論文・総説 - 今井 耕輔

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  1. Akira Nishimura, Yuki Aoki, Yasuyoshi Ishiwata, Takuya Ichimura, Junichi Ueyama, Yuta Kawahara, Takahiro Tomoda, Maiko Inoue, Kazuaki Matsumoto, Kento Inoue, Haruka Hiroki, Shintaro Ono, Motoi Yamashita, Tsubasa Okano, Mari Tanaka-Kubota, Miho Ashiarai, Satoshi Miyamoto, Reiji Miyawaki, Chika Yamagishi, Mari Tezuka, Teppei Okawa, Akihiro Hoshino, Akifumi Endo, Masato Yasuhara, Takahiro Kamiya, Noriko Mitsuiki, Toshiaki Ono, Takeshi Isoda, Masakatsu Yanagimachi, Daisuke Tomizawa, Masayuki Nagasawa, Shuki Mizutani, Michiko Kajiwara, Masatoshi Takagi, Hirokazu Kanegane, Kohsuke Imai, Tomohiro Morio. Hematopoietic Cell Transplantation with Reduced Intensity Conditioning Using Fludarabine/Busulfan or Fludarabine/Melphalan for Primary Immunodeficiency Diseases. J Clin Immunol. 2021.07; 41 (5): 944-957. ( PubMed, DOI )

  2. Yuichi Nagamatsu, Takeshi Isoda, Motoki Inaji, Jun Oyama, Daiki Niizato, Dan Tomomasa, Noriko Mitsuiki, Motoi Yamashita, Takahiro Kamiya, Kohsuke Imai, Hirokazu Kanegane, Tomohiro Morio, Masatoshi Takagi. Intracranial residual lesions following early intensification in a patient with T-cell acute lymphoblastic leukemia: a case report. BMC Pediatr. 2024.05; 24 (1): 304. ( PubMed, DOI )

  3. Masatoshi Takagi, Chihiro Tomoyasu, Junko Yamanaka, Takayuki Hamabata, Takeshi Isoda, Takako Miyamura, Kohsuke Imai. Immunological assessment of a patient with infant acute lymphoblastic leukemia. Pediatr Int. 2024.01; 66 (1): e15738. ( PubMed, DOI )

  4. Motoi Yamashita, Masae Kuroha, Yuko Kinowawki, Nao Kashiwagi, Kotaro Watanabe, Mika Nagase, Daiki Niizato, Noriko Mitsuiki, Takeshi Isoda, Takahiro Kamiya, Atsuko Arisaka, Motoki Inaji, Kenichi Ohashi, Kohsuke Imai, Hirokazu Kanegane, Tomohiro Morio, Masatoshi Takagi. A SAMD5-SASH1 fusion in solitary infantile myofibromatosis. Pediatr Blood Cancer. 2023.03; e30278. ( PubMed, DOI )

  5. Dan Tomomasa, Takeshi Isoda, Noriko Mitsuiki, Kento Inoue, Akira Nishimura, Kazuhiro Uda, Toru Uchiyama, Motoi Yamashita, Takahiro Kamiya, Akifumi Endo, Masatoshi Takagi, Kohsuke Imai, Michiko Kajiwara, Morton J Cowan, Tomohiro Morio, Hirokazu Kanegane. Successful TCRαβ/CD19-Depleted Hematopoietic Cell Transplantation for a Patient With Artemis Deficiency. J Pediatr Hematol Oncol. 2023.02; ( PubMed, DOI )

  6. Aoi Morishita, Tzu-Wen Yeh, Kouki Tomari, Mihoko Furuichi, Kenichi Kashimada, Tomohiro Morio, Masatoshi Takagi, Kohsuke Imai. Transient immune deficiency accompanied with homozygous CBL rare variant. Pediatr Int. 2022.12; e15439. ( PubMed, DOI )

  7. Qian Zhang, Daniela Matuozzo, Jérémie Le Pen, Danyel Lee, Leen Moens, Takaki Asano, Jonathan Bohlen, Zhiyong Liu, Marcela Moncada-Velez, Yasemin Kendir-Demirkol, Huie Jing, Lucy Bizien, Astrid Marchal, Hassan Abolhassani, Selket Delafontaine, Giorgia Bucciol, , Gulsum Ical Bayhan, Sevgi Keles, Ayca Kiykim, Selda Hancerli, Filomeen Haerynck, Benoit Florkin, Nevin Hatipoglu, Tayfun Ozcelik, Guillaume Morelle, Mayana Zatz, Lisa F P Ng, David Chien Lye, Barnaby Edward Young, Yee-Sin Leo, Clifton L Dalgard, Richard P Lifton, Laurent Renia, Isabelle Meyts, Emmanuelle Jouanguy, Lennart Hammarström, Qiang Pan-Hammarström, Bertrand Boisson, Paul Bastard, Helen C Su, Stéphanie Boisson-Dupuis, Laurent Abel, Charles M Rice, Shen-Ying Zhang, Aurélie Cobat, Jean-Laurent Casanova. Recessive inborn errors of type I IFN immunity in children with COVID-19 pneumonia. J Exp Med. 2022.08; 219 (8): ( PubMed, DOI )

  8. Tessa Mollie Campbell, Zhiyong Liu, Qian Zhang, Marcela Moncada-Velez, Laura E Covill, Peng Zhang, Ilad Alavi Darazam, Paul Bastard, Lucy Bizien, Giorgia Bucciol, Sara Lind Enoksson, Emmanuelle Jouanguy, Şemsi Nur Karabela, Taushif Khan, Yasemin Kendir-Demirkol, Andres Augusto Arias, Davood Mansouri, Per Marits, Nico Marr, Isabelle Migeotte, Leen Moens, Tayfun Ozcelik, Isabelle Pellier, Anton Sendel, Mohammad Shahrooei, C I Edvard Smith, Isabelle Vandernoot, Karen Willekens, , Peter Bergman, Laurent Abel, Aurélie Cobat, Jean-Laurent Casanova, Isabelle Meyts, Yenan T Bryceson. Respiratory viral infections in otherwise healthy humans with inherited IRF7 deficiency. J Exp Med. 2022.07; 219 (7): ( PubMed, DOI )

  9. Akira Nishimura, Satoshi Miyamoto, Kohsuke Imai, Tomohiro Morio. Conditioning regimens for inborn errors of immunity: current perspectives and future strategies. Int J Hematol. 2022.07; 116 (1): 7-15. ( PubMed, DOI )

  10. Adela Escudero, Masatoshi Takagi, Franziska Auer, Ulrike Anne Friedrich, Satoshi Miyamoto, Atsushi Ogawa, Kohsuke Imai, Barbara Pascual, María Vela, Polina Stepensky, Layal Yasin, Sarah Elitzur, Arndt Borkhardt, Antonio Pérez-Martínez, Julia Hauer. Clinical and immunophenotypic characteristics of familial leukemia predisposition caused by PAX5 germline variants. Leukemia. 2022.07; ( PubMed, DOI )

  11. Shohei Eto, Yoko Nukui, Miyuki Tsumura, Yu Nakagama, Kenichi Kashimada, Yoko Mizoguchi, Takanori Utsumi, Maki Taniguchi, Fumiaki Sakura, Kosuke Noma, Yusuke Yoshida, Shinichiro Ohshimo, Shintaro Nagashima, Keisuke Okamoto, Akifumi Endo, Kohsuke Imai, Hirokazu Kanegane, Hidenori Ohnishi, Shintaro Hirata, Eiji Sugiyama, Nobuaki Shime, Masanori Ito, Hiroki Ohge, Yasutoshi Kido, Paul Bastard, Jean-Laurent Casanova, Osamu Ohara, Junko Tanaka, Tomohiro Morio, Satoshi Okada. Neutralizing Type I Interferon Autoantibodies in Japanese Patients with Severe COVID-19. J Clin Immunol. 2022.06; ( PubMed, DOI )

  12. Tomoko Niwano, Tadashi Hosoya, Saori Kadowaki, Etsushi Toyofuku, Takuya Naruto, Masaki Shimizu, Hidenori Ohnishi, Ryuji Koike, Tomohiro Morio, Kohsuke Imai, Masayuki Yoshida, Shinsuke Yasuda. An adult case of suspected A20 haploinsufficiency mimicking polyarteritis nodosa. Rheumatology (Oxford). 2022.05; ( PubMed, DOI )

  13. Shohei Eto, Yoko Nukui, Miyuki Tsumura, Yu Nakagama, Kenichi Kashimada, Yoko Mizoguchi, Takanori Utsumi, Maki Taniguchi, Fumiaki Sakura, Kosuke Noma, Yusuke Yoshida, Shinichiro Ohshimo, Shintaro Nagashima, Keisuke Okamoto, Akifumi Endo, Kohsuke Imai, Hirokazu Kanegane, Hidenori Ohnishi, Shintaro Hirata, Eiji Sugiyama, Nobuaki Shime, Masanori Ito, Hiroki Ohge, Yasutoshi Kido, Paul Bastard, Jean-Laurent Casanova, Junko Tanaka, Tomohiro Morio, Satoshi Okada. Neutralizing Type I Interferon Autoantibodies in Japanese Patients With Severe COVID-19. Res Sq. 2022.03; ( PubMed, DOI )

  14. Egg D, Rump IC, Mitsuiki N, Rojas-Restrepo J, Maccari ME, Schwab C, Gabrysch A, Warnatz K, Goldacker S, Patiño V, Wolff D, Okada S, Hayakawa S, Shikama Y, Kanda K, Imai K, Sotomatsu M, Kuwashima M, Kamiya T, Morio T, Matsumoto K, Mori T, Yoshimoto Y, Dybedal I, Kanariou M, Kucuk ZY, Chapdelaine H, Petruzelkova L, Lorenz HM, Sullivan KE, Heimall J, Moutschen M, Litzman J, Recher M, Albert MH, Hauck F, Seneviratne S, Schmid JP, Kolios A, Unglik G, Klemann C, Snapper S, Giulino-Roth L, Svaton M, Platt CD, Hambleton S, Neth O, Gosse G, Reinsch S, Holzinger D, Kim YJ, Bakhtiar S, Atschekzei F, Schmidt R, Sogkas G, Chandrakasan S, Rae W, Derfalvi B, Marquart HV, Ozen A, Kiykim A, Karakoc-Aydiner E, Králíčková P, de Bree G, Kiritsi D, Seidel MG, Kobbe R, Dantzer J, Alsina L, Armangue T, Lougaris V, Agyeman P, Nyström S, Buchbinder D, Arkwright PD, Grimbacher B.. Therapeutic options for CTLA-4 insufficiency. J Allergy Clin Immunol. 2022.02; 149 (2): 736-746. ( PubMed, DOI )

  15. Kay Tanita, Yoshiki Kawamura, Hiroki Miura, Noriko Mitsuiki, Takahiro Tomoda, Kento Inoue, Akihiro Iguchi, Masafumi Yamada, Taro Yoshida, Hideki Muramatsu, Norimasa Tada, Toshihiro Matsui, Motohiro Kato, Katsuhide Eguchi, Masataka Ishimura, Shouichi Ohga, Kohsuke Imai, Tomohiro Morio, Tetsushi Yoshikawa, Hirokazu Kanegane. Case Report: Rotavirus Vaccination and Severe Combined Immunodeficiency in Japan. Front Immunol. 2022.02; 13 786375. ( PubMed, DOI )

  16. Miyamoto S, Umeda K, Kurata M, Yanagimachi M, Iguchi A, Sasahara Y, Okada K, Koike T, Tanoshima R, Ishimura M, Yamada M, Sato M, Takahashi Y, Kajiwara M, Kawaguchi H, Inoue M, Hashii Y, Yabe H, Kato K, Atsuta Y, Imai K, Morio T.. Hematopoietic Cell Transplantation for Inborn Errors of Immunity Other than Severe Combined Immunodeficiency in Japan: Retrospective Analysis for 1985-2016. J Clin Immunol. 2022.01; ( PubMed, DOI )

  17. Tomomasa D, Isoda T, Mitsuiki N, Yamashita M, Morishita A, Tomoda T, Okano T, Endo A, Kamiya T, Yanagimachi M, Imai K, Kanegane H, Takagi M, Morio T . Successful ruxolitinib administration for a patient with steroid-refractory idiopathic pneumonia syndrome following hematopoietic stem cell transplantation: A case report and literature review. Clin Case Rep. 2021.12; 9 (12): e05242. ( PubMed, DOI )

  18. Isshiki K, Kamiya T, Endo A, Okamoto K, Osumi T, Kawai T, Arai K, Tomizawa D, Ohtsuka K, Nagahori M, Imai K, Kato M, Kanegane H. Vedolizumab therapy for pediatric steroid-refractory gastrointestinal acute graft-versus-host disease. Int J Hematol. 2021.11; ( PubMed, DOI )

  19. Toyohara M, Kajiho Y, Toyofuku E, Takahashi C, Owada K, Kanda S, Harita Y, Ohnishi H, Wada T, Imai K, Kanegane H, Morio T, Oka A. An infant with X-linked anhidrotic ectodermal dysplasia with immunodeficiency presenting with Pneumocystis pneumonia: A case report Clin Case Rep. 2021.11; 9 (11): e05093. ( PubMed, DOI )

  20. Ono S, Takeshita K, Kiridoshi Y, Kato M, Kamiya T, Hoshino A, Yanagimachi M, Arai K, Takeuchi I, Toita N, Imamura T, Sasahara Y, Sugita J, Hamamoto K, Takeuchi M, Saito S, Onuma M, Tsujimoto H, Yasui M, Taga T, Arakawa Y, Mitani Y, Yamamoto N, Imai K, Suda W, Hattori M, Ohara O, Morio T, Honda K, Kanegane H.. Hematopoietic Cell Transplantation Rescues Inflammatory Bowel Disease and Dysbiosis of Gut Microbiota in XIAP Deficiency. J Allergy Clin Immunol Pract. 2021.10; 9 (10): 3767-3780. ( PubMed, DOI )

  21. Okano T, Nishimura A, Inoue K, Naruto T, Tokoro S, Tomoda T, Kamiya T, Simbo A, Akutsu Y, Okamoto K, Yeh T, Isoda T, Yanagimachi M, Kajiwara M, Imai K, Kanegane H, Mori M, Morio,T, Takagi M. Somatic mutation in RUNX1 underlies mucocutaneus inflammatory manifestations. Rheumatology (Oxford). 2021.09; ( PubMed, DOI )

  22. Miyamoto S, Umeda K, Kurata M, Nishimura A, Yanagimachi M, Ishimura M, Sato M, Shigemura T, Kato M, Sasahara Y, Iguchi A, Koike T, Takahashi Y, Kajiwara M, Inoue M, Hashii Y, Yabe H, Kato K, Atsuta Y, Imai K, Morio T.. Hematopoietic Cell Transplantation for Severe Combined Immunodeficiency Patients: a Japanese Retrospective Study. J Clin Immunol. 2021.08; 41 (8): 1865-1877. ( PubMed, DOI )

  23. Takaki Asano, Bertrand Boisson, Fanny Onodi, Daniela Matuozzo, Marcela Moncada-Velez, Majistor Raj Luxman Maglorius Renkilaraj, Peng Zhang, Laurent Meertens, Alexandre Bolze, Marie Materna, Sarantis Korniotis, Adrian Gervais, Estelle Talouarn, Benedetta Bigio, Yoann Seeleuthner, Kaya Bilguvar, Yu Zhang, Anna-Lena Neehus, Masato Ogishi, Simon J Pelham, Tom Le Voyer, Jérémie Rosain, Quentin Philippot, Pere Soler-Palacín, Roger Colobran, Andrea Martin-Nalda, Jacques G Rivière, Yacine Tandjaoui-Lambiotte, Khalil Chaïbi, Mohammad Shahrooei, Ilad Alavi Darazam, Nasrin Alipour Olyaei, Davood Mansouri, Nevin Hatipoğlu, Figen Palabiyik, Tayfun Ozcelik, Giuseppe Novelli, Antonio Novelli, Giorgio Casari, Alessandro Aiuti, Paola Carrera, Simone Bondesan, Federica Barzaghi, Patrizia Rovere-Querini, Cristina Tresoldi, Jose Luis Franco, Julian Rojas, Luis Felipe Reyes, Ingrid G Bustos, Andres Augusto Arias, Guillaume Morelle, Kyheng Christèle, Jesús Troya, Laura Planas-Serra, Agatha Schlüter, Marta Gut, Aurora Pujol, Luis M Allende, Carlos Rodriguez-Gallego, Carlos Flores, Oscar Cabrera-Marante, Daniel E Pleguezuelo, Rebeca Pérez de Diego, Sevgi Keles, Gokhan Aytekin, Ozge Metin Akcan, Yenan T Bryceson, Peter Bergman, Petter Brodin, Daniel Smole, C I Edvard Smith, Anna-Carin Norlin, Tessa M Campbell, Laura E Covill, Lennart Hammarström, Qiang Pan-Hammarström, Hassan Abolhassani, Shrikant Mane, Nico Marr, Manar Ata, Fatima Al Ali, Taushif Khan, András N Spaan, Clifton L Dalgard, Paolo Bonfanti, Andrea Biondi, Sarah Tubiana, Charles Burdet, Robert Nussbaum, Amanda Kahn-Kirby, Andrew L Snow, , , , , , , , , , Jacinta Bustamante, Anne Puel, Stéphanie Boisson-Dupuis, Shen-Ying Zhang, Vivien Béziat, Richard P Lifton, Paul Bastard, Luigi D Notarangelo, Laurent Abel, Helen C Su, Emmanuelle Jouanguy, Ali Amara, Vassili Soumelis, Aurélie Cobat, Qian Zhang, Jean-Laurent Casanova. X-linked recessive TLR7 deficiency in ~1% of men under 60 years old with life-threatening COVID-19. Sci Immunol. 2021.08; 6 (62): ( PubMed, DOI )

  24. Imanaka Y, Taniguchi M, Doi T, Tsumura M, Nagaoka R, Shimomura M, Asano T, Kagawa R, Mizoguchi Y, Karakawa S, Arihiro K, Imai K, Morio T, Casanova JL, Puel A, Ohara O, Kamei K, Kobayashi M, Okada S. . Inherited CARD9 Deficiency in a Child with Invasive Disease Due to Exophiala dermatitidis and Two Older but Asymptomatic Siblings. J Clin Immunol. 2021.07; 41 (5): 975-986. ( PubMed, DOI )

  25. Yamashita M, Kuehn HS, Okuyama K, Okada S, Inoue Y, Mitsuiki N, Imai K, Takagi M, Kanegane H, Takeuchi M, Shimojo N, Tsumura M, Padhi AK, Zhang KYJ, Boisson B, Casanova JL, Ohara O, Rosenzweig SD, Taniuchi I, Morio T.. A variant in human AIOLOS impairs adaptive immunity by interfering with IKAROS. Nat Immunol. 2021.07; 22 (7): 893-903. ( PubMed, DOI )

  26. Mushino T, Hiroi T, Yamashita Y, Suzaki N, Mishima H, Ueno M, Kinoshita A, Minami K, Imai K, Yoshiura KI, Sonoki T, Tamura S.. Progressive Massive Splenomegaly in an Adult Patient with Kabuki Syndrome Complicated with Immune Thrombocytopenic Purpura. Intern Med. 2021.06; 60 (12): 1927-1933. ( PubMed, DOI )

  27. Kato T, Tamura Y, Matsumoto H, Kobayashi O, Ishiguro H, Ogawa M, Tsujikawa K, Hasegawa Y, Sakamoto M, Konagaya M, Houzen H, Takagi M, Imai K, Morio T, Yokoseki A, Onodera O, Nonoyama S.. Immunological abnormalities in patients with early-onset ataxia with ocular motor apraxia and hypoalbuminemia. Clin Immunol. 2021.06; 229 108776. ( PubMed, DOI )

  28. Sancho-Shimizu V, Brodin P, Cobat A, Biggs CM, Toubiana J, Lucas CL, Henrickson SE, Belot A, MIS-C@CHGE, Tangye SG, Milner JD, Levin M, Abel L, Bogunovic D, Casanova JL, Zhang SY.. SARS-CoV-2-related MIS-C: A key to the viral and genetic causes of Kawasaki disease? J Exp Med. 2021.06; 218 (6): ( PubMed, DOI )

  29. Dimitrova D, Nademi Z, Maccari ME, Ehl S, Uzel G, Tomoda T, Okano T, Imai K, Carpenter B, Ip W, Rao K, Worth AJJ, Laberko A, Mukhina A, Néven B, Moshous D, Speckmann C, Warnatz K, Wehr C, Abolhassani H, Aghamohammadi A, Bleesing JJ, Dara J, Dvorak CC, Ghosh S, Kang HJ, Markelj G, Modi A, Bayer DK, Notarangelo LD, Schulz A, Garcia-Prat M, Soler-Palacín P, Karakükcü M, Yilmaz E, Gambineri E, Menconi M, Masmas TN, Holm M, Bonfim C, Prando C, Hughes S, Jolles S, Morris EC, Kapoor N, Koltan S, Paneesha S, Steward C, Wynn R, Duffner U, Gennery AR, Lankester AC, Slatter M, Kanakry JA.. International retrospective study of allogeneic hematopoietic cell transplantation for activated PI3K-delta syndrome. J Allergy Clin Immunol. 2021.05; ( PubMed, DOI )

  30. Pilania RK, Rawat A, Vignesh P, Guleria S, Jindal AK, Das G, Suri D, Gupta A, Gupta K, Chan KW, Lau YL, Imai K, Singh S.. Liver Abscess in Chronic Granulomatous Disease-Two Decades of Experience from a Tertiary Care Centre in North-West India. J Clin Immunol. 2021.04; 41 (3): 552-564. ( PubMed, DOI )

  31. Totsune E, Nakano T, Moriya K, Sato D, Suzuki D, Miura A, Katayama S, Niizuma H, Kanno J, van Zelm MC, Imai K, Kanegane H, Sasahara Y, Kure S.. Case Report: Infantile-Onset Fulminant Type 1 Diabetes Mellitus Caused by Novel Compound Heterozygous LRBA Variants Front Immunol. 2021.04; 12 677572. ( PubMed, DOI )

  32. Vignesh P, Loganathan SK, Sudhakar M, Chaudhary H, Rawat A, Sharma M, Shekar A, Vaiphei K, Kumar N, Singh Sachdeva MU, Jindal AK, Suri D, Gupta A, Ray P, Imai K, Ohara O, Nonoyama S, Lau YL, Singh S.. Hemophagocytic Lymphohistiocytosis in Children with Chronic Granulomatous Disease-Single-Center Experience from North India. J Allergy Clin Immunol Pract. 2021.02; 9 (2): 771-782. ( PubMed, DOI )

  33. Kadowaki S, Hashimoto K, Nishimura T, Kashimada K, Kadowaki T, Kawamoto N, Imai K, Okada S, Kanegane H, Ohnishi H.. Functional analysis of novel A20 variants in patients with atypical inflammatory diseases. Arthritis Res Ther. 2021.02; 23 (1): 52. ( PubMed, DOI )

  34. Vignesh P, Rawat A, Kumrah R, Singh A, Gummadi A, Sharma M, Kaur A, Nameirakpam J, Jindal A, Suri D, Gupta A, Khadwal A, Saikia B, Minz RW, Sharma K, Desai M, Taur P, Gowri V, Pandrowala A, Dalvi A, Jodhawat N, Kambli P, Madkaikar MR, Bhattad S, Ramprakash S, Cp R, Jayaram A, Sivasankaran M, Munirathnam D, Balaji S, Rajendran A, Aggarwal A, Singh K, Na F, George B, Mehta A, Lashkari HP, Uppuluri R, Raj R, Bartakke S, Gupta K, Sreedharanunni S, Ogura Y, Kato T, Imai K, Chan KW, Leung D, Ohara O, Nonoyama S, Hershfield M, Lau YL, Singh S.. Clinical, Immunological, and Molecular Features of Severe Combined Immune Deficiency: A Multi-Institutional Experience From India. Front Immunol. 2021.02; 11 619146. ( PubMed, DOI )

  35. Rawat A, Vignesh P, Sudhakar M, Sharma M, Suri D, Jindal A, Gupta A, Shandilya JK, Loganathan SK, Kaur G, Chawla S, Patra PK, Khadwal A, Saikia B, Minz RW, Aggarwal V, Taur P, Pandrowala A, Gowri V, Desai M, Kulkarni M, Hule G, Bargir U, Kambli P, Madkaikar M, Bhattad S, Ginigeri C, Kumar H, Jayaram A, Munirathnam D, Sivasankaran M, Raj R, Uppuluri R, Na F, George B, Lashkari HP, Kalra M, Sachdeva A, Seth S, Sabui T, Gupta A, van Leeuwen K, de Boer M, Chan KW, Imai K, Ohara O, Nonoyama S, Lau YL, Singh S.. Clinical, Immunological, and Molecular Profile of Chronic Granulomatous Disease: A Multi-Centric Study of 236 Patients From India. Front Immunol. 2021.02; 12 625320. ( PubMed, DOI )

  36. Maiko Inoue, Takeshi Isoda, Motoi Yamashita, Takahiro Tomoda, Kento Inoue, Tsubasa Okano, Teppei Ohkawa, Akifumi Endo, Noriko Mitsuiki, Takahiro Kamiya, Masakatsu Yanagimachi, Kouhei Yamamoto, Yuichiro Inaba, Toru Sasaki, Masatoshi Takagi, Hirokazu Kanegane, Kohsuke Imai, Tomohiro Morio. Cytomegalovirus Laryngitis in Primary Combined Immunodeficiency Diseases. J Clin Immunol. 2021.01; 41 (1): 243-247. ( PubMed, DOI )

  37. Tanita K, Sakura F, Nambu R, Tsumura M, Imanaka Y, Ohnishi H, Kato Z, Pan J, Hoshino A, Suzuki K, Yasutomi M, Umetsu S, Okada C, Takagi M, Imai K, Ohara O, Muise AM, Okada S, Morio T, Kanegane H.. Clinical and Immunological Heterogeneity in Japanese Patients with Gain-of-Function Variants in STAT3 J Clin Immunol.. 2021.01; ( PubMed )

  38. Rawat A, Jindal AK, Suri D, Vignesh P, Gupta A, Saikia B, Minz RW, Banday AZ, Tyagi R, Arora K, Joshi V, Mondal S, Shandilya JK, Sharma M, Desai M, Taur P, Pandrowala A, Gowri V, Sawant-Desai S, Gupta M, Dalvi AD, Madkaikar M, Aggarwal A, Raj R, Uppuluri R, Bhattad S, Jayaram A, Lashkari HP, Rajasekhar L, Munirathnam D, Kalra M, Shukla A, Saka R, Sharma R, Garg R, Imai K, Nonoyama S, Ohara O, Lee PP, Chan KW, Lau YL, Singh S.. Clinical and Genetic Profile of X-Linked Agammaglobulinemia: A Multicenter Experience From India. Front Immunol. 2021.01; 11 612323. ( PubMed, DOI )

  39. Miyazaki H, Hoshi N, Kohashi M, Tokunaga E, Ku Y, Takenaka H, Ooi M, Yamamoto N, Uemura S, Nishimura N, Iijima K, Jimbo K, Okano T, Hoshino A, Imai K, Kanegane H, Kobayashi I, Kodama Y.. A case of autoimmune enteropathy with CTLA4 haploinsufficiency. Intest Res. 2021.01; ( PubMed, DOI )

  40. Suri D, Rikhi R, Jindal AK, Rawat A, Sudhakar M, Vignesh P, Gupta A, Kaur A, Sharma J, Ahluwalia J, Bhatia P, Khadwal A, Raj R, Uppuluri R, Desai M, Taur P, Pandrowala AA, Gowri V, Madkaikar MR, Lashkari HP, Bhattad S, Kumar H, Verma S, Imai K, Nonoyama S, Ohara O, Chan KW, Lee PP, Lau YL, Singh S.. Wiskott Aldrich Syndrome: A Multi-Institutional Experience From India. Front Immunol. 2021; 12 627651. ( PubMed, DOI )

  41. Akihiro Hoshino, Etsushi Toyofuku, Noriko Mitsuiki, Motoi Yamashita, Keisuke Okamoto, Michio Yamamoto, Kenji Kanda, Genki Yamato, Dai Keino, Yuri Yoshimoto-Suzuki, Junji Kamizono, Yasuhiro Onoe, Takuya Ichimura, Mika Nagao, Masaru Yoshimura, Koji Tsugawa, Toru Igarashi, Kanako Mitsui-Sekinaka, Yujin Sekinaka, Takehiko Doi, Takahiro Yasumi, Yozo Nakazawa, Masatoshi Takagi, Kohsuke Imai, Shigeaki Nonoyama, Tomohiro Morio, Sylvain Latour, Hirokazu Kanegane. Clinical Courses of IKAROS and CTLA4 Deficiencies: A Systematic Literature Review and Retrospective Longitudinal Study Front Immunol. 2021; 12 784901. ( PubMed, DOI )

  42. Yeh TW, Okano T, Naruto T, Yamashita M, Okamura M, Tanita K, Du L, Pan-Hammarström Q, Mitsuiki N, Okada S, Kanegane H, Imai K, Morio T.. APRIL-dependent lifelong plasmacyte maintenance and immunoglobulin production in humans. J Allergy Clin Immunol. 2020.11; 146 (5): 1109-1120.e4. ( PubMed, DOI )

  43. Osumi T, Yoshimura S, Sako M, Uchiyama T, Ishikawa T, Kawai T, Inoue E, Takimoto T, Takeuchi I, Yamada M, Sakamoto K, Yoshida K, Kimura Y, Matsukawa Y, Matsumoto K, Imadome KI, Arai K, Deguchi T, Imai K, Yuza Y, Matsumoto K, Onodera M, Kanegane H, Tomizawa D, Kato M.. A prospective study of allogeneic hematopoietic stem cell transplantation with post-transplantation cyclophosphamide and anti-thymoglobulin from HLA-mismatched related donors for non-malignant diseases. Biol. Blood Marrow Transplant.. 2020.11; 26 (11): e286-e291. ( PubMed, DOI )

  44. Matsumoto K, Hoshino A, Nishimura A, Kato T, Mori Y, Shimomura M, Naito C, Watanabe K, Hamazaki M, Mitsuiki N, Takagi M, Imai K, Nonoyama S, Kanegane H, Morio T. DNA Ligase IV Deficiency Identified by Chance Following Vaccine-Derived Rubella Virus Infection. Journal of clinical immunology. 2020.11; 40 (8): 1187-1190. ( PubMed, DOI )

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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  206. 江口詩織, 磯田健志, 金田明也, 井上健斗, 星野顕宏, 森下あおい, 山下基, 滝島茂, 柳町昌克, 高木正稔, 金兼弘和, 今井耕輔, 森尾友宏. 原発性線毛機能不全症同胞例に対する高張食塩水吸入療法 日本小児科学会雑誌. 2021.01; 125 (1): 52-58.

  207. 金兼弘和,木村菜美子, 小林弘美, 今井耕輔. 皮下注射免疫グロブリン製剤在宅自己注射治療導入の実際 小児科. 2020.12; 61 (13): 1774-1783.

  208. 原田瑞生, 久保暢大, 高地貴行, 岩渕晴子, 今村勝, 齋藤昭彦, 梅津哉, 山中崇之, 今井耕輔, 岡田賢, 今井千速 . ランゲルハンス細胞組織球症との鑑別を要した播種性BCG感染症を合併したIFN-γR1部分欠損症 2020.11; 57 (3): 309-313.

  209. 今井耕輔. 【抗菌薬の「なぜ?」に答える】抗菌薬を開始する前に!患者さんに免疫不全はありませんか? 小児内科. 2020.10; 52 (10): 1313-1318. ( 医中誌 )

  210. 今井耕輔. 遺伝情報と遺伝カウンセリング 小児科領域別のポイント 免疫不全・自己炎症性疾患 小児内科. 2020.08; 52 (8): 1081-1086. ( 医中誌 )

  211. 大原智子, 宮井健太郎, 谷田けい, 平石知佳, 福山希央, 田村英一郎, 河合利尚, 今井耕輔, 金兼弘和, 清原鋼二. リファンピシン投与に関連してマクロファージ活性化症候群を合併した慢性肉芽腫症 日本小児科学会雑誌. 2020.05; 124 (5): 838-844.

  212. 今井耕輔. 日常診療に活かせるアレルギーの知識 獲得免疫 JOHNS. 2020.03; 36 (3): 285-288. ( 医中誌 )

  213. 今井耕輔. 変わりつつある免疫不全症 免疫不全症の診断 免疫不全症に対する新生児マススクリーニング 小児科診療. 2020.03; 83 (3): 321-327. ( 医中誌 )

  214. 伊藤 佳史, 岡本 健太郎, 荻野 恵, 友田 昴, 井上 真依子, 磯田 健志, 今井 耕輔. 原発性免疫不全症の治療経過中に腸管気腫症をきたし保存的加療で軽快した2例 日本小児外科学会雑誌. 2019.12; 55 (7): 1220. ( 医中誌 )

  215. 今井 耕輔. 新規対象疾患のパイロット研究の現状と課題 TRECとKRECを用いた重症原発性免疫不全症に対する新生児スクリーニングの実現に向けて 日本マス・スクリーニング学会誌. 2019.10; 29 (2): 152. ( 医中誌 )

  216. 花井 潤師, 田中 稔泰, 山田 雅文, 今井 耕輔. 自動核酸抽出機・TREC/KREC同時測定キットによるPIDスクリーニングの基礎検討 日本マス・スクリーニング学会誌. 2019.10; 29 (2): 219. ( 医中誌 )

  217. 金兼弘和,今井耕輔. 原発性免疫不全症候群-最近の話題 原発性免疫不全症候群の診断と遺伝子解析ネットワーク 小児科. 2019.08; 60 (9): 1249-1256.

  218. 今井 耕輔. 原発性免疫不全症候群-最近の話題 原発性免疫不全症候群患者の移行期医療 小児科. 2019.08; 60 (9): 1273-1277. ( DOI 医中誌 )

  219. 末永祐太,吉本優里,大熊喜彰,兼重昌夫,田中瑞恵,瓜生英子,山中純子,水上愛弓,五石圭司,佐藤典子,今井耕輔,金兼弘和,七野浩之. . 血便を初発症状とし、若年性骨髄単球性白血病様所見を 小児科. 2019.04; 60 (4): 417-421.

  220. 伊藤佳史,岡本健太郎, 水野裕貴, 荻野恵, 廣木遥, 今井耕輔, 森尾友宏. 小児外科診療における合併症、偶発症-とっさの処置、その後の対応 中心静脈カテーテルによるフィブリンシース・血栓形成 小児外科. 2019.03; 51 (3): 225-229. ( 医中誌 )

  221. 西村聡, 星野顕宏, 松本和明, 小野真太郎, 田中真理, 石渡泰芳, 安原眞人, 足洗美穂, 満生紀子, 樋口紘平, 井上雅美, 宮村能子, 橋井佳子, 柳町昌克, 磯田健志, 梶原道子, 高木正稔, 水谷修紀, 金兼弘和, 今井耕輔, 森尾友宏. X連鎖高IgM症候群に対するフルダラビン・ブスルファンを用いた強度減弱前処置による造血細胞移植 日本造血細胞移植学会雑誌 . 2019.01; 8 (1): 43-49.

  222. 毛利真理子,金森透,岡本圭祐,田中絵里子,今井耕輔,森尾友宏,岡本健太郎,森雅亮. MSH6遺伝子変異を伴い難治性腸管Behcet病を疑う超早期発症炎症性腸疾患(VEO-IBD)の1例 小児リウマチ. 2018.11; 9 (1): 65-69.

  223. 春谷勇平, 田村志宣, 小畑裕史, 大岩健洋, 山下友佑, 蒸野寿紀, 細井裕樹, 村田祥吾, 西川彰則, 今井耕輔, 森尾友宏, 園木孝志. 臍帯血移植が奏効した成人型分類不能型免疫不全症 臨床血液. 2018.04; 59 (3): 293-299.

  224. 金兼 弘和, 今井 耕輔, 森尾 友宏. 重症複合免疫不全症 その発見から今後の展望 日本臨床免疫学会会誌. 2017.06; 40 (3): 145-154.

  225. 高木 正稔, 緒方 昌平, 上野 浩生, 吉田 健一, 葉 姿ぶん, 朴 今花, 星野 顕宏, 山下 基, 南谷 真衣, 岡野 翼, 村松 秀樹, 奥野 友介, 白石 友一, 千葉 健一, 田中 洋子, 坂東 由紀, 林 泰秀, 宮野 悟, 今井 耕輔, 金兼 弘和, 小川 誠司, 小島 勢二, 森尾 友宏. ALPS責任分子TNFAIP3の同定 日本小児血液・がん学会雑誌. 2017.06; 54 (2): 169. ( 医中誌 )

  226. 廣木遥, 岡野翼, 山下基, 足洗美穂, 宮本智史, 小林千佳, 青木由貴, 高木正稔, 今井耕輔, 金兼弘和, 森尾友宏. Epstein-Barrウイルス関連血球貪食性リンパ組織球症にリツキシマブが奏功したX連鎖リンパ増殖症候群1型の一例 日本小児血液・がん学会雑誌. 2017.04; 54 (1): 25-29. ( 医中誌 )

  227. 山口(藤巻)明日香, 大坂渓, 田中(久保田)真理, 宮本智史, 満生紀子, 高木正稔, 今井耕輔, 窪田満, 金兼弘和, 森尾友宏. 無形成発作を契機に診断されたグルコース-6-リン酸脱水素酵素欠損症の日本男児 日本小児科学会雑誌. 2017.04; 121 (4): 724-728.

  228. 金兼弘和, 今井耕輔, 森尾友宏. 重症複合免役不全症~その発見から今後の展望~ 2017.03; 40 (3): 145-154.

  229. 足洗美穂, 金兼弘和, 今井耕輔, 木村菜美子, 陳菜穂, 岡野翼, 小野真太郎, 田中(久保田)真理, 宮本智史, 小林千佳, 満生紀子, 青木由貴, 田中絵里子, 高木正稔, 森尾友宏. 低または無ガンマグロブリン血症50例に対する皮下注用免疫グロブリン製剤導入. 日本小児科学会雑誌. 2016.12; 120 (12): 1772-1781. ( 医中誌 )

  230. 今井耕輔. B細胞シグナル伝達異常と原発性免疫不全症 炎症と免疫. 2016.10; 24 (6): 67-75.

  231. 岡本圭祐, 今井耕輔. 【血球の増加と減少】白血球 リンパ球減少症 小児内科. 2016.07; 48 (7): 974-978. ( 医中誌 )

  232. 木脇祐子,手束真理,小林大輔,阿部志保,森尾友宏,今井耕輔,北川昌伸. パラインフルエンザウイルス3型(PIV3)感染を契機として肺胞蛋白症を発症した完全型DiGeorge症候群の1剖検例 病理と臨床. 2016.06; 34 (6): 631-636.

  233. 金兼弘和,高島健浩,今井耕輔. 原発性免疫不全症における診断のすすめ方 モダンメディア別冊. 2016.04; 62 (4): 130-137.

  234. 平本梨花,大曽根眞也,今村俊彦,石田宏之,高島健浩,今井耕輔,森尾友宏,細井創. 臍帯血移植にて救命し得た、サイトメガトウイルス感染症合併重症複合型免疫不全症の一例 日本小児血液・がん学会雑誌. 2016.02; 52 (5): 449-453.

  235. 今井耕輔. 免疫グロブリンクラススイッチ異常症(高IgM症候群) 小児内科. 2015.11; 47 713-717.

  236. 辻田 由喜,今井耕輔,野々山 恵章. PI3K異常症および類縁疾患 小児内科. 2015.11; 47 776-778.

  237. 高島 健浩,今井耕輔,森尾友宏. DiGeorge症候群 小児内科. 2015.11; 47 702-704.

  238. 今井耕輔. 免疫グロブリンクラススイッチ症候群(高IgA症候群 小児疾患診療のための病態生理2 改訂第5版. 2015.11; 47 (増刊): 713-717.

  239. 今井耕輔. 原発性免疫不全症 原因探索法・診断法の進歩 2015.08; 22 (9): 1196-1207.

  240. 今井耕輔. ips細胞を用いた難病研究ー臨床病態解明と創薬に向けた研究の最新知見(第4章)血液・免疫疾患 原発性免疫不全症 遺伝子医学 MOOK. 2015.02; (27): 152-157.

  241. 森尾友宏、高島健浩、今井耕輔. 多パラメータ解析による免疫担当細胞亜群同定と機能解析 医学のあゆみ. 2015.01; 252 (1): 48-54. ( 医中誌 )

  242. 今井 耕輔. 見逃しやすい免疫不全 ピンポイント小児医療 免疫系overview 免疫不全症との対応を含めて 小児内科. 2014.10; 46 (10): 1454-1458.

  243. 本間 健一,今井 耕輔, 野々山 恵章. 見逃しやすい免疫不全 ピンポイント小児医療 これからの原発性免疫不全症の新生児マススクリーニングについて 小児内科. 2014.10; 46 (10): 1535-1538.

  244. 高島 健浩. 今井 耕輔,. 見逃しやすい免疫不全 ピンポイント小児医療 ヒト免疫担当細胞サブセット解析の標準化 小児内科. 2014.10; 46 (10): 1539-1544 .

  245. 今井 耕輔. 原発性免疫不全症における遺伝学的検査の取り扱いと諸問題について 日本小児血液・がん学会雑誌 . 2013.10; 50 (3): 415-417.

  246. 本間 健一, 今井 耕輔, 金兼 弘和, 野々山 恵章. MonoMAC症候群(GATA2異常症) 臨床免疫・アレルギー科. 2013.10; 60 (4): 439-446.

  247. 今井 耕輔. 原発性免疫不全症の最新国際分類(2011) 小児科. 2013.10; 54 (11): 1491-1515.

  248. 今井 耕輔. 【子どもの免疫Update】自然免疫について チャイルド ヘルス. 2013.09; 16 (9): 608-613.

  249. 今井 耕輔. 【原発性免疫不全症の診断と治療Update】新生児スクリーニングによる原発性免疫不全症の診断 小児科臨床. 2013.06; 66 (6): 1025-1032.

  250. 今井 耕輔. 【クローズアップ 新しい子どもの病気】免疫不全 新しい診断技術 TREC、KRECによる原発性免疫不全症のスクリーニング 小児内科. 2013.06; 45 (6): 1148-1151.

  251. Takagi M, Imai K, Morio T, Mizutani S.. [Secondary immune thrombocytopenia associated with primary immunodeficiency] Rinsho Ketsueki. 2013.04; 54 (4): 357-364. ( PubMed )

  252. 高木正稔, 今井耕輔, 森尾友宏, 水谷修紀. The Research Front Line of Immune Thrombocytopenia 原発性免疫不全症候群関連の免疫性血小板減少症 臨床血液. 2013.04; 54 (4): 357-364.

  253. 今井 耕輔. 【知っておきたい最新の免疫不全症分類-診断から治療まで】疫学 PIDJと原発性免疫不全症の新生児スクリーニング 小児科診療. 2013.03; 76 (3): 367-375.

  254. 今井 耕輔. 原発性免疫不全症の最新国際分類 臨床免疫・アレルギー科 . 2012.10; 58 (4): 446-466.

  255. 今井 耕輔. 原発性免疫不全症の遺伝子診断・治療 臨床血液. 2012.10; 53 (10): 1865-1873.

  256. 今井 耕輔. 【知っておきたい内科症候群】膠原病・免疫・アレルギー《免疫不全症》 ウィスコット・アルドリッチ症候群 内科. 2012.06; 109 (6): 1501-1503.

  257. 今井 耕輔. 臨床検査の意義と限界 T細胞・B細胞サブセット 小児内科. 2012.04; 44 (4): 645-648.

  258. 今井 耕輔, 中川 紀子, 森西 洋一, 野々山 恵章. 【原発性免疫不全症の新展開】原発性免疫不全症のマススクリーニング 炎症と免疫1. 2011.04; 19 (3): 203-209.

  259. 吉田 裕輔, 西山 光則, 加藤 環, 石渡 隆寛, 山田 謙太郎, 今井 耕輔, 若松 太, 川名 明彦, 野々山 恵章. 【新型インフルエンザ 重症化からの脱却】小児におけるパンデミックインフルエンザA(H1N1)2009 気道感染の特徴と人工呼吸器管理例を含む治療経験 日本胸部臨床. 2010.12; 69 (12): 1103-1117.

  260. 吉田裕輔, 西山光則, 石渡隆寛, 今井耕輔, 若松太, 川名明彦, 野々山恵章. 人工呼吸管理例を含むパンデミックインフルエンザA(H1N1)2009肺炎3例の治療経験 日本小児科学会雑誌. 2010.01; 114 (1): 85-87.

  261. 今井 耕輔. 【小児科医のための思春期医学・医療】思春期へキャリーオーバーした疾患をもつ患者への対応 先天性免疫不全症 小児科. 2009.10; 50 (11): 1899-1909.

  262. 今井 耕輔. わが国の小児科医・研究者によって新たに提唱・発見された疾患、疾患概念、原因の究明された疾患 高IgM症候群(Uracil DNA glycosylase異常による) 小児内科. 2009.06; 41 (6): 942-949.

  263. 富澤 大輔, 今井 耕輔 . 【免疫不全症候群と遺伝子異常】各疾患の遺伝子異常,診断と治療 伴性高IgM症候群(CD40 ligand欠損症) 臨床検査. 2009.05; 53 (5): 575-579.

  264. 森西 洋一, 今井 耕輔. 【免疫不全症候群と遺伝子異常】免疫不全症の臨床検査 TRECs測定による重症複合免疫不全症のマススクリーニング 臨床検査. 2009.05; 53 (5): 553-559.

  265. 今井 耕輔, スジャータ・モハン , 小原 收. 免疫不全症候群と遺伝子異常】免疫不全症候群の遺伝子診断の中央化とデータベース 臨床検査. 2009.05; 53 (5): 533-540.

  266. 本間健一, 辻陽一郎, 今井耕輔, 子川和宏, , 野々山恵章. 骨髄非破壊的前処置にて血縁者間臍帯血移植を施行し、生着が得られた重症再生不良性貧血の1例 日本小児血液学会雑誌. 2009.02; 23 (1): 43-46.

  267. 今井 耕輔. 【原発性免疫不全症候群】いわゆる高IgM症候群(クラススイッチ障害) アレルギー・免疫. 2008.09; 15 (10): 1338-1349.

  268. 今井 耕輔. 【ここまで分かっている免疫不全症候群】PIDJ(日本原発性免疫不全症データベース)プロジェクトについて 小児科臨床. 2008.09; 61 (9): 1811-1816.

  269. 野々山 恵章, 今井 耕輔. 【原発性免疫不全症候群】原発性免疫不全症候群の病因(遺伝子異常) アレルギー・免疫. 2008.09; 15 (10): 1304-1311.

  270. 今井 耕輔, 黒崎 知博, 野々山 恵章. 【分子メカニズムから解き明かす疾患のサイエンス】免疫(アレルギー)疾患 B細胞の終末分化とその障害による原発性免疫不全症 実験医学. 2006.06; 24 (10): 1515-1524.

  271. 今井 耕輔. 【先天性免疫不全症の最近の話題】高IgM症候群と免疫グロブリンクラススイッチ障害 血液フロンティア. 2006.03; 16 (4): 541-557.

  272. 今井 耕輔. 【免疫2005】獲得免疫 UNG欠損による免疫グロブリンクラススイッチ障害 Molecular Medicine. 2004.12; 41 295-304.

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