Sato T - Search Results

1

A novel mutation (Gln433Glu) in exon 12 combined with the G insertion in exon 13 causes severe factor XI deficiency in Japanese patients.

Ishikawa N, Okada S, Sato T, Yasunaga S, Ohtsubo M, Takihara Y, Kobayashi M. Ishikawa N, et al. Among authors: sato t. Blood Coagul Fibrinolysis. 2007 Jul;18(5):519-23. doi: 10.1097/MBC.0b013e328133f553. Blood Coagul Fibrinolysis. 2007. PMID: 17581330

2

A comparison of the defective granulopoiesis in childhood cyclic neutropenia and in severe congenital neutropenia.

Sera Y, Kawaguchi H, Nakamura K, Sato T, Habara M, Okada S, Ishikawa N, Kojima S, Katoh O, Kobayashi M. Sera Y, et al. Among authors: sato t. Haematologica. 2005 Aug;90(8):1032-41. Haematologica. 2005. PMID: 16079102

3

Significance of the detection of antineutrophil antibodies in children with chronic neutropenia.

Kobayashi M, Nakamura K, Kawaguchi H, Sato T, Kihara H, Hiraoka A, Tanihiro M, Taniguchi K, Takata N, Ueda K. Kobayashi M, et al. Among authors: sato t. Blood. 2002 May 1;99(9):3468-71. doi: 10.1182/blood.v99.9.3468. Blood. 2002. PMID: 11964321 Free article.

4

Defects of granulopoiesis in patients with severe congenital neutropenia.

Nakamura K, Kobayashi M, Konishi N, Kawaguchi H, Miyagawa S, Sato T, Katoh O, Ueda K. Nakamura K, et al. Among authors: sato t. Hiroshima J Med Sci. 2002 Sep;51(3):63-74. Hiroshima J Med Sci. 2002. PMID: 12422946

5

Management of advanced-stage neuroblastoma in a patient with 21-hydroxalase deficiency.

Utsunomiya AN, Okada S, Hara K, Miki M, Mizoguchi Y, Kobayashi Y, Miyagawa S, Jinno K, Nakamura K, Sato T, Kobayashi M. Utsunomiya AN, et al. Among authors: sato t. Pediatr Int. 2013 Aug;55(4):e96-9. doi: 10.1111/ped.12093. Pediatr Int. 2013. PMID: 23910817

6

Deficiency of regulatory T cells in children with autoimmune neutropenia.

Nakamura K, Miki M, Mizoguchi Y, Karakawa S, Sato T, Kobayashi M. Nakamura K, et al. Among authors: sato t. Br J Haematol. 2009 Jun;145(5):642-7. doi: 10.1111/j.1365-2141.2009.07662.x. Epub 2009 Mar 26. Br J Haematol. 2009. PMID: 19344427 Free article.

7

Successful treatment with liposteroid followed by reduced intensity stem cell transplantation in an infant with perforin deficiency presenting with hemophagocytic lymphohistiocytosis.

Kobayashi Y, Salih HM, Kajiume T, Nakamura K, Miyagawa S, Sato T, Nishimura S, Kobayashi M. Kobayashi Y, et al. Among authors: sato t. J Pediatr Hematol Oncol. 2007 Mar;29(3):178-82. doi: 10.1097/MPH.0b013e3180335030. J Pediatr Hematol Oncol. 2007. PMID: 17356398

8

Dysregulation of transcriptions in primary granule constituents during myeloid proliferation and differentiation in patients with severe congenital neutropenia.

Kawaguchi H, Kobayashi M, Nakamura K, Konishi N, Miyagawa S, Sato T, Toyoda H, Komada Y, Kojima S, Todoroki Y, Ueda K, Katoh O. Kawaguchi H, et al. Among authors: sato t. J Leukoc Biol. 2003 Feb;73(2):225-34. doi: 10.1189/jlb.0902427. J Leukoc Biol. 2003. PMID: 12554799

9

Short-term culture of umbilical cord blood-derived CD34 cells enhances engraftment into NOD/SCID mice through increased CXCR4 expression.

Ohno N, Kajiume T, Sera Y, Sato T, Kobayashi M. Ohno N, et al. Among authors: sato t. Stem Cells Dev. 2009 Oct;18(8):1221-6. doi: 10.1089/scd.2008.0298. Stem Cells Dev. 2009. PMID: 19113880

10

Efficacy of prophylactic use of trimethoprim-sulfamethoxazole in autoimmune neutropenia in infancy.

Kobayashi M, Sato T, Kawaguchi H, Nakamura K, Kihara H, Hiraoka A, Tanihiro M, Taniguchi K, Takata N, Ueda K. Kobayashi M, et al. Among authors: sato t. J Pediatr Hematol Oncol. 2003 Jul;25(7):553-7. doi: 10.1097/00043426-200307000-00011. J Pediatr Hematol Oncol. 2003. PMID: 12847323

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