Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Kentaro Shinozaki"'
Publikováno v:
Nihon Shoni Jinzobyo Gakkai Zasshi. 17:142-145
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d52b0e334fec0fb6a7eba01d30920c20
https://doi.org/10.3165/jjpn.17.142
https://doi.org/10.3165/jjpn.17.142
Autor:
Toshio Miyawaki, Kentaro Shinozaki, Keiko Nomura, Takeo Kubota, Yue Wang, Satoshi Tsukada, Hiroyoshi Matsukura, Takeshi Futatani, Hirokazu Kanegane
Publikováno v:
Journal of Allergy and Clinical Immunology. 108:1012-1020
Background: X-linked agammaglobulinemia (XLA), caused by mutations in Bruton's tyrosine kinase ( BTK ), is the most common form of inherited antibody deficiency. We previously reported that a flow cytometric evaluation of BTK expression in monocytes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e69da9acda477f732eef1df90e47899c
https://doi.org/10.1067/mai.2001.120133
https://doi.org/10.1067/mai.2001.120133
Autor:
Hiroshi Kimura, Akira Matsui, Toshio Miyawaki, Kentaro Shinozaki, Hiroyoshi Matsukura, Masahiro Tsuchida, Ryo Sumazaki, Hirokazu Kanegane, Maki Osaki, Takashi Fukushima
Publikováno v:
Blood. 98:1268-1270
X-linked lymphoproliferative disease (XLP), a genetic disorder characterized by immunodeficiency to Epstein-Barr virus (EBV) infection, has been linked to mutations in the SH2D1A gene. To search for the occurrence of SH2D1A mutations in Japan, we per
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe6bf277319aa96191b9e7863ef86321
https://doi.org/10.1182/blood.v98.4.1268
https://doi.org/10.1182/blood.v98.4.1268
Autor:
Toshio Miyawaki, Tatsuro Kondoh, Mika Makita, Masahiro Tsuchida, Hiroyoshi Matsukura, Yasuo Kimoto, Hirokazu Kanegane, Hiroyuki Moriuchi, Kentaro Shinozaki, Rie Kanai, Ryo Sumazaki, Kumi Tsumura
Publikováno v:
International immunology. 14(10)
X-linked lymphoproliferative disease (XLP) is an inherited immunodeficiency characterized by extreme vulnerability to Epstein-Barr virus (EBV) infection, resulting in fatal infectious mononucleosis, dysgammaglobulinemia and malignant lymphoma. Recent
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::498541608cb8b775ae0b3f45ea0a7450
https://pubmed.ncbi.nlm.nih.gov/12356686
https://pubmed.ncbi.nlm.nih.gov/12356686
Autor:
Hiro Matsukura, Masanori Hara, Kentaro Shinozaki, Tsuneo Takada, Toshio Miyawaki, Toshio Yanagihara, Susumu Inaba, Takakuni Tanizawa, Akira Higuchi
Publikováno v:
American journal of nephrology. 21(5)
Eighty-six patients (59 males and 27 females) diagnosed with steroid-responsive nephrotic syndrome during childhood were identified. The patients were 20–40 years of age (mean 27.0 ± 5.0) with a mean follow-up period of 19.5 ± 5.9 years. All pati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::955eba403a59e0ccfad88badc5306bed
https://pubmed.ncbi.nlm.nih.gov/11684795
https://pubmed.ncbi.nlm.nih.gov/11684795
Publikováno v:
Pediatric Nephrology. 17:70-70
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d6eef0f9a7e423e9ec57e839bf812245
https://doi.org/10.1007/s004670200012
https://doi.org/10.1007/s004670200012