211ad4
Autor:
Masato Akiyama, Yujiro Mori, Emi Ueda, Shoko Tsukamoto, Takahito Nakama, Kohta Fujiwara, Koh Hei Sonoda, Mitsuru Arima, Eiko Seki
Publikováno v:
Eye (Lond)
Background/objectives The prevalence of myopia is higher in preterm infants who underwent laser photocoagulation (LPC) for retinopathy of prematurity (ROP). The aim of this study was to investigate factors associated with myopia in preterm infants wh
Autor:
Hiroshi Ichise, Shoko Tsukamoto, Tsuyoshi Hirashima, Yoshinobu Konishi, Choji Oki, Shinya Tsukiji, Satoshi Iwano, Atsushi Miyawaki, Kenta Sumiyama, Kenta Terai, Michiyuki Matsuda
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ab3b720876e6ecb16bb514bad273ebd1
https://doi.org/10.7554/elife.76269.sa2
https://doi.org/10.7554/elife.76269.sa2
Publikováno v:
American Journal of Ophthalmology Case Reports
American Journal of Ophthalmology Case Reports, Vol 23, Iss, Pp 101137-(2021)
American Journal of Ophthalmology Case Reports, Vol 23, Iss, Pp 101137-(2021)
Background: Revesz syndrome is a rare type of the dyskeratosis congenita spectrum disorder that is characterized by nail dystrophy, oral leukoplakia, and abnormal skin pigmentation. The retinal features are similar to those of exudative retinopathy w
Autor:
Michiyuki Matsuda, Kenta Terai, Kenta Sumiyama, Atsushi Miyawaki, Satoshi Iwano, Shinya Tsukiji, Choji Oki, Yoshinobu Konishi, Tsuyoshi Hirashima, Shoko Tsukamoto, Hiroshi Ichise
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cfb322da3447312eb394aa7c6a73129d
https://doi.org/10.15252/rc.2022198045
https://doi.org/10.15252/rc.2022198045
Autor:
Shouichi Ohga, Noriyuki Kaku, Shogo Minamikawa, Shoko Tsukamoto, Tomoaki Taguchi, Koh Hei Sonoda, Yoshihiko Maehara, Kandai Nozu, Kei Nishiyama, Michiko Torio, Mitsuru Arima, Yasunari Sakai, Mari Kurokawa, Satoshi Obata
Publikováno v:
BMC Medical Genetics
BMC Medical Genetics, Vol 21, Iss 1, Pp 1-7 (2020)
BMC Medical Genetics, Vol 21, Iss 1, Pp 1-7 (2020)
Background Pierson syndrome (PS) is a rare autosomal recessive disorder, characterized by congenital nephrotic syndrome and microcoria. Advances in renal replacement therapies have extended the lifespan of patients, whereas the full clinical spectrum