Art

J-GLOBAL ID：201802273880292468   Reference number：18A1879678

Successful hemostatic management of major surgery for cervical spondylotic myelopathy in a patient with severe factor XI deficiency

重症第XI因子欠損症における頚椎性脊髄症の大手術の止血管理の成功

Author (12)： OGAWA Yoshiyuki (Gunma Univ. Graduate School of Medicine, Maebashi, JPN) ,  YANAGISAWA Kunio (Gunma Univ. Graduate School of Medicine, Maebashi, JPN) ,  UCHIYAMA Yuri (Gunma Univ. Graduate School of Medicine, Maebashi, JPN) ,  UCHIYAMA Yuri (Yokohama City Univ. Graduate School of Medicine, Yokohama, JPN) ,  AKASHI Naoki (Gunma Univ. Graduate School of Medicine, Maebashi, JPN) ,  MIEDA Tokue (Gunma Univ. Hospital, Maebashi, JPN) ,  IIZUKA Haku (Gunma Univ. Hospital, Maebashi, JPN) ,  INOUE Madoka (Gunma Univ. Hospital, Maebashi, JPN) ,  SHIZUKA Reiko (Gunma Univ. Hospital, Maebashi, JPN) ,  MURAKAMI Masami (Gunma Univ. Graduate School of Medicine, Maebashi, JPN) ,  MATSUMOTO Naomichi (Yokohama City Univ. Graduate School of Medicine, Yokohama, JPN) ,  HANDA Hiroshi (Gunma Univ. Graduate School of Medicine, Maebashi, JPN)
Material： International Journal of Hematology  (Int J Hematol)
Volume： 108  Issue： 4  Page： 443-446  Publication year： Oct. 2018 
JST Material Number： F0888A  ISSN： 0925-5710  CODEN： IJHEEY  Document type： Article
Article type： 短報  Country of issue： Germany, Federal Republic of (DEU)  Language： ENGLISH (EN)

Thesaurus term： *hemophilia ,...
Semi thesaurus term： *INDEL Mutation ,...

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JST classification (3)： Hematologic diseases  (GK03000F) ,  Surgical treatment for nervous system diseases  (GN05030J) ,  Molecular genetics in general  (EC02010J)

Reference (11)：

• Asakai R, Chung DW, Davie EW, Seligsohn U. Factor XI deficiency in Ashkenazi Jews in Israel. N Engl J Med. 1991;325:153-8.
• Kato A, Asakai R, Davie EW, Aoki N. Factor XI gene (F11) is located on the distal end of the long arm of human chromosome 4. Cytogenet Cell Genet. 1989;52:77-8.
• Colakoglu S, Bayhan T, Tavil B, Keskin EY, Cakir V, Gümrük F, et al. Molecular genetic analysis of the F11 gene in 14 Turkish patients with factor XI deficiency: identification of novel and recurrent mutations and their inheritance within families. Blood Transfus. 2016;4:1-8. (Epub).
• James P, Salomon O, Mikovic D, Peyvandi F. Rare bleeding disorders- bleeding assessment tools, laboratory aspects and phenotype and therapy of FXI deficiency. Haemophilia. 2014;20(Suppl. 4):71-5.
• Duga S, Salomon O. Congenital factor XI deficiency: an update. Semin Thromb Hemostasis. 2013;39:621-31.

Terms in the title (7)： 重症 ,  第XI因子 ,  欠損 ,  頚椎性脊髄症 ,  手術 ,  止血 ,  成功