Institute of Science Tokyo · Graduate School of Medical and Dental Sciences · 教授

Research keywords原発性免疫不全症・X連鎖無ガンマグロブリン血症・血球貪食性リンパ組織球症・XIAP欠損症・Griscelli症候群2型・XLP1リンパ増殖性疾患・EBER flow FISH・自己炎症性疾患造血細胞移植・IKZF1ハプロ不全

This is a public-data preview. Personalized fit, contact angles, and saved workflows require sign-in.

• Sagawa H, Hirata K, Katayama S, Shibata H, Toyofuku E, Kaneko S, Katata Y, Takezawa Y, Uematsu M, Onishi I, Yamazaki Y, Hattori T, Yamamoto M, Shimizu M, Imai K, Yasumi T, Morio T, Yokota T, Sasahara Y, Kanegane H. . Two Cases of CLIPPERS-like Syndrome Sharing a Hypomorphic UNC13D Variant. J Clin Immunol. 2026.03; 46 (1): ( PubMed , DOI )2026
• Wakatsuki R, Nishimura M, Tomomasa D, Takahashi S, Suzuki K, Kawaguchi K, Saura R, Inoue S, Takeuchi I, Arai K, Sugiyama M, Narishige Y, Oshima A, Tsumura M, Okada S, Hoshino A, Takagi M, Kanegane H. . Rapid flow cytometric diagnosis of XIAP deficiency. Pediatr Allergy Immunol. 2026.01; 37 (1): e70284. ( PubMed , DOI )2026
• Nishimura A, Uppuluri R, Raj R, Swaminathan VV, Cheng Y, Abu-Arja RF, Fu B, Laberko A, Albert MH, Hauck F, Bucciol G, Bigley V, Elcombe S, Kharya G, Pronk CJH, Wehr C, Neven B, Warnatz K, Meyts I, Morio T, Gennery AR, Kanegane H.. Correction to: An international survey of allogeneic hematopoietic cell transplantation for X-linked agammaglobulinemia. J Clin Immunol. 2026.01; 46 (1): 11. ( PubMed , DOI )2026
• Tanaka T, Sugawara A, Yasuoka R, Sakaguchi K, Natsume O, Haga K, Maruta Y, Kobayashi A, Sato T, Saito E, Minakawa S, Hirata Y, Shibata H, Yasumi T, Shimizu M, Kanegane H, Kudo K, Fukuda M, Teui K.. Functional characterization of Griscelli syndrome type 2 sine albinism in Japanese patients. J Hum Immun. 2026.07; 2 (4): e20250270. ( PubMed , DOI )2026