Caplacizumab in the treatment of acquired thrombotic thrombocytopenic purpura
Author:
Affiliation:
1. 奈良県総合医療センター血液腫瘍内科
Publisher
Japanese Society on Thrombosis and Hemostasis
Link
https://www.jstage.jst.go.jp/article/jjsth/35/4/35_2024_JJTH_35_4_440-447/_pdf
Reference20 articles.
1. 1) Moschcowitz E: Hyaline thrombosis of the terminal arterioles and capillaries: A hitherto undescribed disease. Proc NY Pathol Soc 24: 21–24, 1924.
2. 2) Amorosi EL, Ultmann JE: Thrombotic thrombocytopenic purpura: Report of 16 cases and review of the literature. Medicine 45: 139–159, 1966.
3. 3) Moake JL, Rudy CK, Troll JH, et al.: Unusually large plasma factor VIII: von Willebrand factor multimers in chronic relapsing thrombotic thrombocytopenic purpura. N Engl J Med 307: 1432–1435, 1982.
4. 4) Zheng XL, Chung D, Takayama TK, et al.: Structure of von Willebrand factor cleaving protease (ADAMTS13), a metalloprotease involved in thrombotic thrombocytopenic purpura. J Biol Chem 276: 41059–41063, 2001.
5. 5) Fujimura Y, Matsumoto M: Registry of 919 patients with thrombotic microangiopathies across Japan: Database of Nara Medical University during 1998–2008. Intern Med 49: 7–15, 2010.
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