Zobrazeno 1 - 10
of 78
pro vyhledávání: '"Sumie, Tabata"'
Autor:
Rio Noto, Nozomu Kamiura, Yuichiro Ono, Sumie Tabata, Shigeo Hara, Hideki Yokoi, Akihiro Yoshimoto, Motoko Yanagita
Publikováno v:
BMC Nephrology, Vol 18, Iss 1, Pp 1-6 (2017)
Abstract Background Proliferative glomerulonephritis with monoclonal IgG deposits (PGNMID) is a form of renal involvement by monoclonal IgG deposits that was found in mesangial, subendothelial or subepithelial regions. The distribution of glomerular
Externí odkaz:
https://doaj.org/article/0c655d01c54d497686c3ff3a12f0e3ed
Autor:
Yotaro Ochi, Nobuhiro Hiramoto, Tetsuichi Yoshizato, Yuichiro Ono, June Takeda, Yusuke Shiozawa, Kenichi Yoshida, Nobuyuki Kakiuchi, Yuichi Shiraishi, Hiroko Tanaka, Kenichi Chiba, Yasuhiro Kazuma, Sumie Tabata, Noboru Yonetani, Keiichiro Uehara, Daisuke Yamashita, Yukihiro Imai, Koji Nagafuji, Mitsunori Yamakawa, Satoru Miyano, Akifumi Takaori-Kondo, Seishi Ogawa, Takayuki Ishikawa
Publikováno v:
Haematologica, Vol 103, Iss 11 (2018)
Externí odkaz:
https://doaj.org/article/26fe60a2ffc14949b09bf655a555346a
Autor:
Seishi Ogawa, Toshiyuki Kitano, Shojiro Inano, Kensuke Fujiwara, Junya Kanda, Mizuki Watanabe, Sho Shibata, Naoto Kawasaki, Sumie Tabata, Akiko Fukunaga, Akifumi Takaori-Kondo, Hiroo Ueno, Yasuhito Nannya, Yoko Takiuchi, Yoshio Okamoto
Publikováno v:
International Journal of Hematology. 115:428-434
Shwachman-Diamond syndrome (SDS) is an autosomal recessive inherited disorder characterized by bone marrow failure, exocrine pancreatic dysfunction, and skeletal abnormalities. SDS is typically caused by a pathogenic mutation in the Shwachman-Bodian-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::297ddef744e8b076df05c5a5ed1309d1
https://doi.org/10.1007/s12185-021-03251-2
https://doi.org/10.1007/s12185-021-03251-2
Autor:
Sho Shibata, Yoko Takiuchi, Yoshio Okamoto, Akiko Fukunaga, Toshiyuki Kitano, Sumie Tabata, Naoto Kawasaki, Hajime Morita, Shojiro Inano, Tomomi Endo
Publikováno v:
Internal Medicine
TAFRO syndrome and POEMS syndrome are lymphoproliferative disorders with elevated interleukin-6 and vascular endothelial growth factor (VEGF) levels; however, their underlying pathogenic mechanisms remain unclear. Similarities have been reported in t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2df52ed232334669004c085a262e417b
http://europepmc.org/articles/PMC8188039
http://europepmc.org/articles/PMC8188039
Autor:
Sho Shibata, Akiko Fukunaga, Toshiyuki Kitano, Yoko Takiuchi, Yoshio Okamoto, Sumie Tabata, Shojiro Inano, Kazuyo Yamamoto
Publikováno v:
Journal of Clinical and Experimental Hematopathology : JCEH
Methotrexate, hydrocortisone, vincristine, sobuzoxane, and etoposide (MTX-HOPE) chemotherapy was originally reported in 2007 as a salvage regimen for relapsed or refractory non-Hodgkin's lymphoma. To clarify the safety and efficacy of this regimen, w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::31963edc3055c5a049ddd641141444cd
http://europepmc.org/articles/PMC7337273
http://europepmc.org/articles/PMC7337273
Autor:
Sho Shibata, Yoko Takiuchi, Naoto Kawasaki, Yoshio Okamoto, Shojiro Inano, Akiko Fukunaga, Sumie Tabata, Ayako Arai, Ken-Ichi Imadome, Toshiyuki Kitano
Publikováno v:
International journal of hematology. 115(4)
Chronic active Epstein-Barr virus infection (CAEBV) is a systemic T- or NK-lymphoproliferative disorder (LPD) caused by EBV. Allogenic hematopoietic stem cell transplantation (HSCT) is the only curative therapy for CAEBV, but relapse sometimes occurs
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::756ee570e272f29f47fc2b9dfa08a41e
https://pubmed.ncbi.nlm.nih.gov/35001347
https://pubmed.ncbi.nlm.nih.gov/35001347
Autor:
Sho, Shibata, Shojiro, Inano, Mizuki, Watanabe, Kensuke, Fujiwara, Hiroo, Ueno, Yasuhito, Nannya, Junya, Kanda, Naoto, Kawasaki, Yoshio, Okamoto, Yoko, Takiuchi, Akiko, Fukunaga, Sumie, Tabata, Seishi, Ogawa, Akifumi, Takaori-Kondo, Toshiyuki, Kitano
Publikováno v:
International journal of hematology. 115(3)
Shwachman-Diamond syndrome (SDS) is an autosomal recessive inherited disorder characterized by bone marrow failure, exocrine pancreatic dysfunction, and skeletal abnormalities. SDS is typically caused by a pathogenic mutation in the Shwachman-Bodian-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::bf120f28f6126888c90ba33aad4f78c5
https://pubmed.ncbi.nlm.nih.gov/34704233
https://pubmed.ncbi.nlm.nih.gov/34704233
Autor:
Toshiyuki Kitano, Sumie Tabata, Naoto Kawasaki, Yoko Takiuchi, Yoshio Okamoto, Akiko Aiba, Yuki Oku, Naoki Yuhi, Sho Shibata, Shojiro Inano
Publikováno v:
International journal of hematology. 114(3)
We report a case of acquired hypofibrinogenemia with multiple myeloma presenting λ-type IgG monoclonal protein. The patient had anemia and renal deficiency, and also developed bleeding tendency due to severe coagulopathy. Her fibrinogen level was un
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a5ea4279039edd1834adcd8cb178aedf
https://pubmed.ncbi.nlm.nih.gov/34057670
https://pubmed.ncbi.nlm.nih.gov/34057670
Autor:
Sho, Shibata, Toshiyuki, Kitano, Yoshio, Okamoto, Yoko, Takiuchi, Kazuyo, Yamamoto, Sumie, Tabata, Akiko, Aiba, Yuji, Yoshida, Yasuhito, Nannya, Seishi, Ogawa, Nobuyoshi, Arima
Publikováno v:
[Rinsho ketsueki] The Japanese journal of clinical hematology. 60(12)
In 2003, a 60-year-old man presenting with thrombocytosis was referred to our hospital. Laboratory tests revealed normal white blood cell count and hemoglobin level. Bone marrow examination showed an increased number of megakaryocytes with dysplasia.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::73ee1562532b9637a74944738b314f99
https://pubmed.ncbi.nlm.nih.gov/31902812
https://pubmed.ncbi.nlm.nih.gov/31902812
Autor:
Mitsunori Yamakawa, Koji Nagafuji, Satoru Miyano, Kenichi Chiba, Akifumi Takaori-Kondo, Noboru Yonetani, Yusuke Shiozawa, Sumie Tabata, Yuichi Shiraishi, Kenichi Yoshida, June Takeda, Daisuke Yamashita, Takayuki Ishikawa, Hiroko Tanaka, Seishi Ogawa, Yukihiro Imai, Keiichiro Uehara, Nobuhiro Hiramoto, Tetsuichi Yoshizato, Yasuhiro Kazuma, Yotaro Ochi, Yuichiro Ono, Nobuyuki Kakiuchi
Publikováno v:
Haematologica. 103:e553-e556
Interdigitating dendritic cell sarcoma (IDCS) is a rare neoplasm considered to derive from a dendritic cell. Recent studies have shown that B- or T-lymphoblastic leukemia/lymphomas can develop clonally related histiocytic/dendritic cell (H/DC) neopla
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9cd9bb91e7585c386c20fc93b4a1994b
https://doi.org/10.3324/haematol.2018.193490
https://doi.org/10.3324/haematol.2018.193490