Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Nobuhisa Hirase"'
Publikováno v:
Internal Medicine
Publikováno v:
Modern Rheumatology. 22:284-289
Hemophagocytic syndrome (HPS) is an unusual disorder associated with systemic lupus erythematosus (SLE). A 64-year-old woman was admitted because of fever and urticarial vasculitis. Laboratory data revealed pancytopenia and immunological abnormalitie
Autor:
Hajime Yamagata, Hiroshi Shiozaki, Nobuhisa Hirase, Jiro Watanabe, Haruo Kuwano, Hiroya Yamaguchi
Publikováno v:
Suizo. 21:70-75
症例は83歳男性.心窩部のつっぱり感を自覚し当科受診.血中膵酵素の増加とCTにて膵全体のソーセージ様腫大を認め,自己免疫性膵炎(autoimmune pancreatitis:AIP)が疑われ入院となった.E
Thiazolidinedione suppresses the expression of erythroid phenotype in erythroleukemia cell line K562
Autor:
Toshihiko Yanase, Nobuhisa Hirase, Hajime Nawata, Ryoichi Takayanagi, Tsukuru Umemura, Koichiro Muta, Yi Ming Mu
Publikováno v:
Leukemia Research. 24:393-400
The activation of PPARgamma:RXR nuclear system induces monocytic differentiation of some myelogeneous leukemia cell lines. The present study was undertaken to examine the effect of PPARgamma ligand, TZD (troglitazone or pioglitazone) and/or RXR selec
Autor:
Yuji Yufu, Junji Nishimura, Koichiro Muta, Satoshi Shiokawa, Nobuhisa Hirase, Hajime Nawata, Yasunobu Abe
Publikováno v:
Cancer Genetics and Cytogenetics. 117:113-117
These are the first cases of primary macroglobulinemia (PMG) with t(11;18)(q21;q21) reported in the literature. The first case was a 77-year-old man with macroglobulinemia (serum IgM: 8.36 g/dL). Abnormal lymphoid cells were detected in the blood and
Autor:
Ryoichi Takayanagi, Yi Ming Mu, Tsukuru Umemura, Nobuhisa Hirase, Toshihiko Yanase, Koichiro Muta, Hajime Nawata
Publikováno v:
Oncology. 57:17-26
Thiazolidinedione (TZD) is known to be a potent activator of peroxisome proliferator-activated receptor γ (PPARγ), a nuclear receptor that constitutes a heterodimer with retinoid X receptor (RXR). Since a considerable amount of PPARγ is expressed
Autor:
Aya, Tanaka, Junichi, Tsukada, Hiroaki, Morimoto, Takefumi, Katsuragi, Tsukasa, Nakanishi, Shu, Watanabe, Nobuhisa, Hirase, Seiichi, Motomura
Publikováno v:
[Rinsho ketsueki] The Japanese journal of clinical hematology. 53(1)
We report a 73-year-old Japanese man with early onset pure red cell aplasia (PRCA) caused by subcutaneous administration of recombinant epoetin-β. Two months after the start of epoetin therapy, he developed PRCA. Anti-erythropoietin (EPO) antibody,
Autor:
Guido Luzzatto, Toshiaki Sano, A. Kourakli, G. Leone, Tadaoki Morimoto, K. Havemann, Hajime Nawata, Yoshiyuki Miyamoto, Stephan Falk, Yuji Yufu, S. Sica, Toshiya Suzuki, B. Etuk, Giuseppe Cella, Amos Cohen, Kaoru Nagata, Shiro Saito, Tetsuya Gotoh, Toshiharu Furukawa, Hidemitsu Kurosawa, P. Salutari, F.E. Costa, Kenichi Sugita, F. Sanalioğlu, Robert Fischer, Nobuhisa Hirase, Nobuko Tsuchihashi, R. Cemeroğlu, A. Di Mario, Shuji Tohda, Nicholas C. Zoumbos, Masaaki Kosaka, T.S.I. Sales, Helma Klein, Felix Rueda, K.H. Pflüger, Hitoshi Sakakibara, Moshe Mittelman, Koichiro Muta, Mitsuoki Eguchi, M.B. de Melo, C. Altay, Junji Nishimura, G. Kolb, Yaacov Matzner, Ikuo Murohashi, Hans-Peter Bertsch, A. Rötig, M. Klausmann, U. Kaiser, I. Lorand-Metze, Hiroshi Ideguchi, Yasunobu Abe, Kazuto Okagawa, Argiris Symeonidis, Shingo Sadamura, F. Gümrük, A. Gürgey, Eyoji Hanada, G. Athanassiou, Mikimasa Komaki, Hans-Jochen Stutte, Raya Maran, Nobuo Nara, Yannis F. Missirlis, Juergen Thiele, Makoto Takishita, Yasufumi Imai, Tsukuru Umemura, Meir Djaldetti, Izidore S. Lossos, L. Pagano
Publikováno v:
Acta Haematologica. 87:I-IV
Publikováno v:
Nihon rinsho. Japanese journal of clinical medicine. 64
Publikováno v:
[Rinsho ketsueki] The Japanese journal of clinical hematology. 48(1)
A 74-year-old man presented with anemia, thrombocytopenia and leukocytosis with 41% abnormal cells having cleaved and monocytoid nuclei. The bone marrow was infiltrated with 43.6% abnormal cells that were negative for peroxidase staining and positive