1. Kenichi Kashimada. Faculty Presentation: Nuances in the management of different types of CAH. ISPAE 2023 ( Indian Society for Pediatric and Adolescent Endocrinology) 2023.11.17 Bengaluru, India

  2. Hirokazu Kanegane. Flow cytometry use in Primary Immunodeficiency disorders. Mini-symposium: Inborn errors of immunity 2023.10.27 Bangkok

  3. Hirokazu Kanegane. NK cell assays. APSID 2023 2023.10.26 Singapore

  4. Hirokazu Kanegane. Diagnosis and Management of Primary Atopic Disorder. APAAACI 2023 2023.10.25 Singapore

  5. Morio T. Dissection of the molecular pathogenesis of transcription factor defects using model mice/cell systems. Chang Gung University 2023.10.20 Taipei

  6. Eriko Adachi, Ryuichi Nakagawa, Atsumi Tsuji-Hosokawa, Maki Gau, Shizuka Kirino, Analia Yogi, Hikase Nakatani, Tomomi Yamaguchi, Masanori Murakami, Toshihiro Tajima, Tomonobu Hasegawa, Tetsuya Yamada, Tomohiro Morino, Osamu Ohara, Kenichi Kashimada . Development of a clinically applicable one-step PCR-based CYP21A2 analysis using long read sequences. Human Genetics Asia 2023( 68th Annual Meeting of Japan Society of Human Genetics/ 14th Asia Pacific Conference on Human Genetics/ 22nd Annual meeting of East Asian Union of human Genetics Societies) 2023.10.14 Tokyo, Japan

  7. Masatoshi Takagi, Motoi Yamashita, Takahiro Tomoda, Takeshi Isoda, Makiko Egawa, Masayuki Yoshida, Tsutomu Toki, Ko Kudou, Kiminori Terui, Etsuro Ito, Tomohiro Morio. Transient erythroblastopenia by GATA1 variant in female. . Human Genetics Asia 2023 2023.10.14 Tokyo

  8. Ryo Aoki, Chikako Morioka, Kikuko Oku, Shigeru Takishima, Yoshihiro Minosaki, Tomonori Ichikawa. Pressure Evaluation of Nasal Continuous Positive Airway Pressure Cannula Using a New Connector and Respiratory Simulator. FAOPS 2023; The 22nd Congress of the Federation of Asia and Oceania Perinatal Societies 2023.10.09 Tokyo

  9. Manabu Sugie, Yusuke Noguchi, Nobutoshi Nawa, Ayako Kashimada, Kazuyuki Ito, Tsutomu Kondo, Satoshi Kusuda, Chikako Morioka, Tomohiro Morio, Kenichi Kashimada. Implication of Acquiring Oxidative Stress Resistance in Chorioamnionitis Leading to Reduced Risk of Severe Retinopathy of Prematurity. FAOPS 2023; The 22nd Congress of the Federation of Asia and Oceania Perinatal Societies 2023.10.09 Tokyo

  10. Hirokazu Kanegane. Rare diseases presenting with hemophagocytic lymphohistiocytosis. IEI SCAC 2023 2023.09.15 重慶

  11. Satoshi Miyamoto, Daiki Niizato, Takahiro Kamiya, Takeshi Isoda, Masatoshi Takagi, Shohei Azumi, Shinsuke Hirabayashi, Kenichi Sakamoto, Kenji Kishimoto, Takako Miyamura, Katsutsugu Umeda, Masakatsu Yanagimachi, Kaori Kanda, Yasuhiro Ikawa, Kenichiro Watanabe, Tatsuo Ichinohe, Hirotoshi Sakaguchi, Tomohiro Morio, Hirokazu Kanegane. Allogenic hematopoietic cell transplantation with alemtuzumab in Asian patients with inborn errors of immunity. ICBMT2023 2023.09.01 Busan

  12. Taku Ishii, Keiko Uchida, Susumu Hosokawa, Hidekazu Ishida, Shinichi Takatsuki, Shigetoyo Kogaki, Kei Inai, Hiroyuki Fukushima, Hiroyuki Yamagishi, Shozaburo Doi. Baseline characteristic of pulmonary hypertension patients with congenital heart disease in Japan: Insights from Japanese association of congenital heart disease with pulmonary hypertension registry (JACPHR). PH Korea 2023 with 3rd EASOPH 2023.07.14 Incheon, Korea

  13. Kenichi Kashimada, Taninee Sahakitrungruang. 21OHD/CAH (clinical management, molecular biology, neonatal screening) . APPES-TSPE CME MEETING 2023 2023.06.06 Bangkok, THAILAND

  14. Kaneko S, Shimbo A,Irabu H, Shimizu M, Mori M, Morio T. Clinical significance of serum cytokine profiling for the differentiation of underlying diseases in cytokine storm syndrome. The 2nd International Symposium of Clinical Immunology 2023.05.19 Kanagawa

  15. Dan Tomomasa, Tasuku Suzuki, Ichiro Takeuchi, Kimitoshi Goto, Shin-Ichiro Hagiwara, Dai Keino, Satoshi Saida, Takashi Ishige, Takahiro Kudo, Masataka Ishimura, Motohiro Kato, Yoji Sasahara, Tomohiro Morio, Katsuhiro Arai, Hirokazu Kanegane. Clinical and genetic characteristics of IL10RA deficiency patients in Japan. The 2nd International Symposium of Clinical Immunology 2023.05.19 神奈川

  16. Kenichi Kashimada. Neonatal screening of 21-hydroxylase deficiency using LC-MS/MS. The 52nd Korean Society of Pediatric Endocrinology 2023.05.19 Soul, Korea

  17. Hirokazu Kanegane. HLH associated with inborn errors of metablism and familial hemophagocytic lymphohistiocytosis in adult. 2nd National Congress of Inborn Errors of Immunity and National Forum on Pediatric Immunology (IEI China 2023 and FOPI) 2023.04.26 Web開催

  18. Tomohiro Morio. Novel Gene Discovery. Asia Pacific Society for Immunodeficiencies (APSID) 2023.04.23 Hong Kong

  19. Mahnaz Jamee, Hirokazu Kanegane. Lung Surgery in STAT3 loss-of-function mutation: is it advisable?. APSID 2023 2023.04.22 香港

  20. Shizuka Kirino, Ryuichi Nakagawa, Kei Takasawa, Maki Gau, Atsumi Tsuji-Hosokawa, Liang Zhao, Josephine Bowles, Peter Koopman, Tomohiro Morio, Kenichi Kashimada. Application of Cap analysis of gene expression (CAGE) in genetic analysis of mouse sex differentiation. Ninth International Symposium on the Biology of Vertebrate Sex Determination 2023.04.19 Kailua-Kona, HAWAII

  1. Carolin Escherich, Wenan Chen, Satoshi Miyamoto, Yui Namikawa, Wenjian Yang, David T. Teachey, Zhenhua Li, Elizabeth A. Raetz, Eric C Larsen, Meenakshi Devidas, Paul L. Martin, W Paul Bowman, Gang Wu, Ching-Hon Pui, Stephen P. Hunger, Masatoshi Takagi, Jun J. Yang, Mignon L. Loh. Rare Deleterious TCF3 Germline Variants and Predisposition to Acute Lymphoblastic Leukemia in Children.. The 64th ASH Annual Meeting and Exposition 2022.12.11 New Orleans, US

  2. Hirokazu Kanegane. Advanced therapies: The future of BMT in Asia. IPOPI 4th Regional Asian PID Meeting 2022.11.19 Kuala Lumpur

  3. Hirokazu Kanegane. Finding NEMO. The 1st National IEI Congress of China 2022 2022.11.12 Web開催

  4. Morio T. Dissection of the molecular pathogenesis of transcription factor defects using model mice/cell systems. . The 17th International Symposium on Inborn Errors of Immunity 2022.10.28 Los Angels

  5. Morio T.. IKZF3 deficiency: LOF? DN? Neomorph? . The 20th annual meeting of ESID 2022.10.12 Gothenburg

  6. Eriko Adachi, Kenichi Kashimada, Ryuichi Nakagawa, Kei Takasawa, Akito Sutani, Atsumi Tsuji-Hosokawa, Osamu Ohara. Allele frequency of deletions or large conversions in Japanese 21 hydroxylase deficiency patients was 20%. The 12th Biennial Scientific Meeting of the Asia Pacific Paediatric Endocrine Society 2022 2022.10.06 Seoul, KOREA (Web)

  7. Analia Gisela Yogi, Kenichi Kashimada, Ryosei Iemura, Hisae Nakatani, Kei Takasawa, Maki Gau, Takeru Yamauchi, Masayuki Yoshida, Tomohiro Morio. A case of BMP2 defficiency with short stature. The 12th Biennial Scientific Meeting of the Asia Pacific Paediatric Endocrine Society 2022 2022.10.06 Seoul, KOREA (Web)

  8. Shizuka Kirino, Analia Gisela Yogi, Eriko Adachi, Maki Gau, Hisae Nakatani, Toru Kanamori, Tomohiro Udagawa, Kei Takasawa, Kenichi Kashimada, Tomohiro Morio. The first family case of 46,XX DSD due to pathogenic variant of WT1 Zinc Finger domain 4. The 12th Biennial Scientific Meeting of the Asia Pacific Paediatric Endocrine Society 2022 2022.10.06 Seoul, KOREA (Web)

  9. Atsumi Tsuji-Hosokawa, Kazuhiro Watanabe, Atsuko Hashimoto, Nobuyuki Ishige, Harumi Yajima, Akito Sutani, Hisae Nakatani, Maki Gau, Kei Takasawa, Kenichi Kashimada. The LC-MS/MS pilot study assay for 21-hydroxylase deficiency newborn screening revealed the high relevancy of 21DOF, (4AD + 17αOHP)/F, and 11DOF/17αOHP. The 12th Biennial Scientific Meeting of the Asia Pacific Paediatric Endocrine Society 2022 2022.10.06 Seoul, KOREA (Web)

  10. Miyamoto Satoshi, Koizumi Miho, Hiroki Haruka, Nishimura Akira, Ota Setsuo, Imai Kohsuke, Kanegane Hirokazu, Morio Tomohiro, Honda Hiroaki, Takagi Masatoshi. B細胞性急性リンパ性白血病を合併した分類不能型免疫不全症患者における生殖細胞系列PAX5バリアント(A PAX5 germline variant in a patient with common variable immunodeficiency complicated with B-cell acute lymphoblastic leukemia). 日本小児血液・がん学会雑誌 2022.10.01

  11. Hirokazu Kanegane. Hematopoietic stem cell transplantation for PID. 17th Congress of Asian Society for Pediatric Research (ASPR 2022) 2022.09.17 Web開催

  12. 西村 聡, 佐々木 麻起子, 高木 正稔, 磯田 健志. 非コードRNA転写とスーパーエンハンサー活性化によるゲノムの3次元構造維持機構(Non-coding RNA transcription and super-enhancer activation facilitate 3D genome structure). 日本癌学会総会記事 2022.09.01

  13. 西村 聡, 佐々木 麻起子, 高木 正稔, 磯田 健志. 非コードRNA転写とスーパーエンハンサー活性化によるゲノムの3次元構造維持機構(Non-coding RNA transcription and super-enhancer activation facilitate 3D genome structure). 日本癌学会総会記事 2022.09.01

  14. Hirokazu Kanegane. A B-Cell Deficient Japanese Girl with ZIP7 Deficiency Caused by Novel Compound Heterozygous Variants in SLC39A7. 13th International Congress of Immunodeficiency Diseases 2022.04.24 Web開催

  15. Hirokazu Kanegane. ALPS & ALPS-like and IPEX & IPEX-like. . 4th Asia-Pacific Society for Immunodeficiencies Congress 2022.04.02 Web開催

  16. Hirokazu Kanegane. An Approach to Antibody Deficencies.. 4th Asia-Pacific Society for Immunodeficiencies Congress 2022.04.01 Web開催

  1. Hirokazu Kanegane. Updates in Primary antibody deficiencies. 16th Congress of Asian Society for Pediatric Research (ASPR 2021) 2021.12.11 Web開催

  2. Yoshinaga Masao, Horigome Hitoshi, Ayusawa Mamoru, Yasuda Kazushi, Kogaki Shigetoyo, Doi Shozaburo, Tateno Sigeru, Ohta Kunio, Hokosaki Tatsunori, Nishihara Eiki, Iwamoto Mari, Sumitomo Naokata, Ushinohama Hiroya, Izumida Naomi, Tauchi Nobuo, Kato Yoshiaki, Kato Taichi, Chisaka Toshiyuki, Higaki Takashi, Yoneyama Tatsuya, Abe Katsumi, Nozaki Yoshihiro, Komori Akiko, Kawai Satoru, Ninomiya Yumiko, Tanaka Yuji, Nuruki Norihito, Sonoda Masahiro, Ueno Kentaro, Hazeki Daisuke, Nomura Yuichi, Sato Seiichi, Hirono Keiichi, Hosokawa Susumu, Takechi Fumie, Ishikawa Yuichi, Hata Tadayoshi, Ichida Fukiko, Ohno Seiko, Makita Naomasa, Horie Minoru, Matsushima Shouji, Tsutsui Hiroyuki, Ogata Hiromitsu, Takahashi Hideto, Nagashima Masami. 小児・青年期の診断前および診断後における心電図による肥大型心筋症診断(Electrocardiographic Diagnosis of Hypertrophic Cardiomyopathy in the Pre- and Post-Diagnostic Phases in Children and Adolescents). Circulation Journal 2021.12.01

  3. Matsusaka Taiji, Udagawa Tomohiro, Osafune Kenji, Araoka Toshikazu. Podocyte Damage in Chimeric Kidney Organoids. American Society of Nephrology kidney week 2021 2021.11.02 San Diego, USA

  4. Yohei Yamaguchi, Susumu Hosokawa, Satoshi Nagahara, Ayako Nagashima-Otsuki, Taku Ishii, Tomoyuki Umemoto, Shozaburo Doi. How should we manage women with Kawasaki disease with giant coronary aneurysms who want a child? ~case reports~. The 13th International Kawasaki Disease Symposium 2021.10.29 Web

  5. Masatoshi Takagi, Chitose Ogawa, Tomoko Iehara, Yuki Aoki-Nogami, Eri Isibashi, Minoru Imai, Toshimi Kimura, Masashi Nagata, Masato Yasuhara, Mitsuko Masutani, Kenichi Yoshimura, Daisuke Tomizawa, Atsushi Ogawa, Kan Yonemori, Tetsuro Kihara, Kiyoshi Nobori, Kazuhisa Hasebe, Shuki Mizutani, Tomohiro Morio, Hajime Hosoi, Ryuji Koike. First In Children Phase I Clinical Study Of Oral Olaparib In Pediatric Patients With Refractory Solid Tumors. SIOP2021 2021.10.24 Honolulu(Web)

  6. Ryuichi Nakagawa, Hideya Kawaji, Yasuhiro Murakawa, Shuji Takada, Satoshi Narumi, Maki Fukami, Josephine Bowles, Andrew Sinclair, Peter Koopman, Kenichi Kashimada. Two ovarian enhancer candidates, identified by time series enhancer RNA analyses, harbored rare SNVs identified in ovarian insufficiency. First Virtual International Symposium on Vertebrate Sex Determination 2021.10.04 Web

  7. Dan Tomomasa, Mitsuki Noriko, Isoda Takeshi, Nishimura Akira, Endo Akifumi, Takagi Masatoshi, Kajiwara Michiko, Imai Kohsuke, Morio Tomohiro, Kanegane Hirokazu. Artemis欠損症に対するTCRαβCD19除去移植(Successful TCRABCD19-depleted hematopoietic cell transplantation for a patient with Artemis deficiency). 日本小児血液・がん学会雑誌 2021.10.01

  8. Dan Tomomasa, Mitsuki Noriko, Isoda Takeshi, Nishimura Akira, Endo Akifumi, Takagi Masatoshi, Kajiwara Michiko, Imai Kohsuke, Morio Tomohiro, Kanegane Hirokazu. Artemis欠損症に対するTCRαβCD19除去移植(Successful TCRABCD19-depleted hematopoietic cell transplantation for a patient with Artemis deficiency). 日本小児血液・がん学会雑誌 2021.10.01

  9. Hirokazu Kanegane. Tips of hematopoietic cell transplantation for inborn errors of immunity. Chinese PID Summer School 2021 2021.09.25 Web開催

  10. 足洗 美穂, 西村 聡, 水城 和義, 出口 隆生, 真部 淳, 長谷川 大輔. 芽球性形質細胞様樹状細胞腫瘍の小児に対する造血細胞移植を回避した治療(Treatment in pediatric blastic plasmacytoid dendritic cell neoplasm(BPDCN) without transplantation). 日本血液学会学術集会 2021.09.01

  11. 西村 聡, 横山 和明, 成戸 卓也, 中園 博仁, 木村 俊介, 今村 俊彦, 森尾 友宏, 金井 昭教, 松井 啓隆, 梅田 雄嗣, 佐野 秀樹, 小池 隆志, 頼 晋也, 關中 悠仁, 小川 淳, 木下 明俊, 柴 徳生, 三木 瑞香, 木村 文彦, 中山 秀樹, 中沢 洋三, 多賀 崇, 滝 智彦, 足立 壯一, 真部 淳, 康 勝好, 石田 也寸志, 滝田 順子, 東條 有伸, 高木 正稔. 新規の白血病特性を有するmyeloid/natural killer cell precursor acute leukemia(Myeloid/natural killer(NK) cell precursor acute leukemia as a novel distinctive leukemia entity). 日本血液学会学術集会 2021.09.01

  12. Yohei Yamaguchi, Susumu Hosokawa, Yusuke Kajikawa, Yasuhiro Maejima, Mitsuaki Isobe, Tetsushi Furukawa, Shozaburo Doi. Pathophysiological Role of Dexmedetomidine for Monocrotaline-induced Pulmonary Arterial Hypertension in Rats.. The 8th Congress of the Asia-Pacific Pediatric Cardiac Society - APPCS 2021 2021.07.15

  13. Hirokazu Kanegane. Revisiting X-linked agammaglobulinemia. 12th International Congress of Immunodeficiency Diseases(ICID) 2021.04.27 Web開催

  1. Akihiro Hoshino, Yuya Koda, Jun Kato, Kay Tanita, Hirokazu Kanegane . A plastic anemia as an initial manifestation in a patient with SAP deficiency. The 27th Annual Meeting of the Japan Childhood Aplastic Anemia Study Group 2020.11.08 Web開催

  2. Masaki Shimizu. Macrophage Activation Syndrome: Analysis of various Cytokines. 22nd Asia-Pacific League of Associations for Rheumatology Congress 2020.10.24 Kyoto

  3. K. Tanita, F. Sakura, M. Tsumura, H. Ohnishi, A. Hoshino, K. Suzuki, S. Okada, R. Nambu, S. Umetsu, K. Imai, T. Morio, H. Kanegane. PATIENTS WITH THE GAIN-OF-FUNCTION MUTATIONS IN STAT3 PRESENT WITH A VARIETY OF AUTOIMMUNE DISEASES. 19th Biennial Meeting of The European Society of immunodeficiencies (ESID 2020) 2020.10.14 web

  4. Imanaka Y, Taniguchi M, Doi T, Shimomura M, Tsumura M, Karakawa S, Imai K, Morio T, Puel A, Casanova-L, Ohara O, Kamei K, Kobayashi M, Okada S.. CARD9 DEFICIENCY IN A PATIENT WITH INVASIVE INFECTION DUE TO EXOPHIALA DERMATITIDIS AND THE ASYMPTOMATIC SIBLINGS. 19th Biennial Meeting of The European Society of immunodeficiencies (ESID 2020) 2020.10.14 web

  5. Tomomasa Dan, Isoda Takeshi, Yamashita Motoi, Morishita Aoi, Mitsuiki Noriko, Kamiya Takahiro, Imai Kohsuke, Kanegane Hirokazu, Takagi Masatoshi, Morio Tomohiro. ステロイド抵抗性肺GVHDに対してルキソリチニブを使用した2例(Ruxolitinib administration for two cases with steroid-refractory lung GVHD). 日本小児血液・がん学会雑誌 2020.10.01

  6. Endo Akifumi, Yamashita Motoi, Kamiya Takahiro, Mitsuiki Noriko, Isoda Takeshi, Imai Kohsuke, Takagi Masatoshi, Kajiwara Michiko, Kanegane Hirokazu, Morio Tomohiro. PTCyハプロ移植症例の6例の後方視的検討(A retrospective study of six cases of HLA haplo-identical hematopoietic stem cell transplantation with Post-Transplant Cyclophosphamide). 日本小児血液・がん学会雑誌 2020.10.01

  7. 宮本 智史, 高木 正稔, 大澤 毅, 澁谷 正史, 森尾 友宏, 土田 里香. BMP4におけるMYCNの抑制を介した神経芽腫の増殖阻害効果. 日本癌学会総会記事 2020.10.01

  8. Isoda Takeshi, Nishimura Akira, Morio Tomohiro, Takagi Masatoshi. 血液基礎・核ダイナミクスからnon-coding RNAによる細胞制御 非コードRNA転写による核内局在転換はT細胞への系列決定を誘導しT細胞系腫瘍の抑制に関与する(Non-coding RNA ThymoD transcription specifies T-cell fate and inhibits T-cell malignancies). 日本小児血液・がん学会雑誌 2020.10.01

  9. Isoda Takeshi, Nishimura Akira, Morio Tomohiro, Takagi Masatoshi. 血液基礎・核ダイナミクスからnon-coding RNAによる細胞制御 非コードRNA転写による核内局在転換はT細胞への系列決定を誘導しT細胞系腫瘍の抑制に関与する(Non-coding RNA ThymoD transcription specifies T-cell fate and inhibits T-cell malignancies). 日本小児血液・がん学会雑誌 2020.10.01

  10. Nishimura Akira, Yokoyama Kazuaki, Naruto Takuya, Morio Tomohiro, Kanai Akinori, Imamura Toshihiko, Koh Katsuyoshi, Ishida Yasushi, Tojo Arinobu, Takagi Masatoshi. Myeloid/Natural killer cell precursor acute leukemiaにおける臨床像とゲノム異常(Clinical feature and genetic alteration of Myeloid/Natural killer cell precursor acute leukemia(MNKPL)). 日本小児血液・がん学会雑誌 2020.10.01

  11. 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

  12. 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

  13. Miyaoka Futaba, Toyofuku Etsushi, Isoda Takeshi, Moiro Tomohiro, Kanegane Hirokazu. Influenza-induced hemolytic crisis in glucose-6-phosphate dehydrogenase deficiency(和訳中). Pediatrics International 2020.08.01

  14. Yamaguchi Yohei, Hosokawa Susumu, Kajikawa Yusuke, Maejima Yasuhiro, Isobe Mitsuaki, Furukawa Tetsushi, Doi Shozaburo. ラットにおけるモノクロタリン誘発性肺動脈性肺高血圧症に対するデクスメデトミジンの病態生理学意義(Pathophysiological Role of Dexmedetomidine for Monocrotaline-induced Pulmonary Arterial Hypertension in Rats). 日本循環器学会学術集会抄録集 2020.07.01

  15. 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. The 3rd Annual Scientific Meeting of the Japanese Society for Immunodeficiency and Autoinflammatory Diseases (JSIAD) 2020.02.16 東京

  16. Mikhail A.Rojavin,Tomohiro Morio,Dandan Luo,Gautam Baheti,Jutta Hofmann,Michael A.Tortorici. INDIVIDUAL AND POPULATION-LEVEL PHARMACOKINETIC PROPERTIES OF PRIVIGEN® IN JAPANESE PATIENTS WITH PRIMARY IMMUNODEFICIENCY(PID). The 3rd Annual Scientific Meeting of the Japanese Society for Immunodeficiency and Autoinflammatory Diseases (JSIAD) 2020.02.15 Tokyo

  17. 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

  18. 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.

  19. 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.

  1. Haruka Hiroki, Masatoshi Takagi, Yuko Ishi, Jinhua Piao, Tomohiro Morio. PARP Inhibition Sensitize BCR-ABL1 Positive Cell. 61st American Society of Hematology (ASH) Annual Meeting and Exposition 2019.12.08 Orlando

  2. Satoshi Miyamoto, Takuya Naruto, Tomohiro Morio, Kevin Y Urayama, Atsushi Manabe, Masatoshi Takagi. Association of Germline Variants of TCF3 and PAX5 with Pediatric Acute Lymphoblastic Leukemia Development. 61st American Society of Hematology (ASH) Annual Meeting and Exposition 2019.12.07 Orlando

  3. Kenichi Kashimada. Endocrine Late Effects of childhood cancer. ISPAE PET School 2019 2019.11.26 Kolkata, India

  4. Tomohiro Udagawa, Keiko Tanaka, Toshikazu Araoka, Kenji Osafune, Taiji Matsusaka. Selective podocyte injury model in kidney organoid. American Society of Nephrology Kidney Week 2019.11.07 Washinton DC. USA

  5. 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 (ESID2019) 2019.10.18 Brussels, Belgium

  6. 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 (ESID2019) 2019.10.18 Brussels, Belgium

  7. 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 (ESID2019) 2019.10.18 Brussels, Belgium

  8. 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 2019.10.18 Brussels, Belgium

  9. 井上 久美,石澤 未来,窪田 哲朗. 細胞外のdsDNAは抗DNA抗体によってリンパ球にも取り込まれる.. 第47回日本臨床免疫学会総会 2019.10.18 札幌

  10. Nunoda Issei, Tomoda Takahiro, Kamiya Takahiro, Okano Tsubasa, Hatano Maho, Yoshimoto Yuri, Muramatsu Hideki, Morishita Aoi, Inoue Kento, Yamashita Motoi, Endo Akifumi, Yanagimachi Masakatsu, Isoda Takeshi, Kanegane Hirokazu, Takagi Masatoshi, Imai Kohsuke, Morio Tomohiro. GATA2異常症に伴うMDSに対するAzacitidineの有効性(Efficacy of Azacitidine for MDS due to germline GATA2 haploinsufficiency). 日本小児血液・がん学会雑誌 2019.10.01

  11. Miyamoto Satoshi, Takagi Masatoshi, Osawa Tsuyoshi, Shibuya Masabumi, Morio Tomohiro, Tsuchida Rika. BMP4におけるMYCNの抑制を介した神経芽腫の増殖阻害効果(BMP4 suppresses the tumor growth of neuroblastoma via MYCN downregulation). 日本小児血液・がん学会雑誌 2019.10.01

  12. Hatano Maho, Tomoda Takahiro, Okano Tsubasa, Nunoda Issei, Morishita Aoi, Inoue Kento, Yamashita Motoi, Endo Akifumi, Kamiya Takahiro, Isoda Takeshi, Yanagimachi Masakatsu, Takagi Masatoshi, Kanegane Hirokazu, Okuno Keisuke, Imai Kohsuke, Morio Tomohiro. 非血縁者間骨髄移植後早期にバンコマイシン自然耐性腸球菌性髄膜炎に罹患した活性型PI3Kδ症候群2型の1例(Intrinsically Vancomycin resistant enterococcal(Enterococcus gallinarum) meningitis occurred early after hematopoietic stem cell transplantation for activated PI3K delta syndrome type2). 日本小児血液・がん学会雑誌 2019.10.01

  13. Tomoda Takahiro, Nishimura Akira, Ono Rintaro, Isoda Takeshi, Inoue Maiko, Kamiya Takahiro, Yanagimachi Masakatsu, Imai Kohsuke, Kanegane Hirokazu, Hasegawa Daisuke, Morio Tomohiro, Manabe Atsushi, Takagi Masatoshi. 急性骨髄性白血病からT細胞型急性リンパ性白血病へclonal evolutionを起こしたMLL-AF9陽性乳児白血病の一例(Clonal evolution of leukemia with MLL-AF9 from myeloid to T-lineage). 日本小児血液・がん学会雑誌 2019.10.01

  14. Ashiarai Miho, Hasegawa Daisuke, Nishimura Akira, Mizuki Kazuyoshi, Yamamoto Kaoru, Yamamoto Shunsuke, Ono Rintaro, Hirabayashi Shinsuke, Hosoya Yosuke, Manabe Atsushi. 肝脾T細胞リンパ腫に対するハプロ末梢血幹細胞移植(Haploidentical hematopoietic stem cell transplantation for hepatosplenic T-cell lymphoma). 日本小児血液・がん学会雑誌 2019.10.01

  15. Tomoda Takahiro, Nishimura Akira, Ono Rintaro, Isoda Takeshi, Inoue Maiko, Kamiya Takahiro, Yanagimachi Masakatsu, Imai Kohsuke, Kanegane Hirokazu, Hasegawa Daisuke, Morio Tomohiro, Manabe Atsushi, Takagi Masatoshi. 急性骨髄性白血病からT細胞型急性リンパ性白血病へclonal evolutionを起こしたMLL-AF9陽性乳児白血病の一例(Clonal evolution of leukemia with MLL-AF9 from myeloid to T-lineage). 日本小児血液・がん学会雑誌 2019.10.01

  16. Nishimura Akira, Miyakawa Yuichi, Murakoshi Miki, Shimbo Asami, Ishiguro Rika, Kajiwara Michiko, Shibuya Atsushi, Ogura Hiromi, Kanno Hitoshi, Koh Katsuyoshi, Minosaki Yoshihiro, Nishioka Masato, Shimohira Masayuki. ANK1変異とSLC4A1バリアントを有する重症貧血が遷延する遺伝性球状赤血球症の1例(A case of hereditary spherocytosis with ANK1 mutation and SLC4A1 variant with persistent severe anemia). 日本小児血液・がん学会雑誌 2019.10.01

  17. Nishimura A, Naruto T, Hoshino A, Amano K, Iwamoto S, Hirayama M, Grigg A, Bosco J J, Migita M, Takagi M, Ohara O, Morio T, van Zelm MC, Kanegane H. Genomics Analysis of Leukemia Predisposition in X-Linked Agammaglobulinemia. 2019 Focused Meeting of the European Society of Immunodeficiencies (ESID2019) 2019.09.20 Brussels

  18. Morio T, Gotoh K, Imagawa T, Morita K, Ohnishi H, Yasui K, Hofmann J, Lawo JP, Shebl A, Rojavin MA. Safety and Tolerability of IgPro10 (PRIVIGEN®) in Japanese Patients with Primary Immunodeficiency: Data From A Phase 3 Study. 2019 Focused Meeting of the European Society of Immunodeficiencies (ESID2019) 2019.09.20 Brussels

  19. Morio T, Baheti G, Tortorici MA, Hofmann J, Rojavin MA. Pharmacokinetic Properties of IgPro10 in Japanese Patients with Primary Immunodeficiency. 2019 Focused Meeting of the European Society of Immunodeficiencies (ESID2019) 2019.09.20 Brussels

  20. 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 (ESID2019) 2019.09.20 Brussels

  21. Honda Y, Yasumi T, Miyamoto T, Nishitani M, Nihira H, Shiba T, Shibata H, Tanaka T, Kanda K, Izawa K, Kanegane H, Heike T, Takita J, Nishikomori R.. A CTLA-4 Haploinsufficiency Case with Multiple Brain and Pulmonary Lesions - Dilemmas in Management. 19th Biennial Meeting of the European Society of Immunodeficiencies (ESID2019). 2019.09.20 Brussels

  22. 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 (ESID2019) 2019.09.19 Brussels

  23. Cardinez C, Miraghazadeh B, Tanita K, da Silva E, Hoshino A, Okada S, Chand R, Asano T, Tsumura M, Yoshida K, Ohnishi H, Kato Z, Yamazaki M, Okuno Y, Miyano S, Kojima S, Ogawa S, Andrews TD, Field MA, Burgio G, Morio T, Vinuesa CG, Kanegane H, Cook M. Gain-of-Function IKBKB Mutation Causes Human Combined Immune Deficiency. 2019 Focused Meeting of the European Society of Immunodeficiencies (ESID2019) 2019.09.19 Brussels

  24. 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 (ESID2019) 2019.09.19 Brussels

  25. Morio T. Disorders caused by a defect in IKAROS family protein. 2019 Samsung Medeikal Center Primary Immunodeficiency Symposium 2019.07.06 Seoul

  26. Kanegane H. Revisit X-linked agammaglobulinemia. 2019 Samsung Medical Center Primary Immunodeficiency Symposium. 2019.07.06 Seoul

  27. Morio T. Primary immunodeficiency disorders caused by a mutation in IKAROS family gene. RIKEN IMS-JSI International Symposium on Immunology 2019 2019.06.25 Tokyo

  28. Kenichi Kashimada. Diagnosis and clinical management of DSD in past and present. Pediatric Academic Societies Meeting 2019.04.28 Baltimore, USA

  29. 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 2019.03.25 Frankfurt

  30. Yeh TW, Okano T, Okamoto K, Yamashita M, Takashima T, Mitsuiki N, Okada S, Kanegane H, Imai . APRIL deficiency as a cause of common variable immunodeficiency. 第2回日本免疫不全・自己炎症学会総会・学術集会 2019.02.02 東京

  31. Tanita K, Cardinez C, Miraghanzadeh B, Hoshino A, Okada S, Asano T, Tsumura M, Ohnishi H, Kato Z, Morio T, Vinuesa CG, Kanegane H, Cook MC. Gain-of-function IKBKB mutation causes human combined immune deficiency. 第2回日本免疫不全・自己炎症学会総会・学術集会 2019.02.02 東京

  32. Yamada Y, Cho K, Agematsu K, Kanegane H, Miyake N, Ueki M, Akimoto T, Kobayashi N, Ikemoto S, Tanino M, Fujita A, Hayasaka I, Miyamoto S, Tanaka-Kubota M, Nakata K, Shiina M, Ogata K, Minakami H, Matsumoto N, Ariga T. Heterozygous mutations in OAS1 cause infantile-onset pulmonary alveolar proteinosis with hypogammaglobulinemia. 第2回日本免疫不全・自己炎症学会総会・学術集会 2019.02.02 東京

  1. Tzu-wen Yeh, Okano T, Okamoto K, Yamashita M, Takashima T, Mitsuiki N, Okada S, Kanegane H, Imai K, Morio T. APRIL deficiency as a cause of common variable immunodeficiency. 第47回日本免疫学会総会学術集会 2018.12.12 福岡

  2. Nishimura A, Yokoyama K, Yamagishi C, Naruto T, Morio T, Kanai A, Matsui H, Higuchi N, Takada A, Okuno H, Saito S, Karakawa S, Kobayashi S, Sano H, Koike T, Hasegawa D, Fujisaki H, Hasegawa D, Koike K, Ogawa A, Kinoshita A, Shiba N, Miki M, Nakayama H, Nakazawa Y, Imamura T, Taga T, Adachi S, Koh K, Manabe A, Taki T, Ishida Y, Tojo A, Takagi M. Clinical Feature and Genetic Alterations in Myeloid/Natural Killer (NK) Cell Precursor Acute Leukemia and Myeloid/NK Cell Acute Leukemia. 60st American society of Hematology Annual Meeting & Exposition 2018.12.02 San Diego

  3. Lin HT, Kubara K, Yamazaki K, Takagi M, Naruto T, Morio T, Okumura T, Otsu M. Enhanced Selective Inhibition of KRAS Mutant Hematopoietic Progenitor Cell Expansion By MEK and Bcl-2 Inhibition . 60st American society of Hematology Annual Meeting & Exposition 2018.12.01 San Diego

  4. Isoda Takeshi, Murre Cornelis. 免疫応答のエピジェネティック調節 非コードRNA ThymoD転写は、T細胞の運命を特定し、T細胞悪性疾患を抑制するために核構造を修飾する(Epigenetic regulation of immune response Non-coding RNA ThymoD transcription modulates nuclear architecture to specify T-cell fate and inhibits T-cell malignancies). 日本免疫学会総会・学術集会記録 2018.12.01

  5. Isoda T, Nishimura A, Miyamoto S, Morio T, Takagi M, Murre C. Non-Coding RNA thymod transcription modulates nuclear architecture to Orchestratet-Cell fate and block T-Cell malignancies. SIOP2018 2018.11.17 Kyoto

  6. Inoue Maiko, Isoda Takeshi, Matsumoto Kazuaki, Inoue Kento, Kamiya Takahiro, Yanagimachi Masakatsu, Takagi Masatoshi, Kanegane Hirokazu, Imai Kohsuke, Morio Tomohiro. 原発性複合免疫不全症におけるサイトメガロウイルス喉頭炎(Cytomegalovirus laryngitis in primary combined immunodeficiency diseases). 日本小児感染症学会総会・学術集会プログラム・抄録集 2018.11.01

  7. Inoue Maiko, Isoda Takeshi, Matsumoto Kazuaki, Inoue Kento, Kamiya Takahiro, Yanagimachi Masakatsu, Takagi Masatoshi, Kanegane Hirokazu, Imai Kohsuke, Morio Tomohiro. 原発性複合免疫不全症におけるサイトメガロウイルス喉頭炎(Cytomegalovirus laryngitis in primary combined immunodeficiency diseases). 日本小児感染症学会総会・学術集会プログラム・抄録集 2018.11.01

  8. Inoue Maiko, Isoda Takeshi, Matsumoto Kazuaki, Inoue Kento, Kamiya Takahiro, Yanagimachi Masakatsu, Takagi Masatoshi, Kanegane Hirokazu, Imai Kohsuke, Morio Tomohiro. 原発性複合免疫不全症におけるサイトメガロウイルス喉頭炎(Cytomegalovirus laryngitis in primary combined immunodeficiency diseases). 日本小児感染症学会総会・学術集会プログラム・抄録集 2018.11.01

  9. Kanegane H.. Modification of cellular and humoral immunity by somatically reverted T cells in XLP1. XLP Symposium 2018. 2018.10.29 London

  10. 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 2018.10.25 Lisbon

  11. Okano T, Cho K, Kwamura S, Onai N, Fujii W, Kakuta S, Kanai-Azuma M, Ohteki T, Otsu M, Ariga T, Morio T. . Induced Pluripotent Stem Cell (IPSC)-Derived Macrophages Recapitulate the Pathological Features of Pulmonary Alveolar Proteinosis Caused by OAS1 Mutation.. 18th Biennial Meeting of the European Society of Immunodeficiencies (ESID2018) 2018.10.25 Lisbon

  12. Leiding J,Vogel T, Heimall J, Gignon Jadoul V, Mhaskar R, Cooper M, O`Sullivan M, Giovannini-Chami L, Thatayatikom B, Bauer C, Hamalainen S, Taskinen M, Seppanen M,Adeli M, Formankova R, Heeg M, Pozos T, Szabolcs P, Morio T, Chua I, Hague R, Hambleton S, Tangye S, Gennery A, Cunningham-Rundles C, Su H, Rao K, Milner J, Ehl S, Forbes L.. The Natural Hisory of STAT3-GOF-The Range of Clinical Manifestations and Treatment Options.. 18th Biennial Meeting of the European Society of Immunodeficiencies (ESID2018) 2018.10.25 Lisbon

  13. 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

  14. Miyamoto Satoshi, Naruto Takuya, Morio Tomohiro, Urayama Kevin, Manabe Atsushi, Takagi Masatoshi. 小児B前駆細胞性急性リンパ性白血病患者におけるTCF3のバリアント(TCF3 inherited variants in children with B-cell precursor acute lymphoblastic leukemia). 日本小児血液・がん学会雑誌 2018.10.01

  15. Hirabayashi Shinsuke, Yamamoto Shunsuke, Yamamoto Kaoru, Yamamoto Kazuki, Aiga Saori, Daida Atsuro, Ono Rintaro, Ashiarai Miho, Nishimura Akira, Hosoya Yosuke, Hasegawa Daisuke, Manabe Atsushi. ダサチニブ併用低減集中化学療法を用いたダウン症候群合併フィラデルフィア染色体陽性急性リンパ性白血病(Dasatinib-combined less intensive chemotherapy for Philadelphia chromosome-positive acute lymphoblastic leukemia in Down syndrome). 日本小児血液・がん学会雑誌 2018.10.01

  16. Nishimura Akira, Hirabayashi Shinsuke, Yamamoto Shunsuke, Aiga Saori, Nishitani Misa, Hosoya Yosuke, Mori Shinichiro, Hasegawa Daisuke, Manabe Atsushi. Diamond-Blackfan貧血に対する強度減弱前処置を用いた骨髄移植(Bone marrow transplantation with reduced intensity conditioning for Diamond-Blackfan anemia). 日本小児血液・がん学会雑誌 2018.10.01

  17. Nakatani H, Miyai K, Takasawa K, Kashimada K, Morimorto A, nagasawa M, Oshiba A. A case of central diabetes insipidus developed 4 years after the non-CNS-risk unifocal bone lesion of Langerhans cell histiocytosis. ESPE2018 2018.09.28 Greece

  18. Yamauchi T, Sugie M, Takasawa K, Imamura M, Kashimada K. Prematurity of 23 or less weeks' gestation is a risk for transient late-onset hyperglycemia in neonates. ESPE 2018 2018.09.28 Greece

  19. Yuji Sugawara, Takeshi Hasegawa, Toshihiro Nomura, Kengo Moriyama, Tomoko Mizuno, Daisuke Kobayashi, Motoki Inaji, Taketoshi Maehara. Temporo-polar gray/white matter blurring prior to febrile seizure status in temporal lobe epilepsy. 19th annual Meeting of Infantile Seizure Soceity (ISSET International Symposium on Severe Infantile Epilepsy Treatment) 2018.09.22 Roma, Italy

  20. Morio T, Nakajima K, Okado H.. Benzodiazepine-resistant status epilepticus in children: Alteration in GABAAR signal in children and its potential preventive measure. The World Federation of Societies of Biological Psychiatry (WFSBP). 2018.09.07 Kobe

  21. 磯田 健志, 高木 正稔. エピゲノム異常とトランスレーショナルリサーチ 非コードRNA転写による核内構造変換はT細胞への系列決定を誘導しT細胞系腫瘍の抑制に寄与する(Epigenome abnormalities and translational research Non-coding RNA transcription modulates nuclear architecture to specify T-cell fate and blocks T-cell malignancies). 日本癌学会総会記事 2018.09.01

  22. 宮本 智史, 成戸 卓也, 森尾 友宏, 浦山 ケビン, 真部 淳, 高木 正稔. 小児B前駆細胞性急性リンパ性白血病の疾患感受性に関連するTCF3のバリアント(Association of a TCF3 germline variant with pediatric B-cell precursor ALL development). 臨床血液 2018.09.01

  23. 長谷川 大輔, 平林 真介, 宮本 智史, 木村 俊介, 吉本 優里, 細谷 要介, 吉田 健一, 小川 誠司, 真部 淳. 急激な臨床経過を辿ったT細胞/骨髄性混合形質型急性白血病/リンパ腫(T/Myeloid mixed phenotype leukemia/lymphoma presenting aggressive clinical course). 臨床血液 2018.09.01

  24. 磯田 健志, 西村 聡, 宮本 智史, 森尾 友宏, 高木 正稔, ミュア・コーネリウス . 非コードRNA転写による核内構造変換はT細胞への系列決定を誘導しT細胞系腫瘍の抑制に寄与する(ThymoD modulates nuclear architecture to specify T-cell fate and blocks T-cell malignancies). 臨床血液 2018.09.01

  25. 磯田 健志, 西村 聡, 宮本 智史, 森尾 友宏, 高木 正稔, ミュア・コーネリウス . 非コードRNA転写による核内構造変換はT細胞への系列決定を誘導しT細胞系腫瘍の抑制に寄与する(ThymoD modulates nuclear architecture to specify T-cell fate and blocks T-cell malignancies). 臨床血液 2018.09.01

  26. 西村 聡, 平林 真介, 金淵 昭一郎, 山本 薫, 相賀 咲央莉, 細谷 要介, 大木 健太郎, 清河 信敬, 長谷川 大輔, 真部 淳. 診断後10年で再発をきたしたTCF3-ZNF384陽性急性リンパ性白血病の1例(TCF3-ZNF384 positive acute lymphoblastic leukemia recurring 10 years after diagnosis). 臨床血液 2018.09.01

  27. 平林 真介, 西村 聡, 山本 薫, 山本 俊亮, 細谷 要介, 野崎 太希, 長谷川 大輔, 真部 淳. 急性前骨髄球性白血病に生じた髄注後の亜急性白質脳症の一例(Subacute leukoencephalopathy after intrathecal methotrexate in a patient with APL). 臨床血液 2018.09.01

  28. 磯田 健志, 西村 聡, 宮本 智史, 森尾 友宏, 高木 正稔, ミュア・コーネリウス . 非コードRNA転写による核内構造変換はT細胞への系列決定を誘導しT細胞系腫瘍の抑制に寄与する(ThymoD modulates nuclear architecture to specify T-cell fate and blocks T-cell malignancies). 臨床血液 2018.09.01

  29. 磯田 健志, 高木 正稔. エピゲノム異常とトランスレーショナルリサーチ 非コードRNA転写による核内構造変換はT細胞への系列決定を誘導しT細胞系腫瘍の抑制に寄与する(Epigenome abnormalities and translational research Non-coding RNA transcription modulates nuclear architecture to specify T-cell fate and blocks T-cell malignancies). 日本癌学会総会記事 2018.09.01

  30. 磯田 健志, 高木 正稔. エピゲノム異常とトランスレーショナルリサーチ 非コードRNA転写による核内構造変換はT細胞への系列決定を誘導しT細胞系腫瘍の抑制に寄与する(Epigenome abnormalities and translational research Non-coding RNA transcription modulates nuclear architecture to specify T-cell fate and blocks T-cell malignancies). 日本癌学会総会記事 2018.09.01

  31. Tomohiro Morio. Overview and Updates on PID. 2018 Samsung Medeikal Center Primary Immunodeficiency Symposium 2018.07.14 Seoul,Korea

  32. 稲毛 章郎, 水野 直和, 吉敷 香菜子, 小林 匠, 石井 卓, 浜道 裕二, 上田 知実, 矢崎 諭, 嘉川 忠博. Feature tracking MR strainによる術後ファロー四徴症の右室心筋deformationと三尖弁変位の評価. 日本小児循環器学会雑誌 2018.07.01

  33. Kanegane H. Epstein-Barr related Primary Immunodeficiency. CME Lecture 2018.05.21 Singapore

  34. Kanegane H. Chronic Active Epstein-Barr Virus & Epstein-Barr Virus associated with Haemophagocytic Lymphohistiocytosis. CME Lecture 2018.05.21 Singapore

  35. Kanegane H. Management of HLH and XLP. APSID 2018 Summer School 2018.05.07 Chonquing, China

  36. 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

  37. Kanegane H. EBV associated PID. The 2nd APSID Scientific Congress 2018.05.07 Chonquing, China

  38. 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

  39. 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

  40. Virachith S, Inoue K, Saito M, Kubota T.. Some anti-CL-beta2-GPI antibodies induce a prothrombotic state by the dual reactivity with DNA and internalization into live cells.. The 62nd Annual Scientific Meeting of the Japan College of Rheumatology 2018.04.28 Tokyo, Japan

  41. Kashimada K, Nomura R, Suzuki H, Zhao L, Tsuji-Hosokawa A, Kanai Y, Yagita H, Bowles J, Koopman P, kanai-Azuma M, Morio T. Enforced expression of Nr5a1/Ad4bp/Sf1 in mouse fetal ovaries causes premature ovarian insufficiency by dysregulating Notch signaling. 8th International Symposium on the Biology of Vertebrate Sex determination 2018.04.16 Hawaii

  42. Tsuji-Hosokawa A, Kato T, Ogawa Y, Nomura R, Lavery R, Takasawa K, Harley V, Morio T, Takeda S, Kashimada K. SOX9 and FOXL2 Antagonistically Regulate Peptidyl Arginine Deiminase 2 (PADI2) Expression during testicular Development. 8th International Symposium on the Biology of Vertebrate Sex determination 2018.04.16 Kona

  43. Inage Akio, Kishiki Kanako, Mizuno Naokazu, Ishii Taku, Uyeda Tomomi, Yazaki Satoshi. Feature tracking MR Programを用いて評価したファロー四徴症修復術後患者における右室心筋変形と三尖弁偏位(Evaluation of Right Ventricular Myocardial Deformation and Tricuspid Valve Displacement in Repaired Tetralogy of Fallot Using Feature Tracking MR Program). 日本循環器学会学術集会抄録集 2018.03.01

  44. Inage Akio, Kishiki Kanako, Mizuno Naokazu, Kobayashi Takumi, Ishii Taku, Hamamichi Yuuji, Ueda Tomomi, Yazaki Satoshi, Yoshikawa Tadahiro. ファロー四徴症再建手術後のRV心筋奇形の心臓MRIによる評価(Assess RV myocardial deformation in repaired tetralogy of Fallot by cardiac MRI). 日本小児科学会雑誌 2018.02.01

  45. Tomohiro Morio. Multi-virus specific T cell therapy for drug-resistant viral infection following hematopoietic cell transplantation. The 5th IMSUT-CGCT Symposium 2018.01.30 Tokyo

  1. Tomohiro Morio. Molecular and cellular basis of systemic immune disease.. The 46th Annual Meeting of The Japanese Society for Immunology 2017.12.13 Miyagi

  2. Motoi Yamashita. B cell differentiation defect caused by IKZF3 mutation. 第46回日本免疫学会学術集会 2017.12.12 仙台

  3. Morio T. Investigational Gene Analysis for Primary Immunodeficiency Diseases. Asia Pacific Society for Immunodeficiencies(APSID) 2017.10.10 Hong Kong

  4. Morio T. Hematopoietic Cell Transplantation for Primary Immunodeficiency Diseases.: Current Situation and Future Direction. Asia Pacific Society for Immunodeficiencies(APSID) 2017.10.10 Hong Kong

  5. Takasawa K. Patient choice of growth hormone device improves child and adolescent adherence, and effects of growth hormone therapy. Novo Nordisk Global Expert Panel Meeting: Role of Patient Autonomy and Shared Decision Making 2017.10.08 London, UK

  6. Miyamoto Satoshi, Takagi Masatoshi, Nishimura Akira, Tanaka Mari, Ono Shintaro, Ashiarai Miho, Mitsuiki Noriko, Hoshino Akihiro, Yanagimachi Masakatsu, Aoki Yuki, Tomizawa Daisuke, Imai Kohsuke, Kajiwara Michiko, Kanegane Hirokazu, Morio Tomohiro. 頻回再発に対する複数回造血細胞移植により寛解を維持している乳児白血病の7歳女児例(A 7-year-old girl who maintains complete remission after multiple hematopoietic cell transplantation for frequent relapse of infant leukemia). 日本小児血液・がん学会雑誌 2017.10.01

  7. Nishimura Akira, Arakawa Ayumu, Hosoya Yosuke, Hirabayashi Shinsuke, Yoshihara Hiroki, Kikuta Atsushi, Matsumoto Seiichi, Kawamori Jiro, Hasegawa Daisuke, Kumamoto Tadashi, Ogawa Chitose, Manabe Atsushi. 骨盤内原発Ewing肉腫における集学的治療の検討(Multimodality treatment for pelvic Ewing sarcoma). 日本小児血液・がん学会雑誌 2017.10.01

  8. Miyamoto Satoshi, Takagi Masatoshi, Nishimura Akira, Tanaka Mari, Ono Shintaro, Ashiarai Miho, Mitsuiki Noriko, Hoshino Akihiro, Yanagimachi Masakatsu, Aoki Yuki, Tomizawa Daisuke, Imai Kohsuke, Kajiwara Michiko, Kanegane Hirokazu, Morio Tomohiro. 頻回再発に対する複数回造血細胞移植により寛解を維持している乳児白血病の7歳女児例(A 7-year-old girl who maintains complete remission after multiple hematopoietic cell transplantation for frequent relapse of infant leukemia). 日本小児血液・がん学会雑誌 2017.10.01

  9. Motoi Yamashita, Noriko Mitsuiki, Yuzaburo Inoue, Satoshi Okada, Aditya K. Padhi, Kam Y. Zhang, Osamu Ohara, Ichiro Taniuchi, Tomohiro Morio. Heterozygous IKZF3 Mutation in Patients with B cell Deficiency. ESID 2017 2017.09.14

  10. Yamashita M, Mitsuiki N, Inoue Y, Okada S, Padhi A.K, Zhang K.Y, Ohara O, Taniuchi I, Morio T. Heterozygous IKZF3 Mutation in Patients with B cell Deficiency. ESID 2017 2017.09.14 Edinburgh,UK

  11. Cho K, Yamada M, Agematsu K, Kanegane H, Miyake N, Ueki M, Akimoto T, Kobayashi N, Ikemoto S, Tanino M, Fujita A, Hayasaka I, Miyamoto S, Nakata K, Shiina M, Ogata K, Minakami H, Matsumoto N, Ariga T. A New Type of Primary Immunodeficiency with Pulmonary Alveolar Proteinosis due to OAS1 Dysfunction. ESID 2017 2017.09.13 Edinburgh, UK

  12. Kodawaki 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

  13. Kumaki E, Ono S, Shiota M, Saito N, Kanazawa N, Ida H, Oda H, Nishikomori R, Saito M, Lin H.T, Otsu M, Morio T. Neutrophil Function in PSTPIP1 Mutations.. ESID 2017 2017.09.13 Edinburg,UK

  14. 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

  15. 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 P13Kγ Syndrome Rescued by Hematopoietic. ESID 2017 2017.09.12 Edinburgh, UK

  16. 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

  17. Taniguchi Maki, Kato Motohiro, Osumi Tomoo, Nakabayashi Kazuhiko, Tsujimoto Shin-ichi, Kimura Yui, Yoshida Kaoru, Shirai Ryota, Miyamoto Satoshi, Yoshida Masanori, Yamada Yuji, Shioda Yoko, Kiyotani Chikako, Terashima Keita, Kiyokawa Nobutaka, Hata Kenichiro, Tomizawa Daisuke, Matsumoto Kimikazu. MECOM遺伝子変異による橈骨異常を伴わない先天性骨髄不全症(Congenital bone marrow failure without radial abnormality by germline mutation of MECOM). 臨床血液 2017.09.01

  18. Matsumoto Kazuaki, Takagi Masatoshi, Ishiwata Yasuyoshi, Aoki Yuki, Miyamoto Satoshi, Hoshino Akihiro, Nishimura Akira, Tanaka Mari, Yanagimachi Masakatsu, Mitsuiki Noriko, Imai Kohsuke, Kanegane Hirokazu, Kajiwara Michiko, Takikawa Kanako, Mae Tsukasa, Tomita Osamu, Fujimura Junya, Yasuhara Masato, Tomizawa Daisuke, Mizutani Shuki, Morio Tomohiro. 小児難治性血液腫瘍に対するクロファラビンおよびブスルファンを用いた前処置による血縁HLA半合致移植(HLA haploidentical HCT using clofarabine and busulfan for refractory pediatric leukemia). 臨床血液 2017.09.01

  19. Matsumoto Kazuaki, Takagi Masatoshi, Ishiwata Yasuyoshi, Aoki Yuki, Miyamoto Satoshi, Hoshino Akihiro, Nishimura Akira, Tanaka Mari, Yanagimachi Masakatsu, Mitsuiki Noriko, Imai Kohsuke, Kanegane Hirokazu, Kajiwara Michiko, Takikawa Kanako, Mae Tsukasa, Tomita Osamu, Fujimura Junya, Yasuhara Masato, Tomizawa Daisuke, Mizutani Shuki, Morio Tomohiro. 小児難治性血液腫瘍に対するクロファラビンおよびブスルファンを用いた前処置による血縁HLA半合致移植(HLA haploidentical HCT using clofarabine and busulfan for refractory pediatric leukemia). 臨床血液 2017.09.01

  20. 稲毛 章郎, 水野 直和, 齋藤 美香, 浜道 裕二, 石井 卓, 上田 知実, 嘉川 忠博, 矢崎 諭. Feature tracking磁気共鳴によって評価された右心系疾患における心筋機能障害の臨床的意義. 日本小児循環器学会雑誌 2017.07.01

  21. 稲毛 章郎, 水野 直和, 齋藤 美香, 浜道 裕二, 石井 卓, 上田 知実, 嘉川 忠博, 矢崎 諭. Feature tracking磁気共鳴ストレインによるFontan循環における右室型及び左室型単心室の心筋機能の比較. 日本小児循環器学会雑誌 2017.07.01

  22. Virachith S, Inoue K, Tamura S, Saito M, Kubota T.. Some anti-caldiolipin-beta2-GPI antibodies bring thrombophilic diathesis by the dual reactivity to DNA and internalization to live cells accompanying DNA.. 12th International Congress on SLE 2017.05.02 Melbourne, Australia

  23. Cell and Gene Therapy for Hematological Disorders. The 8th JSH International Symposium 2017 2017.05.01 Miyazaki, Japan

  24. Udagawa Tomohiro, Miura Kenichiro, Kanda Shoichiro, Saito Akihiko, Harita Yutaka. Amnionless遺伝子変異はcubilin-amnionless複合体形成障害を介して尿細管性タンパク尿を引き起こす(Mutations of Amnionless gene cause tubular proteinuria through defect in formation of cubilin-amnionless complex). 日本小児腎臓病学会雑誌 2017.05.01

  25. 稲毛 章郎, 石井 卓, 上田 知実, 矢崎 諭. Feature tracking磁気共鳴ストレイン、ストレインレート、および壁運動遅延分析によるフォンタン術後の右室機能の生理学的評価(Assessment of Right Ventricular Function in Fontan Physiology Using Feature Tracking Magnetic Resonance Strain, Strain Rate and Wall Motion Delay). 日本循環器学会学術集会抄録集 2017.03.01

  26. 稲毛 章郎, 水野 直和, 齋藤 美香, 浜道 裕二, 石井 卓, 上田 知実, 矢崎 諭, 嘉川 忠博. フォンタン手術後における大動脈肺動脈側副血行発達因子についての検討(Development factors of aortopulmonary collaterals after Fontan completions). 日本小児科学会雑誌 2017.02.01

  1. Kei Takasawa, et al.. Mortality and incidence of misidentification of sex assignment in patients with congenital 21-hydroxylase deficiency identified by a newborn screening program in Japan (2001-2015).. The 9th biennial scientific meeting of the Asia Pacific Paediatric Endocrine Society 2016.11.18 Tokyo, Japan

  2. Ryuichi Nakagawa, Akito Sutani, Tsuji Atsumi, Yohei Matsubara, Shigeru Takishima, Kei Takasawa, Kentaro Miyai, Makoto Ono, Toshikaza Oonishi, Kenichi Kashimada, Tomohiro Morio. The level of LH and FSH would be a monitoring marker for adult male 21-OHD patient. The 9th Biennial Scientific Meeting of the Asia Pacific Endocrine Society/ The 50th Annual Meeting of the Japanese Society for Pediatric Endocrinology 2016.11.17 Tokyo, Japan

  3. Kazuhisa Akiba, Masahiro Goto, Yoshihiko Morikawa, Kenichi Kashimada, Koji Muroya, Masayoshi Adachi, Yukihiro Hasegawa. Hydrocortisone dose between 180 and 360 days may change Ht- SDS during the first 1 year of life with 21 OHD. The 9th Biennial Scientific Meeting of the Asia Pacific Endocrine Society/ The 50th Annual Meeting of the Japanese Society for Pediatric Endocrinology 2016.11.17 Tokyo, Japan

  4. Risa Nomura, Maki Gau, Takeru Yamauchi, Akito Sutani, Atsumi Tsji-Hosokawa, Yohei Matsubara, Kentaro Miyai, Susumu Hosokawa, Gen Nishimura, Kenichi Kashimada. Myhre syndrome: a progressive connective tissue disorder with short stature. The 9th Biennial Scientific Meeting of the Asia Pacific Endocrine Society/ The 50th Annual Meeting of the Japanese Society for Pediatric Endocrinology 2016.11.17 Tokyo, Japan

  5. Akito Sutani, Takeru Yamauchi, Ryuichi Nakagawa, Nozomi Matsuda, Yuichi Miyakawa, Risa Nomura, Atsumi Tsuji-Hosokawa, Shigeru Takishima, Yohei Matsubara, Kei Takasawa, Misako Nagatsuma, Makoto Ono, Kenichi Kashimada, Tomohiro Morio. Fifty cases of congenital hypothyroidism re-evaluation taken in our hospital. The 9th Biennial Scientific Meeting of the Asia Pacific Endocrine Society/ The 50th Annual Meeting of the Japanese Society for Pediatric Endocrinology 2016.11.17 Tokyo, Japan

  6. Maki Igarashi, Kei Takasawa, Akiko Hakoda, Junko Kanno, Shuji Takada, Mami Miyado, Toshihiro Tajima, Ryohei Sekido, Tsutomu Ogata, Kenichi Kashimada, Maki Fukami. Identical NR5A1 Missense Mutations in Two Unrelated 46, XX Individuals with Testicular Tissues. The 9th Biennial Scientific Meeting of the Asia Pacific Endocrine Society/ The 50th Annual Meeting of the Japanese Society for Pediatric Endocrinology 2016.11.17 Tokyo, Japan

  7. Masahiro Goto, Kazuhisa Akiba, Kenichi Kashimada, Koji Muroya, Masanori Adachi, Tsuyoshi Isojima, Yukhiro Hasegawa. Infantile body weight gain up to 60 days of age is associated with height at 1 year of age in classical 21-hydroxylase deficiency. The 9th Biennial Scientific Meeting of the Asia Pacific Endocrine Society/ The 50th Annual Meeting of the Japanese Society for Pediatric Endocrinology 2016.11.17 Tokyo, Japan

  8. Yuichi Miyakwa, Akito Sutani, Atsumi Tsuji, Tomohiro Morio, Kenichi Kashimada. A case of Atypical Pubertal Development Caused by Dopamine Antagonist. The 9th Biennial Scientific Meeting of the Asia Pacific Endocrine Society/ The 50th Annual Meeting of the Japanese Society for Pediatric Endocrinology 2016.11.17 Tokyo, Japan

  9. Tomoda T, Okuno M, Sutani A, Tsuji-Hosokawa A, Imai K, Kashimada K, Urakami T, MorioT. Combined Therapy with pump and long acting insulin for type 1 diabetes mellitus caused by STAT1 mutation. The 9th Beinnial Scientific Meeting of the Asia Pacific Paediatric Endocrine Society/ The 50th Annual Meeting of the Japanese Society for Pediatric Endocrinology 2016.11.17 Tokyo, Japan

  10. Atsumi Tsuji, Kei Takasawa, Risa Nomura, Yuichi Miyakawa, Chikahiko Numakura, Atsushi Hijikata, Tsuyoshi Shirai, Yoshihiro Ogawa, Kashimada, Tomohiro Morio. Molecular mechanisms of insulin resistance in two cases of primary insulin receptor defect-associated diseases. The 9th biennial scientific meeting of the Asia Pacific Paediatric Endocrine Society 2016.10.19 Tokyo, Japan

  11. Virachith S, Inoue K, Tamura S, Saito M, Kubota T. Anti-DNA antibodies are internalized into live cells via cell surface DNA.. The 13th International Workshop on Autoantibodies and Autoimmunity 2016.10.13 Kyoto, Japan

  12. Kanegane H. Recent advances in primary antibody immunodeficiency and immunoglobulin replacement therapy. 21th Congress of Chinese Pediatric Society 2016.10 Zhuhai, PRC

  13. 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, UK

  14. 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, UK

  15. 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

  16. 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

  17. 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. I B-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

  18. 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

  19. 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

  20. 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 Immunodeficiency 2016.09.22 Barcelona, Spain

  21. 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 PI3 Kinase Delta Syndrome (APDS)-Like Immunodeficiency Caused by PTEN Mutation. 17th Biennial Meeting of the European Society for Immunodeficiencies 2016.09.22 Barcelona, Spain

  22. 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

  23. 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

  24. 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,Mori T,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

  25. 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

  26. Kanegane H. Immunoglobulin Replacement for Agammaglobulinemia – Intravenous or Subcutaneous?. ASPID Spring School 2016.05.01 HongKong

  27. Kanegane H. Use of Flow Cytometry in PID diagnosis.. APSID Spring School 2016.04.28 Hong Kong

  28. Motoi Yamashita, Kohsuke Imai, Tamaki Kato, Shingo Yamanishi, Nobuko Mayumi, Mayuri Tanaka, Tsubasa Okano, Keisuke Tanaka, Tzuwen Yeh, Akihiro Hoshino, Hirokazu Kanegane, Shigeaki Nonoyama, Tomohiro Morio. A novel synonymous mutation in the IL2RG gene results in abnormal splicing, leading to γc deficiency in 16-year-old boy with diffuse warts: a case report. Asia Pacific Society for Immunodeficiencies Congress 2016.04 Hong Kong, China

  29. Virachith S, Inoue K, Kato Y, Kubota T. Internalization of anti-DNA antibodies into live cells: one of the possible pathogenic mechanisms in SLE.. The 60th Annual Meeting of the Japan College of Rheumatology 2016.04 Yokohama, Japan

  30. 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

  1. Kenichi Kashimada. CAH newborn screening in Japan. ISNS-9th Asia Pacific Regional Meeting 2015.12.18 Penang, Malaysia

  2. Kajikawa Y, Hosokawa S, Wakabayashi K, Maejima Y, Isobe M, Doi S. Dexmedetomidine Ameliorates Monocrotaline Induced Pulmonary Arterial Hypertension in Rats. American Heart Association Scientific Sessions 2015 2015.11.10 Orland, USA

  3. Akihito Sutani, Yuichi Miyakawa, Atsumi Tsuji, Yuki Aoki, Kei Takasawa, Masatoshi Takagi, Kosuke Imai, Kenichi Kashimada, Tomohiro Morio. The late effects after the hematopoietic stem cells transplantation (HSCT) for patients with non-neoplastic disease. ESPE 2015.10.01 Barcelona

  4. Ryuichi Nakagawa, Atsumi Tsuji, Yuki Aoki, Keisuke Nakajima, Akito Sutani, Yuichi Miyakawa, Kei Takazawa, Daisuke Tomizawa, Masatoshi Takagi, Kenichi Kashimada, Tomohiro Morio. Total-Body Irradiation is a major risk factor for young adult onset diabetes mellitus and hyperlipidemia i childhood cancer survivors after hematopoietic stem cell transplantation. ESPE 2015.10.01 Barcelona

  5. Miyamoto Satoshi, Okawa Teppei, Mitsuiki Noriko, Isoda Takeshi, Aoki Yuki, Takagi Masatoshi, Kajiwara Michiko, Imai Kohsuke, Kanegane Hirokazu, Nagasawa Masayuki, Morio Tomohiro. 先天性角化不全症に対する非血縁同種骨髄移植 2症例報告(Unrelated allogenic bone marrow transplantation for dyskeratosis congenita: two case reports). 臨床血液 2015.09.01

  6. Kenichi Kashimada, Yohei Matsubara, Tomoko Kato, Takashi Nakasuji, Hiromitsu Tanaka, Zhou Zhi, Shizuko Ichinose, Tomoki Chiba, Yoshiaki Ito, Yumiko Saga, Tomohiro Morio, Shuji Takada, Hiroshi Asahara. TALEN-Mediated Gene Disruption on Y Chromosome Reveals Critical Role of EIF2S3Y in Mouse Spermatogenesis. Germinal Stem Cell Biology, Gordon Research Conference 2015.05.31

  7. Hirokazu Kanegane. XLP (X-linked lympho proliferative syndrome) and Epstein-Barr virus infection.. V Simpósio Internacional de Immunodeficiências Primárias—SIDEP, 5 2015.05.20

  8. 細川奨, 原口剛, 前嶋康浩, 磯部光章, 土井庄三郎. The synergistic effects of Incretin-related drugs for the treatment of pulmonary arterial hypertension. 第79回日本循環器学会学術集会 2015.04.25 大阪

  9. Takasawa K, Kashimada K, Pelosi E, Takagi M, Morio T, Asahara H, Schlessinger D, Mizutani S, Koopman P. FOXL2 transcriptionally represses Sf1 expression by antagonizing WT1 during ovarian development in mice.. 7th International Symposium on Vertebrate Sex Determination 2015.04.13 Hawaii

  10. Doi S, Matsumura Y, Kuranobu D, Kajikawa Y, Hosokawa S. Two pediatric cases with severe PAH in Japan that active early induction, rapid dose-up and relatively high dose maintenance of PGI2 remarkably worked for. 13th International Pulmonary Hypertension Forum 2015.03.28 Copenhagen, Denmark

  11. Morio T. Cell processing facility. International regulatory endeavor towards sound development of human cell therapy products. 2015.02.18 Tokyo

  12. Ogashiwa T, Kunisaki R, Yasuhara H, Tsuda S, Koh R, Yazawa K, Gotoh K, Kimura H, Sugita A, Mori M, Tanaka M, Kanegane H, Maeda S. Clinical, Morphological and Histological Features of X-linked Lymphoproliferative Syndrome Type 2 Enteritis Diagnosed in three Cases with Childhood Onset Inflammatory Bowel Disease. 10th Congress of ECCO - Inflammatory Bowel Diseases. 10th Congress of ECCO - Inflammatory Bowel Diseases 2015.02.18 Barcelona

  1. Kanegane H. Whole exome sequencing reveals atypical phenotype of X-linked lymphoproliferative syndrome.. A symposium for researchers and clinicians on XLP WAS 2014.11.03 London, UK

  2. Susumu Hosokawa, Go Haraguchi, Yasuhiro Maejima, Shozaburo Doi, Mitsuaki Isobe. The synergistic effects of Incretin-related drugs for the treatment of pulmonary arterial hypertension. American Heart Association Scientific Session s 2014 2014.11 Chicago, USA

  3. H. Takada, T. Takimoto, M. Ishimura, M. Urata, T. Morio, T. Hara. Wiskott-aldrich syndrome in a girl caused by heterozygous wasp mutation and extremely skewed x-chromosome inactivation:an association of non-randome x-chromosome inactivation and uniparental isodisomy 6. 16th Biennial Meeting of the European society for immunodeficiencies 2014.10.31 Prague, Czech Republic

  4. 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

  5. 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

  6. 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

  7. 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

  8. 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

  9. Yang X, Nishida N, Hoshino A, Goi K, Kanzaki T, Yoshida K, Muramatsu H, Ogawa S, Kojima S, Kanegane H. X-linked dysgammaglobulinemia associated with somatically reverted memory T cells in a family with X-linked lymphoproliferative syndrome type 1. 16th Biennial Meeting of the European Society of Immunodeficiencies 2014.10 Prague, Czech Rep

  10. Aguilar C, Lenoir C, Lambert N, Begue B, Brousse N, Canioni D, Berrebi D, Roy M, Gerart S, Chapel H, Schwerd T, Siproudhis L, Schappi M, Al-Ahmari A, Yamaide A, Mori M, Galicier L, Neven B, Routes J, Ulhig H, Koletzko S, Patel S, Kanegane H, Picard C, Fischer A, Cerf Bensussan N, Ruemmele F, Hugot J.P, Latour S. Characterization of crohn disease in X-linked inhibitor of apoptosis protein-deficient male patients and female symptomatic carriers. 16th Biennial Meeting of the European Society of Immunodeficiencies 2014.10 Prague, Czech Rep

  11. Mitsuiki N, Yang X, Bartol S, Kosaka Y, Takada H, Imai K, Kanegane H, Mizutani S, Van der Burg M, Van Zelm M, Ohara O, Morio T. Mutations in Bruton’s tyrosine kinase impair IgA responses. 16th Biennial Meeting of the European Society of Immunodeficiencies 2014.10 Prague, Czech Rep

  12. Hoshino A, Okuno Y, Migita M, Ban H, Yang X, Kiyokawa N, Kojima S, Ohara O, Kanegane H. B-precursor acute lymphoblastic leukemia in a patient with X-linked agammaglobulinemia. 16TH Biennial Meeting of the European Society of Immunodeficiencies 2014.10

  13. Nishida N, Yang X, Hoshino A, Kanegane H. Inflammatory bowel disease in Japanese patients with xiap deficiency. 16th Biennial Meeting of the European Society of Immunodeficiencies 2014.10 Prague, Czech Rep

  14. Kanegane H, Imai K, Yamada M, Takada H, Ariga T, Hara T, Rojavin M, Hu W, Hubsch A, Nonoyama S. Safety and tolerability of hizentra in patients with primary immunodeficiency in Japan, Europe and the US. 16th Biennial Meeting of the European Society of Immunodeficiencies 2014.10 Prague, Czech Rep

  15. Takashima T, Tsujita Y, Yeh T.W, Mitsuiki N, Kanegane H, Kracker S, Durandy A, Nonoyama S, Morio T, Imai K. Clinical and immunological features of patients with Gain-of-Function PIK3CD mutations in Japan. 16th Biennial Meeting of the European Society of Immunodeficiencies 2014.10 Prague, Czech Rep

  16. 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.

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

  1. Atsumi Tsuji, Kaoru Konishi, Satomi Hasegawa, Akira Anazawa, Teruo Kitagawa, Shuki Mizutani, Kenichi Kashimada. Newborn screening for congenital adrenal hyperplasia(CAH) in Tokyo, Japan: Lessons learned from 23 years’ experience. the 9th Joint Meeting of Paediatric Endocrinology 2013.09.20 Milan, Italy

  2. 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

  3. 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

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

  1. 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

  2. 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

  3. 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

  4. 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.

  5. 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.

  6. 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.

  7. 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.

  8. 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.

  9. 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.

  10. Hirata O, Tsumura M, Mizoguchi Y, Okada S, Minegishi S, Morio T, Kobayashi M. . Gain-of-function mutations of STAT1 in Japanese patients with CMCD.. 15th Biennial Meeting of the European Society of Immunodeficiencies (ESID2012). 2012.10 Florence, Italy.

  11. Sato T, Kuramitsu M, Sato-Otsubo A, Yoshida K, Toki T, Terui K, Wang R, Kanno H, Morio T, Ohga S, Ohara A, Kitoh T, Kudo K, Kojima S, Ogawa S, Hamaguchi I,. Frequent mutations in the RPS17 gene in Japanese DBA Patients.. 第74回日本血液学会学術集会 2012.10 京都

  12. Kumaki S, Sasahara Y, Kamachi Y, Muramatsu H, Morio T, Goi K, SugitaK, Urabe T, Takada H, Tsuchiya S, Hara T. . Long-term B cell function after unrelated CBT using a RIC regimen in patients with X-SCID.. 第74回日本血液学会学術集会 2012.10 京都

  13. Hayase T, Morimoto A, Ikeda T, Katsube N, Kawahara Y, Fukuda T. Kasii Y, Morio T, Momoi M.. HLA-matched unrelated CBT without conditioning in a SCID patient with Artemis abnormality. . 第74回日本血液学会学術集会 2012.10 京都

  14. 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

  15. 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

  16. 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.

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

  18. Nagasawa Masayuki, Ookawa Teppei, Endo Akifumi, Mitsuiki Noriko, Ono Toshiaki, Aoki Yuki, Isoda Takeshi, Tomizawa Daisuke, Imai Kohsuke, Takagi Masatoshi, Kajiwara Michiko, Morio Tomohiro, Mizutani Shuki. トロンボモジュリン-αは同種異系SCT後の凝固不全を伴うTRMを改善する(Thrombomodulin-alpha improves the coagulation disorder associated TRM after allogeneic SCT). 臨床血液 2012.09.01

  19. 磯田 健志, 高木 正稔, 森尾 友宏, 水谷 修紀. ATM欠損早期T細胞分化における14番染色体TCRd鎖切断と転座形成の可視化(Visualization of chromosome 14 breaks and translocations involving TCRd loci during early T-cell development lacking ATM). 日本癌学会総会記事 2012.08.01

  20. 磯田 健志, 高木 正稔, 森尾 友宏, 水谷 修紀. ATM欠損早期T細胞分化における14番染色体TCRd鎖切断と転座形成の可視化(Visualization of chromosome 14 breaks and translocations involving TCRd loci during early T-cell development lacking ATM). 日本癌学会総会記事 2012.08.01

  21. 磯田 健志, 高木 正稔, 森尾 友宏, 水谷 修紀. ATM欠損早期T細胞分化における14番染色体TCRd鎖切断と転座形成の可視化(Visualization of chromosome 14 breaks and translocations involving TCRd loci during early T-cell development lacking ATM). 日本癌学会総会記事 2012.08.01

  22. Takasawa K, Kashimada K, Ono M, Matsubara Y, Hijikata A, Katsumata N, Takagi M, Morio T, Ohara O, Mizutani S.. Two Novel Hsd3b2 Miss-Sense Mutations With Different Enzymatic Activity For Δ5 Steroids: Possible Cause For Elevated Levels Of 17-Hydroxyprogesterone (17-OHP) In 3β-Hydroxysteroid Dehydrogenase (3Β-HSD) Deficiency Patients.. ENDO 2012 (The Endocrine Society’s 94th Annual Meeting & Expo). 2012.06 Houston, Texas, USA.

  23. Isoda T, Takagi M, Piao J, Nakagama S, Sato M, Masuda K, Ikawa T, Azuma M, Morio T, Kawamoto H, Mizutani S.. Immune defect and visualization of chromosome 14 breaks and translocations involving TCRa/d loci during early T-cell development lacking ATM. . 17th congress of the European Hematology Association (EHA). 2012.06 Amsterdam, Netherlands.

  24. Motoyoshi Y, Udagawa T, Chiga M, Yoshida Y, Fujimura Y, Nagasawa M, Morio T, Mizutani S, Nagata M. . A case of atypical hemolytic uremic syndrome successfully treated with anti-C5 antibody. Continuous Professional Development program of International Pediatric Nephrology Association.. Japan-Korea The 10th Pediatric Nephrology Seminar 2012. 2012.05 Tokyo, Japan.

  25. Morio T.. An old and new regulator of ROS production in neutrophils. . Seminar of Brain Korea 21 Project for Functional Foods and Nutrigenomics. 2012.03 Seoul, Korea.

  26. Isoda T, Takagi M, Piao J, Sato M, Masuda K, Ikawa T, Azuma M, Morio T, Kawamoto H, Mizutani S. Visualization of chromosomal translocation and early T-cell development failure in ATM deficiency.. Ataxia telangiectagia workshop. 2012.02 New Delhi, INDIA.

  1. Isoda T, Takagi M, Piao J, Nakagama S, Sato M, Masuda K, Ikawa T, Azuma M, Morio T, Kawamoto H, Mizutani S.. T-Cell Development Failure At β-Selection Checkpoint and TCRα/δ Locus Break Formation Associated with Chromosome 14 Translocation in Ataxia-Telangiectagia Mutated Deficient Mice.. 53rd American society of hematology, annual meeting. 2011.12 San Diego, California, USA.

  2. Nagasawa M, Okawa T, Endo A, Mitsuiki N, Aoki Y, Ono T, Isoda T, Tomizawa D, Takagi M, Morio T, Mizutani S, Kajiwara M, Ishiwata Y, Yasuhara M.. Retrospective PK/PD analysis of oral and intravenous busulfan in pediatric patient having SCT.. 第73回日本血液学会学術集会 2011.10 名古屋

  3. Nagasawa M, Miyatake H, Hayakawa T, Hayashi Y, Katsumoto Y, Takagi M, Morio T, Ohmori S, Mizutani S. . Analysis of dielectricity and membrane proteins of erythrocytes in patient having allogenic SCT.. 第73回日本血液学会学術集会 2011.10 名古屋

  4. Isoda T, Takagi M, Piao J, Masuda K, Ikawa T, Azuma M, Morio T, Kawamoto H, Mizutani S.. DN3 T-cell development failure in Ataxia telangiectagia (AT).. 第73回日本血液学会学術集会 2011.10 名古屋

  5. Kuramitsu M, Matsubara A, Morio T, Takagi M, Toki T, Terui K, Wang R, Kanno H, Ohga S, Ohara A, Masumi A, Momose H, Mizukami T, Takizawa K, Yamaguchi K, Ogawa S, Ito E, Hamaguchi I. Extensive gene deletions in Japanese patients with Diamond Blackfan anemia.. Extensive gene deletions in Japanese patients with Diamond Blackfan anemia. . 第73回日本血液学会学術集会 2011.10 名古屋

  6. Nagasawa Masayuki, Okawa Teppei, Endo Akifumi, Mitsuiki Noriko, Aoki Yuki, Ono Toshiaki, Isoda Takeshi, Tomizawa Daisuke, Takagi Masatoshi, Morio Tomohiro, Mizutani Shuki, Kajiwara Michiko, Ishiwata Yasuyoshi, Yasuhara Masato. SCT施行小児患者におけるbusulfan経口投与および静脈内投与の後向きPK/PD解析(Retrospective PK/PD analysis of oral and intravenous busulfan in pediatric patients having SCT). 臨床血液 2011.09.01

  7. Isoda T, Ford A, Tomizawa D, Frederik van Delft, David Gonzalez De Castro, Score J, Takagi M, Morio T, Greaves M, Mizutani S. . Transmission and Ingenious Clonal Evolution of Maternal Cancer Cells in the Infant. . PAS/ASPR (Pediatric Academic Societies and Asian Society for Pediatric Research) 2011. 2011.05 Denver, Colorado, USA.

  8. Imai K, Mitsui K, Kajiwara M, Tomizawa D, Nagasawa M, Kogawa K, Morio T, Nonoyama S.. Retrospective analysis of stem cell transplantations for X-linked hyper-IgM syndrome. . 37th Annual Meeting of the European Group for Blood and Marrow Transplantation. 2011.04 Paris, France.

  9. Morio T. . Dissection of Common Variable immunodeficiency With Distinct Phenotype. . 2011 Pediatric Academic Societies &Asian Society for Pediatric Research Joint Meeting. 2011.04 Denver, Colorado, USA.

  10. renal lesions of japanese tuberous sclerosis. asian congress of pediatric nephrology 2011

  1. 高木 正稔, 烏野 初萌, 磯田 健志, 杉本 昌隆, 安田 章夫, 水谷 修紀. DNA損傷応答と細胞代謝におけるATMファミリー蛋白質の新側面 ATMは細胞分化を制御する(Novel Aspect of ATM family proteins in DNA damage responses and cellular metabolism ATM regulates cell differentiation). 日本生化学会大会・日本分子生物学会年会合同大会講演要旨集 2010.12.01

  2. Isoda Takeshi. 免疫学的に無症候性癌クローンの母から子に対する伝達(Immunologically silent cancer clone transmission from mother to offspring). 小児がん 2010.12.01

  3. Kuramitsu M, Morio T, Takagi M, Toki T, Terui K, RuNan Wang, , Masumi A, Mizukami T, Momose H, Takizawa K, Yamaguchi K, Ito E, Hamaguchi I. . New Determination Method for Extensive Gene Deletions In Diamond-Blackfan Anemia. . The 52nd ASH Annual Meeting. 2010.12 Orlando, Florida, USA.

  4. Morio T.. Unrelated umbilical cord blood transplantation for patients with primary immunodeficiency in Japan. . The 52nd ASH Annual Meeting. 2010.12 Orlando, Florida, USA.

  5. Erika Asai, Taizo Wada, Yasuhisa Sakakibara, Tomoko Toma, Takashi Shimizu, Kohsuke Imai, Shigeyuki Nonoyama, Tomohiro Morio, Yoshiro Kamachi, Osamu Ohara, Akihiro Yachie. Analysis of mutations and recombination activity in patients with rag 1/2 deficiency. XIVth meeting of the European Society for Immunodeficiencies. 2010.10 Isutanbul, Republic of Turkey.

  6. Morio T. . Btk Controls ROS Production and Apoptosis in Human Neutrophils.. XIVth meeting of the European Society for Immunodeficiencies. 2010.10 Isutanbul, Republic of Turkey.

  7. Kuramitsu M, Morio T, Takagi M, Ozeki M, Masumi A, Mizukami T, Momose H, Takizawa K, Ito E, Yamaguchi K, Hamaguchi I. . A novel method to analyze genomic copy number of Diamond Blacfan anemia responsible gene.. 第72回日本血液学会学術集会 2010.09 横浜

  8. Morio T. . 臍帯血移植における免疫モニタリングとT細胞免疫療法. 第2回 韓国-日本 臍帯血移植シンポジウム 2010.09

  9. Motoyoshi Y, Endo A, Takagi M, Nagasawa M, Morio T, Mizutani S, Nagata M.. Thrombotic microangiopathy in allogenic bone marrow transplantation in acute leukemia.. The 15th Congress of the International Pediatric Nephrology Association. 2010.08 New York.

  10. Shin M J, Shim J, Lee J, Chae W, Lee H, Morio T, Park J H, Chang E, Lee S.. PP-059-37 - Functional analysis of Fas-mediated activation signaling pathways in T cells.. 14th International Congress of Immunology 2010. 2010.08 Kobe in Japan.

  11. Honda F, Ikeda Y, Takahashi1 N, Lee S, Mizutani S, Morio T.. WS/PP-034-04 - Btk controls ROS production and apoptosis in human neutrophil.. 14th International Congress of Immunology 2010. 2010.08 Kobe in Japan.

  12. Okamoto K, Iwai Y, Oh-hora M, Yamamoto M, Morio T, Jetten A M, Akira S, Muta T, Takayanag H.. WS/PP-014-02 - IκBζ is required for the transcriptional program in Th17 development.. 14th International Congress of Immunology 2010. 2010.08 Kobe in Japan.

  13. Morio T. . PP-102-32 - Impaired CD4 and CD8 Effector Function and Decreased Memory T-cell Populations in ICOS-deficient Patients.. 14th International Congress of Immunology 2010. 2010.08 Kobe, Japan.

  14. Morio T. . Common variable immunodeficiency (CVID): Molecular basis of immunedysfunction: . The 2nd Symposium for PID in Asia. 2010.02 Chiba, Japan.

  15. long-term outcome of ideopathic steroid resistant nephrotic syndrome in children. congress of internationla pediatric nephrology association 2010

  1. Takagi M, Unno J, Kiyono T, Honda F, Teraoka H, Maeda D, Masutani M, Morio T, Mizutani S.. LA DNA Double-Strand Break Formation Induced by Replication Arrest Depend On Artemis. . 51th American Society of Hematology Annual meeting 2009. 2009.12 New Orleans.

  2. Isoda T, Ford A, Tomizawa D, van Delft FW, Gonzalez de Castro D, Mitsuiki N, Score J, Taki T, Morio T, Takagi M, Saji H, Mizutani S, Greaves M.. Loss of non-inherited maternal MHC and materno-fetal transmission of p190 type BCR-ABL leukemia.. 51st Annual Meeting of the American Society of Hematology. 2009.12 New Orleans, USA

  3. 磯田健志、高木正稔、長澤正之、森尾友宏、滝 智彦、谷脇雅史、水谷修紀. Materno-fetal transmission and loss of non-inherited maternal MHC in p190 type BCR-ABL leukemia. . 第68回日本癌学会 2009.10.02 横浜

  4. Aoki Y, Mitsuiki N, Endo A, Ono T, Takagi M, Kajiwara M, Nagasawa M, Morio T, Mizutani S, Imadome K. . A case of SLE 10years following cord blood transplantation for JMML with mixed chimerism. . 第71回日本血液学会 2009.10 京都

  5. Isoda T, Mitsuiki N, Aoki Y, Tomizawa D, Takagi M, Nagasawa M, Morio T, Ochiai N, Taki T, Taniwaki M, Saji H, Mizutani S.. Loss of NIMA as a possible role of materno-fetal transmission of p190 type BCR-ABL leukemia.. 第71回日本血液学会 2009.10 京都

  6. Isoda Takeshi, Mitsuiki Noriko, Aoki Yuki, Tomizawa Daisuke, Takagi Masatoshi, Nagasawa Masayuki, Morio Tomohiro, Ochiai Nakaba, Taki Tomohiko, Taniwaki Masafumi, Saji Hiroh, Mizutani Shuki. p190型BCR-ABL白血病の母児移行の原因としてのNIMAの欠失(Loss of NIMA as a possible role of materno-fetal transmission of p190 type BCR-ABL leukemia). 臨床血液 2009.09.01

  7. 磯田 健志, 高木 正稔, 長澤 正之, 森尾 友宏, 滝 智彦, 谷脇 雅史, 水谷 修紀. p190型BCR-ABL白血病における母児間転移と非遺伝母HLAアレル(NIMA)欠損(Materno-fetal transmission and loss of non-inherited maternal MHC in p190 type BCR-ABL leukemia). 日本癌学会総会記事 2009.08.01

  8. 磯田 健志, 高木 正稔, 長澤 正之, 森尾 友宏, 滝 智彦, 谷脇 雅史, 水谷 修紀. p190型BCR-ABL白血病における母児間転移と非遺伝母HLAアレル(NIMA)欠損(Materno-fetal transmission and loss of non-inherited maternal MHC in p190 type BCR-ABL leukemia). 日本癌学会総会記事 2009.08.01

  9. 磯田 健志, 高木 正稔, 長澤 正之, 森尾 友宏, 滝 智彦, 谷脇 雅史, 水谷 修紀. p190型BCR-ABL白血病における母児間転移と非遺伝母HLAアレル(NIMA)欠損(Materno-fetal transmission and loss of non-inherited maternal MHC in p190 type BCR-ABL leukemia). 日本癌学会総会記事 2009.08.01

  10. Morio T. . ROS induced DNA damage response. Symposium: “ROS and NO”. The 46th Meeting of Korean Society of Biochemistry and Molecular Biology. 2009.05 Seoul, Korea.

  11. Tanaka E,Mukai J, Morio T, Mizutani S.. A case of Wiskott-Aldrich syndrome with purpura nephritis: Improvement in renal pathology after immunosuppressants and bone marrow transplantation.. 7th Japan-Korean pediatric nephrology seminar. 2009.04 Kyunggi-Do, Korea.

  1. Isoda T, Mitsuiki N, Aoki Y, Tomizawa D, Takagi M, Kajiwara M, Nagasawa M, Ochiai H, Taki T, Morio T, Mizutani S. An eleven-month-old girl who developed malignant lymphoma derived from maternal BCR-ABL positive clone.. 第11回乳児白血病講演会 2008.04.19 東京

  2. Watanabe F, Morio T, Ogigami N, Kiyono T, Delia D, Mizutani S.. Stability of Artemis protein is regulated by Hsp72. . Ataxia-Telangiectasia Workshop 2008. 2008.04 Otsu, Shiga,

  3. Unno J, Takagi M, Watanabe F, Sato M, Takahashi N, Morio T, Teraoka H, Mizutani S. . Generation of DNA double-stranded breaks in stalled DNA replication forks: an essential step initiated by Artemis toward a second wave of DNA damage response and ATM activation.. Ataxia-Telangiectasia Workshop 2008. 2008.04 Otsu, Shiga,

  4. Mizutani S, Unno J, Watanabe F, Takagi M ,Morio T, Teraoka H, Domenico D.. Regulation of Artemis/ATM-related DNA damage response network.. Ataxia-Telangiectasia Workshop 2008. 2008.04 Otsu, Shiga,

  5. Nakamura K, Morio T, Mizutani S,. Identification of Novel Mutation in Japanese Patients with Ataxia Telangiectasia ; Absence of Founder Mutations.. Ataxia- TelangiectasiaWorkshop 2008. 2008.04 Otsu, Shiga,

  6. Morio T. . Ataxia telangiectasia: Involvement of ATM in immunodeficiency and leukemogenesis.. International symposium on Recent Advances in Cell Function and Defense Mechanisim. 2008.04 Seoul, Korea.

  7. Morio T. . Immunodefiencies with impaired DNA damage response.. Recent Advances in DNA Damage Response. 2008.04

  8. Morio T. . Ataxia-Telangiectasia in Japan:Phenotypic variations in affected siblings with Ataxia-Telangiectasia. . Ataxia-Telangiectasia Workshop 2008. 2008.04 Otsu, Shiga

  1. Morio T. . Strategy to combat opportunistic infections after umbilical cord stem cell transplantation.. The 5th Annual International Umbilical Cord Blood Transplantation Symposium. 2007.05 California, USA.

  2. Morio T. . Immunity & Nutrition, Its importance in post-transplantation period.. Symposium on Infection, Immunity and Nutrition. 2007.03 Seoul, Korea

  1. Morio T. . Strategy to combat opportunistic infections aft Seoul, Korea.er stem cell transplantation. . The 11th Congress of Asian-Pacific Bone Marrow Transplantation. 2006.10 Nagoya, Japan.

  1. Morio T. . Cell cycle checkpoint. DNA repair system. and Carcinogenesis. . International Symposium on Gastrointestinal Disorders: Molecular Mechanisms of Pathogenesis. in Commemoration of 120th Anniversary of Yonsei Univeisity. College of Medicine. 2005.06 Seoul, Korea.

  1. Morio T. . Activated T-Cell transfusion for opportunistic infection in immunodeficient patients and for post-transplant infections.. The 10th Meeting of Transplantation/ Immunoregulation 21. 2003.11 Tokyo, Japan.

  2. Morio T. . Activated T-Cell Transfusion for Opportunistic Infection in Immunodeficient Patients and for Post-transplant Infections.. The 2nd International Symposium "New Challenges in the Post Genome Era 2003" 2003.11 Seoul, Korea.

  3. Morio T. . Activated T-Cell Transfusion for Opportunistic Infection in Immunodeficient Patients.. Nihon University School of Medicine Symposium “Cell Biology of Virus Infection” 2003.10 Tokyo, Japan.

  4. Morio T. . Molecular Basis of Primary Immunodeficiency.. The 46th Meeting of Korean Association of Immunobiologists 2003.04 Seoul, Korea.

  1. Morio T. . Ku70/80, A DNA Repair Protein Involved in Cellular Survival, Transformation, and Death.. 2002 International Symposium on Exocrine Pancreas 2002.08 Seoul, Korea.

  1. Morio T. . Proteomics approach for elucidating signal transduction pathway. Symposium: "Genomics and Proteomics in Pharmacology". Annual Meeting of Korean Society of Pharmacology 2001.04 Seoul, Korea.

  2. Morio T. . Proteomics approach for elucidating signal transduction pathway. Symposium: "Genomics and Proteomics in Pharmacology" . Annual Meeting of Korean Society of Pharmacology 2001.04 Seoul, Korea.

  1. Morio T. . Identification of CD40-associated protein by protein microsequencing and ESI-MS.. In Proteomics and Genomics in Biotechnology, The 8th Bioproduct Research Center International Symposium. 2000.06 Seoul, Korea.

  1. Yoko Miyoshi, Makiko Tachibana, Naoko Nagai, Tadashi Akao, Masanori Adachi, Junko Ito, Kenichi Kashimada, Junko Kanno, Takeshi Sato, Shizuyo Nagai, Tomohiro Hori, Reiko Horikawa, Koji Muroya, Shuntaro Morikawa, Satoshi Okada, . Questionnaire survey for pediatric endocrinologists regarding nutritional management in childhood and AYA cancer patients. The 56th JSPE Saitama 2023.10.19 Saitama

  2. Kanshi Minamitani, Kentaro Shiga, Asako Tajima, Kenichi Kashimada, Yasusada Kawada, Ken Fukuda, Yumiko Kotani, Miyuki Kitamura, Junnosuke Miura, Ikuko Takahashi, Hanako Tajima, Ichiro Yokota, Shigetaka Sugihara, Toru Kikuchi . Thyroid function in pediatric fulminant type 1 diabetes mellitus. The 56th JSPE Saitama 2023.10.19 Saitama

  3. Shogo Akahoshi, Tomohiro Nagata, Masako Tomotsune, Hiroaki Zukeran, Kento Ikegawa, Marie Konno, Yoshihiko Morikawa, Shigeru Takishima, Yukihiro Hasegawa. Feedback Sheet for Type 1 Diabetes Care: Interim Report( Derivation Study) and Invitation to Collaborate( Validation Study) . The 56th JSPE Saitama 2023.10.19 Saitama

  4. Ryosei Iemura, Haruki Yamano, Haruka Iwata, Kazuyuki Itou, Manabu Sugie, Chikako Morioka, Kei Takasawa, Kenichi Kashimada, Tomohiro Morio . A neonate with chromosome Xp21 deletion syndrome presenting as severe adrenal insufficiency. The 56th JSPE Saitama 2023.10.19 Saitama

  5. Nozomi Matsuda, Shigeru Takishima, Kaoru Sato, Kenichi Kashimada, Takeshi Hasegawa. A study of central precocious puberty before and after the COVID-19 pandemic.. The 56th JSPE Saitama 2023.10.19 Saitama

  6. Shizuka Kirino, Ryuichi Nakagawa, Kei Takazawa, Maki Gau, Kenichi Kashimada . Sequencing of Functionally Active Enhancers Reveals a Novel Transcriptional Regulatory Mechanism in Gonadogenesis . The 56th JSPE Saitama 2023.10.19 Saitama

  7. Hideyuki Iwayama, Saiki Sugimoto, Makoto Ono, Sachiko Kitagawa, Kohei Kawahara, Kiyoshi Yamakawa, Ryosuike Miyamoto, Kenichiro Kaneko, Shogo Nakano, Yasushi Fujimoto, Junko Takagi, Akihisa Okumura, Chiyoe Shirota, Takahisa Tainaka, Hiroo Uchida, Shigeru Takishima, Kei Takazawa, Misako Nagatsuma, Kenichi Kashimada. Pathogenic bacteria and their antibiotic resistance in uncomplicated acute suppurative thyroiditis in Japan. The 56th JSPE Saitama 2023.10.19 Saitama

  8. Eriko Adachi, Ryuichi Nakagawa, Atsumi Tsuji, Maki Gau, Shizuka Kirino, Analia Yogi, Hisae Nakatani, Kei Takasawa, Tomomi Yamaguchi, Tomoki Kosho, Masanori Murakami, Toshihiro Tajima, Tomonobu Hasegawa, Tetsuya Yamada, Tomohiro Morio, Osamu Ohara, Kenichi Kashimada . Development of a clinically applicable one-step PCR-based CYP21A2 analysis using long read sequences, identifying a novel structural abnormality. The 56th JSPE Saitama 2023.10.19 Saitama

  9. Kenichi Kashimada. Preconception Care for Pediatric Patients with Endocrine Diseases. The 56th JSPE Saitama 2023.10.19

  10. Haruki Yamano, Ryosei Iemura, Shizuka Kirino, Kumi Shuno, Yoko Saitou, Eriko Adachi, Hanako Tajima, Tomohiro Morio, Kenichi Kashimada, Kei Takazawa . A new treatment strategy for congenital hyperinsulinism using lanreotide and continuous glucose monitoring. The 56th JSPE Saitama 2023.10.19 Saitama

  11. Kenichi Kashimada, Ichiro Miyata, Takuo Kubota, Jun Mori, Kayo Ozaki, Yosuke Nonaka, Yoshikazu Nakamura, Toya Ohashi, Keiichi Ohzono . Designing early phase Ⅱ study of anti-FGF2 RNA aptamer in children with achondroplasia. The 56th JSPE Saitama 2023.10.19 Saitama

  12. Lessons from CAH Newborn Screening by LC-MS/MS assay. Japanese Journal of Neonatal Screening 2023.08.26

  13. A novel RNF213 gene de novo variant is involved in systemic vasculopathy. 2023.05.27

  14. Two cases of late-onset familial hemophagocytic lymphohistiocytosis type 3 presenting with CLIPPERS-like syndrome. 2023.02.12

  15. Wiskott-Aldrich syndrome due to chromosomal structural abnormalities. 2023.02.12

  16. Allogenic HCT with alemtuzumab in pediatric patients with inborn errors of immunity. 2023.02.12

  17. A case of A20 haploinsufficiency diagnosed by recurrent fever and vomiting attacks during follow-up as initial diagnosis of oligoarticular juvenile idiopathic arthritis . 2023.02.12

  18. Investigation of calprotectin suppressive therapy using disease-specific iPS cells in a pathological model of PAMI syndrome. 2023.02.12

  19. Hematopoietic cell transplantation for patients with inborn errors of immunity. 2023.02.11

  20. The potential of baricitinib as a treatment for Aicardi-Goutiēres syndrome type 7. 2023.02.11

  21. Efficacy of JAK inhibitors for patients with gain-of-function mutation of STAT3. 2023.02.11

  22. Comparison of adult and pediatric cases with hyper-IgE syndrome caused by function in STAT3. 2023.02.11

  23. Support for adolescent patients and their families by HSC coordinators in fertility preservation. 2023.02.11

  24. A case of relapsed AML maintained complete remission by re-transplantation using clofarabine. 2023.02.11

  1. A case of unrelated bone marrow transplantation with alemtuzumab-based conditioning regimen for XIAP deficiency. 2022.11.26

  2. EBV reactivation and nephrotic syndrome associated with chronic GVHD after allogeneic hematopoietic cell transplantation for GATA2 deficiency. 2022.11.26

  3. Sinusoidal obstruction syndrome during induction remission therapy for FUS-ERG-positive BCP-ALL. 2022.11.26

  4. Cytokine monitoring for disease status evaluation in a patient with chronic active Epstein-Barr virus infection. 2022.11.25

  5. Umbilical cord blood transplantation for a patient with CHARGE syndrome and severe combined immunodeficiency. 2022.11.25

  6. BCP-ALL Inotuzumab ozogamicin successfully controlled the TCF3-HLF-positive acute lymphoblastic leukemia before hematopoietic cell transplantation. 2022.11.25

  7. A PAX5 germline variant in a patient with common variable immunodeficiency complicated with B-cell acute lymphoblastic leukemia. 2022.11.25

  8. Polatuzumab vedotin, bendamustine and rituximab (Pola-BR) for diffuse large B cell lymphoma in a patient with Bloom syndrome. 2022.11.25

  9. Non-coding RNA transcription and super-enhancer activation facilitate 3D genome structure. 2022.09.29

  10. Stem cell transplantation for XLP1 with EBV-associated hemophagocytic lymphohistiocytosis. 2022.05.14

  11. Role of Hematopoietic Cell Transplant Coordinator in transition from childhood to adulthood. 2022.05.14

  12. Alemtuzumab-containing reduced intensity conditioning for two cases with PI3K-delta syndrome. 2022.05.13

  13. Allogeneic hematopoietic cell transplantation for asymptomatic patients with SAP deficiency. 2022.05.13

  14. International retrospective study of allogeneic HCT for X-linked agammaglobulinemia. 2022.05.13

  15. Cellular therapy within the framework of regenerative medicine. 2022.05.12

  16. A case of bone marrow transplantation to activated P13KDelta syndrome type 1 (APDS1). 2022.02.12

  17. A nation-wide study of congenital complement deficiency in Japan. 2022.02.12

  18. Infection prevention for patients with inborn errors of immunity; second report from a nationwide survey in Japan. 2022.02.12

  1. Endeavor toward constant supply of human raw materials for industrial use in Japan. 2021.12.10

  2. Epstein-Barr Virus-negative granulomatous disease due to SAP deficiency; a case report. 2021.11.25

  3. Successful TCRABCD 19-depleted hematopoietic cell transplantation for a patient with Artemis deficiency. 2021.11.25

  4. First in children phase I clinical study of oral olaparib in pediatric patients with refractory solid tumors. 2021.11.25

  5. Utlization and prospects of single-cell RNA sequencing -Aiming to elucidate heterogeneity of cancer cells-. 2021.11.25

  6. Rare Diseases and Regenerative Medicine. 2021.03.12

  7. A study of adenosine deaminase 2 deficiency by multi-omics analysis. 2021.02.07

  8. Delayed recovery of chimeric status after non-myeloablative cord blood transplantation in a patient with DNA ligase IV deficiency. 2021.02.06

  9. Inborn Errors of Immunity : Lessons learnt from outliers. 2021.01.26

  1. Challenges and Opportunities in Processing of Raw Materials and Cellular and Tissue-based Products at Hospitals. 5th DIA Cell and Gene Therapy Products Symposium in Japan(DIA) 2020.12.11

  2. Allogeneic hematopoietic stem cell transplantation from haploidentical donors for non-malignant diseases with post-transplantation cyclophosphamide and anti-thymoglobulin. 2020.11.22

  3. A retrospective study of six cases of HLA haplo-identical hematopoietic stem cell transplantation with Post-Transplant Cyclophosphamide. 2020.11.22

  4. Ruxolitinib administration for two cases with steroid-refractory lung GVHD. 2020.11.22

  5. Inflammatory bowel disease associated with XIAP deficiency can be cured by allogeneic hematopoietic cell transplantation. 2020.11.22

  6. Salvage haploidentical bone marrow transplant using post-transplant cyclophosphamide for graft failure in a patient with EDA-ID due to NEMO deficiency. 2020.11.22

  7. Non-coding RNA ThymoD transcription specifies T-cell fate and inhibits T-cell malignancies. 2020.11.21

  8. Clinical feature and genetic alteration of Myeloid/Natural killer cell precursor acute leukemia (MNKPL). 2020.11.21

  9. CAR-T Therapy Practice: Through experience under various situations. 2020.11.21

  10. A case of relapsed infant ALL with MLL rearrangement who underwent CAR-T cell therapy. 2020.11.21

  11. Analysis of viral antigen-specific T memory stem cells induced by HTLV-I infection. Japanese Society of Immunotherapy for Hematological Disorders (JSIHD) 2020.09.12

  12. Genomics analysis of leukemia predisposition in X-linked agammaglobulinemia. 2020.02.16

  13. A case of rheumatoid arthritis associated with IKAROS deficiency treated with abatacept. 2020.02.16

  14. 175 cases of genetic testing by health insurance for primary immunodeficiency in Japan. 2020.02.16

  15. An adult case of A20 haploinsufficiency diagnosed by the development of myocardial infarction due to coronary arteritis. 2020.02.15

  16. Two cases identifield CARD11 mutation with atopic dermatitis and susceptibility to infection. 2020.02.15

  17. A PHASE 3 STUDY OF SAFETY AND TOLERABILITY OF IgPro10(PRIVIGEN®) IN JAPANESE PATIENTS WITH PRIMARY IMMUNODEFICIENCY. 2020.02.15

  1. Pay attention to selective Immunoglobulin G2 deficiency - a case of Invasive pneumococcal infection after allogenic hematopietic stem cell transplantation. 2019.11.16

  2. Usefulness of respiratory infection early diagnosis with multiplex PCR method for immunocompromised patients. 2019.11.16

  3. Succesful case of donor lymphocyte infusion for refractory T cell acute lymphoblastic leukemia which lead to one year of remission. 2019.11.16

  4. Intrinsically Vancomycin resistant enterococcal (Enterococcus gallinarum) meningitis occurred early after hematopoietic stem cell transplantation for activated PI3K delta syndrome type2. 2019.11.16

  5. BMP4 suppresses the tumor growth of neuroblastoma via MYCN downregulation. 2019.11.15

  6. A case with relapsed acute lymphoblastic leukemia treated with blinatumomab under the active GVHD after unrelated bone marrow transplantation. 2019.11.15

  7. A case of type 1 hyper-IgE syndrome with leukemoid reaction in an infant. 2019.11.14

  8. PARP inhibition sensitize BCR-ABL1 positive cell. 2019.11.14

  9. Treatment of platelet transfusion refractoriness in patients with Wiskott-Aldrich syndrome. 2019.11.14

  10. Efficacy of Azacitidine for MDS due to germline GATA2 haploinsufficiency. 2019.11.14

  11. BRAFV600E-POSITIVE PRECURSORS AS MOLECULAR MARKERS OF BONE MARROW INVOLVEMENT IN PEDIATRIC LANGERHANS CELL HISTIOCYTOSIS. 2019.11.14

  12. Clonal evolution of leukemia with MLL-AF9 from myeloid to T-lineage. 2019.11.14

  13. Genetic test for the suspected patients of inborn errors of immunity. 2019.11.07

  14. Influence of genetic mutation of CGD on the outcome of HSCT (a collaboration of JDCHCT and PIDJ). 2019.03.08

  15. Impact of GVHD on the clinical outcome of allogeneic HSCT for non-malignant diseases. 2019.03.08

  16. Multivirus specific T cell therapy for refractory viral infection after HSCT. 2019.03.08

  17. An experience of allogenic stem cell transplantation for NFKB1 deficiency. 2019.02.03

  18. Three families with X-linked agammaglobulinemia caused by transcriptional. 2019.02.03

  19. Combined immunodeficiency of ICF syndrome. 2019.02.03

  20. An adult case of cytotoxic T-lymphocyte antigen 4 (CTLA-4) insufficiency treated successfully with abatacept. 2019.02.03

  21. Hematopoietic cell transplantation with reduced intensity conditioning regimen using fludarabine/busulfan and fludarabine/melphalan for primary immunodeficiency diseases . 2019.02.02

  1. TCF3 inherited variants in children with B-cell precursor acute lymphoblastic leukemia. 2018.11.15

  1. A case of CTLA4 hapioinsufficiency found by lymphadenopathy. 2017.11.11

  2. A 7-year-old girl who maintain complete remission after multiple hematopoietic cell transplantation for frequent relapse of infant leukemia. 2017.11.11

  3. A case of T-cell hymphoblastic lymphoma/leukemia complicated by gait inability during combination chemotherapy with nelarabine. 2017.11.10

  4. Kudo K, Maeda M, Suzuki N, Kanegane H, Ohga S, Ishii E, Shioda Y, Imamura T, Imashuku S, Tsunematu Y, Endo M, Shimada A, Koga Y, Hashii Y, Inagaki J, Inoue M, Tabuchi K, Morimoto A. Hematopoietic stem cell transplamtation in children with refractory Langerhans cell histiocytosis. 2017.11.09

  5. Central venous catheter-related cylindrical thrombosis in right atrium after bone marrow transplantation for X-linked anhidrotic ectodermal dysplasia with immunodeficiency(XL-EDA-ID). 2017.11.09

  6. Sutani A, Hosokawa S, Takasawa K, Shima H, Suzuki E, Doi S, Fukami M, Kashimada K, Morio T. A boy with WDR11 mutation who represented CHARGE syndrome loke phenotype. The 51st Annual Scientific Meeting of JSPE 2017.09.30 Osaka

  7. Takasawa K, Igarashi M, Takada S, Yamataka A, Ogata T, Fukami M, Kashimada K. Various phenotypes of 46, XX DSD due to the p.R92W variant of NR5A1. The 51st Annual Scientific Meeting of JSPE 2017.09.30 Osaka

  8. Takishima S, Nakajima K, Nomura R, Tsuji A, Matsuda N, Matsubara Y, Ono M, Miyai K, Takasawa K, Morio T, Hasegawa Y, Kasimada K. Lower body weight and BMI at birth were associated with early adiposity rebound in 21-hydroxylase deficiency patients. The 51st Annual Scientific Meeting of JSPE 2017.09.30 Osaka

  9. Nakagawa R, Takasawa K, Yeh TW, Imai K, kashimada K, Morio T. A case of Type 1 diabetes mellitus developed by gain of function mutation in P13K delta. The 51st Annual Scientific Meeting of JSPE 2017.09.30 Osaka

  10. Gau M, Matsuda N, Miyakawa Y, Hayata M, Ito K, Sato C, MinosakiY, Kashimada K, Takasawa K. Diazoxide treatment with CGM for syndrome congenital hyperinsulinism. The 51st Annual Scientific Meeting of JSPE 2017.09.29 Osaka

  11. Saito Y, Nakagawa R, Nomura R, Kasimada K, Miyai K. Induction of thyroid remission using carbamazepine in a patient with Graves' disease: A case report. The 51st Annual Scientific Meeting of JSPE 2017.09.29

  12. Miyakawa Y, Matsubara Y, Takasawa K, Ohtsu Y, Kitsuda K, Sato M, Mochizuki H, Yokota I, Hasegawa Y, Kashimada K. Pseudohypoparathyroidism Type 1a (PHP1a) with Delayed Language Development during Early Childhood. The 51st Annual Scientific Meeting of JSPE 2017.09.29 Osaka

  13. Matsuda N, Takishima S, Gau M, Miyagawa Y, Fujiwara M, Ohata Y, Kashimada K, Ozono K, Takasawa K. To investigate the implication of TNSALPc.787T>C mutation. The 51st Annual Scientific Meeting of JSPE 2017.09.28 Osaka

  14. Nagatsuma M, tuji A, Takasawa K, Kashimada K. A polymorphism of calcium sensing receptor (CaSR), R990G, could cause mild hypoparathyroidism during childhood. The 51st Annual Scientific Meeting of JSPE 2017.09.28 Osaka

  15. Kashimada K. Clinical Practice od DSD from Understanding Molecular Mechanism if Sexual Differentiation. The 51st Annual Scientific Meeting of JSPE 2017.09.28 Osaka

  16. Tomoko Mizuno, Satoko, Kumada, Hiroya Nishida, Tetsuharu Kamioka, Shumpei Uchino, Eiji Kurihara. A case of opsoclonus-myoclonus syndrome associated with laryngeal stridor during sleep. The 59th Annual Meeting of the Japanese Society of Child Neurology 2017.06.15 Osaka

  17. Takasawa K, Tsuji A, Nomura R, Miyakawa Y, Numakura C, Kashimada K, Morio T. Molecular mechanism of insulin resistance: two cases of insulin receptoropathy. The 120th Annual Meeting of the JPS 2017.02.01 Tokyo

  1. Akihiro Hoshino, Satoshi Okada, Kenichi Yoshida, Yusuke Okuno, Miyuki Tsumura, Shiho Nishimura, Sonoko Sakata, Masatoshi Takagi, Kohsuke Imai, Yuichi Shiraishi, Kenichi Chiba, Hiroko Tanaka, Satoru Miyano, Seishi Ogawa, Seiji Kojima, Shigeaki Nonoyama, Tomohiro Morio, Hirokazu Kanegane. ABNORMAL HEMATOPOIESIS AND AUTOIMMUNITY IN HUMANS WITH GERMLINE IKZF1 MUTATIONS. 2016.12.16

  2. Akihiro Hoshino, Satoshi Okada, Kenichi Yoshida, Naonori Nishida, Yusuke Okuno, Hiroo Ueno, Motoi Yamashita, Tsubasa Okano, Miyuki Tsumura, Shiho Nishimura, Sonoko Sakata, Masatoshi Takagi, Kohsuke Imai, Yuichi Shiraishi, Kenichi Chiba, Hiroko Tanaka, Satoru Miyano, Seishi Ogawa, Seiji Kojima, Shigeaki Nonoyama, Tomohiro Morio, Hirokazu Kanegane. ABNORMAL HEMATOPOIESIS AND AUTOIMMUNITY IN HUMANS WITH GERMLINE IKZF1 MUTATIONS. 2016.10.21

  3. Akihiro Hoshino, Hirokazu Kanegane. ABNORMAL HEMATOPOIESIS AND AUTOIMMUNITY IN HUMANS WITH GERMLINE IKZF1 MUTATIONS. 2016.05.27

  1. Ataxia Telangiectasia patient with intractable Cytomegalovirus encephalitis. The 118th Annual Meeting of the Japan Pediatric Society 2015.04.19 Osaka

  2. epilepsy in acute lymphoblastic leukemia. The 118th Annual Meeting of the Japan Pediatric Society 2015.04.18 Osaka

  1. The role of inflammation for a development process of pulmonary arterial hypertension. 2014.10

  2. Generation of Multivirus-specific T cells by a single stimulation of PBMCs with a peptide mixture utilizing serum free medium. 2014.09.06

  3. Morioka Chikako. A novel therapy for Periventricular leucomalacia using mesenchymal stem cell . 2014.07.13

  1. Infections and Immune Defects in Down Syndrome.. 2013.06.29

  1. Pediatric Hodgkin's lymphoma subsequently diagnosed as common variable immunodeficiency with FAS mutation. 2020.11.22

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