川村信明 (Nobuaki Kawamura) - マイポータル - researchmap

基本情報

所属: 北海道大学大学院医学研究科医科学専攻生殖発達医学講座小児科学分野准教授

学位: 医学博士

J-GLOBAL ID: 200901089405428619
researchmap会員ID: 1000246181

研究キーワード

4

研究分野

2

MISC

40

Central nervous system manifestations after steroid pulse therapy in systemic lupus erythematosus

Y Tabata, Kobayashi, I, N Kawamura, M Okano, K Kobayashi

EUROPEAN JOURNAL OF PEDIATRICS 161(9) 503-504 2002年9月
KL-6 is a potential marker for interstitial lung disease associated with juvenile dermatomyositis

Kobayashi, I, S Ono, N Kawamura, M Okano, K Miyazawa, H Shibuya, K Kobayashi

JOURNAL OF PEDIATRICS 138(2) 274-276 2001年2月
Novel mutations of FOXP3 in two Japanese patients with immune dysregulation, polyendocrinopathy, enteropathy, X linked syndrome (IPEX)

J Med Genet 38: 874-876 2001年
A long-term survivor with the immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome.

N Engl J Med 345(13):999-1000 2001年
Combined immunodeficiency, chromosomal instability, and postnatal growth deficiency in a japanese girl

Am J Med Genet 15: 9-12 2001年
T-cell lines from 2 patients with adenosine deaminase (ADA) deficiency showed the restoration of ADA activity resulted from the reversion of an inherited mutation.

Blood 97: 2896-2899 2001年
Anti-alpha-fodrin autoantibody is an early diagnostic marker for childhood primary Sjogren's syndrome.

J Rheumatol 28: 363-365 2001年
Elevated serum levels of soluble interleukin-2 receptor in juvenile dermatomyositis.

Pediatr Int 43:109-111 2001年
Gene-transferred oligoclonal T cells predominantly persist in peripheral blood from an adenosine deaminase-deficient patient during gene therapy.

Molecular therapy 3: 24-27 2001年
Platelet-specific hemophagocytosis in a patient with juvenile dermatomyositis

Kobayashi, I, M Yamada, N Kawamura, R Kobayashi, M Okano, K Kobayashi

ACTA PAEDIATRICA 89(5) 617-619 2000年5月
Genetic studies of three Japanese patients with p22-phox-deficient chronic granulomatous disease: detection of a possible common mutant CYBA allele in Japan and a genotype-phenotype correlation in these patients

M Yamada, T Ariga, N Kawamura, M Ohtsu, S Imajoh-Ohmi, E Ohshika, O Tatsuzawa, K Kobayashi, Y Sakiyama

BRITISH JOURNAL OF HAEMATOLOGY 108(3) 511-517 2000年3月
Genetic studies of three Japanese patients with p22-phox-deficient chronic granulomatous disease: detection of a possible common mutant CYBA allele in Japan and a genotype-phenotype correlation in these patients.

Br J Haematol 108: 511-517 2000年
Platelet-specific hemophagocytosis in a patient with juvenile dermatomyositis.

Acta Pediatr 89: 617-619 2000年
Determination of carrier status for the Wiskott-Aldrich syndrome (WAS) by flow cytometric analysis of WASP expression in peripheral blood mononuclear cells.

J Immunol 165: 1119-1122 2000年
Improved dysgammaglobulinemia in congenital rubella syndrome after immunoglobulin therapy: correlation with CD154 expression.

Eur J Pediatr 159: 764-766 2000年
Induction of IgE synthesis by genetically modified CD8+ T cells of a patient with adenosine deaminase deficiency

Y. Yanagihara, K. Kajiwara, Y. Basaki, K. Ikizawa, M. Mori, K. Akiyama, N. Kawamura, Y. Sakiyama

Allergology International 49(3) 195-204 2000年
Determination of carrier status for the Wiskott-Aldrich syndrome(WAS) by flow cytometric analysis of WASP expression in peripheral blood mononuclear cells.

The Journal of Immunology 165 1119-1122 2000年
Successful treatment with methylprednisolone pulse therapy for a life-threatening pulmonary insufficiency in a patient with chronic granulomatous disease following pulmonary invasive Aspergillosis and Burkholderia cepacia infection

M Okano, M Yamada, M Ohtsu, N Kawamura, Y Sakiyama, K Aoi, S Gandoh, M Fujita, K Kobayashi

RESPIRATION 66(6) 551-554 1999年11月
In vivo kinetics of transduced cells in peripheral T cell-directed gene therapy: Role of CD8(+) cells in improved immunological function in an adenosine deaminase (ADA)-SCID patient

N Kawamura, T Ariga, M Ohtsu, Kobayashi, I, M Yamada, A Tame, H Furuta, M Okano, M Egashira, N Niikawa …

JOURNAL OF IMMUNOLOGY 163(4) 2256-2261 1999年8月
Flow cytometric analysis of Wiskott-Aldrich Syndrome (WAS) protein in lymphocytes from WAS patients and their famillial carriers.

Blood 93: 756-757 1999年

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所属学協会

5

共同研究・競争的資金等の研究課題

5