Kawamura N - Search Results

1

Fusarium falciforme infection in a patient with chronic granulomatous disease: Unique long-term course of epidural abscess.

Okura Y, Kawamura N, Okano M, Toita N, Takezaki S, Yamada M, Kobayashi I, Ariga T. Okura Y, et al. Among authors: kawamura n. Pediatr Int. 2015;57(1):e4-6. doi: 10.1111/ped.12458. Pediatr Int. 2015. PMID: 25711271

2

Somatic mosaicism in two unrelated patients with X-linked chronic granulomatous disease characterized by the presence of a small population of normal cells.

Yamada M, Okura Y, Suzuki Y, Fukumura S, Miyazaki T, Ikeda H, Takezaki S, Kawamura N, Kobayashi I, Ariga T. Yamada M, et al. Among authors: kawamura n. Gene. 2012 Apr 10;497(1):110-5. doi: 10.1016/j.gene.2012.01.019. Epub 2012 Jan 28. Gene. 2012. PMID: 22305980

3

Stem cell transplantation in primary immunodeficiency disease patients.

Sato T, Kobayashi R, Toita N, Kaneda M, Hatano N, Iguchi A, Kawamura N, Ariga T. Sato T, et al. Among authors: kawamura n. Pediatr Int. 2007 Dec;49(6):795-800. doi: 10.1111/j.1442-200X.2007.02468.x. Pediatr Int. 2007. PMID: 18045274

4

Early diagnosis for polyarthritis of juvenile idiopathic arthritis using systemic gallium scintigraphy.

Yamazaki S, Okano M, Toita N, Hatano N, Kobayashi I, Kawamura N, Kobayashi K. Yamazaki S, et al. Among authors: kawamura n. Pediatr Int. 2009 Aug;51(4):587-90. doi: 10.1111/j.1442-200X.2009.02873.x. Pediatr Int. 2009. PMID: 19674372 No abstract available.

5

X-linked agammaglobulinemia in a 10-year-old boy with a novel non-invariant splice-site mutation in Btk gene.

Maekawa K, Yamada M, Okura Y, Sato Y, Yamada Y, Kawamura N, Ariga T. Maekawa K, et al. Among authors: kawamura n. Blood Cells Mol Dis. 2010 Apr 15;44(4):300-4. doi: 10.1016/j.bcmd.2010.01.004. Epub 2010 Feb 1. Blood Cells Mol Dis. 2010. PMID: 20122858

6

Determination of the deletion breakpoints in two patients with contiguous gene syndrome encompassing CYBB gene.

Yamada M, Arai T, Oishi T, Hatano N, Kobayashi I, Kubota M, Suzuki N, Yoda M, Kawamura N, Ariga T. Yamada M, et al. Among authors: kawamura n. Eur J Med Genet. 2010 Nov-Dec;53(6):383-8. doi: 10.1016/j.ejmg.2010.08.003. Epub 2010 Sep 21. Eur J Med Genet. 2010. PMID: 20813210

7

Anti-melanoma differentiation-associated gene 5 antibody is a diagnostic and predictive marker for interstitial lung diseases associated with juvenile dermatomyositis.

Kobayashi I, Okura Y, Yamada M, Kawamura N, Kuwana M, Ariga T. Kobayashi I, et al. Among authors: kawamura n. J Pediatr. 2011 Apr;158(4):675-7. doi: 10.1016/j.jpeds.2010.11.033. Epub 2011 Jan 13. J Pediatr. 2011. PMID: 21232756

8

Novel compound heterozygous mutations in the C3 gene: hereditary C3 deficiency.

Okura Y, Yamada M, Takezaki S, Nawate M, Takahashi Y, Kida M, Kawamura N, Ariga T. Okura Y, et al. Among authors: kawamura n. Pediatr Int. 2011 Apr;53(2):e16-9. doi: 10.1111/j.1442-200X.2010.03259.x. Pediatr Int. 2011. PMID: 21501302 No abstract available.

9

Arthritis associated with Kawasaki disease: MRI findings and serum matrix metalloproteinase-3 profiles.

Izumi G, Narugami M, Saita Y, Matsuzawa T, Sugawara O, Kawamura N, Kobayashi I. Izumi G, et al. Among authors: kawamura n. Pediatr Int. 2011 Dec;53(6):1087-9. doi: 10.1111/j.1442-200X.2011.03393.x. Pediatr Int. 2011. PMID: 22181570 No abstract available.

10

Elevated serum levels of soluble interleukin-2 receptor in juvenile dermatomyositis.

Kobayashi I, Ono S, Kawamura N, Okano M, Kobayashi K. Kobayashi I, et al. Among authors: kawamura n. Pediatr Int. 2001 Feb;43(1):109-11. doi: 10.1046/j.1442-200x.2001.01367.x. Pediatr Int. 2001. PMID: 11208016 No abstract available.

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