Novel mutations in a Japanese patient with CD19 deficiency von Kanegane, H, Agematsu, K, Futatani, T, Sira, M M, Suga, K, Sekiguchi, T, van Zelm, M C, Miyawaki, T

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A novel immunoregulatory protein in human colostrum, syntenin-1, for promoting the development of IgA-producing cells from cord blood B cells von Sira, Mostafa M., Yoshida, Taketoshi, Takeuchi, Makoto, Kashiwayama, Yoshinori, Futatani, Takeshi, Kanegane, Hirokazu, Sasahara, Akiko, Ito, Yasunori, Mizuguchi, Mineyuki, Imanaka, Tsuneo, Miyawaki, Toshio

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Detection of Bruton's tyrosine kinase mutations in hypogammaglobulinaemic males registered as common variable immunodeficiency (CVID) in the Japanese Immunodeficiency Registry von Kanegane, H., Tsukada, S., Iwata, T., Futatani, T., Nomura, K., Yamamoto, J., Yoshida, T., Agematsu, K., Komiyama, A., Miyawaki, T.

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Neutrophils and mononuclear cells express vascular endothelial growth factor in acute Kawasaki disease : Its possible role in progression of coronary artery lesions von HAMAMICHI, Yuji, ICHIDA, Fukiko, MIYAWAKI, Toshio, YU, Xianyi, HIRONO, Kei-Ichi, UESE, Kei-Ichiro, HASHIMOTO, Ikuo, TSUBATA, Shinichi, YOSHIDA, Taketoshi, FUTATANI, Takeshi, KANEGANE, Hirokazu

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Predominance of Th2-promoting dendritic cells in early human pregnancy decidua von Miyazaki, Satomi, Tsuda, Hiroshi, Sakai, Masatoshi, Hori, Shinichi, Sasaki, Yasushi, Futatani, Takeshi, Miyawaki, Toshio, Saito, Shigeru

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Early inhaled steroid use in extremely low birthweight infants: a randomised controlled trial von Nakamura, Tomohiko, Yonemoto, Naohiro, Nakayama, Masahiro, Hirano, Shinya, Aotani, Hirofumi, Kusuda, Satoshi, Fujimura, Masanori, Tamura, Masanori

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Genetic analysis in patients with left ventricular noncompaction and evidence for genetic heterogeneity von Xing, Yanlin, Ichida, Fukiko, Matsuoka, Taro, Isobe, Takeshi, Ikemoto, Yumiko, Higaki, Takashi, Tsuji, Tohru, Haneda, Noriyuki, Kuwabara, Atsushi, Chen, Rui, Futatani, Takeshi, Tsubata, Shinichi, Watanabe, Sayaka, Watanabe, Kazuhiro, Hirono, Keiichi, Uese, Keiichiro, Miyawaki, Toshio, Bowles, Karla R., Bowles, Neil E., Towbin, Jeffrey A.

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Bruton tyrosine kinase gene mutations in Turkish patients with presumed X-linked agammaglobulinemia von Wang, Yue, Kanegane, Hirokazu, Sanal, Ozden, Ersoy, Fügen, Tezcan, Ilhan, Futatani, Takeshi, Tsukada, Satoshi, Miyawaki, Toshio

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Survival of wild polio by a patient with XLA von Sarpong, Sampson, Skolnick, Helen S., Ochs, Hans D., Futatani, T., Winkelstein, Jerry A.

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A case of body stalk anomaly arising in the second baby of a triplet pregnancy after in-vitro fertilization and embryo transfer von HIROKAWA, S, UOTANI, H, FUTATANI, T, SASAKI, Y, OGAWA, J, SAKAI, M, TSUKADA, K, SAITO, S

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Toll-like receptor signaling is impaired in dendritic cells from patients with X-linked agammaglobulinemia von Taneichi, Hiromichi, Kanegane, Hirokazu, Mohamed Sira, Mostafa, Futatani, Takeshi, Agematsu, Kazunaga, Sako, Masahiro, Kaneko, Hideo, Kondo, Naomi, Kaisho, Tsuneyasu, Miyawaki, Toshio

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Role of transforming growth factor-β in breast milk for initiation of IgA production in newborn infants von Ogawa, Jiro, Sasahara, Akiko, Yoshida, Taketoshi, Sira, Mostafa Mohamed, Futatani, Takeshi, Kanegane, Hirokazu, Miyawaki, Toshio

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Ganciclovir Therapy for Congenital Cytomegalovirus Infection in Six Infants von Tanaka-Kitajima, Naoko, Sugaya, Naomi, Futatani, Takeshi, Kanegane, Hirokazu, Suzuki, Chizuko, Oshiro, Makoto, Hayakawa, Masahiro, Futamura, Masahide, Morishima, Tsuneo, Kimura, Hiroshi

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Absence of Memory B Cells in Patients with Common Variable Immunodeficiency von Agematsu, Kazunaga, Futatani, Takeshi, Hokibara, Sho, Kobayashi, Norimoto, Takamoto, Masaya, Tsukada, Satoshi, Suzuki, Harumi, Koyasu, Shigeo, Miyawaki, Toshio, Sugane, Kazuo, Komiyama, Atsushi, Ochs, Hans D.

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Clinical and mutational characteristics of X-linked agammaglobulinemia and its carrier identified by flow cytometric assessment combined with genetic analysis von Kanegane, Hirokazu, Futatani, Takeshi, Wang, Yue, Nomura, Keiko, Shinozaki, Kentaro, Matsukura, Hiroyoshi, Kubota, Takeo, Tsukada, Satoshi, Miyawaki, Toshio

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Severe neutropenia in Japanese patients with x-linked agammaglobulinemia von Kanegane, Hirokazu, Taneichi, Hiromichi, Nomura, Keiko, Futatani, Takeshi, Miyawaki, Toshio

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Bruton's tyrosine kinase is present in normal platelets and its absence identifies patients with X‐linked agammaglobulinaemia and carrier females von Futatani, Takeshi, Watanabe, Chiaki, Baba, Yoshihiro, Tsukada, Satoshi, Ochs, Hans D.

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Deficient expression of Bruton's tyrosine kinase in monocytes from X-linked agammaglobulinemia as evaluated by a flow cytometric analysis and its clinical application to carrier de... von FUTATANI, T, MIYAWAKI, T, IWATA, T, TSUCHIYA, S, TATSUZAWA, O, YOSHIZAKI, K, KISHIMOTO, T, TSUKADA, S, HASHIMOTO, S, KUNIKATA, T, ARAI, S, KURIMOTO, M, NIIDA, Y, MATSUOKA, H, SAKIYAMA, Y

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Neutrophil-derived S100A12 is profoundly upregulated in the early stage of acute Kawasaki disease von Ye, Fei, Foell, Dirk, Hirono, Kei-ich, Vogl, Thomas, Rui, Chen, Yu, Xianyi, Watanabe, Sayaka, Watanabe, Kazuhiro, Uese, Kei-ichiro, Hashimoto, Ikuo, Roth, Johannes, Ichida, Fukiko, Miyawaki, Toshio

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Contiguous X-chromosome deletion syndrome encompassing the BTK, TIMM8A, TAF7L, and DRP2 genes von Sedivá, Anna, Smith, C I Edvard, Asplund, A Charlotta, Hadac, Jan, Janda, Ales, Zeman, Jirí, Hansíková, Hana, Dvoráková, Lenka, Mrázová, Lenka, Velbri, Sirje, Koehler, Carla, Roesch, Karin, Sullivan, Kathleen E, Futatani, Takeshi, Ochs, Hans D

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