Zobrazeno 1 - 10
of 90
pro vyhledávání: '"Hideki Uchiumi"'
Autor:
Yohei Osaki, Akihiko Yokohama, Akio Saito, Kenichi Tahara, Kunio Yanagisawa, Yoshiyuki Ogawa, Takuma Ishizaki, Takeki Mitsui, Hiromi Koiso, Makiko Takizawa, Hideki Uchiumi, Takayuki Saitoh, Hiroshi Handa, Hirokazu Murakami, Norifumi Tsukamoto, Yoshihisa Nojima
Publikováno v:
PLoS ONE, Vol 8, Iss 11, p e81722 (2013)
Blastic plasmacytoid dendritic cell neoplasm (BPDCN) is a rare hematological malignancy. Plasmacytoid DCs (pDCs), which are defined as lineage marker (Lin)(-)HLA-DR(+)CD56(-)CD123(+)CD11c(-) cells, are considered to be the normal counterpart of BPDCN
Externí odkaz:
https://doaj.org/article/e71289c0988c4bd9ab721881e57a7dac
Autor:
Masahiro Ieko, Takuma Ishizaki, Takeki Mitsui, Hiroshi Handa, Yoshiyuki Ogawa, Hideki Uchiumi, Akitada Ichinose, Yoshihisa Nojima, Fumito Gouda, Kunio Yanagisawa
Publikováno v:
International Journal of Hematology. 106:82-89
Acquired hemophilia A (AHA), which is caused by autoantibodies against coagulation factor VIII (FVIII) is a rare, life-threatening bleeding disorder, the incidence of which appears to be increasing in Japan as the population ages. However, the clinic
Autor:
Kunio Yanagisawa, Yoshiyuki Ogawa, Tetsuya Shikawa, Fumito Gohda, Hideki Uchiumi, Hiroshi Handa
Publikováno v:
Kansenshogaku Zasshi. 91:25-30
An HIV-infected man in his 30s was transferred to our hospital after the discontinuation of antiretroviral therapy (ART) for 4 years. An intraoral tumor was identified, and a biopsy was performed. The diagnosis was Kaposi's sarcoma (KS) and dissemina
Autor:
Akihiro Nakamura, Koumei Hoshikawa, Toshimasa Hayashi, Morio Sawamura, Kunio Yanagisawa, Tomoko Kodama, Hideki Uchiumi, Yoshihisa Nojima, Yoshimi Ishizaki, Fumito Gohda, Akihiro Tago, Mizue Kobayashi, Yoshiyuki Ogawa, Hiroshi Handa
Publikováno v:
The Kitakanto Medical Journal. 67:135-141
Autor:
Kunio Yanagisawa, Akitada Ichinose, Hiroshi Handa, Yoshiyuki Ogawa, Chiaki Naito, Hiroaki Shimizu, Takuma Ishizaki, Hideki Uchiumi, Fumito Gohda, Masahiro Ieko
Publikováno v:
International journal of hematology. 111(4)
Acquired hemophilia A (AHA) is a rare, life-threatening bleeding disorder caused by autoantibodies against coagulation factor VIII (FVIII). Immunosuppressive therapy for AHA aims to arrest bleeding by eliminating FVIII inhibitors. Factor VIII activit
Autor:
Ikuko, Matsumura, Kunio, Yanagisawa, Yoshiyuki, Ogawa, Hiroaki, Shimizu, Takuma, Ishizaki, Takeki, Mitsui, Hideki, Uchiumi, Yuri, Uchiyama, Naomichi, Matsumuto, Hiroshi, Handa
Publikováno v:
[Rinsho ketsueki] The Japanese journal of clinical hematology. 59(3)
Hemophilic pseudotumors can occur in patients with hemophilia because of recurrent bleeding and poor hemostasis. A man in his 30s with hemophilia B and human immunodeficiency virus/hepatitis C virus co-infection complicated by liver cirrhosis present
Autor:
Fumito Gohda, Tomonori Nakamura, Yoshiyuki Ogawa, Koujirou Yamamoto, Hideki Uchiumi, Daisuke Nagano, Takuya Araki, Hiroshi Handa, Kunio Yanagisawa
Publikováno v:
European journal of clinical pharmacology. 74(8)
The clinical efficacies of some antiretroviral drugs are known to not depend on its concentration in blood. To establish a method of dosage adjustment for darunavir (DRV) based on pharmacokinetic theory, we analyzed the correlation between DRV levels
Autor:
Hirokazu Murakami, Hideki Uchiumi, Takuma Ishizaki, Hiromi Koiso, Yoshihisa Nojima, Takayuki Saitoh, Takeki Mitsui, Akihiko Yokohama, Kunio Yanagisawa, Norifumi Tsukamoto, Hiroshi Handa, Yoshiyuki Ogawa, Makiko Takizawa
Publikováno v:
The Kitakanto Medical Journal. 65:187-191
Autor:
Yoshiyuki Ogawa, Takuya Araki, Tetsuya Shigehara, Daisuke Nagano, Kazuhisa Saruki, Yoshihisa Nojima, Hiroshi Handa, Kunio Yanagisawa, Koujirou Yamamoto, Hideki Uchiumi
Publikováno v:
AIDS. 30:970-972
Autor:
Nobuhiko, Kobayashi, Yoshiyuki, Ogawa, Kunio, Yanagisawa, Takuma, Ishizaki, Hideki, Uchiumi, Nobuaki, Suzuki, Tadashi, Matsushita, Akitada, Ichinose, Hiroshi, Handa
Publikováno v:
[Rinsho ketsueki] The Japanese journal of clinical hematology. 58(6)
Acquired von Willebrand syndrome (AvWS) is a rare bleeding disorder with laboratory findings resembling those of congenital von Willebrand disease. AvWS usually occurs in association with a variety of underlying disorders, such as lymphoproliferative