講演・口頭発表等 - 森尾　友宏

81. N. Mitsuiki, X. Yang, S. Bartol, Y.Kosaka, H.Takada, K. Imai, H. Kanegane, S. Mizutani, M. Van der Burg, M. Van Zelm, O. Ohara, T. Morio. Mutations in bruton's tyrosine kinase impair IgA responses. 16th Biennial Meeting of the European society for immunodeficiencies 2014.10.30 Prague, Czech Republic

82. K. Imai, Y. Tsujita, K. Mitsui-Sekinaka, N. Mitsuiki, T. Takashima, T. Okano, Y. Aoki, F. Kimoto, M. Inoue, F. Iwasaki, T. Kaneko, T. Waragai, H. Sano, A. Kikuta, T. Morio, S. Nonoyama. Hematopoietic stem cell transplantation for the patients with activated PI3K-delta syndrome. 16th Biennial Meeting of the European society for immunodeficiencies 2014.10.30 Prague, Czech Republic

83. T.Takashima, Y. Tsujita, T.W.Yeh, N. Mitsuiki, H. Kanegane, S Kracker, A.Durandy, S. Nonoyama, T. Morio, K. Imai. Clinical and immunological features of patients with gain-of-function PIK3CD mutations in japan. 16th Biennial Meeting of the European society for immunodeficiencies 2014.10.30 Prague, Czech Republic

84. L. Gamez-Diaz, D. August, N. Kanariou, S. Seneviratne, C. Speckmann, M. Seidel, M. Noriko, T. Morio, M. Jordan, P. Stepensky, B. Grimbacher. LRBA deficiency:clinical, immunologic and genetic characterization. 16th Biennial Meeting of the European society for immunodeficiencies 2014.10.30 Prague, Czech Republic

85. Morio T, Fujita Y, Ono T, Ochiai N, Leen A.M, and Takahashi S.. Development of simplified method for generation of multivirus-specific T cells.. 2014 International Symposium and Annual Meeting of Korean Society of Microbiology and Biotechnology. 2014.06 Busan, Korea.

86. Morio T.. Primary Immunodeficiency.. Brain Korea 21 Plus Project Seminar. 2014.05

87. Tomohito Takimoto, Hidetoshi Takada, Masataka Ishimura, Tomohiro Morio, Toshiro Hara. A Japanese Female Case of Wiskott-Aldrich Syndrome with Skewed X-chromosome Inactivation. The 4th JSH International Symposium 2013 in EHIME 2013.05 EHIME, Japan

88. Mari Tezuka, Kohsuke Imai, Teppei Okawa, Daisuke Tomizawa, Masatoshi Takagi, Michiko Kajiwara, Masayuki Nagasawa, Tomohiro Morio, and Shuki Mizutani. Fatal Outcome Due to Parainfluenza-3 Pneumonitis in a Patient with Atypical Complete DiGeorge Syndrome. The 4th JSH International Symposium 2013 in EHIME 2013.05 EHIME, Japan

89. Morio T. . Cord blood transplantation for primary immunodeficiency in Japan. . AsiaCORD2013. 2013.04 Kobe,Japan.

90. Takada H, Ishimura M, Imai K, Morio T, Kobayashi M, Nonoyama S, Hara O.. Endocrine complications in primary immunodeficiency diseases in Japan.. 第41回日本免疫学会総会・学術集会 2012.12 神戸

91. Takimoto T, Ishimura M, Takada H, Morio T, Hara T.. A Japanses female case of Wiskott Aldrich syndrome with skewed X-Chromoseme inactivation.. 第41回日本免疫学会総会・学術集会 2012.12 神戸

92. 長澤正之、大川哲平、遠藤明史、満生紀子、青木由貴、小野敏明、磯田健志、富澤大輔、今井耕輔、高木正稔、梶原道子、森尾友宏、水谷修紀. . Thrombomodulin-alpha improves the coagulation disorder associated transplantation-related mortality after allogeneic SCT.. 第74回日本血液学会 2012.10.21 京都

93. Takagi M, Imai K, Nakagawa M, Morio T, Mizutani S. . The Research Front Line of Immune Thrombocytopenia Chronic immune thrombocytopenia as a disease with or without association of defined diseases in children. . 第74回日本血液学会学術集会 2012.10 京都

94. Endou A, Ookawa T, Tomizawa D, Imai K, Takagi M, Nagasawa M, Morio T, Mizutani S. . Acute myeloid leukemia with EWSR1 split signal.. 第74回日本血液学会学術集会 2012.10 京都

95. Morio T. . Primary Immunodeficiencies due the Defect in Signaling Molecules.. 2012 KSMCB Annual Meeting. 2012.10 Seoul, Korea.

96. Honma K, Imai K, Kamae C, Ishida H, Ito Y, Kojima S, Yokosuka T, Kanegane H, Morio T, Sasahara Y, Fujiwara T, Harigae H, Hashii Y, Ohara O, Nonoyama S.. Clinical features and immunological abnormalities of GATA2 deficiency in JAPAN. . 15th Biennial Meeting of the European Society of Immunodeficiencies (ESID2012). 2012.10 Florence, Italy.

97. Isoda T, Takagi M, Morio T, Kawamoto H, Mizutani S.. Visualization of chromosomal translocation and early T-cell development failure in ATM deficiency.. 15th Biennial Meeting of the European Society of Immunodeficiencies (ESID2012). 2012.10 Florence, Italy.

98. Mitsuiki N, Oshim K, Imai K, Ohara O, Morio T, Mizutani S.. Genetic Analysis For 207 Cases With Primary Immunodeficiency (PID) Consulted to A Single Center Through PID Network in JAPAN (PIDJ) in 5 Years (2007-2011).. 15th Biennial Meeting of the European Society of Immunodeficiencies (ESID2012). 2012.10 Florence, Italy.

99. Wada T, Muraoka M, Toma T, Shigemura T, Agematsu K, Moriuchi H, Ohara O, Morio T, Yachie A. Rapid detection of intracellular p47phox and p67phox by flow cytomery in patients with chronic granulomatous disease. . 15th Biennial Meeting of the European Society of Immunodeficiencies (ESID2012). 2012.10 Florence, Italy.

100. Mitsuiki N, Oshima K, Imai K, Ohara O, Morio T, Mizutani S.. Genetic analysis for 207 cases with primary immunodeficiency (PID) consulted to a single center through PID network in Japan (PIDJ) in 5 years (2007-2011).. 15th Biennial Meeting of the European Society of Immunodeficiencies (ESID2012). 2012.10 Florence, Italy.