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Diagnostic challenge of the newborn patients with heritable protein C deficiency.
Ichiyama M, Inoue H, Ochiai M, Ishimura M, Shiraishi A, Fujiyoshi J, Yamashita H, Sato K, Matsumoto S, Hotta T, Uchiumi T, Kang D, Ohga S. Ichiyama M, et al. Among authors: shiraishi a. J Perinatol. 2019 Feb;39(2):212-219. doi: 10.1038/s41372-018-0262-0. Epub 2018 Oct 23. J Perinatol. 2019. PMID: 30353081 Free PMC article.
Progressive B cell depletion in human MALT1 deficiency.
Sonoda M, Ishimura M, Eguchi K, Yada Y, Lenhartová N, Shiraishi A, Tanaka T, Sakai Y, Ohga S. Sonoda M, et al. Among authors: shiraishi a. Clin Exp Immunol. 2021 Dec;206(3):237-247. doi: 10.1111/cei.13662. Epub 2021 Oct 7. Clin Exp Immunol. 2021. PMID: 34559885 Free PMC article.
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: shiraishi a. Front Pediatr. 2019 Feb 4;7:15. doi: 10.3389/fped.2019.00015. eCollection 2019. Front Pediatr. 2019. PMID: 30778380 Free PMC article.
566 results