八角 高裕

最終更新日時: 2019/06/26 20:56:52

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氏名(漢字/フリガナ/アルファベット表記)
八角 高裕/ヤスミ タカヒロ/Yasumi, Takahiro
所属部署・職名(部局/所属/講座等/職名)
医学研究科/医学専攻発生発達医学講座発達小児科学/准教授
学部兼担
部局 所属 講座等 職名
医学部
所属学会(国内)
学会名(日本語) 学会名(英語)
日本小児科学会 Japan Pediatric Society
日本アレルギー学会 Japanese Society of Allergology
日本リウマチ学会 Japn College of Rheumatology
日本小児感染症学会 Japanese Society for Pediatric Infectious Diseases
日本免疫学会 Japanese Society for Immunology
日本小児リウマチ学会 Pediatric Rheumatology Association of Japan
日本小児アレルギー学会 Japanese Society of Pediatric Allergy and Clinical Immunology
日本免疫不全・自己炎症学会 Japanese Society for Immunodeficiency and Autoinflammatory Diseases
所属学会(海外)
学会名(英語) 国名
European Society for Immunodeficiencies EU
取得学位
学位名(日本語) 学位名(英語) 大学(日本語) 大学(英語) 取得区分
博士(医学) 京都大学
使用言語
言語名
英語
researchmap URL
https://researchmap.jp/7000008690
研究テーマ
(日本語)
小児免疫疾患
(英語)
Pediatric Immunological Disorders
研究概要
(日本語)
小児免疫疾患のうち、原発性免疫不全症を中心に研究と臨床に携わっている。特に、感染を主症状とする古典的な免疫不全症では無く、免疫調節機構の障害による過剰炎症を主症状とする家族性血球貪食性リンパ組織球症炎症や自己炎症疾患の研究と臨床に携わっている。これらの疾患の病態を明らかにし、診断や治療に繋げる研究を目指している。
(英語)
My researchy focuses on the study of pediatric immunology, with special emphasis on primary immunodeficiency diseases (PIDs). Among many PIDs, I am particularly interested in familial hemophagocytic lymphohistiocytosis and autoinflammatory disorders, diseases characterized by uncontrolled immune responses that result in excessive inflammation and not by susceptibily to infections commonly seen in classical forms of PIDs. By unraveling the pathogenesis of these disorders, I hope to provide new strategies to diagnose and treat the patients.
研究分野(キーワード)
キーワード(日本語) キーワード(英語)
免疫不全症 Immunodeficiency
論文
著者 著者(日本語) 著者(英語) タイトル タイトル(日本語) タイトル(英語) 書誌情報等 書誌情報等(日本語) 書誌情報等(英語) 出版年月 査読の有無 記述言語 掲載種別 公開
Yanagisawa R, Nakazawa Y, Matsuda K, Yasumi T, Kanegane H, Ohga S, Morimoto A, Hashii Y, Imaizumi M, Okamoto Y, Saito AM, Horibe K, Ishii E, HLH/LCH committee members of the Japan Children’s Cancer Group. Yanagisawa R, Nakazawa Y, Matsuda K, Yasumi T, Kanegane H, Ohga S, Morimoto A, Hashii Y, Imaizumi M, Okamoto Y, Saito AM, Horibe K, Ishii E, HLH/LCH committee members of the Japan Children’s Cancer Group. Yanagisawa R, Nakazawa Y, Matsuda K, Yasumi T, Kanegane H, Ohga S, Morimoto A, Hashii Y, Imaizumi M, Okamoto Y, Saito AM, Horibe K, Ishii E, HLH/LCH committee members of the Japan Children’s Cancer Group. Outcomes in children with hemophagocytic lymphohistiocytosis treated using HLH-2004 protocol in Japan. Outcomes in children with hemophagocytic lymphohistiocytosis treated using HLH-2004 protocol in Japan. Outcomes in children with hemophagocytic lymphohistiocytosis treated using HLH-2004 protocol in Japan. International journal of hematology, 109, 2, 206-213 International journal of hematology, 109, 2, 206-213 International journal of hematology, 109, 2, 206-213 2019/02 公開
Boisson B, Honda Y, Ajiro M, Bustamante J, Bendavid M, Gennery AR, Kawasaki Y, Ichishima J, Osawa M, Nihira H, Shiba T, Tanaka T, Chrabieh M, Bigio B, Hur H, Itan Y, Liang Y, Okada S, Izawa K, Nishikomori R, Ohara O, Heike T, Abel L, Puel A, Saito MK, Casanova JL, Hagiwara M, Yasumi T Boisson B, Honda Y, Ajiro M, Bustamante J, Bendavid M, Gennery AR, Kawasaki Y, Ichishima J, Osawa M, Nihira H, Shiba T, Tanaka T, Chrabieh M, Bigio B, Hur H, Itan Y, Liang Y, Okada S, Izawa K, Nishikomori R, Ohara O, Heike T, Abel L, Puel A, Saito MK, Casanova JL, Hagiwara M, Yasumi T Boisson B, Honda Y, Ajiro M, Bustamante J, Bendavid M, Gennery AR, Kawasaki Y, Ichishima J, Osawa M, Nihira H, Shiba T, Tanaka T, Chrabieh M, Bigio B, Hur H, Itan Y, Liang Y, Okada S, Izawa K, Nishikomori R, Ohara O, Heike T, Abel L, Puel A, Saito MK, Casanova JL, Hagiwara M, Yasumi T Rescue of recurrent deep intronic mutation underlying cell type-dependent quantitative NEMO deficiency. Rescue of recurrent deep intronic mutation underlying cell type-dependent quantitative NEMO deficiency. Rescue of recurrent deep intronic mutation underlying cell type-dependent quantitative NEMO deficiency. The Journal of clinical investigation, 129, 2, 583-597 The Journal of clinical investigation, 129, 2, 583-597 The Journal of clinical investigation, 129, 2, 583-597 2018/11 公開
Hoshino A, Tanita K, Kanda K, Imadome KI, Shikama Y, Yasumi T, Imai K, Takagi M, Morio T, Kanegane H Hoshino A, Tanita K, Kanda K, Imadome KI, Shikama Y, Yasumi T, Imai K, Takagi M, Morio T, Kanegane H Hoshino A, Tanita K, Kanda K, Imadome KI, Shikama Y, Yasumi T, Imai K, Takagi M, Morio T, Kanegane H High frequencies of asymptomatic Epstein-Barr virus viremia in affected and unaffected individuals with CTLA4 mutations. High frequencies of asymptomatic Epstein-Barr virus viremia in affected and unaffected individuals with CTLA4 mutations. High frequencies of asymptomatic Epstein-Barr virus viremia in affected and unaffected individuals with CTLA4 mutations. Clinical immunology (Orlando, Fla.), 195, 45-48 Clinical immunology (Orlando, Fla.), 195, 45-48 Clinical immunology (Orlando, Fla.), 195, 45-48 2018/10 公開
Ono S, Nakayama M, Kanegane H, Hoshino A, Shimodera S, Shibata H, Fujino H, Fujino T, Yunomae Y, Okano T, Yamashita M, Yasumi T, Izawa K, Takagi M, Imai K, Zhang K, Marsh R, Picard C, Latour S, Ohara O, Morio T Ono S, Nakayama M, Kanegane H, Hoshino A, Shimodera S, Shibata H, Fujino H, Fujino T, Yunomae Y, Okano T, Yamashita M, Yasumi T, Izawa K, Takagi M, Imai K, Zhang K, Marsh R, Picard C, Latour S, Ohara O, Morio T Ono S, Nakayama M, Kanegane H, Hoshino A, Shimodera S, Shibata H, Fujino H, Fujino T, Yunomae Y, Okano T, Yamashita M, Yasumi T, Izawa K, Takagi M, Imai K, Zhang K, Marsh R, Picard C, Latour S, Ohara O, Morio T Comprehensive molecular diagnosis of Epstein-Barr virus-associated lymphoproliferative diseases using next-generation sequencing. Comprehensive molecular diagnosis of Epstein-Barr virus-associated lymphoproliferative diseases using next-generation sequencing. Comprehensive molecular diagnosis of Epstein-Barr virus-associated lymphoproliferative diseases using next-generation sequencing. International journal of hematology, 108, 3, 319-328 International journal of hematology, 108, 3, 319-328 International journal of hematology, 108, 3, 319-328 2018/09 公開
Lucchini G, Marsh R, Gilmour K, Worth A, Nademi Z, Rao A, Booth C, Amrolia P, Silva J, Chiesa R, Wynn R, Lehmberg K, Astigarraga I, Gungor T, Stary J, Moshous D, Ifversen M, Zinn D, Jordan M, Kumar A, Yasumi T, Veys P, Rao K Lucchini G, Marsh R, Gilmour K, Worth A, Nademi Z, Rao A, Booth C, Amrolia P, Silva J, Chiesa R, Wynn R, Lehmberg K, Astigarraga I, Gungor T, Stary J, Moshous D, Ifversen M, Zinn D, Jordan M, Kumar A, Yasumi T, Veys P, Rao K Lucchini G, Marsh R, Gilmour K, Worth A, Nademi Z, Rao A, Booth C, Amrolia P, Silva J, Chiesa R, Wynn R, Lehmberg K, Astigarraga I, Gungor T, Stary J, Moshous D, Ifversen M, Zinn D, Jordan M, Kumar A, Yasumi T, Veys P, Rao K Treatment dilemmas in asymptomatic children with primary haemophagocytic lymphohistiocytosis. Treatment dilemmas in asymptomatic children with primary haemophagocytic lymphohistiocytosis. Treatment dilemmas in asymptomatic children with primary haemophagocytic lymphohistiocytosis. Blood, 132, 19, 2088-2096 Blood, 132, 19, 2088-2096 Blood, 132, 19, 2088-2096 2018/08 公開
Kawaguchi K, Umeda K, Hiejima E, Iwai A, Mikami M, Nodomi S, Saida S, Kato I, Hiramatsu H, Yasumi T, Nishikomori R, Kondo T, Takaori-Kondo A, Heike T, Adachi S Kawaguchi K, Umeda K, Hiejima E, Iwai A, Mikami M, Nodomi S, Saida S, Kato I, Hiramatsu H, Yasumi T, Nishikomori R, Kondo T, Takaori-Kondo A, Heike T, Adachi S Kawaguchi K, Umeda K, Hiejima E, Iwai A, Mikami M, Nodomi S, Saida S, Kato I, Hiramatsu H, Yasumi T, Nishikomori R, Kondo T, Takaori-Kondo A, Heike T, Adachi S Influence of post-transplant mucosal-associated invariant T cell recovery on the development of acute graft-versus-host disease in allogeneic bone marrow transplantation. Influence of post-transplant mucosal-associated invariant T cell recovery on the development of acute graft-versus-host disease in allogeneic bone marrow transplantation. Influence of post-transplant mucosal-associated invariant T cell recovery on the development of acute graft-versus-host disease in allogeneic bone marrow transplantation. International journal of hematology, 108, 1, 66-75 International journal of hematology, 108, 1, 66-75 International journal of hematology, 108, 1, 66-75 2018/07 公開
Hiejima E, Shibata H, Yasumi T, Shimodera S, Hori M, Izawa K, Kawai T, Matsuoka M, Kojima Y, Ohara A, Nishikomori R, Ohara O, Heike T Hiejima E, Shibata H, Yasumi T, Shimodera S, Hori M, Izawa K, Kawai T, Matsuoka M, Kojima Y, Ohara A, Nishikomori R, Ohara O, Heike T Hiejima E, Shibata H, Yasumi T, Shimodera S, Hori M, Izawa K, Kawai T, Matsuoka M, Kojima Y, Ohara A, Nishikomori R, Ohara O, Heike T Characterization of a large UNC13D gene duplication in a patient with familial hemophagocytic lymphohistiocytosis type 3. Characterization of a large UNC13D gene duplication in a patient with familial hemophagocytic lymphohistiocytosis type 3. Characterization of a large UNC13D gene duplication in a patient with familial hemophagocytic lymphohistiocytosis type 3. Clinical immunology (Orlando, Fla.), 191, 63-66 Clinical immunology (Orlando, Fla.), 191, 63-66 Clinical immunology (Orlando, Fla.), 191, 63-66 2018/06 公開
Shibata H, Yasumi T, Shimodera S, Hiejima E, Izawa K, Kawai T, Shirakawa R, Wada T, Nishikomori R, Horiuchi H, Ohara O, Ishii E, Heike T Shibata H, Yasumi T, Shimodera S, Hiejima E, Izawa K, Kawai T, Shirakawa R, Wada T, Nishikomori R, Horiuchi H, Ohara O, Ishii E, Heike T Shibata H, Yasumi T, Shimodera S, Hiejima E, Izawa K, Kawai T, Shirakawa R, Wada T, Nishikomori R, Horiuchi H, Ohara O, Ishii E, Heike T Human CTL-based functional analysis shows the reliability of a munc13-4 protein expression assay for FHL3 diagnosis. Human CTL-based functional analysis shows the reliability of a munc13-4 protein expression assay for FHL3 diagnosis. Human CTL-based functional analysis shows the reliability of a munc13-4 protein expression assay for FHL3 diagnosis. Blood, 131, 18, 2016-2025 Blood, 131, 18, 2016-2025 Blood, 131, 18, 2016-2025 2018/05 公開
Tanaka T, Yoshioka K, Nishikomori R, Sakai H, Abe J, Yamashita Y, Hiramoto R, Morimoto A, Ishii E, Arakawa H, Kaneko U, Ohshima Y, Okamoto N, Ohara O, Hata I, Shigematsu Y, Kawai T, Yasumi T, Heike T Tanaka T, Yoshioka K, Nishikomori R, Sakai H, Abe J, Yamashita Y, Hiramoto R, Morimoto A, Ishii E, Arakawa H, Kaneko U, Ohshima Y, Okamoto N, Ohara O, Hata I, Shigematsu Y, Kawai T, Yasumi T, Heike T Tanaka T, Yoshioka K, Nishikomori R, Sakai H, Abe J, Yamashita Y, Hiramoto R, Morimoto A, Ishii E, Arakawa H, Kaneko U, Ohshima Y, Okamoto N, Ohara O, Hata I, Shigematsu Y, Kawai T, Yasumi T, Heike T National survey of Japanese patients with mevalonate kinase deficiency reveals distinctive genetic and clinical characteristics. National survey of Japanese patients with mevalonate kinase deficiency reveals distinctive genetic and clinical characteristics. National survey of Japanese patients with mevalonate kinase deficiency reveals distinctive genetic and clinical characteristics. Modern rheumatology, 1-7 Modern rheumatology, 1-7 Modern rheumatology, 1-7 2018/03 公開
Nihira H, Nakagawa K, Izawa K, Kawai T, Yasumi T, Nishikomori R, Nambu M, Miyagawa-Hayashino A, Nomura T, Kabashima K, Ito M, Iwaki-Egawa S, Sasahara Y, Nakayama M, Heike T Nihira H, Nakagawa K, Izawa K, Kawai T, Yasumi T, Nishikomori R, Nambu M, Miyagawa-Hayashino A, Nomura T, Kabashima K, Ito M, Iwaki-Egawa S, Sasahara Y, Nakayama M, Heike T Nihira H, Nakagawa K, Izawa K, Kawai T, Yasumi T, Nishikomori R, Nambu M, Miyagawa-Hayashino A, Nomura T, Kabashima K, Ito M, Iwaki-Egawa S, Sasahara Y, Nakayama M, Heike T Fever of unknown origin with rashes in early infancy is indicative of adenosine deaminase type 2 deficiency. Fever of unknown origin with rashes in early infancy is indicative of adenosine deaminase type 2 deficiency. Fever of unknown origin with rashes in early infancy is indicative of adenosine deaminase type 2 deficiency. Scandinavian journal of rheumatology, 47, 2, 170-172 Scandinavian journal of rheumatology, 47, 2, 170-172 Scandinavian journal of rheumatology, 47, 2, 170-172 2018/03 公開
Kanegane H, Hoshino A, Okano T, Yasumi T, Wada T, Takada H, Okada S, Yamashita M, Yeh TW, Nishikomori R, Takagi M, Imai K, Ochs HD, Morio T Kanegane H, Hoshino A, Okano T, Yasumi T, Wada T, Takada H, Okada S, Yamashita M, Yeh TW, Nishikomori R, Takagi M, Imai K, Ochs HD, Morio T Kanegane H, Hoshino A, Okano T, Yasumi T, Wada T, Takada H, Okada S, Yamashita M, Yeh TW, Nishikomori R, Takagi M, Imai K, Ochs HD, Morio T Flow cytometry-based diagnosis of primary immunodeficiency diseases. Flow cytometry-based diagnosis of primary immunodeficiency diseases. Flow cytometry-based diagnosis of primary immunodeficiency diseases. Allergology international : official journal of the Japanese Society of Allergology, 67, 1, 43-54 Allergology international : official journal of the Japanese Society of Allergology, 67, 1, 43-54 Allergology international : official journal of the Japanese Society of Allergology, 67, 1, 43-54 2018/01 公開
Hasegawa D, Saito A, Nino N, Uemura S, Takafuji S, Yokoi T, Kozaki A, Ishida T, Kawasaki K, Yasumi T, Sakata N, Ohtsuka Y, Hirase S, Mori T, Nishimura N, Kusumoto M, Ogawa Y, Tominaga K, Nakagawa T, Kanda K, Tanaka R, Kosaka Y Hasegawa D, Saito A, Nino N, Uemura S, Takafuji S, Yokoi T, Kozaki A, Ishida T, Kawasaki K, Yasumi T, Sakata N, Ohtsuka Y, Hirase S, Mori T, Nishimura N, Kusumoto M, Ogawa Y, Tominaga K, Nakagawa T, Kanda K, Tanaka R, Kosaka Y Hasegawa D, Saito A, Nino N, Uemura S, Takafuji S, Yokoi T, Kozaki A, Ishida T, Kawasaki K, Yasumi T, Sakata N, Ohtsuka Y, Hirase S, Mori T, Nishimura N, Kusumoto M, Ogawa Y, Tominaga K, Nakagawa T, Kanda K, Tanaka R, Kosaka Y Successful Treatment of Transplantation-associated Atypical Hemolytic Uremic Syndrome With Eculizumab. Successful Treatment of Transplantation-associated Atypical Hemolytic Uremic Syndrome With Eculizumab. Successful Treatment of Transplantation-associated Atypical Hemolytic Uremic Syndrome With Eculizumab. Journal of pediatric hematology/oncology, 40, 1, e41-e44 Journal of pediatric hematology/oncology, 40, 1, e41-e44 Journal of pediatric hematology/oncology, 40, 1, e41-e44 2018/01 英語 研究論文(学術雑誌) 公開
Kusunoki T, Takeuchi J, Morimoto T, Sakuma M, Yasumi T, Nishikomori R, Higashi A, Heike T Kusunoki T, Takeuchi J, Morimoto T, Sakuma M, Yasumi T, Nishikomori R, Higashi A, Heike T Kusunoki T, Takeuchi J, Morimoto T, Sakuma M, Yasumi T, Nishikomori R, Higashi A, Heike T Fruit intake reduces the onset of respiratory allergic symptoms in schoolchildren. Fruit intake reduces the onset of respiratory allergic symptoms in schoolchildren. Fruit intake reduces the onset of respiratory allergic symptoms in schoolchildren. Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology, 28, 8, 793-800 Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology, 28, 8, 793-800 Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology, 28, 8, 793-800 2017/12 公開
Hiejima E, Yasumi T, Nakase H, Matsuura M, Honzawa Y, Higuchi H, Okafuji I, Yorifuji T, Tanaka T, Izawa K, Kawai T, Nishikomori R, Heike T Hiejima E, Yasumi T, Nakase H, Matsuura M, Honzawa Y, Higuchi H, Okafuji I, Yorifuji T, Tanaka T, Izawa K, Kawai T, Nishikomori R, Heike T Hiejima E, Yasumi T, Nakase H, Matsuura M, Honzawa Y, Higuchi H, Okafuji I, Yorifuji T, Tanaka T, Izawa K, Kawai T, Nishikomori R, Heike T Tricho-hepato-enteric syndrome with novel SKIV2L gene mutations: A case report. Tricho-hepato-enteric syndrome with novel SKIV2L gene mutations: A case report. Tricho-hepato-enteric syndrome with novel SKIV2L gene mutations: A case report. Medicine, 96, 46, e8601 Medicine, 96, 46, e8601 Medicine, 96, 46, e8601 2017/11 公開
Kawai T, Hiejima E, Oda H, Izawa K, Yasumi T, Nishikomori R, Okamoto S, Heike T Kawai T, Hiejima E, Oda H, Izawa K, Yasumi T, Nishikomori R, Okamoto S, Heike T Kawai T, Hiejima E, Oda H, Izawa K, Yasumi T, Nishikomori R, Okamoto S, Heike T Reply to Walsh et al. Reply to Walsh et al. Reply to Walsh et al. European journal of human genetics : EJHG, 25, 8, 907 European journal of human genetics : EJHG, 25, 8, 907 European journal of human genetics : EJHG, 25, 8, 907 2017/08 英語 研究論文(学術雑誌) 公開
Hashimoto M, Ogata S, Yamaguchi A, Kawada K, Kenmochi M, Ebato T, Nomoto K, Bando Y, Shimodera S, Shibata H, Ono S, Nakayama M, Yasumi T, Ishii M Hashimoto M, Ogata S, Yamaguchi A, Kawada K, Kenmochi M, Ebato T, Nomoto K, Bando Y, Shimodera S, Shibata H, Ono S, Nakayama M, Yasumi T, Ishii M Hashimoto M, Ogata S, Yamaguchi A, Kawada K, Kenmochi M, Ebato T, Nomoto K, Bando Y, Shimodera S, Shibata H, Ono S, Nakayama M, Yasumi T, Ishii M Hemophagocytic lymphohistiocytosis with high serum levels of IL-18 and predominant lymphocyte activation in a neonate born to a mother with adult-onset Still's disease. Hemophagocytic lymphohistiocytosis with high serum levels of IL-18 and predominant lymphocyte activation in a neonate born to a mother with adult-onset Still's disease. Hemophagocytic lymphohistiocytosis with high serum levels of IL-18 and predominant lymphocyte activation in a neonate born to a mother with adult-onset Still's disease. Clinical immunology (Orlando, Fla.), 180, 95-96 Clinical immunology (Orlando, Fla.), 180, 95-96 Clinical immunology (Orlando, Fla.), 180, 95-96 2017/07 英語 研究論文(学術雑誌) 公開
Nakayama M, Oda H, Nakagawa K, Yasumi T, Kawai T, Izawa K, Nishikomori R, Heike T, Ohara O Nakayama M, Oda H, Nakagawa K, Yasumi T, Kawai T, Izawa K, Nishikomori R, Heike T, Ohara O Nakayama M, Oda H, Nakagawa K, Yasumi T, Kawai T, Izawa K, Nishikomori R, Heike T, Ohara O Accurate clinical genetic testing for autoinflammatory diseases using the next-generation sequencing platform MiSeq. Accurate clinical genetic testing for autoinflammatory diseases using the next-generation sequencing platform MiSeq. Accurate clinical genetic testing for autoinflammatory diseases using the next-generation sequencing platform MiSeq. Biochemistry and biophysics reports, 9, 146-152 Biochemistry and biophysics reports, 9, 146-152 Biochemistry and biophysics reports, 9, 146-152 2017/03 公開
Hori M, Yasumi T, Shimodera S, Shibata H, Hiejima E, Oda H, Izawa K, Kawai T, Ishimura M, Nakano N, Shirakawa R, Nishikomori R, Takada H, Morita S, Horiuchi H, Ohara O, Ishii E, Heike T Hori M, Yasumi T, Shimodera S, Shibata H, Hiejima E, Oda H, Izawa K, Kawai T, Ishimura M, Nakano N, Shirakawa R, Nishikomori R, Takada H, Morita S, Horiuchi H, Ohara O, Ishii E, Heike T Hori M, Yasumi T, Shimodera S, Shibata H, Hiejima E, Oda H, Izawa K, Kawai T, Ishimura M, Nakano N, Shirakawa R, Nishikomori R, Takada H, Morita S, Horiuchi H, Ohara O, Ishii E, Heike T A CD57<sup>+</sup> CTL Degranulation Assay Effectively Identifies Familial Hemophagocytic Lymphohistiocytosis Type 3 Patients. A CD57<sup>+</sup> CTL Degranulation Assay Effectively Identifies Familial Hemophagocytic Lymphohistiocytosis Type 3 Patients. A CD57<sup>+</sup> CTL Degranulation Assay Effectively Identifies Familial Hemophagocytic Lymphohistiocytosis Type 3 Patients. Journal of clinical immunology, 37, 1, 92-99 Journal of clinical immunology, 37, 1, 92-99 Journal of clinical immunology, 37, 1, 92-99 2017/01 英語 研究論文(学術雑誌) 公開
Nanishi E, Hoshina T, Takada H, Ishimura M, Nishio H, Uehara T, Mizuno Y, Hasegawa S, Ohga S, Nagao M, Igarashi M, Yajima S, Kusumoto Y, Onishi N, Sasahara Y, Yasumi T, Heike T, Hara T, PID-Infection Study Group. Nanishi E, Hoshina T, Takada H, Ishimura M, Nishio H, Uehara T, Mizuno Y, Hasegawa S, Ohga S, Nagao M, Igarashi M, Yajima S, Kusumoto Y, Onishi N, Sasahara Y, Yasumi T, Heike T, Hara T, PID-Infection Study Group. Nanishi E, Hoshina T, Takada H, Ishimura M, Nishio H, Uehara T, Mizuno Y, Hasegawa S, Ohga S, Nagao M, Igarashi M, Yajima S, Kusumoto Y, Onishi N, Sasahara Y, Yasumi T, Heike T, Hara T, PID-Infection Study Group. A nationwide survey of common viral infections in childhood among patients with primary immunodeficiency diseases. A nationwide survey of common viral infections in childhood among patients with primary immunodeficiency diseases. A nationwide survey of common viral infections in childhood among patients with primary immunodeficiency diseases. The Journal of infection, 73, 4, 358-368 The Journal of infection, 73, 4, 358-368 The Journal of infection, 73, 4, 358-368 2016/10 英語 研究論文(学術雑誌) 公開
Hiejima E, Nakase H, Matsuura M, Honzawa Y, Higuchi H, Saida S, Umeda K, Hiramatsu H, Adachi S, Izawa K, Kawai T, Yasumi T, Nishikomori R, Heike T Hiejima E, Nakase H, Matsuura M, Honzawa Y, Higuchi H, Saida S, Umeda K, Hiramatsu H, Adachi S, Izawa K, Kawai T, Yasumi T, Nishikomori R, Heike T Hiejima E, Nakase H, Matsuura M, Honzawa Y, Higuchi H, Saida S, Umeda K, Hiramatsu H, Adachi S, Izawa K, Kawai T, Yasumi T, Nishikomori R, Heike T Diagnostic accuracy of endoscopic features of pediatric acute gastrointestinal graft-versus-host disease. Diagnostic accuracy of endoscopic features of pediatric acute gastrointestinal graft-versus-host disease. Diagnostic accuracy of endoscopic features of pediatric acute gastrointestinal graft-versus-host disease. Digestive endoscopy : official journal of the Japan Gastroenterological Endoscopy Society, 28, 5, 548-555 Digestive endoscopy : official journal of the Japan Gastroenterological Endoscopy Society, 28, 5, 548-555 Digestive endoscopy : official journal of the Japan Gastroenterological Endoscopy Society, 28, 5, 548-555 2016/07 英語 研究論文(学術雑誌) 公開
Saida S, Umeda K, Yasumi T, Matsumoto A, Kato I, Hiramatsu H, Ohara O, Heike T, Adachi S Saida S, Umeda K, Yasumi T, Matsumoto A, Kato I, Hiramatsu H, Ohara O, Heike T, Adachi S Saida S, Umeda K, Yasumi T, Matsumoto A, Kato I, Hiramatsu H, Ohara O, Heike T, Adachi S Successful reduced-intensity stem cell transplantation for GATA2 deficiency before progression of advanced MDS. Successful reduced-intensity stem cell transplantation for GATA2 deficiency before progression of advanced MDS. Successful reduced-intensity stem cell transplantation for GATA2 deficiency before progression of advanced MDS. Pediatric transplantation, 20, 2, 333-336 Pediatric transplantation, 20, 2, 333-336 Pediatric transplantation, 20, 2, 333-336 2016/03 英語 研究論文(学術雑誌) 公開
Kusunoki T, Takeuchi J, Morimoto T, Sakuma M, Mukaida K, Yasumi T, Nishikomori R, Heike T Kusunoki T, Takeuchi J, Morimoto T, Sakuma M, Mukaida K, Yasumi T, Nishikomori R, Heike T Kusunoki T, Takeuchi J, Morimoto T, Sakuma M, Mukaida K, Yasumi T, Nishikomori R, Heike T Sports activities enhance the prevalence of rhinitis symptoms in schoolchildren. Sports activities enhance the prevalence of rhinitis symptoms in schoolchildren. Sports activities enhance the prevalence of rhinitis symptoms in schoolchildren. Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology, 27, 2, 209-213 Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology, 27, 2, 209-213 Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology, 27, 2, 209-213 2016/03 英語 研究論文(学術雑誌) 公開
Oda H, Sato T, Kunishima S, Nakagawa K, Izawa K, Hiejima E, Kawai T, Yasumi T, Doi H, Katamura K, Numabe H, Okamoto S, Nakase H, Hijikata A, Ohara O, Suzuki H, Morisaki H, Morisaki T, Nunoi H, Hattori S, Nishikomori R, Heike T Oda H, Sato T, Kunishima S, Nakagawa K, Izawa K, Hiejima E, Kawai T, Yasumi T, Doi H, Katamura K, Numabe H, Okamoto S, Nakase H, Hijikata A, Ohara O, Suzuki H, Morisaki H, Morisaki T, Nunoi H, Hattori S, Nishikomori R, Heike T Oda H, Sato T, Kunishima S, Nakagawa K, Izawa K, Hiejima E, Kawai T, Yasumi T, Doi H, Katamura K, Numabe H, Okamoto S, Nakase H, Hijikata A, Ohara O, Suzuki H, Morisaki H, Morisaki T, Nunoi H, Hattori S, Nishikomori R, Heike T Exon skipping causes atypical phenotypes associated with a loss-of-function mutation in FLNA by restoring its protein function. Exon skipping causes atypical phenotypes associated with a loss-of-function mutation in FLNA by restoring its protein function. Exon skipping causes atypical phenotypes associated with a loss-of-function mutation in FLNA by restoring its protein function. European journal of human genetics : EJHG, 24, 3, 408-414 European journal of human genetics : EJHG, 24, 3, 408-414 European journal of human genetics : EJHG, 24, 3, 408-414 2016/03 英語 研究論文(学術雑誌) 公開
八角 高裕, 平家 俊男 八角 高裕, 平家 俊男 新規膠原病関連小児慢性特定疾病としての自己炎症性疾患 新規膠原病関連小児慢性特定疾病としての自己炎症性疾患 臨床免疫・アレルギー科, 65, 1, 57-64 臨床免疫・アレルギー科, 65, 1, 57-64 , 65, 1, 57-64 2016/01 日本語 公開
Yasumi T, Shibata H, Shimodera S, Heike T Yasumi T, Shibata H, Shimodera S, Heike T Yasumi T, Shibata H, Shimodera S, Heike T [Heterogeneity of HLH pathophysiology and treatment strategies]. [Heterogeneity of HLH pathophysiology and treatment strategies]. [Heterogeneity of HLH pathophysiology and treatment strategies]. [Rinsho ketsueki] The Japanese journal of clinical hematology, 56, 10, 2248-2257 [Rinsho ketsueki] The Japanese journal of clinical hematology, 56, 10, 2248-2257 [Rinsho ketsueki] The Japanese journal of clinical hematology, 56, 10, 2248-2257 2015/10 公開
Yasumi T, Hori M, Hiejima E, Shibata H, Izawa K, Oda H, Yoshioka K, Nakagawa K, Kawai T, Nishikomori R, Ohara O, Heike T Yasumi T, Hori M, Hiejima E, Shibata H, Izawa K, Oda H, Yoshioka K, Nakagawa K, Kawai T, Nishikomori R, Ohara O, Heike T Yasumi T, Hori M, Hiejima E, Shibata H, Izawa K, Oda H, Yoshioka K, Nakagawa K, Kawai T, Nishikomori R, Ohara O, Heike T Laboratory parameters identify familial haemophagocytic lymphohistiocytosis from other forms of paediatric haemophagocytosis. Laboratory parameters identify familial haemophagocytic lymphohistiocytosis from other forms of paediatric haemophagocytosis. Laboratory parameters identify familial haemophagocytic lymphohistiocytosis from other forms of paediatric haemophagocytosis. British journal of haematology, 170, 4, 532-538 British journal of haematology, 170, 4, 532-538 British journal of haematology, 170, 4, 532-538 2015/08 英語 研究論文(学術雑誌) 公開
Hiejima E, Kawai T, Nakase H, Tsuruyama T, Morimoto T, Yasumi T, Taga T, Kanegane H, Hori M, Ohmori K, Higuchi T, Matsuura M, Yoshino T, Ikeuchi H, Kawada K, Sakai Y, Kitazume MT, Hisamatsu T, Chiba T, Nishikomori R, Heike T Hiejima E, Kawai T, Nakase H, Tsuruyama T, Morimoto T, Yasumi T, Taga T, Kanegane H, Hori M, Ohmori K, Higuchi T, Matsuura M, Yoshino T, Ikeuchi H, Kawada K, Sakai Y, Kitazume MT, Hisamatsu T, Chiba T, Nishikomori R, Heike T Hiejima E, Kawai T, Nakase H, Tsuruyama T, Morimoto T, Yasumi T, Taga T, Kanegane H, Hori M, Ohmori K, Higuchi T, Matsuura M, Yoshino T, Ikeuchi H, Kawada K, Sakai Y, Kitazume MT, Hisamatsu T, Chiba T, Nishikomori R, Heike T Reduced Numbers and Proapoptotic Features of Mucosal-associated Invariant T Cells as a Characteristic Finding in Patients with Inflammatory Bowel Disease. Reduced Numbers and Proapoptotic Features of Mucosal-associated Invariant T Cells as a Characteristic Finding in Patients with Inflammatory Bowel Disease. Reduced Numbers and Proapoptotic Features of Mucosal-associated Invariant T Cells as a Characteristic Finding in Patients with IBD. Inflammatory bowel diseases, 21, 7, 1529-1540 Inflammatory bowel diseases, 21, 7, 1529-1540 Inflammatory bowel diseases, 21, 7, 1529-1540 2015/07 英語 研究論文(学術雑誌) 公開
Matsumoto A, Umeda K, Kawaguchi K, Kawada K, Maeda S, Kinehara T, Saida S, Kato I, Hiramatsu H, Watanabe K, Yasumi T, Heike T, Tsujikawa A, Uji A, Usami I, Ito K, Adachi S Matsumoto A, Umeda K, Kawaguchi K, Kawada K, Maeda S, Kinehara T, Saida S, Kato I, Hiramatsu H, Watanabe K, Yasumi T, Heike T, Tsujikawa A, Uji A, Usami I, Ito K, Adachi S Matsumoto A, Umeda K, Kawaguchi K, Kawada K, Maeda S, Kinehara T, Saida S, Kato I, Hiramatsu H, Watanabe K, Yasumi T, Heike T, Tsujikawa A, Uji A, Usami I, Ito K, Adachi S Development of CMV retinitis in an antigenemia-negative infant after cord blood transplantation. Development of CMV retinitis in an antigenemia-negative infant after cord blood transplantation. Development of CMV retinitis in an antigenemia-negative infant after cord blood transplantation. [Rinsho ketsueki] The Japanese journal of clinical hematology, 56, 5, 506-510 [Rinsho ketsueki] The Japanese journal of clinical hematology, 56, 5, 506-510 [Rinsho ketsueki] The Japanese journal of clinical hematology, 56, 5, 506-510 2015/05 公開
Yang X, Hoshino A, Taga T, Kunitsu T, Ikeda Y, Yasumi T, Yoshida K, Wada T, Miyake K, Kubota T, Okuno Y, Muramatsu H, Adachi Y, Miyano S, Ogawa S, Kojima S, Kanegane H Yang X, Hoshino A, Taga T, Kunitsu T, Ikeda Y, Yasumi T, Yoshida K, Wada T, Miyake K, Kubota T, Okuno Y, Muramatsu H, Adachi Y, Miyano S, Ogawa S, Kojima S, Kanegane H Yang X, Hoshino A, Taga T, Kunitsu T, Ikeda Y, Yasumi T, Yoshida K, Wada T, Miyake K, Kubota T, Okuno Y, Muramatsu H, Adachi Y, Miyano S, Ogawa S, Kojima S, Kanegane H A female patient with incomplete hemophagocytic lymphohistiocytosis caused by a heterozygous XIAP mutation associated with non-random X-chromosome inactivation skewed towards the wild-type XIAP allele. A female patient with incomplete hemophagocytic lymphohistiocytosis caused by a heterozygous XIAP mutation associated with non-random X-chromosome inactivation skewed towards the wild-type XIAP allele. A female patient with incomplete hemophagocytic lymphohistiocytosis caused by a heterozygous XIAP mutation associated with non-random X-chromosome inactivation skewed towards the wild-type XIAP allele. Journal of clinical immunology, 35, 3, 244-248 Journal of clinical immunology, 35, 3, 244-248 Journal of clinical immunology, 35, 3, 244-248 2015/04 英語 研究論文(学術雑誌) 公開
Iwatani S, Uemura K, Mizobuchi M, Yoshimoto S, Kawasaki K, Kosaka Y, Hori M, Yasumi T, Nakao H Iwatani S, Uemura K, Mizobuchi M, Yoshimoto S, Kawasaki K, Kosaka Y, Hori M, Yasumi T, Nakao H Iwatani S, Uemura K, Mizobuchi M, Yoshimoto S, Kawasaki K, Kosaka Y, Hori M, Yasumi T, Nakao H Familial Hemophagocytic Lymphohistiocytosis Presenting as Hydrops Fetalis. Familial Hemophagocytic Lymphohistiocytosis Presenting as Hydrops Fetalis. Familial Hemophagocytic Lymphohistiocytosis Presenting as Hydrops Fetalis. AJP reports, 5, 1, e22-4 AJP reports, 5, 1, e22-4 AJP reports, 5, 1, e22-4 2015/04 英語 研究論文(学術雑誌) 公開
Nakagawa K, Gonzalez-Roca E, Souto A, Kawai T, Umebayashi H, Campistol JM, Cañellas J, Takei S, Kobayashi N, Callejas-Rubio JL, Ortego-Centeno N, Ruiz-Ortiz E, Rius F, Anton J, Iglesias E, Jimenez-Treviño S, Vargas C, Fernandez-Martin J, Calvo I, Hernández-Rodríguez J, Mendez M, Dordal MT, Basagaña M, Bujan S, Yashiro M, Kubota T, Koike R, Akuta N, Shimoyama K, Iwata N, Saito MK, Ohara O, Kambe N, Yasumi T, Izawa K, Kawai T, Heike T, Yagüe J, Nishikomori R, Aróstegui JI Nakagawa K, Gonzalez-Roca E, Souto A, Kawai T, Umebayashi H, Campistol JM, Cañellas J, Takei S, Kobayashi N, Callejas-Rubio JL, Ortego-Centeno N, Ruiz-Ortiz E, Rius F, Anton J, Iglesias E, Jimenez-Treviño S, Vargas C, Fernandez-Martin J, Calvo I, Hernández-Rodríguez J, Mendez M, Dordal MT, Basagaña M, Bujan S, Yashiro M, Kubota T, Koike R, Akuta N, Shimoyama K, Iwata N, Saito MK, Ohara O, Kambe N, Yasumi T, Izawa K, Kawai T, Heike T, Yagüe J, Nishikomori R, Aróstegui JI Nakagawa K, Gonzalez-Roca E, Souto A, Kawai T, Umebayashi H, Campistol JM, Cañellas J, Takei S, Kobayashi N, Callejas-Rubio JL, Ortego-Centeno N, Ruiz-Ortiz E, Rius F, Anton J, Iglesias E, Jimenez-Treviño S, Vargas C, Fernandez-Martin J, Calvo I, Hernández-Rodríguez J, Mendez M, Dordal MT, Basagaña M, Bujan S, Yashiro M, Kubota T, Koike R, Akuta N, Shimoyama K, Iwata N, Saito MK, Ohara O, Kambe N, Yasumi T, Izawa K, Kawai T, Heike T, Yagüe J, Nishikomori R, Aróstegui JI Somatic NLRP3 mosaicism in Muckle-Wells syndrome. A genetic mechanism shared by different phenotypes of cryopyrin-associated periodic syndromes. Somatic NLRP3 mosaicism in Muckle-Wells syndrome. A genetic mechanism shared by different phenotypes of cryopyrin-associated periodic syndromes. Somatic NLRP3 mosaicism in Muckle-Wells syndrome. A genetic mechanism shared by different phenotypes of cryopyrin-associated periodic syndromes. Annals of the rheumatic diseases, 74, 3, 603-610 Annals of the rheumatic diseases, 74, 3, 603-610 Annals of the rheumatic diseases, 74, 3, 603-610 2015/03 英語 研究論文(学術雑誌) 公開
Yokoyama K, Ikeya M, Umeda K, Oda H, Nodomi S, Nasu A, Matsumoto Y, Izawa K, Horigome K, Kusaka T, Tanaka T, Saito MK, Yasumi T, Nishikomori R, Ohara O, Nakayama N, Nakahata T, Heike T, Toguchida J Yokoyama K, Ikeya M, Umeda K, Oda H, Nodomi S, Nasu A, Matsumoto Y, Izawa K, Horigome K, Kusaka T, Tanaka T, Saito MK, Yasumi T, Nishikomori R, Ohara O, Nakayama N, Nakahata T, Heike T, Toguchida J Yokoyama K, Ikeya M, Umeda K, Oda H, Nodomi S, Nasu A, Matsumoto Y, Izawa K, Horigome K, Kusaka T, Tanaka T, Saito MK, Yasumi T, Nishikomori R, Ohara O, Nakayama N, Nakahata T, Heike T, Toguchida J Enhanced chondrogenesis of induced pluripotent stem cells from patients with neonatal-onset multisystem inflammatory disease occurs via the caspase 1-independent cAMP/protein kinase A/CREB pathway. Enhanced chondrogenesis of induced pluripotent stem cells from patients with neonatal-onset multisystem inflammatory disease occurs via the caspase 1-independent cAMP/protein kinase A/CREB pathway. Enhanced chondrogenesis of induced pluripotent stem cells from patients with neonatal-onset multisystem inflammatory disease occurs via the caspase 1-independent cAMP/protein kinase A/CREB pathway. Arthritis & rheumatology (Hoboken, N.J.), 67, 1, 302-314 Arthritis & rheumatology (Hoboken, N.J.), 67, 1, 302-314 Arthritis & rheumatology (Hoboken, N.J.), 67, 1, 302-314 2015/01 英語 研究論文(学術雑誌) 公開
八角高裕 八角高裕 見逃しやすい免疫不全 血球貪食性リンパ組織球症と免疫不全症 見逃しやすい免疫不全 血球貪食性リンパ組織球症と免疫不全症 小児内科, 46, 10, 1513-1517 小児内科, 46, 10, 1513-1517 , 46, 10, 1513-1517 2014/10 日本語 公開
Wada T, Yasumi T, Toma T, Hori M, Maeda S, Umeda K, Heike T, Adachi S, Usami I, Yachie A Wada T, Yasumi T, Toma T, Hori M, Maeda S, Umeda K, Heike T, Adachi S, Usami I, Yachie A Wada T, Yasumi T, Toma T, Hori M, Maeda S, Umeda K, Heike T, Adachi S, Usami I, Yachie A Munc13-4 deficiency with CD5 downregulation on activated CD8+ T cells. Munc13-4 deficiency with CD5 downregulation on activated CD8+ T cells. Munc13-4 deficiency with CD5 downregulation on activated CD8+ T cells. Pediatrics international : official journal of the Japan Pediatric Society, 56, 4, 605-608 Pediatrics international : official journal of the Japan Pediatric Society, 56, 4, 605-608 Pediatrics international : official journal of the Japan Pediatric Society, 56, 4, 605-608 2014/08 英語 研究論文(学術雑誌) 公開
Oda H, Nakagawa K, Abe J, Awaya T, Funabiki M, Hijikata A, Nishikomori R, Funatsuka M, Ohshima Y, Sugawara Y, Yasumi T, Kato H, Shirai T, Ohara O, Fujita T, Heike T Oda H, Nakagawa K, Abe J, Awaya T, Funabiki M, Hijikata A, Nishikomori R, Funatsuka M, Ohshima Y, Sugawara Y, Yasumi T, Kato H, Shirai T, Ohara O, Fujita T, Heike T Oda H, Nakagawa K, Abe J, Awaya T, Funabiki M, Hijikata A, Nishikomori R, Funatsuka M, Ohshima Y, Sugawara Y, Yasumi T, Kato H, Shirai T, Ohara O, Fujita T, Heike T Aicardi-Goutières syndrome is caused by IFIH1 mutations. Aicardi-Goutières syndrome is caused by IFIH1 mutations. Aicardi-Goutières syndrome is caused by IFIH1 mutations. American journal of human genetics, 95, 1, 121-125 American journal of human genetics, 95, 1, 121-125 American journal of human genetics, 95, 1, 121-125 2014/07 英語 研究論文(学術雑誌) 公開
西小森隆太, 中川権史, 粟屋美絵, 河合朋樹, 八角高裕, 平家俊男 西小森隆太, 中川権史, 粟屋美絵, 河合朋樹, 八角高裕, 平家俊男 自己炎症性疾患の新展開 自己炎症性疾患の新展開 臨床リウマチ, 26, 2, 79-87 臨床リウマチ, 26, 2, 79-87 , 26, 2, 79-87 2014/06 日本語 公開
Abe J, Nakamura K, Nishikomori R, Kato M, Mitsuiki N, Izawa K, Awaya T, Kawai T, Yasumi T, Toyoshima I, Hasegawa K, Ohshima Y, Hiragi T, Sasahara Y, Suzuki Y, Kikuchi M, Osaka H, Ohya T, Ninomiya S, Fujikawa S, Akasaka M, Iwata N, Kawakita A, Funatsuka M, Shintaku H, Ohara O, Ichinose H, Heike T Abe J, Nakamura K, Nishikomori R, Kato M, Mitsuiki N, Izawa K, Awaya T, Kawai T, Yasumi T, Toyoshima I, Hasegawa K, Ohshima Y, Hiragi T, Sasahara Y, Suzuki Y, Kikuchi M, Osaka H, Ohya T, Ninomiya S, Fujikawa S, Akasaka M, Iwata N, Kawakita A, Funatsuka M, Shintaku H, Ohara O, Ichinose H, Heike T Abe J, Nakamura K, Nishikomori R, Kato M, Mitsuiki N, Izawa K, Awaya T, Kawai T, Yasumi T, Toyoshima I, Hasegawa K, Ohshima Y, Hiragi T, Sasahara Y, Suzuki Y, Kikuchi M, Osaka H, Ohya T, Ninomiya S, Fujikawa S, Akasaka M, Iwata N, Kawakita A, Funatsuka M, Shintaku H, Ohara O, Ichinose H, Heike T A nationwide survey of Aicardi-Goutières syndrome patients identifies a strong association between dominant TREX1 mutations and chilblain lesions: Japanese cohort study. A nationwide survey of Aicardi-Goutières syndrome patients identifies a strong association between dominant TREX1 mutations and chilblain lesions: Japanese cohort study. A nationwide survey of Aicardi-Goutières syndrome patients identifies a strong association between dominant TREX1 mutations and chilblain lesions: Japanese cohort study. Rheumatology (Oxford, England), 53, 3, 448-458 Rheumatology (Oxford, England), 53, 3, 448-458 Rheumatology (Oxford, England), 53, 3, 448-458 2014/03 英語 研究論文(学術雑誌) 公開
Wada T, Sakakibara Y, Nishimura R, Toma T, Ueno Y, Horita S, Tanaka T, Nishi M, Kato K, Yasumi T, Ohara O, Yachie A Wada T, Sakakibara Y, Nishimura R, Toma T, Ueno Y, Horita S, Tanaka T, Nishi M, Kato K, Yasumi T, Ohara O, Yachie A Wada T, Sakakibara Y, Nishimura R, Toma T, Ueno Y, Horita S, Tanaka T, Nishi M, Kato K, Yasumi T, Ohara O, Yachie A Down-regulation of CD5 expression on activated CD8+ T cells in familial hemophagocytic lymphohistiocytosis with perforin gene mutations. Down-regulation of CD5 expression on activated CD8+ T cells in familial hemophagocytic lymphohistiocytosis with perforin gene mutations. Down-regulation of CD5 expression on activated CD8+ T cells in familial hemophagocytic lymphohistiocytosis with perforin gene mutations. Human immunology, 74, 12, 1579-1585 Human immunology, 74, 12, 1579-1585 Human immunology, 74, 12, 1579-1585 2013/12 英語 研究論文(学術雑誌) 公開
Yoshioka T, Nishikomori R, Hara J, Okada K, Hashii Y, Okafuji I, Nodomi S, Kawai T, Izawa K, Ohnishi H, Yasumi T, Nakahata T, Heike T Yoshioka T, Nishikomori R, Hara J, Okada K, Hashii Y, Okafuji I, Nodomi S, Kawai T, Izawa K, Ohnishi H, Yasumi T, Nakahata T, Heike T Yoshioka T, Nishikomori R, Hara J, Okada K, Hashii Y, Okafuji I, Nodomi S, Kawai T, Izawa K, Ohnishi H, Yasumi T, Nakahata T, Heike T Autosomal dominant anhidrotic ectodermal dysplasia with immunodeficiency caused by a novel NFKBIA mutation, p.Ser36Tyr, presents with mild ectodermal dysplasia and non-infectious systemic inflammation. Autosomal dominant anhidrotic ectodermal dysplasia with immunodeficiency caused by a novel NFKBIA mutation, p.Ser36Tyr, presents with mild ectodermal dysplasia and non-infectious systemic inflammation. Autosomal dominant anhidrotic ectodermal dysplasia with immunodeficiency caused by a novel NFKBIA mutation, p.Ser36Tyr, presents with mild ectodermal dysplasia and non-infectious systemic inflammation. Journal of clinical immunology, 33, 7, 1165-1174 Journal of clinical immunology, 33, 7, 1165-1174 Journal of clinical immunology, 33, 7, 1165-1174 2013/10 英語 研究論文(学術雑誌) 公開
八角高裕 八角高裕 自己炎症症候群:稀な遺伝性疾患からリウマチ・アレルギー疾患へのメッセージ IV.高IgD症候群(hyperimmunoglobulinemia D and periodic fever syndrome:HIDS) 自己炎症症候群:稀な遺伝性疾患からリウマチ・アレルギー疾患へのメッセージ IV.高IgD症候群(hyperimmunoglobulinemia D and periodic fever syndrome:HIDS) アレルギー・免疫, 20, 10, 1424-1430 アレルギー・免疫, 20, 10, 1424-1430 , 20, 10, 1424-1430 2013/09 日本語 公開
Kusunoki T, Morimoto T, Sakuma M, Mukaida K, Yasumi T, Nishikomori R, Heike T Kusunoki T, Morimoto T, Sakuma M, Mukaida K, Yasumi T, Nishikomori R, Heike T Kusunoki T, Morimoto T, Sakuma M, Mukaida K, Yasumi T, Nishikomori R, Heike T Effect of eczema on the association between season of birth and food allergy in Japanese children. Effect of eczema on the association between season of birth and food allergy in Japanese children. Effect of eczema on the association between season of birth and food allergy in Japanese children. Pediatrics international : official journal of the Japan Pediatric Society, 55, 1, 7-10 Pediatrics international : official journal of the Japan Pediatric Society, 55, 1, 7-10 Pediatrics international : official journal of the Japan Pediatric Society, 55, 1, 7-10 2013/02 英語 研究論文(学術雑誌) 公開
Abe J, Izawa K, Nishikomori R, Awaya T, Kawai T, Yasumi T, Hiragi N, Hiragi T, Ohshima Y, Heike T Abe J, Izawa K, Nishikomori R, Awaya T, Kawai T, Yasumi T, Hiragi N, Hiragi T, Ohshima Y, Heike T Abe J, Izawa K, Nishikomori R, Awaya T, Kawai T, Yasumi T, Hiragi N, Hiragi T, Ohshima Y, Heike T Heterozygous TREX1 p.Asp18Asn mutation can cause variable neurological symptoms in a family with Aicardi-Goutieres syndrome/familial chilblain lupus. Heterozygous TREX1 p.Asp18Asn mutation can cause variable neurological symptoms in a family with Aicardi-Goutieres syndrome/familial chilblain lupus. Heterozygous TREX1 p.Asp18Asn mutation can cause variable neurological symptoms in a family with Aicardi-Goutieres syndrome/familial chilblain lupus. Rheumatology (Oxford, England), 52, 2, 406-408 Rheumatology (Oxford, England), 52, 2, 406-408 Rheumatology (Oxford, England), 52, 2, 406-408 2013/02 英語 研究論文(学術雑誌) 公開
八角高裕 八角高裕 家族性血球貪食症候群のスクリーニング検査 家族性血球貪食症候群のスクリーニング検査 血液フロンティア Vol.23 No.1 2013 血液フロンティア Vol.23 No.1 2013 2013/01/30 日本語 公開
Yanagimachi MD, Niwa A, Tanaka T, Honda-Ozaki F, Nishimoto S, Murata Y, Yasumi T, Ito J, Tomida S, Oshima K, Asaka I, Goto H, Heike T, Nakahata T, Saito MK Yanagimachi MD, Niwa A, Tanaka T, Honda-Ozaki F, Nishimoto S, Murata Y, Yasumi T, Ito J, Tomida S, Oshima K, Asaka I, Goto H, Heike T, Nakahata T, Saito MK Yanagimachi MD, Niwa A, Tanaka T, Honda-Ozaki F, Nishimoto S, Murata Y, Yasumi T, Ito J, Tomida S, Oshima K, Asaka I, Goto H, Heike T, Nakahata T, Saito MK Robust and highly-efficient differentiation of functional monocytic cells from human pluripotent stem cells under serum- and feeder cell-free conditions. Robust and highly-efficient differentiation of functional monocytic cells from human pluripotent stem cells under serum- and feeder cell-free conditions. Robust and highly-efficient differentiation of functional monocytic cells from human pluripotent stem cells under serum- and feeder cell-free conditions. PloS one, 8, 4, e59243 PloS one, 8, 4, e59243 PloS one, 8, 4, e59243 2013 英語 研究論文(学術雑誌) 公開
Hiejima E, Yasumi T, Kubota H, Ohmori K, Ohshima K, Nishikomori R, Nakase H, Chiba T, Heike T Hiejima E, Yasumi T, Kubota H, Ohmori K, Ohshima K, Nishikomori R, Nakase H, Chiba T, Heike T Hiejima E, Yasumi T, Kubota H, Ohmori K, Ohshima K, Nishikomori R, Nakase H, Chiba T, Heike T Gastric ulcer and gastroenteritis caused by Epstein-Barr virus during immunosuppressive therapy for a child with systemic juvenile idiopathic arthritis. Gastric ulcer and gastroenteritis caused by Epstein-Barr virus during immunosuppressive therapy for a child with systemic juvenile idiopathic arthritis. Gastric ulcer and gastroenteritis caused by Epstein-Barr virus during immunosuppressive therapy for a child with systemic juvenile idiopathic arthritis. Rheumatology (Oxford, England), 51, 11, 2107-2109 Rheumatology (Oxford, England), 51, 11, 2107-2109 Rheumatology (Oxford, England), 51, 11, 2107-2109 2012/11 英語 研究論文(学術雑誌) 公開
Tsumura M, Okada S, Sakai H, Yasunaga S, Ohtsubo M, Murata T, Obata H, Yasumi T, Kong XF, Abhyankar A, Heike T, Nakahata T, Nishikomori R, Al-Muhsen S, Boisson-Dupuis S, Casanova JL, Alzahrani M, Shehri MA, Elghazali G, Takihara Y, Kobayashi M Tsumura M, Okada S, Sakai H, Yasunaga S, Ohtsubo M, Murata T, Obata H, Yasumi T, Kong XF, Abhyankar A, Heike T, Nakahata T, Nishikomori R, Al-Muhsen S, Boisson-Dupuis S, Casanova JL, Alzahrani M, Shehri MA, Elghazali G, Takihara Y, Kobayashi M Tsumura M, Okada S, Sakai H, Yasunaga S, Ohtsubo M, Murata T, Obata H, Yasumi T, Kong XF, Abhyankar A, Heike T, Nakahata T, Nishikomori R, Al-Muhsen S, Boisson-Dupuis S, Casanova JL, Alzahrani M, Shehri MA, Elghazali G, Takihara Y, Kobayashi M Dominant-negative STAT1 SH2 domain mutations in unrelated patients with Mendelian susceptibility to mycobacterial disease. Dominant-negative STAT1 SH2 domain mutations in unrelated patients with Mendelian susceptibility to mycobacterial disease. Dominant-negative STAT1 SH2 domain mutations in unrelated patients with Mendelian susceptibility to mycobacterial disease. Human mutation, 33, 9, 1377-1387 Human mutation, 33, 9, 1377-1387 Human mutation, 33, 9, 1377-1387 2012/09 英語 研究論文(学術雑誌) 公開
Kawai T, Saito M, Nishikomori R, Yasumi T, Izawa K, Murakami T, Okamoto S, Mori Y, Nakagawa N, Imai K, Nonoyama S, Wada T, Yachie A, Ohmori K, Nakahata T, Heike T Kawai T, Saito M, Nishikomori R, Yasumi T, Izawa K, Murakami T, Okamoto S, Mori Y, Nakagawa N, Imai K, Nonoyama S, Wada T, Yachie A, Ohmori K, Nakahata T, Heike T Kawai T, Saito M, Nishikomori R, Yasumi T, Izawa K, Murakami T, Okamoto S, Mori Y, Nakagawa N, Imai K, Nonoyama S, Wada T, Yachie A, Ohmori K, Nakahata T, Heike T Multiple reversions of an IL2RG mutation restore T cell function in an X-linked severe combined immunodeficiency patient. Multiple reversions of an IL2RG mutation restore T cell function in an X-linked severe combined immunodeficiency patient. Multiple reversions of an IL2RG mutation restore T cell function in an X-linked severe combined immunodeficiency patient. Journal of clinical immunology, 32, 4, 690-697 Journal of clinical immunology, 32, 4, 690-697 Journal of clinical immunology, 32, 4, 690-697 2012/08 英語 研究論文(学術雑誌) 公開
堀内久徳, 白川龍太郎, 八角高裕 堀内久徳, 白川龍太郎, 八角高裕 血小板顆粒放出の分子メカニズム 血小板顆粒放出の分子メカニズム 臨床血液, 53, 7, 664-671 (J-STAGE) 臨床血液, 53, 7, 664-671 (J-STAGE) , 53, 7, 664-671 (J-STAGE) 2012/07 日本語 研究論文(学術雑誌) 公開
Kawai T, Nishikomori R, Izawa K, Murata Y, Tanaka N, Sakai H, Saito M, Yasumi T, Takaoka Y, Nakahata T, Mizukami T, Nunoi H, Kiyohara Y, Yoden A, Murata T, Sasaki S, Ito E, Akutagawa H, Kawai T, Imai C, Okada S, Kobayashi M, Heike T Kawai T, Nishikomori R, Izawa K, Murata Y, Tanaka N, Sakai H, Saito M, Yasumi T, Takaoka Y, Nakahata T, Mizukami T, Nunoi H, Kiyohara Y, Yoden A, Murata T, Sasaki S, Ito E, Akutagawa H, Kawai T, Imai C, Okada S, Kobayashi M, Heike T Kawai T, Nishikomori R, Izawa K, Murata Y, Tanaka N, Sakai H, Saito M, Yasumi T, Takaoka Y, Nakahata T, Mizukami T, Nunoi H, Kiyohara Y, Yoden A, Murata T, Sasaki S, Ito E, Akutagawa H, Kawai T, Imai C, Okada S, Kobayashi M, Heike T Frequent somatic mosaicism of NEMO in T cells of patients with X-linked anhidrotic ectodermal dysplasia with immunodeficiency. Frequent somatic mosaicism of NEMO in T cells of patients with X-linked anhidrotic ectodermal dysplasia with immunodeficiency. Frequent somatic mosaicism of NEMO in T cells of patients with X-linked anhidrotic ectodermal dysplasia with immunodeficiency. Blood, 119, 23, 5458-5466 Blood, 119, 23, 5458-5466 Blood, 119, 23, 5458-5466 2012/06 英語 研究論文(学術雑誌) 公開
Nishi M, Nishimura R, Suzuki N, Sawada A, Okamura T, Fujita N, Kanai R, Yano J, Adachi S, Yasumi T, Sato E, Yasutomo K, Ishii E, Ohga S Nishi M, Nishimura R, Suzuki N, Sawada A, Okamura T, Fujita N, Kanai R, Yano J, Adachi S, Yasumi T, Sato E, Yasutomo K, Ishii E, Ohga S Nishi M, Nishimura R, Suzuki N, Sawada A, Okamura T, Fujita N, Kanai R, Yano J, Adachi S, Yasumi T, Sato E, Yasutomo K, Ishii E, Ohga S Reduced-intensity conditioning in unrelated donor cord blood transplantation for familial hemophagocytic lymphohistiocytosis. Reduced-intensity conditioning in unrelated donor cord blood transplantation for familial hemophagocytic lymphohistiocytosis. Reduced-intensity conditioning in unrelated donor cord blood transplantation for familial hemophagocytic lymphohistiocytosis. American journal of hematology, 87, 6, 637-639 American journal of hematology, 87, 6, 637-639 American journal of hematology, 87, 6, 637-639 2012/06 英語 研究論文(学術雑誌) 公開
Kusunoki T, Mukaida K, Morimoto T, Sakuma M, Yasumi T, Nishikomori R, Heike T Kusunoki T, Mukaida K, Morimoto T, Sakuma M, Yasumi T, Nishikomori R, Heike T Kusunoki T, Mukaida K, Morimoto T, Sakuma M, Yasumi T, Nishikomori R, Heike T Birth order effect on childhood food allergy. Birth order effect on childhood food allergy. Birth order effect on childhood food allergy. Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology, 23, 3, 250-254 Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology, 23, 3, 250-254 Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology, 23, 3, 250-254 2012/05 英語 研究論文(学術雑誌) 公開
Izawa K, Hijikata A, Tanaka N, Kawai T, Saito MK, Goldbach-Mansky R, Aksentijevich I, Yasumi T, Nakahata T, Heike T, Nishikomori R, Ohara O Izawa K, Hijikata A, Tanaka N, Kawai T, Saito MK, Goldbach-Mansky R, Aksentijevich I, Yasumi T, Nakahata T, Heike T, Nishikomori R, Ohara O Izawa K, Hijikata A, Tanaka N, Kawai T, Saito MK, Goldbach-Mansky R, Aksentijevich I, Yasumi T, Nakahata T, Heike T, Nishikomori R, Ohara O Detection of base substitution-type somatic mosaicism of the NLRP3 gene with &gt;99.9% statistical confidence by massively parallel sequencing. Detection of base substitution-type somatic mosaicism of the NLRP3 gene with &gt;99.9% statistical confidence by massively parallel sequencing. Detection of base substitution-type somatic mosaicism of the NLRP3 gene with &gt;99.9% statistical confidence by massively parallel sequencing. DNA research : an international journal for rapid publication of reports on genes and genomes, 19, 2, 143-152 DNA research : an international journal for rapid publication of reports on genes and genomes, 19, 2, 143-152 DNA research : an international journal for rapid publication of reports on genes and genomes, 19, 2, 143-152 2012/04 英語 研究論文(学術雑誌) 公開
Sakai H, Okafuji I, Nishikomori R, Abe J, Izawa K, Kambe N, Yasumi T, Nakahata T, Heike T Sakai H, Okafuji I, Nishikomori R, Abe J, Izawa K, Kambe N, Yasumi T, Nakahata T, Heike T Sakai H, Okafuji I, Nishikomori R, Abe J, Izawa K, Kambe N, Yasumi T, Nakahata T, Heike T The CD40-CD40L axis and IFN-γ play critical roles in Langhans giant cell formation. The CD40-CD40L axis and IFN-γ play critical roles in Langhans giant cell formation. The CD40-CD40L axis and IFN-γ play critical roles in Langhans giant cell formation. International immunology, 24, 1, 5-15 International immunology, 24, 1, 5-15 International immunology, 24, 1, 5-15 2012/01 英語 研究論文(学術雑誌) 公開
Tahara M, Sakai H, Nishikomori R, Yasumi T, Heike T, Nagata I, Inui A, Fujisawa T, Shigematsu Y, Nishijima K, Kuwakado K, Watabe S, Kameyama J Tahara M, Sakai H, Nishikomori R, Yasumi T, Heike T, Nagata I, Inui A, Fujisawa T, Shigematsu Y, Nishijima K, Kuwakado K, Watabe S, Kameyama J Tahara M, Sakai H, Nishikomori R, Yasumi T, Heike T, Nagata I, Inui A, Fujisawa T, Shigematsu Y, Nishijima K, Kuwakado K, Watabe S, Kameyama J Patient with neonatal-onset chronic hepatitis presenting with mevalonate kinase deficiency with a novel MVK gene mutation. Patient with neonatal-onset chronic hepatitis presenting with mevalonate kinase deficiency with a novel MVK gene mutation. Patient with neonatal-onset chronic hepatitis presenting with mevalonate kinase deficiency with a novel MVK gene mutation. Modern rheumatology, 21, 6, 641-645 Modern rheumatology, 21, 6, 641-645 Modern rheumatology / the Japan Rheumatism Association, 21, 6, 641-645 2011/12 英語 研究論文(学術雑誌) 公開
Tanaka N, Izawa K, Saito MK, Sakuma M, Oshima K, Ohara O, Nishikomori R, Morimoto T, Kambe N, Goldbach-Mansky R, Aksentijevich I, de Saint Basile G, Neven B, van Gijn M, Frenkel J, Aróstegui JI, Yagüe J, Merino R, Ibañez M, Pontillo A, Takada H, Imagawa T, Kawai T, Yasumi T, Nakahata T, Heike T Tanaka N, Izawa K, Saito MK, Sakuma M, Oshima K, Ohara O, Nishikomori R, Morimoto T, Kambe N, Goldbach-Mansky R, Aksentijevich I, de Saint Basile G, Neven B, van Gijn M, Frenkel J, Aróstegui JI, Yagüe J, Merino R, Ibañez M, Pontillo A, Takada H, Imagawa T, Kawai T, Yasumi T, Nakahata T, Heike T Tanaka N, Izawa K, Saito MK, Sakuma M, Oshima K, Ohara O, Nishikomori R, Morimoto T, Kambe N, Goldbach-Mansky R, Aksentijevich I, de Saint Basile G, Neven B, van Gijn M, Frenkel J, Aróstegui JI, Yagüe J, Merino R, Ibañez M, Pontillo A, Takada H, Imagawa T, Kawai T, Yasumi T, Nakahata T, Heike T High incidence of NLRP3 somatic mosaicism in patients with chronic infantile neurologic, cutaneous, articular syndrome: results of an International Multicenter Collaborative Study. High incidence of NLRP3 somatic mosaicism in patients with chronic infantile neurologic, cutaneous, articular syndrome: results of an International Multicenter Collaborative Study. High incidence of NLRP3 somatic mosaicism in patients with chronic infantile neurologic, cutaneous, articular syndrome: results of an International Multicenter Collaborative Study. Arthritis and rheumatism, 63, 11, 3625-3632 Arthritis and rheumatism, 63, 11, 3625-3632 Arthritis and rheumatism, 63, 11, 3625-3632 2011/11 英語 研究論文(学術雑誌) 公開
八角高裕 八角高裕 血球貪食症候群の発症機構に迫る  家族性血球貪食症候群の病態と診断―細胞障害活性による免疫応答の調節 血球貪食症候群の発症機構に迫る  家族性血球貪食症候群の病態と診断―細胞障害活性による免疫応答の調節 医学のあゆみ, 238, 11, 1048-1052 医学のあゆみ, 238, 11, 1048-1052 , 238, 11, 1048-1052 2011/09/10 日本語 公開
Ohta H, Miyashita E, Hirata I, Matsumura R, Yoshida H, Hashii Y, Higashiura T, Yasumi T, Murata Y, Heike T, Yang X, Kanegane H, Ohara O, Ozono K Ohta H, Miyashita E, Hirata I, Matsumura R, Yoshida H, Hashii Y, Higashiura T, Yasumi T, Murata Y, Heike T, Yang X, Kanegane H, Ohara O, Ozono K Ohta H, Miyashita E, Hirata I, Matsumura R, Yoshida H, Hashii Y, Higashiura T, Yasumi T, Murata Y, Heike T, Yang X, Kanegane H, Ohara O, Ozono K Hematopoietic stem cell transplantation with reduced intensity conditioning from a family haploidentical donor in an infant with familial hemophagocytic lymphohistocytosis. Hematopoietic stem cell transplantation with reduced intensity conditioning from a family haploidentical donor in an infant with familial hemophagocytic lymphohistocytosis. Hematopoietic stem cell transplantation with reduced intensity conditioning from a family haploidentical donor in an infant with familial hemophagocytic lymphohistocytosis. International journal of hematology, 94, 3, 285-290 International journal of hematology, 94, 3, 285-290 International journal of hematology, 94, 3, 285-290 2011/09 英語 研究論文(学術雑誌) 公開
Murata Y, Yasumi T, Shirakawa R, Izawa K, Sakai H, Abe J, Tanaka N, Kawai T, Oshima K, Saito M, Nishikomori R, Ohara O, Ishii E, Nakahata T, Horiuchi H, Heike T Murata Y, Yasumi T, Shirakawa R, Izawa K, Sakai H, Abe J, Tanaka N, Kawai T, Oshima K, Saito M, Nishikomori R, Ohara O, Ishii E, Nakahata T, Horiuchi H, Heike T Murata Y, Yasumi T, Shirakawa R, Izawa K, Sakai H, Abe J, Tanaka N, Kawai T, Oshima K, Saito M, Nishikomori R, Ohara O, Ishii E, Nakahata T, Horiuchi H, Heike T Rapid diagnosis of FHL3 by flow cytometric detection of intraplatelet Munc13-4 protein. Rapid diagnosis of FHL3 by flow cytometric detection of intraplatelet Munc13-4 protein. Rapid diagnosis of FHL3 by flow cytometric detection of intraplatelet Munc13-4 protein. Blood, 118, 5, 1225-1230 Blood, 118, 5, 1225-1230 Blood, 118, 5, 1225-1230 2011/08 英語 研究論文(学術雑誌) 公開
Kusunoki T, Morimoto T, Sakuma M, Mukaida K, Yasumi T, Nishikomori R, Fujii T, Heike T Kusunoki T, Morimoto T, Sakuma M, Mukaida K, Yasumi T, Nishikomori R, Fujii T, Heike T Kusunoki T, Morimoto T, Sakuma M, Mukaida K, Yasumi T, Nishikomori R, Fujii T, Heike T Total and low-density lipoprotein cholesterol levels are associated with atopy in schoolchildren. Total and low-density lipoprotein cholesterol levels are associated with atopy in schoolchildren. Total and low-density lipoprotein cholesterol levels are associated with atopy in schoolchildren. The Journal of pediatrics, 158, 2, 334-336 The Journal of pediatrics, 158, 2, 334-336 The Journal of pediatrics, 158, 2, 334-336 2011/02 英語 研究論文(学術雑誌) 公開
八角高裕 八角高裕 マクロファージ活性化症候群と血球貪食性リンパ組織球症 マクロファージ活性化症候群と血球貪食性リンパ組織球症 医学のあゆみ Vol.235 Nos.12,13 2010 医学のあゆみ Vol.235 Nos.12,13 2010 2010/12/25 日本語 公開
Mukaida K, Kusunoki T, Morimoto T, Yasumi T, Nishikomori R, Heike T, Fujii T, Nakahata T Mukaida K, Kusunoki T, Morimoto T, Yasumi T, Nishikomori R, Heike T, Fujii T, Nakahata T Mukaida K, Kusunoki T, Morimoto T, Yasumi T, Nishikomori R, Heike T, Fujii T, Nakahata T The effect of past food avoidance due to allergic symptoms on the growth of children at school age. The effect of past food avoidance due to allergic symptoms on the growth of children at school age. The effect of past food avoidance due to allergic symptoms on the growth of children at school age. Allergology international : official journal of the Japanese Society of Allergology, 59, 4, 369-374 Allergology international : official journal of the Japanese Society of Allergology, 59, 4, 369-374 Allergology international : official journal of the Japanese Society of Allergology, 59, 4, 369-374 2010/12 英語 研究論文(学術雑誌) 公開
Nagai K, Yamamoto K, Fujiwara H, An J, Ochi T, Suemori K, Yasumi T, Tauchi H, Koh K, Sato M, Morimoto A, Heike T, Ishii E, Yasukawa M Nagai K, Yamamoto K, Fujiwara H, An J, Ochi T, Suemori K, Yasumi T, Tauchi H, Koh K, Sato M, Morimoto A, Heike T, Ishii E, Yasukawa M Nagai K, Yamamoto K, Fujiwara H, An J, Ochi T, Suemori K, Yasumi T, Tauchi H, Koh K, Sato M, Morimoto A, Heike T, Ishii E, Yasukawa M Subtypes of familial hemophagocytic lymphohistiocytosis in Japan based on genetic and functional analyses of cytotoxic T lymphocytes. Subtypes of familial hemophagocytic lymphohistiocytosis in Japan based on genetic and functional analyses of cytotoxic T lymphocytes. Subtypes of familial hemophagocytic lymphohistiocytosis in Japan based on genetic and functional analyses of cytotoxic T lymphocytes. PloS one, 5, 11, e14173 PloS one, 5, 11, e14173 PloS one, 5, 11, e14173 2010/11 英語 研究論文(学術雑誌) 公開
西小森隆太, 八角高裕, 平家俊男 西小森隆太, 八角高裕, 平家俊男 自己炎症性疾患の最近の進歩 自己炎症性疾患の最近の進歩 Front Rheumatol Clin Immunol, 4, 1, 49-51 Front Rheumatol Clin Immunol, 4, 1, 49-51 , 4, 1, 49-51 2010/02 日本語 公開
Kusunoki T, Morimoto T, Nishikomori R, Yasumi T, Heike T, Mukaida K, Fujii T, Nakahata T Kusunoki T, Morimoto T, Nishikomori R, Yasumi T, Heike T, Mukaida K, Fujii T, Nakahata T Kusunoki T, Morimoto T, Nishikomori R, Yasumi T, Heike T, Mukaida K, Fujii T, Nakahata T Breastfeeding and the prevalence of allergic diseases in schoolchildren: Does reverse causation matter? Breastfeeding and the prevalence of allergic diseases in schoolchildren: Does reverse causation matter? Breastfeeding and the prevalence of allergic diseases in schoolchildren: Does reverse causation matter? Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology, 21, 1 Pt 1, 60-66 Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology, 21, 1 Pt 1, 60-66 Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology, 21, 1 Pt 1, 60-66 2010/02 英語 研究論文(学術雑誌) 公開
Sakai H, Ito S, Nishikomori R, Takaoka Y, Kawai T, Saito M, Okafuji I, Yasumi T, Heike T, Nakahata T Sakai H, Ito S, Nishikomori R, Takaoka Y, Kawai T, Saito M, Okafuji I, Yasumi T, Heike T, Nakahata T Sakai H, Ito S, Nishikomori R, Takaoka Y, Kawai T, Saito M, Okafuji I, Yasumi T, Heike T, Nakahata T A case of early-onset sarcoidosis with a six-base deletion in the NOD2 gene. A case of early-onset sarcoidosis with a six-base deletion in the NOD2 gene. A case of early-onset sarcoidosis with a six-base deletion in the NOD2 gene. Rheumatology (Oxford, England), 49, 1, 194-196 Rheumatology (Oxford, England), 49, 1, 194-196 Rheumatology (Oxford, England), 49, 1, 194-196 2010/01 英語 研究論文(学術雑誌) 公開
Kusunoki T, Morimoto T, Nishikomori R, Yasumi T, Heike T, Fujii T, Nakahata T Kusunoki T, Morimoto T, Nishikomori R, Yasumi T, Heike T, Fujii T, Nakahata T Kusunoki T, Morimoto T, Nishikomori R, Yasumi T, Heike T, Fujii T, Nakahata T Changing prevalence and severity of childhood allergic diseases in kyoto, Japan, from 1996 to 2006. Changing prevalence and severity of childhood allergic diseases in kyoto, Japan, from 1996 to 2006. Changing prevalence and severity of childhood allergic diseases in kyoto, Japan, from 1996 to 2006. Allergology international : official journal of the Japanese Society of Allergology, 58, 4, 543-548 Allergology international : official journal of the Japanese Society of Allergology, 58, 4, 543-548 Allergology international : official journal of the Japanese Society of Allergology, 58, 4, 543-548 2009/12 英語 研究論文(学術雑誌) 公開
Matangkasombut P, Marigowda G, Ervine A, Idris L, Pichavant M, Kim HY, Yasumi T, Wilson SB, DeKruyff RH, Faul JL, Israel E, Akbari O, Umetsu DT Matangkasombut P, Marigowda G, Ervine A, Idris L, Pichavant M, Kim HY, Yasumi T, Wilson SB, DeKruyff RH, Faul JL, Israel E, Akbari O, Umetsu DT Matangkasombut P, Marigowda G, Ervine A, Idris L, Pichavant M, Kim HY, Yasumi T, Wilson SB, DeKruyff RH, Faul JL, Israel E, Akbari O, Umetsu DT Natural killer T cells in the lungs of patients with asthma. Natural killer T cells in the lungs of patients with asthma. Natural killer T cells in the lungs of patients with asthma. The Journal of allergy and clinical immunology, 123, 5, 1181-1185 The Journal of allergy and clinical immunology, 123, 5, 1181-1185 The Journal of allergy and clinical immunology, 123, 5, 1181-1185 2009/05 英語 研究論文(学術雑誌) 公開
Koh YI, Kim HY, Meyer EH, Pichavant M, Akbari O, Yasumi T, Savage PB, DeKruyff RH, Umetsu DT Koh YI, Kim HY, Meyer EH, Pichavant M, Akbari O, Yasumi T, Savage PB, DeKruyff RH, Umetsu DT Koh YI, Kim HY, Meyer EH, Pichavant M, Akbari O, Yasumi T, Savage PB, Dekruyff RH, Umetsu DT Activation of nonclassical CD1d-restricted NK T cells induces airway hyperreactivity in beta 2-microglobulin-deficient mice. Activation of nonclassical CD1d-restricted NK T cells induces airway hyperreactivity in beta 2-microglobulin-deficient mice. Activation of nonclassical CD1d-restricted NK T cells induces airway hyperreactivity in beta 2-microglobulin-deficient mice. Journal of immunology (Baltimore, Md. : 1950), 181, 7, 4560-4569 Journal of immunology (Baltimore, Md. : 1950), 181, 7, 4560-4569 Journal of immunology (Baltimore, Md. : 1950), 181, 7, 4560-4569 2008/10 英語 研究論文(学術雑誌) 公開
Matangkasombut P, Pichavant M, Yasumi T, Hendricks C, Savage PB, Dekruyff RH, Umetsu DT Matangkasombut P, Pichavant M, Yasumi T, Hendricks C, Savage PB, Dekruyff RH, Umetsu DT Matangkasombut P, Pichavant M, Yasumi T, Hendricks C, Savage PB, Dekruyff RH, Umetsu DT Direct activation of natural killer T cells induces airway hyperreactivity in nonhuman primates. Direct activation of natural killer T cells induces airway hyperreactivity in nonhuman primates. Direct activation of natural killer T cells induces airway hyperreactivity in nonhuman primates. The Journal of allergy and clinical immunology, 121, 5, 1287-1289 The Journal of allergy and clinical immunology, 121, 5, 1287-1289 The Journal of allergy and clinical immunology, 121, 5, 1287-1289 2008/05 英語 研究論文(学術雑誌) 公開
八角高裕 八角高裕 Th1とTh2の相互制御 Th1とTh2の相互制御 臨床免疫, 44, 1, 97-99 臨床免疫, 44, 1, 97-99 , 44, 1, 97-99 2005/07 日本語 研究論文(学術雑誌) 公開
Yasumi T, Katamura K, Okafuji I, Yoshioka T, Meguro TA, Nishikomori R, Kusunoki T, Heike T, Nakahata T Yasumi T, Katamura K, Okafuji I, Yoshioka T, Meguro TA, Nishikomori R, Kusunoki T, Heike T, Nakahata T Yasumi T, Katamura K, Okafuji I, Yoshioka T, Meguro TA, Nishikomori R, Kusunoki T, Heike T, Nakahata T Limited ability of antigen-specific Th1 responses to inhibit Th2 cell development in vivo. Limited ability of antigen-specific Th1 responses to inhibit Th2 cell development in vivo. Limited ability of antigen-specific Th1 responses to inhibit Th2 cell development in vivo. Journal of immunology (Baltimore, Md. : 1950), 174, 3, 1325-1331 Journal of immunology (Baltimore, Md. : 1950), 174, 3, 1325-1331 Journal of immunology (Baltimore, Md. : 1950), 174, 3, 1325-1331 2005/02 英語 研究論文(学術雑誌) 公開
Tanaka T, Matsubara H, Adachi S, Chang H, Fujino H, Higashi Y, Yasumi T, Kobayashi M, Watanabe K, Takahashi M, Kobayashi Y, Maruya E, Saji H, Nakahata T Tanaka T, Matsubara H, Adachi S, Chang H, Fujino H, Higashi Y, Yasumi T, Kobayashi M, Watanabe K, Takahashi M, Kobayashi Y, Maruya E, Saji H, Nakahata T Tanaka T, Matsubara H, Adachi S, Chang H, Fujino H, Higashi Y, Yasumi T, Kobayashi M, Watanabe K, Takahashi M, Kobayashi Y, Maruya E, Saji H, Nakahata T Second transplantation from HLA 2-loci-mismatched mother for graft failure due to hemophagocytic syndrome after cord blood transplantation. Second transplantation from HLA 2-loci-mismatched mother for graft failure due to hemophagocytic syndrome after cord blood transplantation. Second transplantation from HLA 2-loci-mismatched mother for graft failure due to hemophagocytic syndrome after cord blood transplantation. International journal of hematology, 80, 5, 467-469 International journal of hematology, 80, 5, 467-469 International journal of hematology, 80, 5, 467-469 2004/12 英語 研究論文(学術雑誌) 公開
Nishikomori R, Akutagawa H, Maruyama K, Nakata-Hizume M, Ohmori K, Mizuno K, Yachie A, Yasumi T, Kusunoki T, Heike T, Nakahata T Nishikomori R, Akutagawa H, Maruyama K, Nakata-Hizume M, Ohmori K, Mizuno K, Yachie A, Yasumi T, Kusunoki T, Heike T, Nakahata T Nishikomori R, Akutagawa H, Maruyama K, Nakata-Hizume M, Ohmori K, Mizuno K, Yachie A, Yasumi T, Kusunoki T, Heike T, Nakahata T X-linked ectodermal dysplasia and immunodeficiency caused by reversion mosaicism of NEMO reveals a critical role for NEMO in human T-cell development and/or survival. X-linked ectodermal dysplasia and immunodeficiency caused by reversion mosaicism of NEMO reveals a critical role for NEMO in human T-cell development and/or survival. X-linked ectodermal dysplasia and immunodeficiency caused by reversion mosaicism of NEMO reveals a critical role for NEMO in human T-cell development and/or survival. Blood, 103, 12, 4565-4572 Blood, 103, 12, 4565-4572 Blood, 103, 12, 4565-4572 2004/06 英語 研究論文(学術雑誌) 公開
Yasumi T, Katamura K, Yoshioka T, Meguro TA, Nishikomori R, Heike T, Inobe M, Kon S, Uede T, Nakahata T Yasumi T, Katamura K, Yoshioka T, Meguro TA, Nishikomori R, Heike T, Inobe M, Kon S, Uede T, Nakahata T Yasumi T, Katamura K, Yoshioka T, Meguro TA, Nishikomori R, Heike T, Inobe M, Kon S, Uede T, Nakahata T Differential requirement for the CD40-CD154 costimulatory pathway during Th cell priming by CD8 alpha+ and CD8 alpha- murine dendritic cell subsets. Differential requirement for the CD40-CD154 costimulatory pathway during Th cell priming by CD8 alpha+ and CD8 alpha- murine dendritic cell subsets. Differential requirement for the CD40-CD154 costimulatory pathway during Th cell priming by CD8 alpha+ and CD8 alpha- murine dendritic cell subsets. Journal of immunology (Baltimore, Md. : 1950), 172, 8, 4826-4833 Journal of immunology (Baltimore, Md. : 1950), 172, 8, 4826-4833 Journal of immunology (Baltimore, Md. : 1950), 172, 8, 4826-4833 2004/04 英語 研究論文(学術雑誌) 公開
Imai T, Adachi S, Nishijo K, Ohgushi M, Okada M, Yasumi T, Watanabe K, Nishikomori R, Nakayama T, Yonehara S, Toguchida J, Nakahata T Imai T, Adachi S, Nishijo K, Ohgushi M, Okada M, Yasumi T, Watanabe K, Nishikomori R, Nakayama T, Yonehara S, Toguchida J, Nakahata T Imai T, Adachi S, Nishijo K, Ohgushi M, Okada M, Yasumi T, Watanabe K, Nishikomori R, Nakayama T, Yonehara S, Toguchida J, Nakahata T FR901228 induces tumor regression associated with induction of Fas ligand and activation of Fas signaling in human osteosarcoma cells. FR901228 induces tumor regression associated with induction of Fas ligand and activation of Fas signaling in human osteosarcoma cells. FR901228 induces tumor regression associated with induction of Fas ligand and activation of Fas signaling in human osteosarcoma cells. Oncogene, 22, 58, 9231-9242 Oncogene, 22, 58, 9231-9242 Oncogene, 22, 58, 9231-9242 2003/12 英語 研究論文(学術雑誌) 公開
八角高裕 八角高裕 樹状細胞の多様性 CD8α+, CD8α- マウス樹状細胞によるヘルパーT細胞の機能的分化 樹状細胞の多様性 CD8α+, CD8α- マウス樹状細胞によるヘルパーT細胞の機能的分化 臨床免疫, 40, 2, 155-159 臨床免疫, 40, 2, 155-159 , 40, 2, 155-159 2003/08 日本語 研究論文(学術雑誌) 公開
八角高裕, 片村憲司 八角高裕, 片村憲司 樹状細胞サブセットとヘルパーT細胞の機能的分化 樹状細胞サブセットとヘルパーT細胞の機能的分化 臨床免疫, 37, 5, 621-625 臨床免疫, 37, 5, 621-625 , 37, 5, 621-625 2002/05 日本語 研究論文(学術雑誌) 公開
Iio J, Katamura K, Takeda H, Ohmura K, Yasumi T, Meguro TA, Ohshima Y, Nakahata T Iio J, Katamura K, Takeda H, Ohmura K, Yasumi T, Meguro TA, Ohshima Y, Nakahata T Iio J, Katamura K, Takeda H, Ohmura K, Yasumi T, Meguro TA, Ohshima Y, Nakahata T Lipid A analogue, ONO-4007, inhibits IgE response and antigen-induced eosinophilic recruitment into airways in BALB/c mice. Lipid A analogue, ONO-4007, inhibits IgE response and antigen-induced eosinophilic recruitment into airways in BALB/c mice. Lipid A analogue, ONO-4007, inhibits IgE response and antigen-induced eosinophilic recruitment into airways in BALB/c mice. International archives of allergy and immunology, 127, 3, 217-225 International archives of allergy and immunology, 127, 3, 217-225 International archives of allergy and immunology, 127, 3, 217-225 2002/03 英語 研究論文(学術雑誌) 公開

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タイトル言語:
Misc
著者 著者(日本語) 著者(英語) タイトル タイトル(日本語) タイトル(英語) 書誌情報等 書誌情報等(日本語) 書誌情報等(英語) 出版年月 査読の有無 記述言語 掲載種別 公開
柴田 洋史, 八角 高裕 柴田 洋史, 八角 高裕 【小児臨床検査のポイント2017】 免疫・アレルギー検査 急性期反応物質 急性期反応蛋白、赤血球沈降速度、CRP、血清アミロイドA、プロカルシトニン、(高サイトカイン血症の病態との関係から)血中・尿中β2ミクログロブリン 【小児臨床検査のポイント2017】 免疫・アレルギー検査 急性期反応物質 急性期反応蛋白、赤血球沈降速度、CRP、血清アミロイドA、プロカルシトニン、(高サイトカイン血症の病態との関係から)血中・尿中β2ミクログロブリン 小児内科, 49, 増刊, 268-272 小児内科, 49, 増刊, 268-272 , 49, 増刊, 268-272 2017/11 日本語 公開
八角 高裕 八角 高裕 【血球の増加と減少】 汎血球減少 血球貪食性リンパ組織球症 【血球の増加と減少】 汎血球減少 血球貪食性リンパ組織球症 小児内科, 48, 7, 1054-1058 小児内科, 48, 7, 1054-1058 , 48, 7, 1054-1058 2016/07 日本語 公開
八角 高裕 八角 高裕 【小児疾患診療のための病態生理2 改訂第5版】 免疫不全 家族性血球貪食性リンパ組織球症 【小児疾患診療のための病態生理2 改訂第5版】 免疫不全 家族性血球貪食性リンパ組織球症 小児内科, 47, 増刊, 722-726 小児内科, 47, 増刊, 722-726 , 47, 増刊, 722-726 2015/11 日本語 公開
八角 高裕, 柴田 洋史, 下寺 佐栄子, 平家 俊男 八角 高裕, 柴田 洋史, 下寺 佐栄子, 平家 俊男 HLH病態の多様性と治療戦略の展望 HLH病態の多様性と治療戦略の展望 臨床血液, 56, 10, 2248-2257 臨床血液, 56, 10, 2248-2257 , 56, 10, 2248-2257 2015/10 日本語 公開
八角 高裕 八角 高裕 【自己炎症症候群とその類縁疾患】 慢性再発性多発性骨髄炎 【自己炎症症候群とその類縁疾患】 慢性再発性多発性骨髄炎 リウマチ科, 54, 2, 185-190 リウマチ科, 54, 2, 185-190 , 54, 2, 185-190 2015/08 日本語 公開
八角 高裕 八角 高裕 【見逃しやすい免疫不全】 ピンポイント小児医療 血球貪食性リンパ組織球症と免疫不全症 【見逃しやすい免疫不全】 ピンポイント小児医療 血球貪食性リンパ組織球症と免疫不全症 小児内科, 46, 10, 1513-1517 小児内科, 46, 10, 1513-1517 , 46, 10, 1513-1517 2014/10 日本語 公開
八角 高裕 八角 高裕 【自己炎症症候群:稀な遺伝性疾患からリウマチ・アレルギー疾患へのメッセージ】 高IgD症候群(hyperimmunoglobulinemia D and periodic fever syndrome:HIDS) 【自己炎症症候群:稀な遺伝性疾患からリウマチ・アレルギー疾患へのメッセージ】 高IgD症候群(hyperimmunoglobulinemia D and periodic fever syndrome:HIDS) アレルギー・免疫, 20, 10, 1424-1430 アレルギー・免疫, 20, 10, 1424-1430 , 20, 10, 1424-1430 2013/09 日本語 公開
八角 高裕 八角 高裕 【血球貪食症候群の病態と診療の新展開】 家族性血球貪食症候群のスクリーニング検査 【血球貪食症候群の病態と診療の新展開】 家族性血球貪食症候群のスクリーニング検査 血液フロンティア, 23, 1, 27-32 血液フロンティア, 23, 1, 27-32 , 23, 1, 27-32 2012/12 日本語 公開
堀内 久徳, 白川 龍太郎, 八角 高裕 堀内 久徳, 白川 龍太郎, 八角 高裕 血栓止血学・血管生物学の最近の進歩 血小板顆粒放出の分子メカニズム 血栓止血学・血管生物学の最近の進歩 血小板顆粒放出の分子メカニズム 臨床血液, 53, 7, 664-671 臨床血液, 53, 7, 664-671 , 53, 7, 664-671 2012/07 日本語 公開
八角 高裕 八角 高裕 【自己炎症性疾患 発熱性疾患における認知】 マクロファージの活性化と血球貪食性リンパ組織球症 【自己炎症性疾患 発熱性疾患における認知】 マクロファージの活性化と血球貪食性リンパ組織球症 医学のあゆみ, 235, 12-13, 1203-1205 医学のあゆみ, 235, 12-13, 1203-1205 , 235, 12-13, 1203-1205 2010/12 日本語 公開
八木 英哉, 田口 周馬, 田中 篤志, 藤野 寿典, 八角 高裕, 澤田 眞智子, 西小森 隆太, 平家 俊男, 中畑 龍俊 八木 英哉, 田口 周馬, 田中 篤志, 藤野 寿典, 八角 高裕, 澤田 眞智子, 西小森 隆太, 平家 俊男, 中畑 龍俊 カプセル内視鏡で診断した小腸クローン病の小児例 カプセル内視鏡で診断した小腸クローン病の小児例 日本小児科学会雑誌, 114, 6, 966-970 日本小児科学会雑誌, 114, 6, 966-970 , 114, 6, 966-970 2010/06 日本語 公開
西小森 隆太, 八角 高裕 西小森 隆太, 八角 高裕 【小児におけるリウマチ・免疫疾患と生物学的製剤】 生物学的製剤の特徴と有用性・安全性のエビデンス サイトカインを標的とする生物学的製剤 抗インターロイキン(IL)製剤 抗IL-1抗体 【小児におけるリウマチ・免疫疾患と生物学的製剤】 生物学的製剤の特徴と有用性・安全性のエビデンス サイトカインを標的とする生物学的製剤 抗インターロイキン(IL)製剤 抗IL-1抗体 アレルギー・免疫, 17, 2, 222-227 アレルギー・免疫, 17, 2, 222-227 , 17, 2, 222-227 2010/01 日本語 公開
森脇 里香, 横山 瑞香, 塩田 光隆, 安田 謙二, 八角 高裕, 石岡 千寛, 藤村 二郎, 田井 道夫, 三浦 弘資 森脇 里香, 横山 瑞香, 塩田 光隆, 安田 謙二, 八角 高裕, 石岡 千寛, 藤村 二郎, 田井 道夫, 三浦 弘資 術前超音波検査が有用であった腸間膜リンパ管腫の1例 術前超音波検査が有用であった腸間膜リンパ管腫の1例 松江赤十字病院医学雑誌, 11, 1, 63-68 松江赤十字病院医学雑誌, 11, 1, 63-68 , 11, 1, 63-68 1999/05 日本語 公開
横山 瑞香, 八角 高裕, 小倉 加恵子, 原 茂登, 塩田 光隆, 安田 謙二, 藤脇 建久, 石岡 千寛 横山 瑞香, 八角 高裕, 小倉 加恵子, 原 茂登, 塩田 光隆, 安田 謙二, 藤脇 建久, 石岡 千寛 耳介後部リンパ節原発のLangerhans Cell Histiocytosis(LCH)の1例 耳介後部リンパ節原発のLangerhans Cell Histiocytosis(LCH)の1例 松江赤十字病院医学雑誌, 11, 1, 77-81 松江赤十字病院医学雑誌, 11, 1, 77-81 , 11, 1, 77-81 1999/05 日本語 公開
平松 信, 中村 明彦, 喜多村 真治, 能勢 聡一郎, 浜家 一雄, 矢吹 満佐江, 渡辺 茂, 八角 高裕 平松 信, 中村 明彦, 喜多村 真治, 能勢 聡一郎, 浜家 一雄, 矢吹 満佐江, 渡辺 茂, 八角 高裕 バセドウ病,寒冷凝集素症に合併した半月体形成を伴うループス腎炎の1症例 バセドウ病,寒冷凝集素症に合併した半月体形成を伴うループス腎炎の1症例 岡山済生会総合病院雑誌, 30, 28-33 岡山済生会総合病院雑誌, 30, 28-33 , 30, 28-33 1999/01 日本語 公開
渡辺 健一郎, 山崎 恭一, 八角 高裕 渡辺 健一郎, 山崎 恭一, 八角 高裕 胎便吸引症候群と新生児仮死の症例の臨床的検討 胎便吸引症候群と新生児仮死の症例の臨床的検討 松江赤十字病院医学雑誌, 8, 1, 41-44 松江赤十字病院医学雑誌, 8, 1, 41-44 , 8, 1, 41-44 1996/03 日本語 公開

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タイトル言語:
講演・口頭発表等
タイトル タイトル(日本語) タイトル(英語) 会議名 会議名(日本語) 会議名(英語) 主催者 主催者(日本語) 主催者(英語) 開催年月日 記述言語 会議種別 公開
FHL and Lymphocyte Homeostasis[招待あり] FHL and Lymphocyte Homeostasis [招待あり] FHL and Lymphocyte Homeostasis [招待あり] PAS/ASPR 2014 PAS/ASPR 2014 PAS/ASPR 2014 2014/05/04 英語 シンポジウム・ワークショップパネル(指名) 公開
Familial Hemophagocytic Lymphohistiocytosis May Present with Atypical Features in Adolescence and Adulthood.[招待あり] Familial Hemophagocytic Lymphohistiocytosis May Present with Atypical Features in Adolescence and Adulthood. [招待あり] Familial Hemophagocytic Lymphohistiocytosis May Present with Atypical Features in Adolescence and Adulthood. [招待あり] The 4th JSH International Symposium 2013 The 4th JSH International Symposium 2013 The 4th JSH International Symposium 2013 2013/05/24 英語 シンポジウム・ワークショップパネル(指名) 公開
タイトル言語:
書籍等出版物
著者 著者(日本語) 著者(英語) タイトル タイトル(日本語) タイトル(英語) 出版社 出版社(日本語) 出版社(英語) 出版年月 記述言語 担当区分 公開
八角 高裕 八角 高裕 自己炎症症候群の臨床 自己炎症症候群の臨床 新興医学出版社 新興医学出版社 2015/04 日本語 分担執筆 公開
八角 高裕 八角 高裕 Takahiro Yasumi ネルソン小児科学 ネルソン小児科学 Nelson Textbook of Pediatrics ELSEVIER ELSEVIER ELSEVIER 2015/04 日本語 共訳 公開
八角高裕 八角高裕 自己炎症性疾患・自然免疫不全症とその近縁疾患 自己炎症性疾患・自然免疫不全症とその近縁疾患 診断と治療社 診断と治療社 2012/11 日本語 分担執筆 公開
八角高裕、平家俊男 八角高裕、平家俊男 小児の発熱 A to Z 小児の発熱 A to Z 診断と治療社 診断と治療社 2012/04 日本語 分担執筆 公開
タイトル言語:
外部資金:競争的資金・科学研究費補助金
種別 代表/分担 テーマ(日本語) テーマ(英語) 期間
基盤研究(C) 代表 家族性血球貪食症候群の迅速診断法確立と細胞工学的手法を用いた病態解明 2010〜2012
基盤研究(C) 代表 分子病態に基づく血球貪食性リンパ組織球症の新規診療基盤開発 2014〜2016
難治性疾患等政策研究事業(難治性疾患政策研究事業) 分担 (平成29年度分) 2017/04/01〜2018/03/31
難治性疾患等克服研究事業(難治性疾患等政策研究事業(免疫アレルギー疾患等政策研究事業(免疫アレルギー疾患政策研究分野))) 分担 (平成30年度分) 2018/04/01〜2019/03/31
担当科目
講義名(日本語) 講義名(英語) 開講期 学部/研究科 年度
生体応答解析学 Analysis of Biological Response 通年 医学部(人間健康科学科) 2014/04〜2015/03
生体応答解析学 Analysis of Biological Response 通年 医学部(人間健康科学科) 2015/04〜2016/03
生体応答解析学 Analysis of Biological Response 通年 医学部(人間健康科学科) 2016/04〜2017/03
生体応答解析学 Analysis of Biological Response 通年 医学部(人間健康科学科) 2017/04〜2018/03
臨床内科疾病論Ⅱ Clinical Overview of Internal Medicine II 後期 医学部(人間健康科学科) 2017/04〜2018/03
生体応答解析学 Analysis of Biological Response 通年 医学部(人間健康科学科) 2018/04〜2019/03
臨床疾病論D Clinical Overview of Medicine D 前期後半 医学部(人間健康科学科) 2018/04〜2019/03
臨床疾病論D Clinical Overview of Medicine D 前期後半 薬学部 2018/04〜2019/03
臨床疾病論D Clinical Overview of Medicine D 前期後半 医学部(人間健康科学科) 2019/04〜2020/03
臨床疾病論D Clinical Overview of Medicine D 前期後半 薬学部 2019/04〜2020/03