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Page 1
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.
Ariga T, Oda N, Yamaguchi K, Kawamura N, Kikuta H, Taniuchi S, Kobayashi Y, Terada K, Ikeda H, Hershfield MS, Kobayashi K, Sakiyama Y. Ariga T, et al. Among authors: kobayashi y, kobayashi k. Blood. 2001 May 1;97(9):2896-9. doi: 10.1182/blood.v97.9.2896. Blood. 2001. PMID: 11313286 Free article.
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.
Yamada M, Ariga T, Kawamura N, Ohtsu M, Imajoh-Ohmi S, Ohshika E, Tatsuzawa O, Kobayashi K, Sakiyama Y. Yamada M, et al. Among authors: kobayashi k. Br J Haematol. 2000 Mar;108(3):511-7. doi: 10.1046/j.1365-2141.2000.01857.x. Br J Haematol. 2000. PMID: 10759707 Free article.
[Leukocyte adhesion deficiency, type I].
Kawamura N, Kobayashi K. Kawamura N, et al. Among authors: kobayashi k. Ryoikibetsu Shokogun Shirizu. 2000;(32):170-2. Ryoikibetsu Shokogun Shirizu. 2000. PMID: 11212679 Review. Japanese. No abstract available.
[Leukocyte adhesion deficiency, type II].
Kawamura N, Kobayashi K. Kawamura N, et al. Among authors: kobayashi k. Ryoikibetsu Shokogun Shirizu. 2000;(32):173-6. Ryoikibetsu Shokogun Shirizu. 2000. PMID: 11212680 Review. Japanese. No abstract available.
Determination of carrier status for the Wiskott-Aldrich syndrome by flow cytometric analysis of Wiskott-Aldrich syndrome protein expression in peripheral blood mononuclear cells.
Yamada M, Ariga T, Kawamura N, Yamaguchi K, Ohtsu M, Nelson DL, Kondoh T, Kobayashi I, Okano M, Kobayashi K, Sakiyama Y. Yamada M, et al. Among authors: kobayashi i, kobayashi k. J Immunol. 2000 Jul 15;165(2):1119-22. doi: 10.4049/jimmunol.165.2.1119. J Immunol. 2000. PMID: 10878391
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