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Makiko Egawa, Kohsuke Imai, Masaaki Mori, Naoyuki Miyasaka, Tetsuo Kubota. Placental Transfer of Canakinumab in a Patient with Muckle-Wells Syndrome J. Clin. Immunol. 2017.05; 37 (4): 339-341. ( PubMed, DOI )

Fumihiro Goto, Toru Uchiyama, Yumiko Nakazawa, Kohsuke Imai, Toshinao Kawai, Masafumi Onodera. Persistent Impairment of T-Cell Regeneration in a Patient with Activated PI3K δ Syndrome J. Clin. Immunol. 2017.05; 37 (4): 347-350. ( PubMed, DOI )

Amit Rawat, Pandiarajan Vignesh, Avinash Sharma, Jitendra K Shandilya, Madhubala Sharma, Deepti Suri, Anju Gupta, Vikas Gautam, Pallab Ray, Shivaprakash M Rudramurthy, Arunaloke Chakrabarti, Kohsuke Imai, Shigeaki Nonoyama, Osamu Ohara, Yu L Lau, Surjit Singh. Infection Profile in Chronic Granulomatous Disease: a 23-Year Experience from a Tertiary Care Center in North India J. Clin. Immunol. 2017.04; 37 (3): 319-328. ( PubMed, DOI )

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Horiuchi K, Imai K, Mitsui-Sekinaka K, Yeh TW, Ochs HD, Durandy A, Nonoyama S.. Analysis of somatic hypermutations in the IgM switch region in human B cells. J. Allergy Clin. Immunol.. 2014.08; 134 (2): 411-419. ( PubMed, DOI )

Hoshino A, Imai K, Ohshima Y, Yasutomi M, Kasai M, Terai M, Ishigaki K, Morio T, Miyawaki T, Kanegane H.. Pneumothorax in patients with severe combined immunodeficiency. Pediatr Int. 2014.08; 56 510-514. ( PubMed )

Endo A, Watanabe K, Ohye T, Suzuki K, Matsubara T, Shimizu N, Kurahashi H, Yoshikawa T, Katano H, Inoue N, Imai K, Takagi M, Morio T, Mizutani S. Molecular and virological evidence of viral activation from chromosomally integrated HHV-6A in a patient with X-SCID Clin Infect Dis. 2014.08; 59 545-548. ( PubMed, DOI )

Kracker S, Curtis J, Ibrahim MAA, Sediva A, Salisbury J, Campr V, Debré M, Edgar JD, Imai K, Picard C, Casanova JL, Fischer A, Nejentsev S, Durandy A. Occurrence of B-cell lymphomas in patients with Activated Phosphoinositide 3-Kinase δ syndrome (APDS) J Allergy Clin Immunol. 2014.07; 134 233-236. ( PubMed )

Hasegawa S, Imai K, Yoshida K, Okuno Y, Muramatsu H, Shiraishi Y, Chiba K, Tanaka H, Miyano S, Kojima S, Ogawa S, Morio T, Mizutani S, Takagi M. Whole-exome sequence analysis of ataxia telangiectasia-like phenotype. J Neurol Sci.. 2014.05; 15 86-90. ( PubMed, DOI )

Mizoguchi Y, Tsumura M, Okada S, Hirata O, Minegishi S, Imai K, Hyakuna N, Muramatsu H, Kojima S, Ozaki Y, Imai T, Takeda S, Okazaki T, Ito T, Yasunaga S, Takihara Y, Bryant VL, Kong XF, Cypowyj S, Boisson-Dupuis S, Puel A, Casanova JL, Morio T, Kobayashi M. Simple diagnosis of STAT1 gain-of-function alleles in patients with chronic mucocutaneous candidiasis J Leukoc Biol. 2014.04; 95 667-676. ( PubMed )

Zahn A1, Eranki AK, Patenaude AM, Methot SP, Fifield H, Cortizas EM, Foster P, Imai K, Durandy A, Larijani M, Verdun RE, Di Noia JM.. Activation induced deaminase C-terminal domain links DNA breaks to end protection and repair during class switch recombination. Proc. Natl. Acad. Sci. U.S.A.. 2014.03; 111 (11): E988-E997. ( PubMed, DOI )

Kanegane H, Imai K, Yamada M, Takada H, Ariga T, Bexon M, Rojavin M, Hu W, Kobayashi M, Lawo JP, Nonoyama S, Hara T, Miyawaki T. Efficacy and safety of IgPro20, a subcutaneous immunoglobulin, in Japanese patients with primary immunodeficiency diseases. J Clin Immunol. 2014.02; 34 204-211. ( PubMed )

Rawat A, Singh S, Suri D, Gupta A, Saikia B, Minz RW, Sehgal S, Vaiphei K, Kamae C, Honma K, Nakagawa N,Imai K, Nonoyama S, Oshima K, Mitsuiki N, Ohara O, Chan KW, Lau YL. Chronic Granulomatous Disease: Two Decades of Experience From a Tertiary Care Centre in North West India. J Clin Immunol. 2014.01; 34 58-67. ( PubMed )

Koura U, Sakaki-Nakatsubo H, Otsubo K, Nomura K, Oshima K, Ohara O, Wada T, Yachie A, Imai K, Morio T, Miyawaki T, Kanegane H. . Successful treatment of systemic cytomegalovirus infection in severe combined immunodeficiency using allogeneic bone marrow transplantation followed by adoptive immunotherapy J Investig Allergol Clin Immunol. 2014; 24 (3): 200-202. ( PubMed )

Machida S1, Tomizawa D, Tamaichi H, Okawa T, Endo A, Imai K, Nagasawa M, Morio T, Mizutani S, Takagi M.. Successful treatment of diffuse large B-cell lymphoma in a patient with ataxia telangiectasia using rituximab. J. Pediatr. Hematol. Oncol.. 2013.08; 35 (6): 482-485. ( PubMed, DOI )

Kamae C, Nakagawa N, Sato H, Honma K, Mitsuiki N, Ohara O, Kanegane H, Pasic S, Pan-Hammarström Q, van Zelm MC, Morio T, Imai K, Nonoyama S. Common variable immunodeficiency classification by quantifying T-cell receptor and immunoglobulin κ-deleting recombination excision circles. J. Allergy Clin. Immunol.. 2013.05; 131 (5): 1437-40.e5. ( PubMed, DOI )

Yoshimi A, Kamachi Y, Imai K, Watanabe N, Nakadate H, Kanazawa T, Ozono S, Kobayashi R, Yoshida M, Kobayashi C, Hama A, Muramatsu H, Sasahara Y, Jakob M, Morio T, Ehl S, Manabe A, Niemeyer C, Kojima S.. Wiskott-Aldrich syndrome presenting with a clinical picture mimicking juvenile myelomonocytic leukaemia. Pediatr Blood Cancer. 2013.05; 60 (5): 836-841. ( PubMed, DOI )

Kawasaki Y, Toyoda H, Otsuki S, Iwasa T, Iwamoto S, Azuma E, Itoh-Habe N, Wada H, Fujimura Y, Morio T, Imai K, Mitsuiki N, Ohara O, Komada Y.. A novel Wiskott-Aldrich syndrome protein mutation in an infant with thrombotic thrombocytopenic purpura. Eur. J. Haematol.. 2013.02; 90 (2): 164-168. ( PubMed, DOI )

Kanegane H, Taneichi H, Nomura K, Wada T, Yachie A, Imai K, Ariga T, Santisteban I, Hershfield MS, Miyawaki T.. Successful bone marrow transplantation with reduced intensity conditioning in a patient with delayed-onset adenosine deaminase deficiency. Pediatr Transplant. 2013.02; 17 (1): E29-E32. ( PubMed, DOI )

Nozaki T, Takada H, Ishimura M, Ihara K, Imai K, Morio T, Kobayashi M, Nonoyama S, Hara T.. Endocrine complications in primary immunodeficiency diseases in Japan. Clin. Endocrinol. (Oxf). 2012.10; 77 (4): 628-634. ( PubMed, DOI )

Kawai T, Saito M, Nishikomori R, Yasumi T, Izawa K, Murakami T, Okamoto S, Mori Y, Nakagawa N, Imai K, Nonoyama S, Wada T, Yachie A, Ohmori K, Nakahata T, Heike T.. Multiple reversions of an IL2RG mutation restore T cell function in an X-linked severe combined immunodeficiency patient. J. Clin. Immunol.. 2012.08; 32 (4): 690-697. ( PubMed, DOI )

Kobayashi D, Kogawa K, Imai K, Tanaka T, Sada A, Nonoyama S.. Hyper-eosinophilia in granular acute B-cell lymphoblastic leukemia with myeloid antigen expression. Pediatr Int. 2012.08; 54 (4): 543-546. ( PubMed, DOI )

Hiroyuki Ishida, Kosuke Imai, Kenichi Honma, Shin-Ichi Tamura, Toshihiko Imamura, Masafumi Ito, Shigeaki Nonoyama. GATA-2 anomaly and clinical phenotype of a sporadic case of lymphedema, dendritic cell, monocyte, B- and NK-cell (DCML) deficiency, and myelodysplasia. Eur J Pediatr. 2012.08; 171 (8): 1273-1276. ( PubMed, DOI )

Oshima K, Nagase T, Imai K, Nonoyama S, Obara M, Mizukami T, Nunoi H, Kanegane H, Kuribayashi F, Amemiya S, Ohara O.. A Dual Reporter Splicing Assay Using HaloTag-containing Proteins. Curr Chem Genomics. 2012.07; 6 27-37. ( PubMed, DOI )

Nakaoka H, Kanegane H, Taneichi H, Miya K, Yang X, Nomura K, Takezaki S, Yamada M, Ohara O, Kamae C, Imai K, Nonoyama S, Wada T, Yachie A, Hershfield MS, Ariga T, Miyawaki T.. Delayed onset adenosine deaminase deficiency associated with acute disseminated encephalomyelitis. Int. J. Hematol.. 2012.06; 95 (6): 692-696. ( PubMed, DOI )

Yang X, Kanegane H, Nishida NImamura T, Hamamoto K, , Miyashita R, Imai K, Nonoyama S, Sanayama K, Yamaide A, Kato F, Nagai K, Ishii E, van Zelm MC, Latour S, Zhao XD, Miyawaki T.. Clinical and genetic characteristics of XIAP deficiency in Japan. J. Clin. Immunol.. 2012.06; 32 (3): 411-420. ( PubMed, DOI )

Suri D, Singh S, Rawat A, Gupta A, Kamae C, Honma K, Nakagawa N, Imai K, Nonoyama S, Oshima K, Mitsuiki N, Ohara O, Bilhou-Nabera C, Proust A, Ahluwalia J, Dogra S, Saikia B, Minz RW, Sehgal S.. Clinical profile and genetic basis of Wiskott-Aldrich syndrome at Chandigarh, North India. Asian Pac. J. Allergy Immunol.. 2012.03; 30 (1): 71-78. ( PubMed )

D Kobayashi, K Kogawa, K Imai, T Tanaka, S Hiroi, H Satoh, K Tanaka-Taya, S Nonoyama. Quantitation of human herpesvirus-6 (HHV-6) DNA in a cord blood transplant recipient with chromosomal integration of HHV-6. Transpl Infect Dis. 2011.12; 13 (6): 650-653. ( PubMed, DOI )

Nakagawa N, Imai K, Kanegane H, Sato H, Yamada M, Kondoh K, Okada S, Kobayashi M, Agematsu K, Takada H, Mitsuiki N, Oshima K, Ohara O, Suri D, Rawat A, Singh S, Pan-Hammarström Q, Hammarström L, Reichenbach J, Seger R, Ariga T, Hara T, Miyawaki T, Nonoyama S.. Quantification of κ-deleting recombination excision circles in Guthrie cards for the identification of early B-cell maturation defects. J. Allergy Clin. Immunol.. 2011.07; 128 (1): 223-225.e2. ( PubMed, DOI )

Okura Y, Yamada M, Kobayashi I, Santisteban I, Arredondo-Santisteban G, Kato Z, Iguchi A, Yoshida M, Ohara O, Nakagawa N, Imai K, Hershfield MS, Ariga T.. ADA-SCID with 'WAZA-ARI' mutations that synergistically abolished ADA protein stability. Br. J. Haematol.. 2011.06; 153 (5): 675-676. ( PubMed, DOI )

Göksel Leblebisatan, Ali Bay, Noriko Mitsuiki, Osamu Ohara, Kenichi Honma, Kohsuke İmai, Shigeaki Nonoyama. Wiskott-Aldrich syndrome mutation in two Turkish siblings with X-linked thrombocytopenia. Turk J Haematol. 2011.06; 28 (2): 139-141. ( PubMed, DOI )

Asai E, Wada T, Sakakibara Y, Toga A, Toma T, Shimizu T, Nampoothiri S, Imai K, Nonoyama S, Morio T, Muramatsu H, Kamachi Y, Ohara O, Yachie A.. Analysis of mutations and recombination activity in RAG-deficient patients. Clin. Immunol.. 2011.02; 138 (2): 172-177. ( PubMed, DOI )

Zhao M, Kanegane H, Kobayashi C, Nakazawa Y, Ishii E, Kasai M, Terui K, Gocho Y, Imai K, Kiyasu J, Nonoyama S, Miyawaki T.. Early and rapid detection of X-linked lymphoproliferative syndrome with SH2D1A mutations by flow cytometry. Cytometry B Clin Cytom. 2011.01; 80 (1): 8-13. ( PubMed, DOI )

Yoshiko Hashii, Hisao Yoshida, Sato Kuroda, Shigenori Kusuki, Emiko Sato, Sadao Tokimasa, Hideaki Ohta, Yasutaka Matsubara, Seiji Kinoshita, Noriko Nakagawa, Kohsuke Imai, Shigeaki Nonoyama, Koichi Oshima, Osamu Ohara, Keiichi Ozono. Hemophagocytosis after bone marrow transplantation for JAK3-deficient severe combined immunodeficiency. Pediatr Transplant. 2010.12; 14 (8): E105-E109. ( PubMed, DOI )

I Tsuge, Y Kondo, Y Nakajima, N Nakagawa, K Imai, S Nonoyama, K Oshima, O Ohara, M Hatanaka, E Kitano, H Kitamura, A Urisu. Hyper IgM syndrome and complement Clq deficiency in an individual with systemic lupus erythematosus-like disease. Clin Exp Rheumatol. 2010.07; 28 (4): 558-560. ( PubMed )

A Aghamohammadi, K Imai, K Moazzami, H Abolhassani, M Tabatabaeiyan, N Parvaneh, R Nasiri Kalmarzi, N Nakagawa, K Oshima, O Ohara, S Nonoyama, N Rezaei. Ataxia-telangiectasia in a patient presenting with hyper-immunoglobulin M syndrome. J Investig Allergol Clin Immunol. 2010; 20 (5): 442-445. ( PubMed )

Shivakumar Keerthikumar, Sahely Bhadra, Kumaran Kandasamy, Rajesh Raju, Y L Ramachandra, Chiranjib Bhattacharyya, Kohsuke Imai, Osamu Ohara, Sujatha Mohan, Akhilesh Pandey. Prediction of candidate primary immunodeficiency disease genes using a support vector machine learning approach. DNA Res. 2009.12; 16 (6): 345-351. ( PubMed, DOI )

Naoki Uchisaka, Naomi Takahashi, Masaki Sato, Akira Kikuchi, Shinji Mochizuki, Kohsuke Imai, Shigeaki Nonoyama, Osamu Ohara, Fumiaki Watanabe, Shuki Mizutani, Ryoji Hanada, Tomohiro Morio. Two brothers with ataxia-telangiectasia-like disorder with lung adenocarcinoma. J Pediatr. 2009.09; 155 (3): 435-438. ( PubMed, DOI )

Shivakumar Keerthikumar, Rajesh Raju, Kumaran Kandasamy, Atsushi Hijikata, Subhashri Ramabadran, Lavanya Balakrishnan, Mukhtar Ahmed, Sandhya Rani, Lakshmi Dhevi N Selvan, Devi S Somanathan, Somak Ray, Mitali Bhattacharjee, Sashikanth Gollapudi, Y L Ramachandra, Sahely Bhadra, Chiranjib Bhattacharyya, Kohsuke Imai, Shigeaki Nonoyama, Hirokazu Kanegane, Toshio Miyawaki, Akhilesh Pandey, Osamu Ohara, Sujatha Mohan. RAPID: Resource of Asian Primary Immunodeficiency Diseases. Nucleic Acids Res. 2009.01; 37 (Database issue): D863-D867. ( PubMed, DOI )

Yoichiro Tsuji, Issei Tokimatsu, Takashi Sugita, Masatoshi Nozaki, Daisuke Kobayashi, Kohsuke Imai, Kazuhiro Kogawa, Shigeaki Nonoyama. Quantitative PCR assay used to monitor serum Trichosporon asahii DNA concentrations in disseminated trichosporonosis. Pediatr Infect Dis J. 2008.11; 27 (11): 1035-1037. ( PubMed, DOI )

Fujimoto M, Imai K, Hirata K, Kashiwagi R, Morinishi Y, Kitazawa K, Sasaki S, Arinami T, Nonoyama S, Noguchi E.. Immunological profile in a family with nephrogenic diabetes insipidus with a novel 11 kb deletion in AVPR2 and ARHGAP4 genes. 2008.05; ( PubMed )

Yoichiro Tsuji, Kazuhiro Kogawa, Kohsuke Imai, Hirokazu Kanegane, Junichiro Fujimoto, Shigeaki Nonoyama. Evans syndrome in a patient with Langerhans cell histiocytosis: possible pathogenesis of autoimmunity in LCH. Int J Hematol. 2008.01; 87 (1): 75-77. ( PubMed, DOI )

Yoichiro Tsuji, Kohsuke Imai, Yoichi Morinishi, Kazuhiro Kogawa, Masaaki Morino, Shigeaki Nonoyama. Successful unrelated cord blood transplantation for a patient with CD40 ligand deficiency. Haematologica. 2007.12; 92 (12): 1727-1728. ( PubMed, DOI )

Tomoharu Tokutomi, Shin Hayashi, Kohsuke Imai, Ayako Chida, Takahiro Ishiwata, Yuh Asano, Johji Inazawa, Shigeaki Nonoyama. dup(8p)/del(8q) recombinant chromosome in a girl with hepatic focal nodular hyperplasia. Am J Med Genet A. 2007.06; 143A (12): 1334-1337. ( PubMed, DOI )

Sophie Péron, Qiang Pan-Hammarström, Kohsuke Imai, Likun Du, Nadine Taubenheim, Ozden Sanal, Laszlo Marodi, Anne Bergelin-Besançon, Malika Benkerrou, Jean-Pierre de Villartay, Alain Fischer, Patrick Revy, Anne Durandy. A primary immunodeficiency characterized by defective immunoglobulin class switch recombination and impaired DNA repair. J Exp Med. 2007.05; 204 (5): 1207-1216. ( PubMed, DOI )

Yoshiyuki Minegishi, Masako Saito, Tomohiro Morio, Ken Watanabe, Kazunaga Agematsu, Shigeru Tsuchiya, Hidetoshi Takada, Toshiro Hara, Nobuaki Kawamura, Tadashi Ariga, Hideo Kaneko, Naomi Kondo, Ikuya Tsuge, Akihiro Yachie, Yukio Sakiyama, Tsutomu Iwata, Fumio Bessho, Tsutomu Ohishi, Kosuke Joh, Kohsuke Imai, Kazuhiro Kogawa, Miwa Shinohara, Mikiya Fujieda, Hiroshi Wakiguchi, Srdjan Pasic, Mario Abinun, Hans D Ochs, Eleonore D Renner, Annette Jansson, Bernd H Belohradsky, Ayse Metin, Norio Shimizu, Shuki Mizutani, Toshio Miyawaki, Shigeaki Nonoyama, Hajime Karasuyama. Human tyrosine kinase 2 deficiency reveals its requisite roles in multiple cytokine signals involved in innate and acquired immunity. Immunity. 2006.11; 25 (5): 745-755. ( PubMed, DOI )

Y Tsuji, K Imai, M Kajiwara, Y Aoki, T Isoda, D Tomizawa, M Imai, S Ito, H Maeda, Y Minegishi, H Ohkawa, J Yata, N Sasaki, K Kogawa, M Nagasawa, T Morio, S Nonoyama, S Mizutani. Hematopoietic stem cell transplantation for 30 patients with primary immunodeficiency diseases: 20 years experience of a single team. Bone Marrow Transplant. 2006.03; 37 (5): 469-477. ( PubMed, DOI )

Kavli B, Andersen S, Otterlei M, Liabakk NB, Imai K, Fischer A, Durandy A, Krokan HE, Slupphaug G.. B cells from hyper-IgM patients carrying UNG mutations lack ability to remove uracil from ssDNA and have elevated genomic uracil. J. Exp. Med.. 2005.06; 201 (12): 2011-2021. ( PubMed, DOI )

Anne Durandy, Patrick Revy, Kohsuke Imai, Alain Fischer. Hyper-immunoglobulin M syndromes caused by intrinsic B-lymphocyte defects. Immunol Rev. 2005.02; 203 67-79. ( PubMed, DOI )

Mansour Akbari, Marit Otterlei, Javier Peña-Diaz, Per Arne Aas, Bodil Kavli, Nina B Liabakk, Lars Hagen, Kohsuke Imai, Anne Durandy, Geir Slupphaug, Hans E Krokan. Repair of U/G and U/A in DNA by UNG2-associated repair complexes takes place predominantly by short-patch repair both in proliferating and growth-arrested cells. Nucleic Acids Res. 2004.10; 32 (18): 5486-5498. ( PubMed, DOI )

Daisuke Tomizawa, Kohsuke Imai, Sukeyuki Ito, Michiko Kajiwara, Yoshiyuki Minegishi, Masayuki Nagasawa, Tomohiro Morio, Shigeaki Nonoyama, Shuki Mizutani. Allogeneic hematopoietic stem cell transplantation for seven children with X-linked hyper-IgM syndrome: a single center experience. Am J Hematol. 2004.05; 76 (1): 33-39. ( PubMed, DOI )

Nadia Catalan, Françoise Selz, Kohsuke Imai, Patrick Revy, Alain Fischer, Anne Durandy. The block in immunoglobulin class switch recombination caused by activation-induced cytidine deaminase deficiency occurs prior to the generation of DNA double strand breaks in switch mu region. J Immunol. 2003.09; 171 (5): 2504-2509. ( PubMed, DOI )

Van-Thanh Ta, Hitoshi Nagaoka, Nadia Catalan, Anne Durandy, Alain Fischer, Kohsuke Imai, Shigeaki Nonoyama, Junko Tashiro, Masaya Ikegawa, Satomi Ito, Kazuo Kinoshita, Masamichi Muramatsu, Tasuku Honjo. AID mutant analyses indicate requirement for class-switch-specific cofactors. Nat Immunol. 2003.09; 4 (9): 843-848. ( PubMed, DOI )

Hirokazu Inoue, Hidemitsu Kurosawa, Shigeaki Nonoyama, Kohsuke Imai, Hisami Kumazaki, Takayuki Matsunaga, Yuya Sato, Kenichi Sugita, Mitsuoki Eguchi. X-linked thrombocytopenia in a girl. Br J Haematol. 2002.09; 118 (4): 1163-1165. ( PubMed, DOI )

戸谷剛, 富澤大輔, 中田慎一郎, 今井雅子, 今井耕輔, 梶原道子, 長沢正之, 森尾友宏, 野々山恵章, 水谷修紀, 清水則夫, 山本興太郎, 関根暉彬. 化学療法回復期HPSの対応に苦慮した慢性活動性EBV感染症・NKリンパ腫症例 血液・腫瘍科. 2001.12; 43 (6): 483-484.

Y Jin, S Nonoyama, T Morio, K Imai, H D Ochs, S Mizutani. Characterization of soluble CD40 ligand released from human activated platelets. J Med Dent Sci. 2001.03; 48 (1): 23-27. ( PubMed )

S Kumaki, N Ishii, M Minegishi, Y Ohashi, I Hakozaki, S Nonoyama, K Imai, T Morio, I Tsuge, Y Sakiyama, A Miyanoshita, J Miura, M Mayumi, T Heike, K Katamura, H Takada, I Izumi, J Kamizono, S Hibi, H Sasaki, M Kimura, A Kikuta, Y Date, M Sako, H Tanaka, K Sano, K Sugamura, S Tsuchiya. Characterization of the gammac chain among 27 unrelated Japanese patients with X-linked severe combined immunodeficiency (X-SCID). Hum Genet. 2000.10; 107 (4): 406-408. ( PubMed, DOI )

M Nagasawa, M Imai, K Imai, S Itoh, M Kajiwara, T Morio, S Nonoyama. In vivo class switch of B cells after cord blood stem cell transplantation in severe combined immune deficient (SCID) patient. Am J Hematol. 2000.10; 65 (2): 176-177. ( PubMed, DOI )

S Itoh, S Nonoyama, T Morio, K Imai, H Okawa, H D Ochs, M Shimadzu, J Yata. Mutations of the WASP gene in 10 Japanese patients with Wiskott-Aldrich syndrome and X-linked thrombocytopenia. Int J Hematol. 2000.01; 71 (1): 79-83. ( PubMed )

M Kajiwara, S Nonoyama, M Eguchi, T Morio, K Imai, H Okawa, M Kaneko, M Sako, S Ohga, M Maeda, S Hibi, H Hashimito, A Shibuya, H D Ochs, T Nakahata, J I Yata. WASP is involved in proliferation and differentiation of human haemopoietic progenitors in vitro. Br J Haematol. 1999.11; 107 (2): 254-262. ( PubMed, DOI )

M Kato, H Miki, K Imai, S Nonoyama, T Suzuki, C Sasakawa, T Takenawa. Wiskott-Aldrich syndrome protein induces actin clustering without direct binding to Cdc42. J Biol Chem. 1999.09; 274 (38): 27225-27230. ( PubMed, DOI )

Y Baba, S Nonoyama, M Matsushita, T Yamadori, S Hashimoto, K Imai, S Arai, T Kunikata, M Kurimoto, T Kurosaki, H D Ochs, J i Yata, T Kishimoto, S Tsukada. Involvement of wiskott-aldrich syndrome protein in B-cell cytoplasmic tyrosine kinase pathway. Blood. 1999.03; 93 (6): 2003-2012. ( PubMed )

P. Vignesh, A. Rawat, A. Singh, R. Kumrah, A. Gummadi, A. Kaur, S. Bhattad, A. Mehta, D. Suri, A. Jinda, D. Leung, S. Ramprakash, R. Cp, K.W. Chan, Y. Ogura, K. Imai, O. Ohara, S. Nonoyama, M. Hershfield, Y. Lau, S. Singh. CLINICAL, IMMUNOLOGICAL, AND MOLECULAR FEATURES OF SEVERE COMBINED IMMUNE DEFICIENCY: A REPORT OF 87 PATIENTS FROM 3 TERTIARY CARE CENTRES IN INDIA. 19th Biennial Meeting of The European Society of immunodeficiencies (ESID 2020) 2020.10.14 web

Satoshi Miyamoto , Masakatsu Yanagimachi , Katsutsugu Umeda , Akihiro Iguchi , Yoji Sasahara , Hidetoshi Takada , Masafumi Yamada , Masataka Ishimura ,Takashi Koike , Masahiro Yasui , Yoshiyuki Takahashi , Hiroshi Kawaguchi , Michiko Kajiwara , Masami Inoue , Koji Kato, Yoshiko Hashii, Yoshiko Atsuta , Hiromasa Yabe , Kohsuke Imai , Tomohiro Morio. Hematopoietic stem cell transplantation for inborn errors of immunity in Japan: overview of a nationwide retrospective analysis. 46th Annual Meeting of the European Society for Blood and Marrow Transplantation (EBMT 2020 Virtual) 2020.08.29 WEB

Satoshi Miyamoto, Masakatsu Yanagimachi, Katsutsugu Umeda, Akihiro Iguchi, Yoji Sasahara, Hidetoshi Takada, Yoshiyuki Takahashi, Michiko Kajiwara, Masami Inoue, Koji Kato, Yoshiko Hashii, Yoshiko Atsuta, Hiromasa Yabe, Kohsuke Imai, Tomohiro Morio. Hematopoietic stem cell transplantation for severe combined immunodeficiency in Japan: a nationwide retrospective analysis. 46th Annual Meeting of the European Society for Blood and Marrow Transplantation (EBMT 2020 Virtual) 2020.08.29 WEB

Yoonsun Yoon, Ji-man Kang, Junsik Choi, Kangmo Ahn, Keon Hee Yoo, Eun-Suk Kang, Kyoung-Mee Kim, Jung Eun Lee, Geum-Youn gawk, Kihyun Kim, Kosuke Imai, Hirokazu Kanegane, Yae-jean Kim.. Cancer development in a Korean family with CTLA-4 haploinsufficiency. 第3回日本免疫不全・自己炎症学会総会・学術集会 2020.02.16 東京

Miko Okamura, Kay Tanita, Hidetoshi Takada, Tetsuo Mitsui, Yoshiyuki Minegishi, Kohsuke Imai, Tomohiro Morio, Hirokazu Kanegane. Somatically reverted T cells in dedicator of cytokinesis 8 deficiency modify cellular immunity. 3rd Scientific Congress of Asia Pacific Society for Immunodeficiencies 2020.02.09 Chandigarh, India

Takahiro Tomoda, Tsubasa Okano, Kento Inoue, Motoi Yamashita, Takahiro Kamiya, Takeshi Isoda Masakatsu Yanagimachi, Hirokazu Kanegane, Masatoshi Takagi, Tomohiro Morio, Kohsuke Imai. Second transplantation rescued the graft failure after hematopoietic stem cell transplantation. 3rd Scientific Congress of Asia Pacific Society for Immunodeficiencies 2020.02.09 Chandigarh, India.

Imai K. Viral infections in patients with hypogammaglobulinemia - What is our current understanding. 3rd Scientific Congress of Asia Pacific Society for Immunodeficiencies 2020.02.09 Chandigarh, India.

Imai K. How I Approach A Patient With Combined Immunodeficiency?. APSID2020 2020.02.06 India

Takahiro Tomoda, Tsubasa Okano, Kento Inoue, Motoi Yamashita, Takahiro Kamiya, Takeshi Isoda, Masakatsu Yanagimachi, Hirokazu Kanegane, Masatoshi Takagi, Tomohiro Morio, Kohsuke Imai. An intractable case of hyper IgE syndrome. APSID (Asia Pacific Society for Immunodeficiencies) School cum Workshop 2020.02.06 Chandigarh, India.

Imai K. Hematopoietic stem cell transplantation in PIDs. 3rd Scientific Congress of Asia Pacific Society for Immunodeficiencies 2020.02 India

Okamura M, Terada N, Mitsuiki N, Ishii T, Morio T, Imai K. The first Cernunnos deficiency patient in Japan. 3rd Scientific Congress of Asia Pacific Society for Immunodeficiencies 2020.02 India

Miyamoto T, Imai K. Japanese experience with UCBT in　SCID. IEWP 2019.10.11 London

Hoshino A, Okano T, Matsumoto K, Nishimura A, Shintaku H, Tokoro S, Okamoto H, Wada T, Mitsuiki N, Kajiwara M, Takagi M, Imai K, Kanegane H, Morio T. Plasmacytoma-Like Post-Transplant Lymphoproliferative Disorder with Multiple Autoantibodies in a XIAP Deficient Patient. 2019 Focused Meeting of the European Society of Immunodeficiencies (ESID 2019) 2019.09.20 Brussels

Okano T, Imai K, Naruto T, Okada S, Okamoto K, Yamashita M, Yeh T. W, Takagi M, Kanegane H, Morio T. Diagnostic Approach by Whole Exome Sequencing for 141 Patients of Inborn Errors of Immunity. 2019 Focused Meeting of the European Society of Immunodeficiencies (ESID 2019) 2019.09.19 Brussels

Sakata S, Okada S, Matsubayashi T, Tamaura M, Tsumura M, Okano T, Imai K, Bustamante J, Morio T, Casanova JL, Kobayashi M. . The First Intronic Mutations Which Caused Autosomal Recessive Complete STAT1 Deficiency. 2019 Focused Meeting of the European Society of Immunodeficiencies (ESID 2019) 2019.09.19 Brussels,Belgium

Nishimura Akira, Aoki Yuki, Ishiwata Yasuyoshi, Inoue Maiko, Ichimura Takuya, Ueyama Junichi, Matsumoto Kazuaki, Inoue Kento, Hiroki Haruka, Ono Shintaro, Okano Tsubasa, Tanaka Mari, Miyamoto Satoshi, Ashiarai Miho, Miyawaki Reiji, Yamagishi Chika, Tezuka Mari, Okawa Teppei, Hoshino Akihiro, Endo Akifumi, Yasuhara Masato, Kamiya Takahiro, Mitsuiki Noriko, Ono Toshiaki, Yanagimachi Masakatsu, Isoda Takeshi, Tomizawa Daisuke, Nagasawa Masayuki, Kajiwara Michiko, Takagi Masatoshi, Mizutani Shuki, Kanegane Hirokazu, Imai Kohsuke, Morio Tomohiro. Hematopoietic cell transplantation with reduced intensity conditioning regimen using fludarabine/busulfan and fludarabine/melphalan for primary immunodeficiency diseases . The 45th Annual Meeting of the European Society for Blood and Marrow Transplantation 2019.03.24 Frankfurt

Yeh T. W, Okano T, Okamoto K, Yamashita M, Takashima T, Mitsuki N, Okada S, Kanegane H, Imai K, Morio T.. April Deficiency as a Cause of Common Variable Immunodeficiency. . 18th Biennial Meeting of the European Society of Immunodeficiencies (ESID2018) 2018.10.25 Lisbon

Imai K. Antibody deficiency: a diagnostic and management challenge. APSID Autumn School 2018.10.11 Bangkok

Imai K. Newborn Screening for primary immunodeficiency (PID)　in Japan and Asia. European Society for Blood and Marrow Transplantation 2018.09.27 Leiden

Imai.k. PIDJ:primary immunodeficiency in japan project.. 2018samsung Medical Center Primary Immunodeficiency Symposium. 2018.07.14 seoul

Imai K. Newborn Screening of PID in Japan. 7th Singapore Paediatric and Perinatal Annual Congress (SiPPAC) 2018.06.27 Singapore

Imai K. Primary Antibody Deficiencies.. 7th Singapore Paediatric and Perinatal Annual Congress (SiPPAC). 2018.06.27 Singapore

Imai K. PID research and clinical care in japan.. 2018samsung Medical Center Primary Immunodeficiency Symposium. 2018.05.08 Chongqing

Imai K. Hematopoietic stem cell transplantation for radiosensible severe combined immunodeficiency. APSID 2018 Summer School 2018.05.08 Chongqing

Yeh TW, Okano T, Okamoto K, Yamashta M, Takashima T, Mitusiki N, Okada S, Kaneganwe H, Imai K, Morio T. APRIL deficiency a as a cause of common variable immunodeficiency. The 2nd APSID Scientific Congress 2018.05.07 Chonquing, China

Okamoto K, Shigemizu D, Okano T, Yeh TW, Takashima T, Yamashita M, Ono S, Mitsuiki N, Takagi M, Mori M, Kanegane H, Tsunoda T, Imai K, Morio T. whole exome sequence analysis using the known and candidate genes for primary immunodeficiency diseases. The 2nd APSID Scientific Congress 2018.05.07 Chonquing, China

Imai K. HSCT for radiosensitive SCID. APSID2018 Summer School 2018.05.05 Chongqing

田村志宣、春谷勇平、小畑裕史、山下友佑、蒸野寿紀、細井裕樹、村田祥吾、西川彰則、吉浦孝一郎、今井耕輔、森尾友宏、園木孝志. Successful cord blood transplantation in a patient with adult-onset common variable immunodeficiency. 第1回日本免疫不全・自己炎症学会総会学術集会 2018.01.20 東京

山下基, 満生紀子, 岡田賢, 井上裕三朗, 中世古知昭, Aditya K. Padhi, Kam Y Zhang, 小原收, 今井耕輔, 高木正稔, 金兼弘和, 谷内一郎, 森尾友宏. IKZF3ヘテロ結合型ミスセンス変異によるB細胞欠損症. 第1回日本免疫不全・自己炎症学会総会・学術集会 2018.01.20 東京

Imai K. Hematopoietic stem cell transplantation for primary immunodeficiency in Japan. KSPHO 2018 Seoul

今井耕輔. 原発性免疫不全症・自己炎症性疾患において考慮すべき遺伝医療の特性と課題. 第59回日本小児血液・がん学会学術集会 2017.11.09

井上健斗, 星野顕宏, 三浦浩樹, 朴明子, 今井耕輔, 吉川哲史, 金兼弘和, 森尾友宏. X連鎖リンパ増殖症候群2型におけるHHV-6 DNA高コピー数は再活性化か？ . 第49回日本小児感染症学会学術集会 2017.10.21 石川

Matsumoto K, Takagi M, Ishiwata Y, Aoki Y, Miyamoto S, Hoshino A, Nishimura A, Tanaka M, Yanagimachi M, Mitsuiki N, Imai K, Kanegnane H, Kajiwara M, Takikawa K, Mae T, Tomiota O, Fujimura J, Yasuhara M, Tomizawa D, Mizutani S, Morio T. HLA haploidentical HCT using clofarabine and busulfan for refractory pediatric leukemia. JSH 2017 2017.10.20 東京

Imai.k. Newborn Screening of PID in japan. APSID 2017 Autumn School 2017.10.10 Hong Kong

Kadawaki T, Ohnishi H, Kanegane H, Kawamoto N, Hori T, Nishimura K, Kobayashi C, Shigemura T, Ogata S, Inoue Y, Kawai T, Hiejima E, Takagi M, Imai K, Nishikomori R, Ito S, Heiki T, Ohara O, Morio T, Fukao T. A Nation-wide Survey of Haploinsufficiency of A20 Reveals the Frequent Coincidence of Autoimmunity in Japan. ESID 2017 2017.09.13 Edinburgh, UK

Ono S, Yanagimachi M, Okano T, Hoshino A, Takagi M, Imai K, Morio T, Kanegane H. Inflammatory Bowel Disease Associated with XIAP Deficiency can be cured by Hematopoietic Stem Cell Transplantation. ESID 2017 2017.09.12 Edinburgh, UK

Okano T, Imai K, Mitui-Sekinaka K, Yeh T.W, Takashima T, Kanegane H, Nonoyama S, Morio T. Combined Immunodeficiency and Progressive Lymphoproliferative Diseases of Activated P13Kδ Syndrome Rescued by Hematopoietic. ESID 2017 2017.09.12 Edinburgh, UK

Okamoto K, Okano T, Kumaki E, Tanaka E, Ono S, Wada T, Ohnishi H, Kato Z, Nunoi N, Imai K, Kanegane H, Mori M, Morio T. A Case of Non-Pulmonary Sarcoidosis Due to Novel Hypomorphic Missense Mutation of NCF2. ESID 2017 2017.09.11 Edinburgh,UK

Imai K. Hematpopoietic stem cell transplantation for P`rimary. The 21st Congress of the Asian Pacific Society of Respirology (APSR 2016) 2016.11.11 Thailand　Bangkok

Imai K. Primary antibody deficiency in Japan:overview and P13K related disorders. XLP-WAS 2016 Symposium-London 2016.09.27 London　England

Ono S, Okano T,　Hoshino　A,　Yanagimachi　M,　Takagi　M,　Imai　K,　Morio　T,　Kanegane H. Hematopoietic　stem　cell　transplantation for XIAP deficiency. XLP-WAS 2016 Symposium-London 2016.09.26 London

Kanegane H, Hoshino A, Takashima T, Yeh T-W, Okano T, Yamashita M, Imai K, Morio T. . Selective dysregulation of Epstein Barr virus infection in hypomorphic ZAP70 mutation. . XLP-WAS 2016 Symposium-London 2016.09.26 London

T. Mizukami,M. Iwata-Okada, T. Nishimura, T. Kawai, M. Onodera, K. Imai, S. Nonoyama, O. Ohara, H. Nunoi. CLINICAL AND GENETIC PROFILES OF CHRONIC GRANULOMATOUS DISEASE IN JAPAN. 17th Biennial Meeting of the European Society for Immunodeficiencies 2016.09.23 Barucelona Spain

Jolles S, Rojavin M, Nelson Jr. R, Wasserman R.L, Borte M, Kanegane H, Imai K.. Efficacy and Safety of HIZENTRA in Patients with Primary Immunodeficiency in Japan, Europe, and the US. 17th Biennial Meeting of17th Biennial Meeting of the European Society for Immunodeficiencies 2016.09.23 Barcelona, Spain

Moriya K, Tanita K, Ohnishi H, Niizuma H, Rikiishi T, Nishikomori R, Ishige T, Imai K, Kanegane H, Sasahara Y, Arakawa H, Kure S, Morio T.. I⃐B-α S32 Mutations Underly Ectodermal Dysplasia with Immunodeficiency Manifestations and Correlation with Immunological Parameters.. 17th Biennial Meeting of the European Society for Immunodeficiencies 2016.09.23 Brcelona, Spain

Schwab C, Gabrysch A, Hoshino M, Slatter M, Hayakawa S, Schubert D, Klemann C, Frede N, Salzer U, Speckmann C, Freiberger T, Lorenz H.M, Hauck F, Klobuch S, Zeissig S, Leichtner A, Van de Veerdonk F, Elemnto O, Giulino-Roth L, Duckers G, Niehues T, Alsina L, Deya-Martinez A, Kanderiva V, Fronkova E, Price C, Patino V, Blumberg R, Yesim Kucuk Z, Seneviratne S, Kanariou M, Lougaris V, Albert M, Giese T, Litzman J, Ehl S, Okada S, Imai K, Dybedai I, Tasken K, Wolff D, Warnatz K, Hambleton S, Arkwright P, Cant A, Kanegane H, Grimbacher B.. The Clinical Spectrum and Treatment Options of 82 Individuals with CTLA-4Deficiency. 17th Biennial Meeting of the European Society for Immunodeficiencies 2016.09.23 Barcelona, Spain

Rojavin M, Kanegane H, Borte H, Imai K, Hubsch A, Jolles S.. Analysis of Patient Treatment Satisfaction from Five Studies of HIZENTRA 20% Subcutaneous Immunoglobulin. 17th Biennial Meeting of the European Society for Immunodeficiencies 2016.09.23 Barcelona, Spain

Okano T, Watanabe E, Takashima T, Nishikawa T, Kawano Y, Tomoda T, Tanaka-Kubota M, Miyamoto S, Yeh T, Yamashita M, Tanaka K, Mitusiki N, Ohara O, Takagi M, Imai K, Kanegane H, Morio T.. IgG1 Gammopathy in X-SCID Caused by Maternal T and B cell Engraftment. 17th Biennial Meeting of the European Society for Immunodeficiencies 2016.09.23 Barcelona, Spain

L.A. Henderson, A.E. O'Connell, J.I. Chu, Y.N. Lee, S. Volpi, M. Armant, I.B. Barlan, A. Ozen, S. Baris, I.C. Hanson, J.M. Despotovic, A. Saitoh, T. Takachi, K. Imai, A. King, S. Arredondo, A. Galy, D.A. Williams,S.Y. Pai, L.D. Notarangelo. GENE THERAPY USING A SELF-INACTIVATING LENTIVIRAL VECTOR AMELIORATES T CELL RECEPTOR REPERTOIRE ABNORMALITIES IN PATIENTS WITH WISKOTT-ALDRICH SYNDROME. 17th Biennial Meeting of the European Society for Immunodeficiency 2016.09.22 Barcelona Spain

S. Singh, A. Rawat, D. Suri, A. Gupta, R. Garg, B. Saikia, R. Minz, S. Sehga, K. Chan, Y. Lau, C. Kamae, K. Honma, N. Nakagawa, K. Imai, S. Nonoyama, K. Oshima, N. Mitsuiki, O. Ohara. SPECTRUM OF BTK GENE MUTATIONS IN A SINGLE-CENTRE COHORT OF X-LINKED AGAMMAGLOBULINEMIA FROM NORTH INDIA. 17th Biennial Meeting of the European Society for Immunodeficiency 2016.09.22 Barcelona Spain

Leiding J,Okada S,Shcherbina A,Abinun M,Pulsipher M,Hagin D,Linemans C,Sullivan K,Bunin N,Kilic S,De La Calle-Martin O,Roiman C,Aldave J.C,Iguchi A,Imai K,Ohkawa T,Gennery A,Slatter M,Ochs H,MorioT,Torgerson T. Hematopoietic Stem cell Transplantation in Patients with Gain of Function STAT1 Mutation. 17th Biennial Meeting of the European Society for Immunodeficiencies 2016.09.22 Barcelona, Spain

Mitsui-Sekinaka K, Imai K, Tsujita Y, Mitsuiki N, Asano T, Sekinaka Y, Kanegane H, Yoshida K, Miyano S, Kojima S, Ogawa S, Ohara O, Okada S, Kobayashi M, Takagi M, Morio T, Nonoyama S.. Activated P13 Kinase Delta Syndrome (APDS)-Like Immunodeficiency Caused by PTEN Mutation. 17th Biennial Meeting of the European Society for Immunodeficiencies 2016.09.22 Barcelona, Spain

Sekinaka Y,Mitsuiki N,Imai K,Yabe M,Mitsui-Sekinaka K,Honma K,Arai A,Yoshida K,Miyano S,Seiji K,Hira A,Takata M,Ohara O,Ogawa S,Morio T,Nonoyama S. Common Variable Immunodeficiency Caused by Fanc Mutations. 17th Biennial Meeting of the European Society for Immunodeficiencies 2016.09.22 Brcelona, Spain

Hoshino A, Okada S, Yoshida K, Nishida N, Yamashita M, Okano T, Tsumura M, Nishimura S, Sakata S, Takagi M, Imai K, Miyano S, Ogawa S, Kojima S, Nonoyama S, Morio T, Kanegane H. . Abnormal Hematopoiesis and Autoimmunity in Humans with Germline IKZF1 Mutations. 17th Biennial Meeting of the European Society for Immunodeficiencies 2016.09.22 Barcelona, Spain

Okano T, Imai K, Tsujita Y, Mitsuiki , Mitsui-Sekinaka K, Takashima T, Kanegane H, Nonoyma S. Broad Spectrum of Clinical Manifestations and Outcome of Hematopoietic Stem Cell Transplantation in Japanese Patients with Activated P13KD Syndrome Type1. ASPID Spring School 2016.05.01 Hong Kong

Imai K. HYPER-IGM SYNDROMES DUE TO CSR DEFECTS-HOW TO TREAT ACCORDING TO GENETIC SUBTYPES?. ASPID Spring School 2016.04.27 HongKong

Imai K. PIDJ AND PIER-PID DATABASE IN JAPAN FOR DOCTORS AND PATIENTS-HOW IT FACILITATES CARE AND RESEARCH?. ASPID Spring School 2016.04.27 HongKong

Mikhail Rojavin, Hirokazu Kanegane, Michael Borte, Imai k , Alphonse P. Hubsch, Helena Soop, Stephen R. Jolles. Pooled Analysis of Patient Treatment Satisfaction from Five Hizentra Studies. 2016 AAAAI ANNUAL MEETING 2016.03.04 Los Angeles

高木正稔,今井耕輔,朴今花,山下基,星野顕宏,岡野翼,金兼弘和,松村秀樹,奥野友介,吉田健一,上野浩生,白石友一,千葉健一,田中洋子,宮野悟,小川誠司,林泰秀,小島勢二,森尾友宏. 自己免疫性リンパ増殖症様疾患に対する全エクソーム解析の経験Whole-exome analysis of autoimmune lymphoproliferative syndrome-like diseases. 第57回日本小児血液・がん学会学術集会 2015.11.29 山梨

小野真太郎,金兼弘和,我有茉希,久保田真理,足洗美穂,宮本智史,小林千佳,満生紀子,今井耕輔,高木正稔,梶原道子,森尾友宏. 炎症性腸疾患を合併したXIAP 欠損症患者に対する骨髄移植成功例Successful bone marrow transplantation in an XIAP-deficient patient associated with inflammatory bowel disease. 第57回日本小児血液・がん学会学術集会 2015.11.29 山梨

T. Wada, T. Toma, M. Yasui, M. Inoue, K. Kawa, K. Imai, T. Morio, A. Yachie. Different leaky phenotype in two siblings with x-linked severe combined immunodeficiency. 16th Biennial Meeting of the European society for immunodeficiencies 2014.10.31 Prague, Czech Republic

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

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

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

今井耕輔. ヒト免疫異常症における免疫担当細胞亜群解析の標準化. 第58回日本リウマチ学会総会・学術集会 2014.04.26

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

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

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

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

H. Takada, M. Ishimura, T. Doi, K. Imai, Y. Sasahara, H Kanegane, R. Nishikomori, T. Morio, T. Heike, M. Kobayashi, T. Ariga, S. Tsuchiya, S. Nonoyama, T. Miyawaki, T. Hara. Nation-wide survey of patients with primary immunodeficiency diseases in japan:2008. 15th Biennial Meeting of the European Society of Immunodeficiencies (ESID2012). 2012.10 Florence, Italy.

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.

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.

Kamae C, Nakagawa N, Sato H, Honma K, Mitsuiki N, Ohara O, Kanegane H, Pasic S, Pan-Hammarström Q, MC van Zelm, Morio T, Imai K, Nonoyama S.. Classification of common variable immunodeficiency by quantification of T cell receptor recombination excision circles (TREC) and Ig kappa-deleting recombination excision circles (KREC). . 15th Biennial Meeting of the European Society of Immunodeficiencies (ESID2012). 2012.10 Florence, Italy.

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.

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