Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Keisei Kawa-Ha"'
Autor:
Noriyuki Aoyagi, Kimihiko Sano, Masuji Yamamoto, Urara Koudera, Keisei Kawa-Ha, Hiroshi Miyata, Keiko Yumura-Yagi, Akio Tawa, Mutsuro Shimodera, Haruki Tanaka, Masahiro Sako, Junichi Hara, Hideo Misu, Park Yd, Osamu Mabuchi, Akira Yoshioka, Yoshiyuki Kosaka, Gaku Hosoi, Makiko Kikkawa
Publikováno v:
International Journal of Hematology. 74:165-172
Between April 1994 and March 1997, 143 children (age range, 1-15 years) with newly diagnosed acute lymphoblastic leukemia (ALL), except for those patients with t(9;22), were treated according to protocol-94 of the Osaka Childhood Leukemia Study Group
Autor:
Yuko Osugi, Shinichi Tagawa, Akio Tawa, Junichi Hara, Michiko Kobayashi, Kenji Takai, Gaku Hosoi, Hiroyuki Fujisaki, Hideaki Ohta, Naoki Sakata, Shintaro Okada, Keisei Kawa-Ha, Yoshiko Matsuda
Publikováno v:
Blood. 89:4100-4103
Hemophagocytic lymphohistiocytosis (HLH) is caused by the hyperactivation of T cells and macrophages. The clinical characteristics associated with this disease result from overproduction of Th1 cytokines including interferon-γ (IFN-γ), interleukin-
Autor:
Masahiro Sako, Junichi Hara, Naoki Sakata, Takayuki Okamura, Keiko Yumura-Yagi, Akio Tawa, Masami Inoue, Keisei Kawa-Ha, Urara Kodera
Publikováno v:
Leukemia & Lymphoma. 26:141-152
To assess the clinical significance of monitoring minimal residual disease in t(8;21)(q22;q22) AML, RT-PCR assay was conducted during the clinical course of 12 patients who had undergone BMT or conventional chemotherapy. Two cases relapsed after BMT
Autor:
Tsuneo Morishima, Shintaro Okada, Shigehiko Ishihara, H Wakiguchi, Keisei Kawa-Ha, T Kurashige
Publikováno v:
Acta Paediatrica. 84:1271-1275
The patients with chronic active Epstein-Barr virus infection (CAEBV) in childhood in Japan are described. Among 39 registered cases, 20 patients were males and 19 were females. Unlike the X-linked lymphoproliferative syndrome, there was no hereditar
Autor:
Bilkis Mahbub, Kiyoshi Kitano, Keisei Kawa-Ha, Fumihiro Ishida, Hikaru Kobayashi, Shigetaka Shimodaira
Publikováno v:
British Journal of Haematology. 90:578-584
The clonal proliferation of large granular lymphocytes can be detected in patients with T-cell-lineage granular lymphocyte-proliferative disorders (T-GLPD) by Southern blotting T-cell receptor genes. However, this cannot be applied to patients with n
Autor:
Junichi Hara, Akio Tawa, Masami Inoue, Keiko Yumura-Yagi, Yuko Osugi, Keisei Kawa-Ha, Shintaro Okada, Hiroki Kurahashi, Naoki Sakata
Publikováno v:
Clinical and Experimental Immunology. 100:543-548
SUMMARY The age-related changes in proportion of various subsets within lymphocytes were investigated in cord blood and peripheral blood from healthy children and adults. The percentages of T and B cells did not show age-related changes, whereas natu
Publikováno v:
Leukemia & Lymphoma. 13:393-400
By immunophenotyping and ultrastructural cytochemistry, the disorders involving megakaryocytic lineage cells have been clarified. These disorders are termed acute megakaryocytic leukemia (AMKL) and transient abnormal myelopoiesis (TAM). The character
Autor:
Yukiko Tsunematsu, Hideaki Mizoguchi, Yoshiaki Hirata, Jun Yokota, Yuichi Sameshima, Masaaki Terada, Keisei Kawa-Ha, Taiji Tsukamoto, Takashi Sugimura, Shaw Watanabe
Publikováno v:
JNCI Journal of the National Cancer Institute. 84:703-707
BACKGROUND Germ-line p53 mutations appear to be inherited among the members of families diagnosed with Li-Fraumeni syndrome (LFS). The mutations detected in those families to date have been clustered in exon 7 of the p53 gene and, typically, have bee
Publikováno v:
Leukemia & Lymphoma. 8:465-475
Recent data have elucidated the pathogenesis of transient abnormal myelopoiesis (TAM) to a great extent. TAM is a monoclonal disorder which resolves spontaneously and the target cell in this disorder is a multipotent stem cell which is capable of dif
Autor:
Masao Mizuki, Yoshihisa Nakamura, Keiko Yumura-Yagi, Junichi Hara, Keisei Kawa-Ha, Shinichi Tagawa, Takako Morita, Junzo Nojima, Teruo Kitani
Publikováno v:
Acta Haematologica. 87:88-93
We recently encountered a patient with acute lymphoblastic leukemia (ALL) who showed temporal monocytosis of an unusually high cell count (5,000-30,000 monocytoid cells/μ1) five times after treatment