Nakakuma H - Search Results

1

Paroxysmal nocturnal haemoglobinuria clones in patients with myelodysplastic syndromes.

Iwanaga M, Furukawa K, Amenomori T, Mori H, Nakamura H, Fuchigami K, Kamihira S, Nakakuma H, Tomonaga M. Iwanaga M, et al. Among authors: nakakuma h. Br J Haematol. 1998 Jul;102(2):465-74. doi: 10.1046/j.1365-2141.1998.00794.x. Br J Haematol. 1998. PMID: 9695961 Free article.

2

NKG2D-mediated immunity underlying paroxysmal nocturnal haemoglobinuria and related bone marrow failure syndromes.

Hanaoka N, Nakakuma H, Horikawa K, Nagakura S, Tsuzuki Y, Shimanuki M, Kojima K, Yonemura Y, Kawaguchi T. Hanaoka N, et al. Among authors: nakakuma h. Br J Haematol. 2009 Sep;146(5):538-45. doi: 10.1111/j.1365-2141.2009.07795.x. Epub 2009 Jul 6. Br J Haematol. 2009. PMID: 19594748 Free article.

3

Paroxysmal nocturnal haemoglobinuria with coexisting deficiency of the ninth component of complement: lack of massive haemolytic attack.

Yonemura Y, Kawakita M, Koito A, Kawaguchi T, Nakakuma H, Kagimoto T, Schichishima T, Terasawa T, Akagaki Y, Inai S. Yonemura Y, et al. Among authors: nakakuma h. Br J Haematol. 1990 Jan;74(1):108-13. doi: 10.1111/j.1365-2141.1990.tb02546.x. Br J Haematol. 1990. PMID: 2310692

4

Establishment of a human T-cell line with deficient surface expression of glycosylphosphatidylinositol (GPI)-anchored proteins from a patient with paroxysmal nocturnal haemoglobinuria.

Masuda T, Yonemura Y, Fujimoto K, Hidaka M, Nagakura S, Nakakuma H, Hata H, Sanada I, Kawakita M, Takatsuki K. Masuda T, et al. Among authors: nakakuma h. Br J Haematol. 1994 May;87(1):24-30. doi: 10.1111/j.1365-2141.1994.tb04865.x. Br J Haematol. 1994. PMID: 7524616

5

Two cases showing clonal progression with full evolution from aplastic anemia-paroxysmal nocturnal hemoglobinuria syndrome to myelodysplastic syndromes and leukemia.

Ishihara S, Nakakuma H, Kawaguchi T, Nagakura S, Horikawa K, Hidaka M, Asou N, Mitsuya H. Ishihara S, et al. Among authors: nakakuma h. Int J Hematol. 2000 Aug;72(2):206-9. Int J Hematol. 2000. PMID: 11039670

6

Apoptosis resistance of blood cells from patients with paroxysmal nocturnal hemoglobinuria, aplastic anemia, and myelodysplastic syndrome.

Horikawa K, Nakakuma H, Kawaguchi T, Iwamoto N, Nagakura S, Kagimoto T, Takatsuki K. Horikawa K, et al. Among authors: nakakuma h. Blood. 1997 Oct 1;90(7):2716-22. Blood. 1997. PMID: 9326238 Free article.

7

Occupancy of whole blood cells by a single PIGA-mutant clone with HMGA2 amplification in a paroxysmal nocturnal haemoglobinuria patient having blood cells with NKG2D ligands.

Hanaoka N, Murakami Y, Nagata M, Horikawa K, Nagakura S, Yonemura Y, Murata S, Sonoki T, Kinoshita T, Nakakuma H. Hanaoka N, et al. Among authors: nakakuma h. Br J Haematol. 2013 Jan;160(1):114-6. doi: 10.1111/bjh.12093. Epub 2012 Oct 18. Br J Haematol. 2013. PMID: 23078078 Free article. No abstract available.

8

Paroxysmal nocturnal hemoglobinuria clone in bone marrow of patients with pancytopenia.

Nakakuma H, Nagakura S, Iwamoto N, Kawaguchi T, Hidaka M, Horikawa K, Kagimoto T, Shido T, Takatsuki K. Nakakuma H, et al. Blood. 1995 Mar 1;85(5):1371-6. Blood. 1995. PMID: 7532041 Free article.

9

Mechanism of intravascular hemolysis in paroxysmal nocturnal hemoglobinuria (PNH).

Nakakuma H. Nakakuma H. Am J Hematol. 1996 Sep;53(1):22-9. doi: 10.1002/(SICI)1096-8652(199609)53:1<22::AID-AJH5>3.0.CO;2-7. Am J Hematol. 1996. PMID: 8813092 Free article. Review.

10

Markedly high plasma erythropoietin and granulocyte-colony stimulating factor levels in patients with paroxysmal nocturnal hemoglobinuria.

Nakakuma H, Nagakura S, Kawaguchi T, Horikawa K, Iwamoto N, Kagimoto T, Takatsuki K. Nakakuma H, et al. Int J Hematol. 1997 Dec;66(4):451-7. doi: 10.1016/s0925-5710(97)00064-9. Int J Hematol. 1997. PMID: 9479872

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