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4,187 results

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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: miyamoto t. 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.
Early hematopoietic cell transplantation for familial hemophagocytic lymphohistiocytosis in a regional treatment network in Japan.
Ishimura M, Eguchi K, Sonoda M, Tanaka T, Shiraishi A, Sakai Y, Yasumi T, Miyamoto T, Voskoboinik I, Hashimoto K, Matsumoto S, Ozono S, Moritake H, Takada H, Ohga S. Ishimura M, et al. Among authors: miyamoto t. Int J Hematol. 2024 May;119(5):592-602. doi: 10.1007/s12185-024-03721-3. Epub 2024 Mar 20. Int J Hematol. 2024. PMID: 38507116
An efficient diagnosis: A patient with X-linked inhibitor of apoptosis protein (XIAP) deficiency in the setting of infantile hemophagocytic lymphohistiocytosis was diagnosed using high serum interleukin-18 combined with common laboratory parameters.
Higuchi T, Izawa K, Miyamoto T, Honda Y, Nishiyama A, Shimizu M, Takita J, Yasumi T. Higuchi T, et al. Among authors: miyamoto t. Pediatr Blood Cancer. 2022 Aug;69(8):e29606. doi: 10.1002/pbc.29606. Epub 2022 Feb 21. Pediatr Blood Cancer. 2022. PMID: 35187790 No abstract available.
Monogenic inflammatory bowel disease with STXBP2 mutations is not resolved by hematopoietic stem cell transplantation but can be alleviated via immunosuppressive drug therapy.
Fujikawa H, Shimizu H, Nambu R, Takeuchi I, Matsui T, Sakamoto K, Gocho Y, Miyamoto T, Yasumi T, Yoshioka T, Arai K. Fujikawa H, et al. Among authors: miyamoto t. Clin Immunol. 2023 Jan;246:109203. doi: 10.1016/j.clim.2022.109203. Epub 2022 Dec 9. Clin Immunol. 2023. PMID: 36503158
Rapid Flow Cytometry-Based Assay for the Functional Classification of MEFV Variants.
Honda Y, Maeda Y, Izawa K, Shiba T, Tanaka T, Nakaseko H, Nishimura K, Mukoyama H, Isa-Nishitani M, Miyamoto T, Nihira H, Shibata H, Hiejima E, Ohara O, Takita J, Yasumi T, Nishikomori R. Honda Y, et al. Among authors: miyamoto t. J Clin Immunol. 2021 Aug;41(6):1187-1197. doi: 10.1007/s10875-021-01021-7. Epub 2021 Mar 17. J Clin Immunol. 2021. PMID: 33733382
Novel AP3B1 mutations in a Hermansky-Pudlak syndrome type2 with neonatal interstitial lung disease.
Matsuyuki K, Ide M, Houjou K, Shima S, Tanaka S, Watanabe Y, Tomino H, Egashira T, Takayanagi T, Tashiro K, Okamura K, Suzuki T, Miyamoto T, Shibata H, Yasumi T, Nishikomori R. Matsuyuki K, et al. Among authors: miyamoto t. Pediatr Allergy Immunol. 2022 Feb;33(2):e13748. doi: 10.1111/pai.13748. Pediatr Allergy Immunol. 2022. PMID: 35212049 No abstract available.
4,187 results