Kimura H - Search Results

1

Fetal origin of the GATA1 mutation in identical twins with transient myeloproliferative disorder and acute megakaryoblastic leukemia accompanying Down syndrome.

Shimada A, Xu G, Toki T, Kimura H, Hayashi Y, Ito E. Shimada A, et al. Among authors: kimura h. Blood. 2004 Jan 1;103(1):366. doi: 10.1182/blood-2003-09-3219. Blood. 2004. PMID: 14684662 Free article. No abstract available.

2

Proinflammatory cytokinemia associated with transient myeloproliferative disorder in down syndrome.

Shimada A, Maruyama K, Shitara T, Kato M, Cho K, Kobayashi T, Fujiu T, Tsuchida Y, Nishida A, Hayashi Y, Minakami H, Kozawa K, Kimura H. Shimada A, et al. Among authors: kimura h. Biol Neonate. 2004;85(3):167-72. doi: 10.1159/000075376. Epub 2003 Dec 10. Biol Neonate. 2004. PMID: 14671434

3

Oligoclonal expansion of T lymphocytes with multiple second-site mutations leads to Omenn syndrome in a patient with RAG1-deficient severe combined immunodeficiency.

Wada T, Toma T, Okamoto H, Kasahara Y, Koizumi S, Agematsu K, Kimura H, Shimada A, Hayashi Y, Kato M, Yachie A. Wada T, et al. Among authors: kimura h. Blood. 2005 Sep 15;106(6):2099-101. doi: 10.1182/blood-2005-03-0936. Epub 2005 Apr 21. Blood. 2005. PMID: 15845893 Free article.

4

Pro-inflammatory cytokinemia is frequently found in Down syndrome patients with hematological disorders.

Shimada A, Hayashi Y, Ogasawara M, Park MJ, Katoh M, Minakami H, Kitoh T, Kojima S, Kawa K, Kimura H. Shimada A, et al. Among authors: kimura h. Leuk Res. 2007 Sep;31(9):1199-203. doi: 10.1016/j.leukres.2006.09.008. Epub 2006 Oct 19. Leuk Res. 2007. PMID: 17055049

5

AML1 mutation and FLT3-internal tandem duplication in leukemia transformed from myelodysplastic syndrome.

Shimada A, Taketani T, Kikuchi A, Hanada R, Arakawa H, Kimura H, Chen Y, Hayashi Y. Shimada A, et al. Among authors: kimura h. J Pediatr Hematol Oncol. 2007 Sep;29(9):666-7. doi: 10.1097/MPH.0b013e318142ac2f. J Pediatr Hematol Oncol. 2007. PMID: 17805050 No abstract available.

6

Omenn syndrome--review of several phenotypes of Omenn syndrome and RAG1/RAG2 mutations in Japan.

Kato M, Kimura H, Seki M, Shimada A, Hayashi Y, Morio T, Kumaki S, Ishida Y, Kamachi Y, Yachie A. Kato M, et al. Among authors: kimura h. Allergol Int. 2006 Jun;55(2):115-9. doi: 10.2332/allergolint.55.115. Allergol Int. 2006. PMID: 17075247 Free article. Review.

7

Cytomegalovirus retinitis during maintenance therapy for T-cell acute lymphoblastic leukemia.

Wakai K, Sano H, Shimada A, Shiozawa Y, Park MJ, Sotomatsu M, Yanagisawa R, Koike K, Kozawa K, Ryo A, Tsukagoshi H, Kimura H, Hayashi Y. Wakai K, et al. Among authors: kimura h. J Pediatr Hematol Oncol. 2013 Mar;35(2):162-3. doi: 10.1097/MPH.0b013e318279e920. J Pediatr Hematol Oncol. 2013. PMID: 23242328 No abstract available.

8

Sustained cytokinemia and chemokinemia concomitant with juvenile myelomonocytic leukemia in an infant with Noonan syndrome.

Okazaki K, Unemoto J, Kondo M, Kusaka T, Kozawa K, Yoshizumi M, Shimada A, Takita J, Kaneko T, Hama T, Kimura H. Okazaki K, et al. Among authors: kimura h. Leuk Res. 2010 Sep;34(9):e226-8. doi: 10.1016/j.leukres.2010.03.018. Epub 2010 Apr 24. Leuk Res. 2010. PMID: 20417558 No abstract available.

9

Role of eosinophils and their clinical significance in allergic inflammation.

Kato M, Suzuki M, Hayashi Y, Kimura H. Kato M, et al. Among authors: kimura h. Expert Rev Clin Immunol. 2006 Jan;2(1):121-33. doi: 10.1586/1744666X.2.1.121. Expert Rev Clin Immunol. 2006. PMID: 20477093

10

Prominent eosinophilia but less eosinophil activation in a patient with Omenn syndrome.

Seki M, Kimura H, Mori A, Shimada A, Yamada Y, Maruyama K, Hayashi Y, Agematsu K, Morio T, Yachie A, Kato M. Seki M, et al. Among authors: kimura h. Pediatr Int. 2010 Aug;52(4):e196-9. doi: 10.1111/j.1442-200X.2010.03135.x. Pediatr Int. 2010. PMID: 20958863 No abstract available.

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