Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Chika, Kawajiri"'
Autor:
Kazunori Imada, Kaoru Kahata, Toshihiro Miyamoto, Toshiaki Yujiri, Yoshiko Atsuta, Jun Taguchi, Chiaki Nakaseko, Tadakazu Kondo, Takehiko Mori, Emiko Sakaida, Makoto Yoshimitsu, Makoto Hirokawa, Chikako Ohwada, Tatsuo Ichinohe, Chika Kawajiri-Manako, Yuichi Hasegawa, Taichi Azuma, Shingo Kurahashi
Publikováno v:
Biology of Blood and Marrow Transplantation. 24:1180-1186
POEMS syndrome is a rare plasma cell dyscrasia presenting with polyneuropathy, λ-type M protein, vascular endothelial growth factor elevation, and systemic manifestations. The standard treatment has not been established, but autologous stem cell tra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d9241e32402d863a30226f205cf8485
https://doi.org/10.1016/j.bbmt.2018.01.026
https://doi.org/10.1016/j.bbmt.2018.01.026
Autor:
Atsushi Iwama, Chiaki Nakaseko, Yusuke Takeda, Masahiro Takeuchi, Koutaro Yokote, Emi Togasaki, Emiko Sakaida, Shuhei Koide, Tomoya Muto, Shokichi Tsukamoto, Tohru Iseki, Yusuke Isshiki, Naoya Mimura, Shio Sakai, Kwangmin Choi, Chikako Ohwada, Daniel T. Starczynowski, Nagisa Hasegawa, Chika Kawajiri-Manako, Kazumasa Aoyama, Yuhei Nagao, Ryo Shimizu
Publikováno v:
Leukemia Research. 50:85-94
Expression of the tumor suppressor gene NR4A3 is silenced in the blasts of acute myeloid leukemia (AML), irrespective of the karyotype. Although the transcriptional reactivation of NR4A3 is considered to have a broad-spectrum anti-leukemic effect, th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::88638ffafd95b623bd0f24262bee693c
https://doi.org/10.1016/j.leukres.2016.09.018
https://doi.org/10.1016/j.leukres.2016.09.018
Autor:
June Takeda, Tohru Iseki, Kensuke Kayamori, Seishi Ogawa, Chiaki Nakaseko, Kenichi Yoshida, Satoru Miyano, Chikako Ohwada, Sonoko Misawa, Yusuke Takeda, Atsunori Saraya, Yusuke Shiozawa, Osamu Ohara, Kenichi Chiba, Emiko Sakaida, Shio Mitsukawa, Koutaro Yokote, Dai Nishijima, Hiroko Tanaka, Yoshinori Hasegawa, Shokichi Tsukamoto, Nagisa Oshima-Hasegawa, Ola Rizq, Masashi Sanada, Shuhei Koide, Chika Kawajiri-Manako, Motohiko Oshima, Satoshi Kuwabara, Kazumasa Aoyama, Yuhei Nagao, Naoya Mimura, Atsushi Iwama, Yuichi Shiraishi, Yusuke Isshiki, Masahiro Takeuchi
Publikováno v:
Leukemia. 33(7)
POEMS syndrome is a rare paraneoplastic disease associated with monoclonal plasma cells; however, the pathogenic importance of plasma cells remains unclear. We performed comprehensive genetic analyses of plasma cells in 20 patients with POEMS syndrom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b5b26b7efe94ffe3eaf2bd9157bb4249
https://pubmed.ncbi.nlm.nih.gov/30635632
https://pubmed.ncbi.nlm.nih.gov/30635632
Autor:
Tomoya Muto, Masahiro Takeuchi, Chikako Ohwada, Sonoko Misawa, Emiko Sakaida, Tohru Iseki, Shokichi Tsukamoto, Naomi Shimizu, Naoya Mimura, Shio Mitsukawa, Emi Togasaki, Chiaki Nakaseko, Yusuke Takeda, Chika Kawajiri-Manako, Yuhei Nagao, Satoshi Kuwabara, Nagisa Oshima-Hasegawa
Publikováno v:
Blood. 131(19)
TO THE EDITOR: Polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, and skin changes (POEMS) syndrome is a rare plasma cell disorder additionally characterized by extravascular volume overload, sclerotic bone lesions, and plasmacytoma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec378c2fa17f559b1c243216df3efbae
https://pubmed.ncbi.nlm.nih.gov/29599110
https://pubmed.ncbi.nlm.nih.gov/29599110
Autor:
Shio Mitsukawa, Sonoko Misawa, Emiko Sakaida, Tohru Iseki, Yuhei Nagao, Masahiro Takeuchi, Chiaki Nakaseko, Koutaro Yokote, Naoya Mimura, Chika Kawajiri-Manako, Hiroe Namba, Shokichi Tsukamoto, Masaki Fukuyo, Ryoh Shimizu, Emi Togasaki, Atsushi Kaneda, Yusuke Takeda, Bahityar Rahmutulla, Nagisa Oshima-Hasegawa, Chikako Ohwada, Satoshi Kuwabara, Makoto Tsuiji
Publikováno v:
American journal of hematology. 93(9)
Polyneuropathy, organomegaly, endocrinopathy, M-protein, and skin changes (POEMS) syndrome is a rare plasma cell dyscrasia characterized by polyneuropathy, organomegaly, endocrinopathy, extravascular fluid overload, M protein, and a myriad of skin ch
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::27e6ad2e26f9c8a1d7fe94c0665823e3
https://pubmed.ncbi.nlm.nih.gov/30015379
https://pubmed.ncbi.nlm.nih.gov/30015379
Autor:
Satoshi Kuwabara, Chika Kawajiri, Satoshi Ota, Chiaki Nakaseko, Naomi Shimizu, Toshiyuki Takagi, Yusuke Takeda, Hiroaki Tanaka, Takeharu Kawaguchi, Shogo Furukawa, Shinichiro Hashimoto, Shoichi Ito
Publikováno v:
Internal Medicine. 54:503-507
Lymphomatoid granulomatosis (LYG) is an angiocentric and angiodestructive lymphoproliferative disease involving extranodal sites. Although LYG cerebral lesions are usually located adjacent to LYG pulmonary lesions, few reports have described the occu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5919dd253a1a9829068160e80f95f23b
https://doi.org/10.2169/internalmedicine.54.2399
https://doi.org/10.2169/internalmedicine.54.2399
Autor:
Koutaro Yokote, Tomoya Muto, Atsuko Yamazaki, Tohru Iseki, Yasumasa Sugita, Ryoh Shimizu, Emiko Sakaida, Chika Kawajiri, Chiaki Nakaseko, Masahiro Takeuchi, Chikako Ohwada, Emi Togasaki, Naoya Mimura, Yusuke Takeda, Shio Sakai, Yuhei Nagao
Publikováno v:
Journal of Clinical and Experimental Hematopathology. 55:163-168
Severe acute lung injury is a rare but life-threatening complication associated with bortezomib. We report a patient with multiple myeloma who developed a severe diffuse alveolar hemorrhage (DAH) immediately after the first bortezomib administration.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::116207e4fcf6e648d9ee0fc896f3e2a4
https://doi.org/10.3960/jslrt.55.163
https://doi.org/10.3960/jslrt.55.163
Autor:
Nagisa Oshima-Hasegawa, Chika Kawajiri-Manako, Chiaki Nakaseko, Emi Togasaki, Masaru Miyazaki, Naomi Shimizu, Masahiro Takeuchi, Yuhei Nagao, Hideyuki Yoshitomi, Naoya Mimura, Ryoh Shimizu, Masayuki Ohtsuka, Shokichi Tsukamoto, Shio Mitsukawa, Yusuke Takeda, Tohru Iseki, Tomoya Muto, Emiko Sakaida, Chikako Ohwada
Publikováno v:
Annals of hematology. 97(4)
Thrombopoietin-receptor agonists have been recently introduced for a second-line treatment of immune thrombocytopenia (ITP). Splenectomy has tended to be avoided because of its complications, but the response rate of splenectomy is 60–80% and it ha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2167b3d4cbb40b16739d98c2a5443525
https://pubmed.ncbi.nlm.nih.gov/29332223
https://pubmed.ncbi.nlm.nih.gov/29332223
Autor:
Tomoya Muto, Naoya Mimura, Emi Togasaki, Yuhei Nagao, Ryo Shimizu, Tohru Iseki, Chika Kawajiri, Shio Sakai, Chiaki Nakaseko, Emiko Sakaida, Shokichi Tsukamoto, Masahiro Takeuchi, Chikako Ohwada, Yusuke Takeda
Publikováno v:
Internal Medicine
Infections of the central nervous system (CNS) with varicella zoster virus (VZV) is a rare occurrence after allogeneic hematopoietic stem cell transplantation. We herein report a case of VZV meningitis, radiculitis and myelitis that developed 8 month
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::66bda3b3025bc02fc596842cd3a85dd9
https://pubmed.ncbi.nlm.nih.gov/28154282
https://pubmed.ncbi.nlm.nih.gov/28154282
Autor:
Kenji Kimura, Chika Kawajiri-Manako, Koutaro Yokote, Nagisa Oshima-Hasegawa, Chiaki Nakaseko, Atsushi Kaneda, Masahiro Takeuchi, Yusuke Takeda, Kenshi Suzuki, Tadao Ishida, Shokichi Tsukamoto, Masaki Fukuyo, Bahityar Rahmutulla, Kanji Miyazaki, Emiko Sakaida, Shio Mitsukawa, Keisuke Matsusaka, Chikako Ohwada, Naoya Mimura, Tohru Iseki
Publikováno v:
Blood. 134:1748-1748
[Introduction] AL amyloidosis is caused by the deposition of abnormally folded clonal immunoglobulin (IG) light chains (LCs, λ:κ = 3:1) made by malignant plasma cells in the bone marrow (BM), which leads to multi-organ dysfunction, often involving
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::00ef4b6e0bc2e33f808b29fe50f0cc93
https://doi.org/10.1182/blood-2019-125028
https://doi.org/10.1182/blood-2019-125028