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First report of inherited protein S deficiency caused by paternal PROS1 mosaicism.
Nagaya S, Maruyama K, Watanabe A, Meguro-Horike M, Imai Y, Hiroshima Y, Horike SI, Kokame K, Morishita E. Nagaya S, et al. Among authors: watanabe a. Haematologica. 2022 Jan 1;107(1):330-333. doi: 10.3324/haematol.2021.278527. Haematologica. 2022. PMID: 34647440 Free PMC article. No abstract available.
Identification and functional analysis of three novel genetic variants resulting in premature termination codons in three unrelated patients with hereditary antithrombin deficiency.
Imai Y, Nagaya S, Araiso Y, Meguro-Horike M, Togashi T, Ohmori K, Makita Y, Sato E, Yujiri T, Nagamori Y, Horike SI, Watanabe A, Morishita E. Imai Y, et al. Among authors: watanabe a. Int J Hematol. 2023 Apr;117(4):523-529. doi: 10.1007/s12185-022-03509-3. Epub 2022 Dec 16. Int J Hematol. 2023. PMID: 36526880
Molecular genetic analysis of inherited protein C deficiency caused by the novel large deletion across two exons of PROC.
Togashi T, Meguro-Horike M, Nagaya S, Sugihara S, Ichinohe T, Araiso Y, Yamaguchi K, Mori K, Imai Y, Kuzasa K, Horike SI, Asakura H, Watanabe A, Morishita E. Togashi T, et al. Among authors: watanabe a. Thromb Res. 2020 Apr;188:115-118. doi: 10.1016/j.thromres.2020.03.009. Epub 2020 Mar 10. Thromb Res. 2020. PMID: 32199175 No abstract available.
Interleukin-23 inhibitors decrease Fibrosis-4 index in psoriasis patients with elevated Fibrosis-4 index but not inteleukin-17 inhibitors.
Takeshima R, Kamata M, Suzuki S, Ito M, Watanabe A, Uchida H, Chijiwa C, Okada Y, Azuma S, Nagata M, Egawa S, Hiura A, Fukaya S, Hayashi K, Fukuyasu A, Tanaka T, Ishikawa T, Tada Y. Takeshima R, et al. Among authors: watanabe a. J Dermatol. 2024 May 28. doi: 10.1111/1346-8138.17277. Online ahead of print. J Dermatol. 2024. PMID: 38804254
4,640 results