Nakamura K - Search Results

1

Heterozygosity for the Y701C STAT1 mutation in a multiplex kindred with multifocal osteomyelitis.

Hirata O, Okada S, Tsumura M, Kagawa R, Miki M, Kawaguchi H, Nakamura K, Boisson-Dupuis S, Casanova JL, Takihara Y, Kobayashi M. Hirata O, et al. Among authors: nakamura k. Haematologica. 2013 Oct;98(10):1641-9. doi: 10.3324/haematol.2013.083741. Epub 2013 Apr 12. Haematologica. 2013. PMID: 23585529 Free PMC article.

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: nakamura k. Haematologica. 2005 Aug;90(8):1032-41. Haematologica. 2005. PMID: 16079102

3

Central nervous system complications and neuroradiological findings in children with chronic active Epstein-Barr virus infection.

Ishikawa N, Kawaguchi H, Nakamura K, Kobayashi M. Ishikawa N, et al. Among authors: nakamura k. Pediatr Int. 2013 Feb;55(1):72-8. doi: 10.1111/ped.12024. Pediatr Int. 2013. PMID: 23240920

4

Identification of the integrin β3 L718P mutation in a pedigree with autosomal dominant thrombocytopenia with anisocytosis.

Kobayashi Y, Matsui H, Kanai A, Tsumura M, Okada S, Miki M, Nakamura K, Kunishima S, Inaba T, Kobayashi M. Kobayashi Y, et al. Among authors: nakamura k. Br J Haematol. 2013 Feb;160(4):521-9. doi: 10.1111/bjh.12160. Epub 2012 Dec 17. Br J Haematol. 2013. PMID: 23253071 Free article.

5

A case of neonatal coxsackie B2 meningo-encephalitis in which serial magnetic resonance imaging findings reveal the development of lesions.

Hirata O, Ishikawa N, Mizoguchi Y, Nakamura K, Kobayashi M. Hirata O, et al. Among authors: nakamura k. Neuropediatrics. 2011 Aug;42(4):156-8. doi: 10.1055/s-0031-1285876. Epub 2011 Aug 29. Neuropediatrics. 2011. PMID: 21877311

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. 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

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: nakamura k. Pediatr Int. 2013 Aug;55(4):e96-9. doi: 10.1111/ped.12093. Pediatr Int. 2013. PMID: 23910817

8

Effective Treatment of a Childhood Blastic Plasmacytoid Dendritic Cell Neoplasm with a Cutaneous Tumor Alone by Stem Cell Transplantation with Reduced Intensity Conditioning.

Shimomura M, Asano T, Furue A, Miki M, Sera Y, Kawaguchi H, Nakamura K, Kobayashi M. Shimomura M, et al. Among authors: nakamura k. Indian J Hematol Blood Transfus. 2016 Jun;32(Suppl 1):26-31. doi: 10.1007/s12288-015-0543-0. Epub 2015 Apr 21. Indian J Hematol Blood Transfus. 2016. PMID: 27408349 Free PMC article.

9

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: nakamura k. Blood. 2002 May 1;99(9):3468-71. doi: 10.1182/blood.v99.9.3468. Blood. 2002. PMID: 11964321 Free article.

10

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. Hiroshima J Med Sci. 2002 Sep;51(3):63-74. Hiroshima J Med Sci. 2002. PMID: 12422946

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