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Kazunori Nakase

Researcher at Mie University

Publications -  79
Citations -  1573

Kazunori Nakase is an academic researcher from Mie University. The author has contributed to research in topics: Leukemia & Myeloid leukemia. The author has an hindex of 21, co-authored 77 publications receiving 1486 citations. Previous affiliations of Kazunori Nakase include Westmead Hospital.

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Phenotypical characteristics of acute myelocytic leukemia associated with the t(8;21)(q22;q22) chromosomal abnormality: frequent expression of immature B-cell antigen CD19 together with stem cell antigen CD34.

TL;DR: The findings indicate that leukemic blasts of t(8;21) AML commonly express CD19 while preserving the stem cell-associated antigens, and differentiate into the granulocytic pathway with discordant maturation such as low CD33 expression.
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Fatal Trichosporon fungemia in patients with hematologic malignancies.

TL;DR: At present, the diagnosis of invasive trichosporonosis depends on blood culture studies, and the mortality of this disease is high; however, azole therapy and control of blood glucose level, together with hematopoietic recovery could help in improving the clinical outcome.
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Clinical Importance of CD7 Expression in Acute Myelocytic Leukemia

TL;DR: In this article, 40 patients with CD7 + acute myelocytic leukemia (AML) were investigated; they were classified into the following subgroups according to French-American-British classification: 15 M1, 18 M2, 3 M4, and 4 MS.
Journal Article

Clinical importance of CD7 expression in acute myelocytic leukemia. The Japan Cooperative Group of Leukemia/Lymphoma

TL;DR: The results presented here indicate the diagnostic importance ofCD7 positivity in AML, suggesting that the cellular and clinical characteristics of CD7+ AML are sufficient for it to be recognized as a distinct category of AML.
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Clinical importance of CD7 expression in acute myelocytic leukemia. The Japan Cooperative Group of Leukemia/Lymphoma [see comments]

TL;DR: Patients with CD7+ acute myelocytic leukemia (AML) were investigated; they were classified into the following subgroups according to French-American-British classification: 15 M1, 18 M2, 3 M4, and 4 M5.