Kodama A - Search Results

1

Karyotypically independent clones with del(11q) and trisomy 10 in acute myeloid leukemia: trisomy 10 may appear as an additional change.

Gotoh M, Sasaki Y, Iguchi T, Fujimoto H, Kodama A, Kiyoi H, Naoe T, Ohyashiki K. Gotoh M, et al. Among authors: kodama a. Int J Hematol. 2008 Jul;88(1):123-124. doi: 10.1007/s12185-008-0109-0. Epub 2008 Jun 20. Int J Hematol. 2008. PMID: 18566741 No abstract available.

2

De novo appearance of t(7;13)(q10;q33) in the leukemic phase of myelodysplastic syndrome: a case report.

Iguchi T, Sashida G, Kawakubo K, Tauchi T, Kodama A, Fukutake K, Ohyashiki K. Iguchi T, et al. Among authors: kodama a. Jpn J Clin Oncol. 2002 Jan;32(1):35-6. doi: 10.1093/jjco/hyf006. Jpn J Clin Oncol. 2002. PMID: 11932362

3

Recurrent der(9;18) in essential thrombocythemia with JAK2 V617F is highly linked to myelofibrosis development.

Ohyashiki K, Kodama A, Ohyashiki JH. Ohyashiki K, et al. Among authors: kodama a. Cancer Genet Cytogenet. 2008 Oct;186(1):6-11. doi: 10.1016/j.cancergencyto.2008.04.021. Cancer Genet Cytogenet. 2008. PMID: 18786436

4

Cytogenetics in myelodysplastic syndromes.

Ohyashiki K, Kodama A, Ohyashiki JH. Ohyashiki K, et al. Among authors: kodama a. Methods Mol Biol. 2011;730:79-88. doi: 10.1007/978-1-61779-074-4_6. Methods Mol Biol. 2011. PMID: 21431635

5

Non-random chromosomal deletion clustering at 20q in Waldenström macroglobulinemia.

Kitahara T, Umezu T, Ando K, Kodama A, Ohyashiki JH, Ohyashiki K. Kitahara T, et al. Among authors: kodama a. Hematology. 2011 May;16(3):139-42. doi: 10.1179/102453311X12953015767338. Hematology. 2011. PMID: 21669052 Free article.

6

Trisomy 10 in acute myeloid leukemia.

Ohyashiki K, Kodama A, Nakamura H, Wakasugi K, Uchida H, Shirota T, Ito H, Toyama K. Ohyashiki K, et al. Among authors: kodama a. Cancer Genet Cytogenet. 1996 Jul 15;89(2):114-7. doi: 10.1016/0165-4608(95)00263-4. Cancer Genet Cytogenet. 1996. PMID: 8697414

7

A sole del(15q) anomaly in post-myelodysplasia acute myeloid leukemia.

Yahata N, Ohyashiki K, Iwase O, Kimura Y, Kodama A, Fukutake K, Toyama K. Yahata N, et al. Among authors: kodama a. Leuk Res. 1998 Sep;22(9):845-7. doi: 10.1016/s0145-2126(98)00019-8. Leuk Res. 1998. PMID: 9716017 Review.

8

Additional cytogenetic changes and previous genotoxic exposure predict unfavorable prognosis in myelodysplastic syndromes and acute myeloid leukemia with der(1;7)(q10;p10).

Hsiao HH, Sashida G, Ito Y, Kodama A, Fukutake K, Ohyashiki JH, Ohyashiki K. Hsiao HH, et al. Among authors: kodama a. Cancer Genet Cytogenet. 2006 Mar;165(2):161-6. doi: 10.1016/j.cancergencyto.2005.09.003. Cancer Genet Cytogenet. 2006. PMID: 16527611

9

Deletion (20q) as the sole abnormality in Waldenström macroglobulinemia suggests distinct pathogenesis of 20q11 anomaly.

Liu YC, Miyazawa K, Sashida G, Kodama A, Ohyashiki K. Liu YC, et al. Among authors: kodama a. Cancer Genet Cytogenet. 2006 Aug;169(1):69-72. doi: 10.1016/j.cancergencyto.2006.03.013. Cancer Genet Cytogenet. 2006. PMID: 16875940

10

Risk factor analysis in myelodysplastic syndrome patients with del(20q): prognosis revisited.

Liu YC, Ito Y, Hsiao HH, Sashida G, Kodama A, Ohyashiki JH, Ohyashiki K. Liu YC, et al. Among authors: kodama a. Cancer Genet Cytogenet. 2006 Nov;171(1):9-16. doi: 10.1016/j.cancergencyto.2006.06.003. Cancer Genet Cytogenet. 2006. PMID: 17074585

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