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American Journal of Medical Genetics|September 11, 1995
Hereditary spherocytic anemia with deletion of the short arm of chromosome 8N Okamoto, Y Wada, Y Nakamura, et al.International Journal of Hematology|February 1, 1994
Combination chemotherapy with MCNU, vindesine, melphalan, and prednisolone (MCNU-VMP therapy) in induction therapy for multiple myeloma. Japan Myeloma Study GroupY Imamura, T Takagi, Y Yawata, et al.Internal Medicine (Tokyo, Japan)|February 1, 1994
Variant type of congenital stomatocytosisH Morita, H Wada, H Tsujinoue, et al.International Journal of Hematology|July 1, 1994
Red cell membrane disorders in the Japanese population: clinical, biochemical, electron microscopic, and genetic studiesY Yawata, A Kanzaki, T Inoue, et al.[Rinsho Ketsueki] the Japanese Journal of Clinical Hematology|July 1, 1989
[Family of hereditary elliptocytosis with abnormalities of spectrin function (Sp alpha 1/74)]E Okino, C Mori, S Yamazaki, et al.International Journal of Cancer|October 15, 1987
Specific abnormalities of chromosome 14 in patients with acute type of adult T-cell leukemia/lymphomaK Miyamoto, N Tomita, A Ishii, et al.Internal Medicine (Tokyo, Japan)|December 1, 1995
Thalassemia incidentally found by marked erythrocytosis due to an ochre mutation at codon 35 in a Japanese manM Yasunaga, Y Fujiyama, A Miyagawa, et al.Cancer Research|March 23, 2000
Estrogen receptors in human myeloma cellsT Otsuki, O Yamada, J Kurebayashi, et al.[Rinsho Ketsueki] the Japanese Journal of Clinical Hematology|September 14, 1999
[B cell acute lymphocytic leukemia with marked leukocytosis and t(3;15)(q27;q2?2)]K Yata, H Wada, T Sugihara, et al.Cancer Research|January 1, 1991
Establishment and characterization of a human leukemic cell line with megakaryocytic features: dependency on granulocyte-macrophage colony-stimulating factor, interleukin 3, or erythropoietin for growth and survivalN Komatsu, H Nakauchi, A Miwa, et al.Pageof 10