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Haploinsufficiency of A20 caused by a novel nonsense variant or entire deletion of TNFAIP3 is clinically distinct from Behçet's disease.
Tsuchida N, Kirino Y, Soejima Y, Onodera M, Arai K, Tamura E, Ishikawa T, Kawai T, Uchiyama T, Nomura S, Kobayashi D, Taguri M, Mitsuhashi S, Mizuguchi T, Takata A, Miyake N, Nakajima H, Miyatake S, Matsumoto N. Tsuchida N, et al. Among authors: tamura e. Arthritis Res Ther. 2019 Jun 4;21(1):137. doi: 10.1186/s13075-019-1928-5. Arthritis Res Ther. 2019. PMID: 31164164 Free PMC article.
Thymitis in chronic granulomatous disease.
Kanamori K, Tamura E, Onodera M, Ishiguro A, Kawai T. Kanamori K, et al. Among authors: tamura e. Pediatr Int. 2019 Apr;61(4):429-431. doi: 10.1111/ped.13810. Epub 2019 Apr 14. Pediatr Int. 2019. PMID: 30983070 No abstract available.
A prospective study of allogeneic transplantation from unrelated donors for chronic granulomatous disease with target busulfan-based reduced-intensity conditioning.
Osumi T, Tomizawa D, Kawai T, Sako M, Inoue E, Takimoto T, Tamura E, Uchiyama T, Imadome KI, Taniguchi M, Shirai R, Yoshida M, Ando R, Tsumura Y, Fuji H, Matsumoto K, Shioda Y, Kiyotani C, Terashima K, Onodera M, Matsumoto K, Kato M. Osumi T, et al. Among authors: tamura e. Bone Marrow Transplant. 2019 Jan;54(1):168-172. doi: 10.1038/s41409-018-0271-9. Epub 2018 Jun 29. Bone Marrow Transplant. 2019. PMID: 29959437 Clinical Trial. No abstract available.
Impact of computer-aided characterization for diagnosis of colorectal lesions, including sessile serrated lesions: Multireader, multicase study.
Kato S, Kudo SE, Minegishi Y, Miyata Y, Maeda Y, Kuroki T, Takashina Y, Mochizuki K, Tamura E, Abe M, Sato Y, Sakurai T, Kouyama Y, Tanaka K, Ogawa Y, Nakamura H, Ichimasa K, Ogata N, Hisayuki T, Hayashi T, Wakamura K, Miyachi H, Baba T, Ishida F, Nemoto T, Misawa M; Collaborators. Kato S, et al. Among authors: tamura e. Dig Endosc. 2024 Mar;36(3):341-350. doi: 10.1111/den.14612. Epub 2023 Jul 13. Dig Endosc. 2024. PMID: 37937532
135 results