Harashima S - Search Results

1

[A case of systemic sclerosis with crescentic glomerulonephritis associated with perinuclear-antineutrophil cytoplasmic antibody (p-ANCA)].

Harashima S, Yoshizawa S, Horiuchi T, Nakashima H, Niho Y, Kusaba T, Hayashida I, Shinozaki M, Katafuchi R, Hirakata H. Harashima S, et al. Nihon Rinsho Meneki Gakkai Kaishi. 1999 Apr;22(2):86-92. doi: 10.2177/jsci.22.86. Nihon Rinsho Meneki Gakkai Kaishi. 1999. PMID: 11126659 Japanese.

2

Analysis of fas ligand gene mutation in patients with systemic lupus erythematosus.

Kojima T, Horiuchi T, Nishizaka H, Sawabe T, Higuchi M, Harashima SI, Yoshizawa S, Tsukamoto H, Nagasawa K, Niho Y. Kojima T, et al. Among authors: harashima si. Arthritis Rheum. 2000 Jan;43(1):135-9. doi: 10.1002/1529-0131(200001)43:1<135::AID-ANR17>3.0.CO;2-Q. Arthritis Rheum. 2000. PMID: 10643709 Free article.

3

Aberrant HS1 molecule in a patient with systemic lupus erythematosus.

Sawabe T, Horiuchi T, Koga R, Tsukamoto H, Kojima T, Harashima S, Kikuchi Y, Otsuka J, Mitoma H, Yoshizawa S, Niho Y, Watanabe T. Sawabe T, et al. Among authors: harashima s. Genes Immun. 2003 Mar;4(2):122-31. doi: 10.1038/sj.gene.6363932. Genes Immun. 2003. PMID: 12618860

4

An NcoI polymorphism in the human complement component 7 (C7) gene.

Horiuchi T, Nishizaka H, Tsukamoto H, Harashima S, Sawabe T, Morita C, Niho Y. Horiuchi T, et al. Among authors: harashima s. J Hum Genet. 1999;44(4):270-1. doi: 10.1007/s100380050159. J Hum Genet. 1999. PMID: 10429371

5

Outside-to-inside signal through the membrane TNF-alpha induces E-selectin (CD62E) expression on activated human CD4+ T cells.

Harashima S, Horiuchi T, Hatta N, Morita C, Higuchi M, Sawabe T, Tsukamoto H, Tahira T, Hayashi K, Fujita S, Niho Y. Harashima S, et al. J Immunol. 2001 Jan 1;166(1):130-6. doi: 10.4049/jimmunol.166.1.130. J Immunol. 2001. PMID: 11123285

6

[A case of Behçet's disease with chronic and repeated sudden hearing loss: successful treatment with intravenous cyclophosphamide pulse therapy].

Hagiwara N, Harashima S, Tukamoto H, Horiuchi T. Hagiwara N, et al. Among authors: harashima s. Ryumachi. 2001 Oct;41(5):858-63. Ryumachi. 2001. PMID: 11729664 Japanese.

7

Association of tumor necrosis factor receptor type II polymorphism 196R with Systemic lupus erythematosus in the Japanese: molecular and functional analysis.

Morita C, Horiuchi T, Tsukamoto H, Hatta N, Kikuchi Y, Arinobu Y, Otsuka T, Sawabe T, Harashima S, Nagasawa K, Niho Y. Morita C, et al. Among authors: harashima s. Arthritis Rheum. 2001 Dec;44(12):2819-27. doi: 10.1002/1529-0131(200112)44:12<2819::aid-art469>3.0.co;2-2. Arthritis Rheum. 2001. PMID: 11762942 Free article.

8

Behçet's disease associated with complement component 9 (C9) deficiency.

Horiuchi T, Tsukamoto H, Sawabe T, Harashima S, Morita C, Kashiwagi Y, Himeji D, Masumoto K, Otsuka T, Kusaba T, Nagasawa K. Horiuchi T, et al. Among authors: harashima s. Mod Rheumatol. 2000 Dec;10(4):276-8. doi: 10.3109/s101650070017. Mod Rheumatol. 2000. PMID: 24383644

9

Mannose binding lectin (MBL) gene mutation is not a risk factor for systemic lupus erythematosus (SLE) and rheumatoid arthritis (RA) in Japanese.

Horiuchi T, Tsukamoto H, Morita C, Sawabe T, Harashima S, Nakashima H, Miyahara H, Hashimura C, Kondo M. Horiuchi T, et al. Among authors: harashima s. Genes Immun. 2000 Oct;1(7):464-6. doi: 10.1038/sj.gene.6363710. Genes Immun. 2000. PMID: 11196679

10

Defect of lck in a patient with common variable immunodeficiency.

Sawabe T, Horiuchi T, Nakamura M, Tsukamoto H, Nakahara K, Harashima SI, Tsuchiya T, Nakano S. Sawabe T, et al. Among authors: harashima si. Int J Mol Med. 2001 Jun;7(6):609-14. doi: 10.3892/ijmm.7.6.609. Int J Mol Med. 2001. PMID: 11351273

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