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J-GLOBAL ID:201902252010913560   Reference number:19A1622298

後天性von Willebrand症候群を合併した骨髄線維症の1例

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Volume: 108  Issue:Page: 1448-1451  Publication year: Jul. 10, 2019 
JST Material Number: F0916A  ISSN: 0021-5384  CODEN: NNGAA  Document type: Article
Article type: 原著論文  Country of issue: Japan (JPN)  Language: JAPANESE (JA)
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Clinical hematology in general 
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Reference (9):
  • 1) Tefferi A: Primary myelofibrosis: 2017 update on diagnosis, risk-stratification, and management. Am J Hematol 91: 1262-1271, 2016.
  • 2) 鈴木伸明: 後天性フォン ヴィレブランド症候群. 血栓止血誌 29: 273-280, 2018.
  • 3) Cervantes F, et al: New prognostic scoring system for primary myelofibrosis based on a study of the International Working Group for Myelofibrosis Research and Treatment. Blood 113: 2895-2901, 2009.
  • 4) Mital A, et al: Acquired von Willebrand syndrome during the course of myelofibrosis: analysis of 32 cases. Adv Clin Exp Med 24: 1001-1006, 2015.
  • 5) Tefferi A, Barbui T: Polycythemia vera and essential thrombocythemia: 2017 update on diagnosis, risk-stratification, and management. Am J Hematol 92: 94-108, 2017.
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