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Epstein-Barr Virus-Associated γδ T-Cell Lymphoproliferative Disorder Associated With Hypomorphic IL2RG Mutation.
Tanita K, Hoshino A, Imadome KI, Kamiya T, Inoue K, Okano T, Yeh TW, Yanagimachi M, Shiraishi A, Ishimura M, Schober T, Rohlfs M, Takagi M, Imai K, Takada H, Ohga S, Klein C, Morio T, Kanegane H. Tanita K, et al. Among authors: hoshino a. Front Pediatr. 2019 Feb 4;7:15. doi: 10.3389/fped.2019.00015. eCollection 2019. Front Pediatr. 2019. PMID: 30778380 Free PMC article.
Dysregulation of Epstein-Barr Virus Infection in Hypomorphic ZAP70 Mutation.
Hoshino A, Takashima T, Yoshida K, Morimoto A, Kawahara Y, Yeh TW, Okano T, Yamashita M, Mitsuiki N, Imai K, Sakatani T, Nakazawa A, Okuno Y, Shiraishi Y, Chiba K, Tanaka H, Miyano S, Ogawa S, Kojima S, Morio T, Kanegane H. Hoshino A, et al. J Infect Dis. 2018 Jul 24;218(5):825-834. doi: 10.1093/infdis/jiy231. J Infect Dis. 2018. PMID: 29684201
Comprehensive molecular diagnosis of Epstein-Barr virus-associated lymphoproliferative diseases using next-generation sequencing.
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, et al. Among authors: hoshino a. Int J Hematol. 2018 Sep;108(3):319-328. doi: 10.1007/s12185-018-2475-6. Epub 2018 May 18. Int J Hematol. 2018. PMID: 29777376
An 18-Year-Old Male With X-linked Lymphoproliferative Syndrome Type 1 Who Developed Primary Central Nervous System Lymphoma 6 Months After Primary Epstein-Barr Virus Infection.
Kusano N, Sakata N, Sugimoto K, Miyazawa T, Ueda S, Okano M, Imadome KI, Hoshino A, Kanegane H, Kimura M, Sato T, Okada M, Takemura T. Kusano N, et al. Among authors: hoshino a. J Pediatr Hematol Oncol. 2019 Nov;41(8):e538-e541. doi: 10.1097/MPH.0000000000001424. J Pediatr Hematol Oncol. 2019. PMID: 30676439
[Inherited lymphoproliferative disorders].
Kanegane H, Hoshino A. Kanegane H, et al. Among authors: hoshino a. Rinsho Ketsueki. 2019;60(6):708-715. doi: 10.11406/rinketsu.60.708. Rinsho Ketsueki. 2019. PMID: 31281164 Review. Japanese.
Haploinsufficiency of TNFAIP3 (A20) by germline mutation is involved in autoimmune lymphoproliferative syndrome.
Takagi M, Ogata S, Ueno H, Yoshida K, Yeh T, Hoshino A, Piao J, Yamashita M, Nanya M, Okano T, Kajiwara M, Kanegane H, Muramatsu H, Okuno Y, Shiraishi Y, Chiba K, Tanaka H, Bando Y, Kato M, Hayashi Y, Miyano S, Imai K, Ogawa S, Kojima S, Morio T. Takagi M, et al. Among authors: hoshino a. J Allergy Clin Immunol. 2017 Jun;139(6):1914-1922. doi: 10.1016/j.jaci.2016.09.038. Epub 2016 Nov 12. J Allergy Clin Immunol. 2017. PMID: 27845235
565 results