Zobrazeno 1 - 10
of 113
pro vyhledávání: '"Tomoyuki Sakai"'
Autor:
Yusuke Ueda, Tomoyuki Sakai, Kazunori Yamada, Kotaro Arita, Yoko Ishige, Daisuke Hoshi, Hiroto Yanagisawa, Haruka Iwao-Kawanami, Takafumi Kawanami, Shuichi Mizuta, Toshihiro Fukushima, Sohsuke Yamada, Akihiro Yachie, Yasufumi Masaki
Publikováno v:
Immunological Medicine, Vol 47, Iss 3, Pp 192-199 (2024)
Hemophagocytic lymphohistiocytosis (HLH) has been recognized as a rare adverse event following the coronavirus disease 2019 (COVID-19) vaccination. We report a case of neuropsychiatric symptoms and refractory HLH in a woman with systemic lupus erythe
Externí odkaz:
https://doaj.org/article/05c2b6655c1f4fa9b5cfc63676225a8c
Autor:
Hiroshi Funaki, Naomi Nojima, Yutaka Takikawa, Kazutoshi Komori, Hajime Hasegawa, Tomoyuki Sakai, Sohsuke Yamada, Yasufumi Masaki
Publikováno v:
Surgical Case Reports, Vol 9, Iss 1, Pp 1-5 (2023)
Abstract Background Extranodal natural killer/T-cell lymphoma, nasal type (ENKL) of the small intestine, is a disease with extremely poor prognosis. We describe treatment in a case which is novel in that it demonstrated long-term survival. Case prese
Externí odkaz:
https://doaj.org/article/d0a029baf30943599721a39b7e2eea62
Autor:
Koichi Kamei, Ryoko Harada, Riku Hamada, Tomoyuki Sakai, Yuko Hamasaki, Hiroshi Hataya, Shuichi Ito, Kenji Ishikura, Masataka Honda
Publikováno v:
PLoS ONE, Vol 11, Iss 3, p e0150885 (2016)
BACKGROUND:Proteinuria is the most important risk factor for IgA nephropathy progression. The purpose of this study is to evaluate the long-term outcome and risk factors for poor prognosis in childhood IgA nephropathy. METHODS:Patients who were diagn
Externí odkaz:
https://doaj.org/article/71103838319446b28b2b05ab7c55f4e5
Autor:
Akio Nakajima, Yasufumi Masaki, Takuji Nakamura, Takafumi Kawanami, Yasuhito Ishigaki, Tsutomu Takegami, Mitsuhiro Kawano, Kazunori Yamada, Norifumi Tsukamoto, Shoko Matsui, Takako Saeki, Kazuichi Okazaki, Terumi Kamisawa, Taiichiro Miyashita, Yoshihiro Yakushijin, Keita Fujikawa, Motohisa Yamamoto, Hideaki Hamano, Tomoki Origuchi, Shintaro Hirata, Hiroto Tsuboi, Takayuki Sumida, Hisanori Morimoto, Tomomi Sato, Haruka Iwao, Miyuki Miki, Tomoyuki Sakai, Yoshimasa Fujita, Masao Tanaka, Toshihiro Fukushima, Toshiro Okazaki, Hisanori Umehara
Publikováno v:
PLoS ONE, Vol 10, Iss 5, p e0126582 (2015)
IgG4-related disease (IgG4-RD) is a new clinical entity of unknown etiology characterized by elevated serum IgG4 and tissue infiltration by IgG4-positive plasma cells. Although aberrancies in acquired immune system functions, including increases in T
Externí odkaz:
https://doaj.org/article/77b0e7d6a84541d3af6199e385ea4d37
Autor:
Yasufumi Masaki, Nozomu Kurose, Motohisa Yamamoto, Hiroki Takahashi, Takako Saeki, Atsushi Azumi, Shinji Nakada, Shoko Matsui, Tomoki Origuchi, Susumu Nishiyama, Kazunori Yamada, Mitsuhiro Kawano, Akira Hirabayashi, Keita Fujikawa, Tomoko Sugiura, Masanobu Horikoshi, Naoto Umeda, Hiroshi Minato, Takuji Nakamura, Haruka Iwao, Akio Nakajima, Miyuki Miki, Tomoyuki Sakai, Toshioki Sawaki, Takafumi Kawanami, Yoshimasa Fujita, Masao Tanaka, Toshihiro Fukushima, Katumi Eguchi, Susumu Sugai, Hisanori Umehara
Publikováno v:
International Journal of Rheumatology, Vol 2012 (2012)
IgG4-related disease is a new disease classification established in Japan in the 21st century. Patients with IgG4-related disease display hyper-IgG4-gammaglobulinemia, massive infiltration of IgG4+ plasma cells into tissue, and good response to gluco
Externí odkaz:
https://doaj.org/article/2c5a55b119ac482cbab259cb7a740320
Autor:
Takafumi Kawanami, Toshioki Sawaki, Tomoyuki Sakai, Miyuki Miki, Haruka Iwao, Akio Nakajima, Takuji Nakamura, Tomomi Sato, Yoshimasa Fujita, Masao Tanaka, Yasufumi Masaki, Toshihiro Fukushima, Yuko Hirose, Makoto Taniguchi, Naotoshi Sugimoto, Toshiro Okazaki, Hisanori Umehara
Publikováno v:
PLoS ONE, Vol 7, Iss 10, p e45689 (2012)
OBJECTIVE: To determine the cytokine production profile of cultured salivary gland epithelial (SGE) cells obtained from patients with Sjögren's syndrome (SS). METHODS: SGE cells obtained from 9 SS patients and 6 normal controls were cultured in the
Externí odkaz:
https://doaj.org/article/3cbbb7f9c387468fae9d56f1b308e39f
Autor:
Tsuyoshi Hamaguchi, Ichizo Nishino, Yasuki Hirano, Nobuaki Uchida, Michiyo Fujita-Nakata, Megumi Nakanishi, Tomoyuki Sakai, Masato Asahina
Publikováno v:
Internal Medicine; 2024, Vol. 63 Issue 19, p2683-2687, 5p
Autor:
Tomoyuki Sakai, Yusuke Ueda, Hiroto Yanagisawa, Kotaro Arita, Haruka Iwao, Kazunori Yamada, Shuichi Mizuta, Hiroshi Kawabata, Toshihiro Fukushima, Katsunori Tai, Shinji Kishi, Koji Morinaga, Jun Murakami, Hiroyuki Takamatsu, Yasushi Terasaki, Nobuyuki Yoshio, Yukio Kondo, Hirokazu Okumura, Matano, Sadaya, Masaki Yamaguchi
Publikováno v:
Global Health & Medicine; Aug2024, Vol. 6 Issue 4, p277-281, 5p
Autor:
Yasufumi Masaki, Yusuke Ueda, Hiroto Yanagisawa, Kotaro Arita, Tomoyuki Sakai, Kazunori Yamada, Shuichi Mizuta, Toshihiro Fukushima, Kazue Takai, Sadao Aoki, Hiroshi Kawabata
Publikováno v:
Internal Medicine. 62:27-32
TAFRO syndrome was first described in 2010, standing for thrombocytopenia, anasarca, fever, reticulin fibrosis and organomegaly. Because the lymph node histopathology of TAFRO syndrome mimics idiopathic multicentric Castleman disease (iMCD), some res
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf5f96088329778bb9883e076f801ca0
https://doi.org/10.2169/internalmedicine.9622-22
https://doi.org/10.2169/internalmedicine.9622-22
Publikováno v:
Annals of Hematology
Although Castleman disease was first described in 1956, this disease includes various conditions, including unicentric Castleman disease with hyaline vascular histology, human herpesvirus-8 (HHV-8) related multicentric Castleman disease, idiopathic m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::87ce38f8ee7aa3e5c324beced4ee3810
https://doi.org/10.1007/s00277-022-04762-6
https://doi.org/10.1007/s00277-022-04762-6