Zobrazeno 1 - 10
of 55
pro vyhledávání: '"Toshihiro Sawai"'
Autor:
Takashi Oda, Toshihiro Sawai
Publikováno v:
Frontiers in Medicine, Vol 10 (2023)
Externí odkaz:
https://doaj.org/article/35be89193b14417499e51889f7598cb7
Autor:
Shereen Shawky, Hesham Safouh, Mona Gamal, Mohammed M. Abbas, Azza Aboul-Enein, Toshihiro Sawai, Yosra Fahmy, Heba Selim
Publikováno v:
International Journal of Nephrology, Vol 2021 (2021)
Background. Atypical hemolytic uremic syndrome (aHUS) is an important cause of acute kidney injury in children. It is primarily caused by dysregulation of the complement alternative pathway due to genetic mutations, mainly in complement factor H gene
Externí odkaz:
https://doaj.org/article/8b0e4b27900e422fa8ee55ee2fe4894b
Autor:
Junji Shimizu, Kazunori Fujino, Toshihiro Sawai, Yasuyuki Tsujita, Takahisa Tabata, Yutaka Eguchi
Publikováno v:
Acute Medicine & Surgery, Vol 8, Iss 1, Pp n/a-n/a (2021)
Aim The complement system is important for defending against pathogens, however, excessive complement activation is associated with a poor prognosis and organ dysfunction in sepsis. Complement factor H (CFH) acts to prevent excessive complement activ
Externí odkaz:
https://doaj.org/article/86f6238fa14b4cadaaffa9165c23e92e
Autor:
Yasuhiro Oda, Yoichiro Ikeda, Hiroyuki Abe, Akinori Hashiguchi, Kazuhito Hatanaka, Toshihiro Sawai, Tetsuo Ushiku, Masaomi Nangaku
Publikováno v:
Internal Medicine; 2023, Vol. 62 Issue 24, p3657-3661, 5p
Autor:
Masataka Honda, Ryoko Harada, Yusuke Okuda, Hiroshi Hataya, Toshihiro Sawai, Tomoyuki Sakai, Kenji Ishikura, Yuko Hamasaki, Riku Hamada, Osamu Uemura
Publikováno v:
Nephrology. 26:763-771
AIM Accurate and precise estimation of glomerular filtration rate (GFR) is essential in kidney disease. We evaluated the usefulness of the mean of creatinine clearance (CCr ) and urea clearance (CUN ) examined over a 1-h urine collection period (1-h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::00b52b9eea4f66c9044af184e2bdb002
https://doi.org/10.1111/nep.13911
https://doi.org/10.1111/nep.13911
Autor:
Yoshihiro Maruo, Yuka Ezumi, Tomoyuki Sakai, Kentaro Ogata, Toshihiro Sawai, Satoko Ichioka, Toshiki Masuda, Kazuna Yamamoto
Publikováno v:
Japanese journal of pediatric nephrology. 34:133-138
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4f6e2efc211afe99b5f0e4f928fb38d2
https://doi.org/10.3165/jjpn.oa.2020.0190
https://doi.org/10.3165/jjpn.oa.2020.0190
Autor:
Yoko Fujita, Masahiko Yazawa, Maho Terashita, Yugo Shibagaki, Katsuki Ohtani, Yukitaka Yamasaki, Toshihiro Sawai, Junichiro Kibayashi, Tomonori Imamura, Yoshihiko Hidaka, Norimitsu Inoue
Publikováno v:
Internal Medicine
Atypical hemolytic uremic syndrome (aHUS) is an extremely rare condition caused by an excessive activation of the complement pathway based on genetic or acquired dysfunctions in complement regulation, leading to thrombotic microangiopathy (TMA). A co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f57406ae0dc502564cbac8eda40c61b
http://hdl.handle.net/10659/00007054
http://hdl.handle.net/10659/00007054
Publikováno v:
Colloids and Surfaces A: Physicochemical and Engineering Aspects. 654:130084
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::653a81171d5f4033ac57ed446c73cea9
https://doi.org/10.1016/j.colsurfa.2022.130084
https://doi.org/10.1016/j.colsurfa.2022.130084
Autor:
Mona Gamal, Toshihiro Sawai, Heba M. Selim, Hesham Safouh, Yosra Aboelnaga Fahmy, Azza Aboul-Enein, Mohammed M. Abbas, Shereen Shawky
Publikováno v:
International Journal of Nephrology
International Journal of Nephrology, Vol 2021 (2021)
International Journal of Nephrology, Vol 2021 (2021)
Background. Atypical hemolytic uremic syndrome (aHUS) is an important cause of acute kidney injury in children. It is primarily caused by dysregulation of the complement alternative pathway due to genetic mutations, mainly in complement factor H gene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a9f52922c60d3d71d796ad22fa089b9
https://pubmed.ncbi.nlm.nih.gov/34840826
https://pubmed.ncbi.nlm.nih.gov/34840826
Autor:
Masafumi Matsuo, Yuko Shima, Eriko Tanaka, Koichi Nakanishi, Yurika Tsuji, Tomohiko Yamamura, China Nagano, Kandai Nozu, Kazumoto Iijima, Yoshinori Araki, Takayuki Okamoto, Hiroaki Nagase, Nana Sakakibara, Yuya Aoto, Eri Okada, Toshihiro Sawai, Shinya Ishiko, Koji Tsugawa, Tomoko Horinouchi, Rini Rossanti
Publikováno v:
Kidney International Reports
Introduction Frasier syndrome (FS) is a rare inherited kidney disease caused by intron 9 splicing variants of WT1. For wild-type WT1, 2 active splice donor sites in intron 9 cause a mixture of 2 essential transcripts (with or without lysine-threonine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::17aac303460bda58eb0a2c04a77bde3d
https://pubmed.ncbi.nlm.nih.gov/34622098
https://pubmed.ncbi.nlm.nih.gov/34622098