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A CD57+ CTL Degranulation Assay Effectively Identifies Familial Hemophagocytic Lymphohistiocytosis Type 3 Patients.
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, et al. Among authors: shibata h. J Clin Immunol. 2017 Jan;37(1):92-99. doi: 10.1007/s10875-016-0357-3. Epub 2016 Nov 28. J Clin Immunol. 2017. PMID: 27896523
A case of fetal-onset type 3 familial hemophagocytic lymphohistiocytosis surviving without severe complications after early diagnosis and treatment.
Matsumoto T, Fukushima H, Fujiyama S, Nagatomo K, Hosaka S, Suzuki R, Yamaki Y, Kanai Y, Shibata H, Yasumi T, Isshiki K, Kato M, Miyazono Y, Takada H. Matsumoto T, et al. Among authors: shibata h. Pediatr Blood Cancer. 2021 Jul;68(7):e29016. doi: 10.1002/pbc.29016. Epub 2021 Mar 26. Pediatr Blood Cancer. 2021. PMID: 33769695 No abstract available.
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.
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, et al. Among authors: shibata h. Clin Immunol. 2017 Jul;180:95-96. doi: 10.1016/j.clim.2017.04.007. Epub 2017 Apr 25. Clin Immunol. 2017. PMID: 28450255 No abstract available.
EBV-associated lymphoproliferative disorder in a patient with X-linked severe combined immunodeficiency with multiple reversions of an IL2RG mutation in T cells.
Wada F, Kondo T, Nakamura M, Uno S, Fujimoto M, Miyamoto T, Honda Y, Shibata H, Izawa K, Yasumi T, Nishikori M, Takaori-Kondo A. Wada F, et al. Among authors: shibata h. EJHaem. 2020 Oct 30;1(2):581-584. doi: 10.1002/jha2.119. eCollection 2020 Nov. EJHaem. 2020. PMID: 35845012 Free PMC article. No abstract available.
2,395 results