dysfibrinogenemia

出典: meddic

異常フィブリノゲン血症

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出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2016/01/23 14:20:40」(JST)

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英文文献

  • Fibrinogen Replacement Therapy for Congenital Fibrinogen Deficiency.
  • Bornikova L, Peyvandi F, Allen G, Bernstein J, Manco-Johnson MJ.SourceHemophilia and Thrombosis Center, Department of Medicine, University of Colorado, Aurora, CO, USA Maggiore Hospital Foundation at the University of Milan, Milan, Italy Rhode Island Hospital, Brown University Medical Center, Providence, RI, USA Children's Center for Cancer and Blood Diseases of Las Vegas, Las Vegas, NV, USA Hemophilia and Thrombosis Center, Department of Pediatrics, University of Colorado, Aurora, CO, USA.
  • Journal of thrombosis and haemostasis : JTH.J Thromb Haemost.2011 Jun 29. doi: 10.1111/j.1538-7836.2011.04424.x. [Epub ahead of print]
  • Background: This review of published studies was conducted to derive data on patients with congenital fibrinogen deficiency (CFD) including dosing of fibrinogen replacement therapy, outcome and adverse events either temporally related or distant to fibrinogen replacement in order to assist clinician
  • PMID 21711446

和文文献

  • Analysis of plasmin generation and clot lysis of plasma fibrinogen purified from a heterozygous dysfibrinogenemia, B beta Gly15Cys (Hamamatsu II)
  • Kamijyo Yuka,Hirota-Kawadobora Masako,Terasawa Fumiko,Honda Takayuki,Ikeya Manae,Okumura Nobuo
  • BLOOD COAGULATION & FIBRINOLYSIS 20(8), 726-732, 2009-12
  • … 20(8):726-732, December 2009.We found a heterozygous dysfibrinogenemia caused by the substitution of B beta Gly15Cys and designated it fibrinogen Hamamatsu II (H-II). … Therefore, we did not clarify an association between the B beta Gly15Cys dysfibrinogenemia and arterial thrombosis. …
  • NAID 120002696304

関連リンク

17 Nov 2009 ... Congenital is a term used to describe a relatively rare condition wherein an inherited abnormality in the fibrin molecule results in defective fibrin clot formation.

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フィブリノゲン異常血症



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