Zobrazeno 1 - 10
of 141
pro vyhledávání: '"Takako Saeki"'
Autor:
Takako Saeki, Takashi Kuroha, Yuya Sato, Maasa Tamura, Akira Iguchi, Tomoyuki Ito, Hajime Yamazaki, Yumi Ito, Kazuhiro Yoshita, Naofumi Imai, Ichiei Narita, Hiroyuki Usuda
Publikováno v:
BMC Nephrology, Vol 20, Iss 1, Pp 1-7 (2019)
Abstract Background Although most cases of tubulointerstitial nephritis in paraproteinemia are monoclonal light chain deposition-mediated, interstitial nephritis as neoplastic interstitial cell infiltration has rarely been described. On the other han
Externí odkaz:
https://doaj.org/article/7e939b55b135437e8a9a6d898d225d68
Autor:
Kazunori Yamada, Motohisa Yamamoto, Takako Saeki, Ichiro Mizushima, Shoko Matsui, Yuhei Fujisawa, Satoshi Hara, Hiroki Takahashi, Hideki Nomura, Shigeyuki Kawa, Mitsuhiro Kawano
Publikováno v:
Arthritis Research & Therapy, Vol 19, Iss 1, Pp 1-10 (2017)
Abstract Background The aim was to further characterize immunoglobulin G4-related disease (IgG4-RD) by a large-scale multicenter study of its clinical and laboratory features conducted by multidisciplinary physicians of IgG4-RD in Japan. Methods Vari
Externí odkaz:
https://doaj.org/article/621cb92bb0a948b5b923451f4109a87e
Autor:
Simona Buelli, Luca Perico, Miriam Galbusera, Mauro Abbate, Marina Morigi, Rubina Novelli, Elena Gagliardini, Chiara Tentori, Daniela Rottoli, Ettore Sabadini, Takao Saito, Mitsuhiro Kawano, Takako Saeki, Carlamaria Zoja, Giuseppe Remuzzi, Ariela Benigni
Publikováno v:
EBioMedicine, Vol 2, Iss 5, Pp 456-466 (2015)
The pathophysiology of glomerular lesions of membranous nephropathy (MN), including seldom-reported IgG4-related disease, is still elusive. Unlike in idiopathic MN where IgG4 prevails, in this patient IgG3 was predominant in glomerular deposits in th
Externí odkaz:
https://doaj.org/article/c067646c7e124486b6bacc964d4a2da5
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:
Mitsuhiro Kawano, Ichiro Mizushima, Yutaka Yamaguchi, Naofumi Imai, Hitoshi Nakashima, Shinichi Nishi, Satoshi Hisano, Nobuaki Yamanaka, Motohisa Yamamoto, Hiroki Takahashi, Hisanori Umehara, Takao Saito, Takako Saeki
Publikováno v:
International Journal of Rheumatology, Vol 2012 (2012)
Although tubulointerstitial nephritis with IgG4+ plasma cell (PC) infiltration is a hallmark of IgG4-related kidney disease (IgG4-RKD), only a few studies are available about the minimum number of IgG4+ PC needed for diagnosis along with IgG4+/IgG+ P
Externí odkaz:
https://doaj.org/article/6bc492996d1b498d976dbb0530252f50
Publikováno v:
Modern Rheumatology Case Reports; Jul2024, Vol. 8 Issue 2, p310-313, 4p
Autor:
Takako Saeki, Tasuku Nagasawa, Yoshifumi Ubara, Yoshinori Taniguchi, Motoko Yanagita, Shinichi Nishi, Michio Nagata, Yutaka Yamaguchi, Takao Saito, Hitoshi Nakashima, Mitsuhiro Kawano
Publikováno v:
Nephrology Dialysis Transplantation. 38:1053-1056
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bb03014862f6c10e3220f772186f14fc
https://doi.org/10.1093/ndt/gfac317
https://doi.org/10.1093/ndt/gfac317
Publikováno v:
Modern Rheumatology. 33:242-251
Recent advances in the management and understanding of immunoglobulin (Ig)G4-related kidney disease (RKD) have emphasized the importance of urgent treatment in IgG4-related tubulointerstitial nephritis. On the other hand, to avoid long-term glucocort
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ace24bbe4968deb49b1643c8fa19fa97
https://doi.org/10.1093/mr/roac065
https://doi.org/10.1093/mr/roac065
Autor:
Mitsuhiro Kawano, Yoh Zen, Takako Saeki, Lingli Dong, Wen Zhang, Emanuel Della-Torre, Philip A. Hart, Judith A. Ferry, John H. Stone
Publikováno v:
A Clinician's Pearls & Myths in Rheumatology ISBN: 9783031234873
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::66d4c586ffc19d61ac6e37b78fe32382
https://doi.org/10.1007/978-3-031-23488-0_50
https://doi.org/10.1007/978-3-031-23488-0_50
