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Recurrent mutations of factor XI gene in Japanese.
Okumura K, Kyotani M, Kawai R, Takagi A, Murate T, Yamamoto K, Takamatsu J, Matsushita T, Saito H, Kojima T. Okumura K, et al. Int J Hematol. 2006 Jun;83(5):462-3. doi: 10.1532/IJH97.06045. Int J Hematol. 2006. PMID: 16787881 No abstract available.
Definite diagnosis in Japanese patients with protein C deficiency by identification of causative PROC mutations.
Takagi A, Tanaka R, Nakashima D, Fujimori Y, Yamada T, Okumura K, Murate T, Yamada M, Horikoshi Y, Yamamoto K, Katsumi A, Matsushita T, Naoe T, Kojima T. Takagi A, et al. Among authors: okumura k. Int J Hematol. 2009 May;89(4):555-557. doi: 10.1007/s12185-009-0312-7. Epub 2009 Apr 17. Int J Hematol. 2009. PMID: 19373522 No abstract available.
L1503R is a member of group I mutation and has dominant-negative effect on secretion of full-length VWF multimers: an analysis of two patients with type 2A von Willebrand disease.
Kashiwagi T, Matsushita T, Ito Y, Hirashima K, Sanda N, Fujimori Y, Yamada T, Okumura K, Takagi A, Murate T, Katsumi A, Takamatsu J, Yamamoto K, Naoe T, Kojima T. Kashiwagi T, et al. Among authors: okumura k. Haemophilia. 2008 May;14(3):556-63. doi: 10.1111/j.1365-2516.2008.01703.x. Epub 2008 Apr 7. Haemophilia. 2008. PMID: 18397285
Assessing the risk factors for surgical site infections after anal reconstruction surgery in patients with anorectal malformations: a retrospective analysis.
Yokoyama S, Ishii D, Sakamura S, Kawahara I, Hashimoto S, Kumata Y, Korai T, Okumura K, Ara M, Kondo T, Ishimura R, Takahashi R, Tsuzaka S, Minato M, Ohba G, Yamamoto H, Honda S, Miyagi H, Nui A. Yokoyama S, et al. Among authors: okumura k. Pediatr Surg Int. 2024 Dec 21;41(1):41. doi: 10.1007/s00383-024-05953-0. Pediatr Surg Int. 2024. PMID: 39708118
3,055 results