Search Results - "ATA, Kazuyuki"

Good prognosis of patients with acute promyelocytic leukemia who achieved second complete remission (CR) with a new retinoid, Am80, after relapse from CR induced by all-trans-retinoic acid by Shinjo, K, Takeshita, A, Ohnishi, K, Sakura, T, Miyawaki, S, Hiraoka, A, Takeuchi, M, Tomoyasu, S, Wakita, H, Ata, K, Fukutani, H, Ueda, R, Ohno, R

“…A new synthetic retinoid, Am80, is effective in treating acute promyelocytic leukemia relapsed from all-trans-retinoic acid-induced complete remission (CR). We…”
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Norwegian scabies in a patient with chronic adult T-cell leukemia by WADA, Hideho, ATA, Kazuyuki, HASHIMOTO, Masashi, SUGIHARA, Takashi, YAMADA, Osamu, YAWATA, Yoshihito

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Ectopic production of amylase by a non-producing type of multiple myeloma by Wada, H, Ohtsuki, T, Sugihara, T, Ata, K, Hashimoto, M, Yamada, O, Yawata, Y, Manabe, T, Miyamoto, K

“…The patient was a 64-year-old woman who was admitted to our hospital because of lumbago. A diagnosis of multiple myeloma (non-producing type) was made, based…”
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Effective vinca-alkaloid slow infusion therapy of refractory idiopathic thrombocytopenic purpura by Wada, H, Ata, K, Shirato, L, Mori, H, Sugihara, T, Yawata, Y

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Hereditary stomatocytosis of the hydrocytosis type: a report of one family and red cell membrane studies by Kida, T, Nakamura, H, Kuroki, T, Mizoguchi, Y, Kobayashi, K, Yamane, T, Im, T, Tatsumi, N, Ata, K, Wada, H

“…A case of hereditary stomatocytosis with hemolytic anemia, increased autohemolysis, increased osmotic fragility, and shortened erythrocyte survival is…”
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An alanine-to-threonine substitution in protein 4.2 cDNA is associated with a Japanese form of hereditary hemolytic anemia (protein 4.2NIPPON) by Bouhassira, E E, Schwartz, R S, Yawata, Y, Ata, K, Kanzaki, A, Qiu, J J, Nagel, R L, Rybicki, A C

“…Erythrocyte (RBC) protein 4.2 (P4.2)-deficiency observed in Japanese individuals results in a hemolytic anemia associated with abnormally shaped (spherocytic,…”
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Molecular characterization and nonradioactive detection of beta-thalassemia in Malaysia by Fucharoen, S, Fucharoen, G, Ata, K, Aziz, S, Hashim, S, Hassan, K, Fukumaki, Y

“…The spectrum of beta-thalassemia mutations in Malaysia has been determined in 45 beta-thalassemia chromosomes using dot blot hybridization of the polymerase…”
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Norwegian scabies in a patient with chronic adult T-cell leukemia by WADA, Hideho, ATA, Kazuyuki, HASHIMOTO, Masashi, SUGIHARA, Takashi, YAMADA, Osamu, YAWATA, Yoshihito

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