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Results: 1-9 |
Results: 9
Long-term outcome of treatment with protocols AL841, AL851, and ALHR88 in children with acute lymphoblastic leukemia: Results obtained by the Kyushu-Yamaguchi Children's Cancer Study Group
Authors: Matsuzaki, A Ishii, E Nagatoshi, Y Eguchi, H Koga, H Yanai, F Inada, H Nibu, K Tamai, Y Akiyoshi, K Nakayama, H Hara, T Take, H Miyazaki, S Okamura, J
Citation: A. Matsuzaki et al., Long-term outcome of treatment with protocols AL841, AL851, and ALHR88 in children with acute lymphoblastic leukemia: Results obtained by the Kyushu-Yamaguchi Children's Cancer Study Group, INT J HEMAT, 73(3), 2001, pp. 369-377
Outcome of acute lymphoblastic leukemia in children with AL90 regimen: Impact of response to treatment and sex difference on prognostic factors
Authors: Ishii, E Eguchi, H Matsuzaki, A Koga, H Yanai, F Kuroda, H Kawakami, K Ayukawa, H Akiyoshi, K Kamizono, J Tamai, Y Kinukawa, N Okamura, J
Citation: E. Ishii et al., Outcome of acute lymphoblastic leukemia in children with AL90 regimen: Impact of response to treatment and sex difference on prognostic factors, MED PED ONC, 37(1), 2001, pp. 10-19
Epstein-Barr virus (EBV) load and cytokine gene expression in activated T cells of chronic active EBV infection
Authors: Ohga, S Nomura, A Takada, H Ihara, K Kawakami, K Yanai, F Takahata, Y Tanaka, T Kasuga, N Hara, T
Citation: S. Ohga et al., Epstein-Barr virus (EBV) load and cytokine gene expression in activated T cells of chronic active EBV infection, J INFEC DIS, 183(1), 2001, pp. 1-7
Truncated mutant B subunit for factor XIII causes its deficiency due to impaired intracellular transportation
Authors: Koseki, S Souri, M Koga, S Yamakawa, M Shitishima, T Maruyama, Y Yanai, F Ichinose, A
Citation: S. Koseki et al., Truncated mutant B subunit for factor XIII causes its deficiency due to impaired intracellular transportation, BLOOD, 97(9), 2001, pp. 2667-2672
Truncated mutant B subunit for factor XIII causes its deficiency due to impaired intracellular transportation (vol 97, pg 2667, 2001)
Authors: Koseki, S Souri, M Koga, S Yamakawa, M Shichishima, T Maruyama, Y Yanai, F Ichinose, A
Citation: S. Koseki et al., Truncated mutant B subunit for factor XIII causes its deficiency due to impaired intracellular transportation (vol 97, pg 2667, 2001), BLOOD, 97(12), 2001, pp. 3712-3712
Treatment of childhood acute myelogenous leukemia with allogeneic and autologous stem cell transplantation during the first remission: A report from the Kyushu-Yamaguchi Children's Cancer Study Group in Japan
Authors: Matsuzaki, A Eguchi, H Ikuno, Y Ayukawa, H Yanai, F Ishii, E Sugimoto, T Inada, H Anami, K Nibu, K Hara, T Miyazaki, S Okamura, J
Citation: A. Matsuzaki et al., Treatment of childhood acute myelogenous leukemia with allogeneic and autologous stem cell transplantation during the first remission: A report from the Kyushu-Yamaguchi Children's Cancer Study Group in Japan, PED HEM ONC, 17(8), 2000, pp. 623-634
Treatment of standard-risk acute lymphoblastic leukemia in children: The results of protocol AL841 from the Kyushu-Yamaguchi Children's Cancer Study Group in Japan
Authors: Matsuzaki, A Okamura, J Ishii, E Ikuno, Y Koga, H Eguchi, H Yanai, F Inada, H Nibu, K Hara, T Take, H Miyazaki, S Tasaka, H
Citation: A. Matsuzaki et al., Treatment of standard-risk acute lymphoblastic leukemia in children: The results of protocol AL841 from the Kyushu-Yamaguchi Children's Cancer Study Group in Japan, PED HEM ONC, 16(3), 1999, pp. 187-199
A G to A transition at the last nucleotide of exon 6 of the gamma c gene (868G -> A) may result in either a splice or missense mutation in patients with X-linked severe combined immunodeficiency (vol 104, pg 36, 1999)
Authors: Kanai, N Yanai, F Hirose, S Nibu, K Izuhara, K Tani, T Kubota, T Mitsudome, A
Citation: N. Kanai et al., A G to A transition at the last nucleotide of exon 6 of the gamma c gene (868G -> A) may result in either a splice or missense mutation in patients with X-linked severe combined immunodeficiency (vol 104, pg 36, 1999), HUM GENET, 104(2), 1999, pp. 196-196
A G to A transition at the last nucleotide of exon 6 of the gamma c gene (868G -> A) may result in either a splice or missense mutation in patients with X-linked severe combined immunodeficiency
Authors: Kanai, N Yanai, F Hirose, S Nibu, K Izuhara, K Tani, T Kubota, T Mitsudome, A
Citation: N. Kanai et al., A G to A transition at the last nucleotide of exon 6 of the gamma c gene (868G -> A) may result in either a splice or missense mutation in patients with X-linked severe combined immunodeficiency, HUM GENET, 104(1), 1999, pp. 36-42
Risultati: 1-9 |