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Nihon Ketsueki Gakkai Zasshi : Journal of Japan Haematological Society|July 1, 1989
Acidified glycerol lysis test (AGLT) studies in JapanN Meyerstein, T Shimomura, K Fujimura, et al.
American Journal of Hematology|January 1, 1978
Glutathione reductase deficiency in a kindred with hereditary spherocytosisK Nakashima, K Yamauchi, S Miwa, et al.
[Rinsho Ketsueki] the Japanese Journal of Clinical Hematology|June 1, 1989
[Multiple myeloma following chronic neutrophilia terminated with acute monocytic leukemia (AML, M 5 b)]K Abe, N Imamura, D M Mtasiwa, et al.
International Journal of Hematology|October 1, 1996
Expression and functional characterization of the P-selectin glycoprotein ligand-1 in various cellsT T Fujimoto, M Noda, T Takafuta, et al.
Thrombosis and Haemostasis|February 19, 1990
Analysis of platelet cytoskeleton assembly during platelet activation in Hermansky-Pudlak syndrome and thrombastheniaK Fujimura, T Fujimoto, M Takemoto, et al.
Nihon Ketsueki Gakkai Zasshi : Journal of Japan Haematological Society|May 1, 1989
[A case of refractory multiple myeloma demonstrating a relationship between the progression of the disease and in vitro myeloma cells activity]K Iwato, H Asaoku, O Tanabe, et al.
Thrombosis and Haemostasis|November 1, 1994
Expression of platelet membrane glycoprotein V in human megakaryocytes and megakaryocytic cell lines: a study using a novel monoclonal antibody against GPVT Takafuta, K Fujimura, H Kawano, et al.
British Journal of Haematology|December 1, 1996
Oligoclonal accumulation of T cells in peripheral blood from patients with idiopathic thrombocytopenic purpuraT Shimomura, K Fujimura, T Takafuta, et al.
[Rinsho Ketsueki] the Japanese Journal of Clinical Hematology|December 1, 1989
[Thrombotic thrombocytopenic purpura which was effectively treated by plasma exchange therapy--involvement of vWF and endothelial cell injury]H Tanaka, S Kusumi, M Takemoto, et al.
Thrombosis and Haemostasis|June 1, 1997
Molecular and genetic analysis of two patients with Bernard-Soulier syndrome--identification of new mutations in glycoprotein Ib alpha geneT Kanaji, T Okamura, M Kurolwa, et al.
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