Zobrazeno 1 - 10
of 34
pro vyhledávání: '"Toshie Ogasawara"'
Autor:
Shunsuke Homma, Toshie Ogasawara, Michie Suga, Yoshiyasu Nakamura, Katsuya Takenaka, Shoko Marshall, Kiyotaka Kawauchi, Naoki Mori, Hajime Kuroda, Naoya Nakamura, Yohei Miyagi, Atsuko Masunaga
Publikováno v:
Journal of Medical Case Reports, Vol 18, Iss 1, Pp 1-7 (2024)
Abstract Background Segregated-nucleus-containing atypical monocytes have recently been identified in mice. Segregated-nucleus-containing atypical monocytes are thought to originate from the bone marrow and induce fibrosis in the drug-injured lung. T
Externí odkaz:
https://doaj.org/article/0b19be3410124971a2457cc59a1cf9c1
Autor:
Toshie Ogasawara, Kiyotaka Kawauchi, Takuya Ono, Shoko Marshall, Kotaro Shide, Kazuya Shimoda, Naoki Mori, Hiroshi Sakura
Publikováno v:
Leukemia Research Reports, Vol 13, Iss , Pp 100194- (2020)
Essential thrombocythemia (ET) is an indolent myeloproliferative neoplasm (MPN) with a transformation to acute myeloid leukemia in
Externí odkaz:
https://doaj.org/article/86621ed111a34cee801160f5d3d2da8e
Publikováno v:
Hematology Reports, Vol 4, Iss 2, Pp e11-e11 (2012)
A 68-year old woman came to our hospital with a severe case of anemia. Serum immunoelectropheresis identified a monoclonal immunoglobulin (Ig) G and κ protein. The serum IgE level was within the nomal range and the amounts of remaining immuno - glob
Externí odkaz:
https://doaj.org/article/199660c2c0914f258cacc75c5668b4e0
Autor:
Ayana Sakurai, Shoko Marshall, Tomoko Ogasawara, Toshie Ogasawara, Yoshikazu Aoka, Hiroshi Sakura, Yasuko Uchigata, Tetsuya Ogawa
Publikováno v:
Journal of Infection and Chemotherapy. 28:943-947
A new treatment for coronavirus disease (COVID-19), REGN-COV2, a cocktail consisting of two neutralizing antibodies against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has been approved for patients at a risk of developing more seve
Autor:
Naoki Mori, Mari Ohwashi-Miyazaki, Kentaro Yoshinaga, Toshie Ogasawara, Shoko Marshall, Masayuki Shiseki, Hiroshi Sakura, Junji Tanaka
Publikováno v:
Journal of Genetics. 101
To elucidate the relevance of genetic alterations, we analysed 17 genes known to be involved in haematological neoplasms in patients with chronic leucocytosis and patients with persistent thrombocytosis. Mutations of the
Autor:
Naoko Tsuyama, Naoki Mori, Kengo Takeuchi, Hirofumi Yamauchi, Noriko Nishimura, Tetsuya Ogawa, Masahiro Yokoyama, Shoko Marshall, Norihito Inoue, Hiroshi Sakura, Yasuhito Terui, Yuko Mishima, Toshie Ogasawara
Publikováno v:
Clinical lymphoma, myelomaleukemia. 21(3)
The R-CHOP regimen (rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisolone) is the standard therapy for patients with diffuse large B-cell lymphoma (DLBCL). However, vincristine is sometimes omitted or reduced owing to side effects.W
Autor:
Toshie, Ogasawara, Nozomiko, Ebata, Julia, Hamasaki, Shoko, Marshall, Kiyotaka, Kawauchi, Koichi, Ohshima, Naoki, Mori, Hiroshi, Sakura
Publikováno v:
[Rinsho ketsueki] The Japanese journal of clinical hematology. 60(6)
Primary adrenal lymphoma is a rare lymphoma, accounting for0.2% of non-Hodgkin lymphoma. The leading histopathological subtype of adrenal lymphoma is diffuse large B-cell lymphoma, and intravascular large B-cell lymphoma (IVLBCL) is rare. Here, we re
Autor:
Takuya Ono, Kiyotaka Kawauchi, Shoko Marshall, Toshie Ogasawara, Naoki Mori, Hiroshi Sakura, Kotaro Shide, Kazuya Shimoda
Publikováno v:
Leukemia Research Reports, Vol 13, Iss, Pp 100194-(2020)
Leukemia Research Reports
Leukemia Research Reports
Essential thrombocythemia (ET) is an indolent myeloproliferative neoplasm (MPN) with a transformation to acute myeloid leukemia in
Autor:
Hiroshi Sakura, Motohiko Aiba, Kiyotaka Kawauchi, Toshie Ogasawara, Masabumi Shibuya, Tsutomu Sanaka, Mariko Fujibayashi
Publikováno v:
European Journal of Haematology. 96:144-151
Primary effusion lymphoma (PEL) is a rare B-cell lymphoma subtype that is characterized by lymphomatous effusion without the presence of masses, and it typically occurs in human immunodeficiency virus (HIV)-infected individuals. Lymphoma cells are un
Autor:
Toshie, Ogasawara, Kiyotaka, Kawauchi, Naoki, Mori, Hiroshi, Sakura, Fumiyo, Katoh, Hitoshi, Kanno, Etsuro, Ito
Publikováno v:
[Rinsho ketsueki] The Japanese journal of clinical hematology. 58(8)
Diamond-Blackfan anemia (DBA) is a rare congenital disease caused by mutations in ribosomal protein genes and is characterized by pure red cell aplasia. While the prognosis is relatively favorable, quality of life (QOL) among DBA patients is negative