Search Results - "Yoshida, Yataro"

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    A Japanese family with X-linked sideroblastic anemia affecting females and manifesting as macrocytic anemia by Katsurada, Tatsuya, Kawabata, Hiroshi, Kawabata, Daiki, Kawahara, Masahiro, Nakabo, Yukiharu, Takaori-Kondo, Akifumi, Yoshida, Yataro

    Published in International journal of hematology (01-06-2016)
    “…X-linked sideroblastic anemia (XLSA) is a rare hereditary disorder that typically manifests in males as microcytic anemia. Here, we report a family with XLSA…”
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    Co-occurrence of monoclonal gammopathy and myelodysplasia: a retrospective study of fourteen cases by Yoshida, Yataro, Oguma, Shigeru, Ohno, Hitoshi, Nakabo, Yukiharu, Katsurada, Tatsuya, Kawahara, Masahiro, Kawabata, Hiroshi

    Published in International journal of hematology (01-06-2014)
    “…We report a series of 14 patients with myelodysplastic syndrome (MDS) accompanied by a monoclonal gammopathy unrelated to therapy. Twelve of these had…”
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    Evolving New Treatment for Myelodysplastic Syndromes by YOSHIDA, Yataro

    Published in International journal of hematology (01-11-2007)
    “…Over the last several years, there has been substantial progress in the definition, diagnosis, and management of myelodysplastic syndromes (MDSs). This…”
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    Absent or Extremely Low Neutrophil Alkaline Phosphatase Activity Levels in Patients with Myelodysplastic Syndromes by Yoshida, Yataro, Katsurada, Tatsuya, Oguma, Shigeru, Nakabo, Yukiharu, Yoshinaga, Noriyoshi, Kawahara, Masahiro, Kawabata, Hiroshi

    Published in Internal Medicine (01-01-2013)
    “…Three patients with myelodysplastic syndrome (MDS) had absent or extremely low levels of neutrophil alkaline phosphatase (NAP) activity (arbitrarily defined as…”
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    Clinical implications of blast immunophenotypes in myelodysplastic syndromes by Ogata, Kiyoyuki, Yoshida, Yataro

    Published in Leukemia & lymphoma (01-09-2005)
    “…Myelodysplastic syndromes (MDS) are malignant disorders of hematopoietic cells. For many neoplasms, immunophenotype data of the neoplastic cells provide…”
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    Immune Pancytopenia Associated with a Leukemic B-Cell Tumor Carrying t(14;18)(q32;q21) Translocation by Mizumoto, Chisaki, Ohno, Hitoshi, Katsurada, Tatsuya, Oguma, Shigeru, Yoshida, Yataro

    Published in Internal Medicine (01-01-2011)
    “…We report a 75-year-old man who was initially suggested to have acute leukemia. The hemoglobin level was 3.8 g/dL, white cell count was 7,700/μL with an…”
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    The duration of functioning of a subcutaneous implantable port for the treatment of hematological tumors: a single institution-based study by Ohno, Hitoshi, Mizumoto, Chisaki, Otsuki, Yoshihiro, Oguma, Shigeru, Yoshida, Yataro

    Published in International journal of clinical oncology (01-04-2010)
    “…Background Although subcutaneous implantable ports have been indicated as venous access for chemotherapy, these devices have not been used routinely for…”
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    Angioimmunoblastic T-Cell Lymphoma Initially Presenting with Replacement of Bone Marrow and Peripheral Plasmacytosis by Sakai, Hisashi, Tanaka, Hideaki, Katsurada, Tatsuya, Yoshida, Yataro, Okamoto, Eiichi, Ohno, Hitoshi

    Published in Internal Medicine (01-01-2007)
    “…A 73-year-old man presented with lymphadenopathy, hepatosplenomegaly, and a variety of hematological and immunological abnormalities. The bone marrow was…”
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    Interferon-alfa Treatment of Essential Thrombocythemia during Pregnancy by Iwashita, Toshiko, Fujitani, Mayumi, Yamamoto, Yoshiaki, Katsurada, Tatsuya, Yoshida, Yataro

    Published in Internal Medicine (01-01-2006)
    “…We report on 2 successful pregnancies in a young woman who has essential thrombocythemia. The platelet count remained well controlled with interferon-alfa…”
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    Polyclonal proliferation of plasma cells associated with marked hypergammaglobulinemia in an elderly patient by OHNO, Hitoshi, TANAKA, Hideaki, SAKAI, Hisashi, KATSURADA, Tatsuya, YOSHIDA, Yataro

    Published in International journal of hematology (01-01-2005)
    “…We describe an 89-year-old woman who presented with prominent plasmacytosis mimicking plasma cell leukemia. The apparent serum M-protein level of > 7 g/dL of…”
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