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Journal Abstract Search

545 related items for PubMed ID: 19598064

  • 1.
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  • 3. Rare inherited disorders of fibrinogen.
    Acharya SS, Dimichele DM.
    Haemophilia; 2008 Nov; 14(6):1151-8. PubMed ID: 19141154
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  • 5. Familial dysfibrinogenemia and thrombophilia. Report on a study of the SSC Subcommittee on Fibrinogen.
    Haverkate F, Samama M.
    Thromb Haemost; 1995 Jan; 73(1):151-61. PubMed ID: 7740487
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  • 6. Epidemiology and treatment of congenital fibrinogen deficiency.
    Peyvandi F.
    Thromb Res; 2012 Dec; 130 Suppl 2():S7-11. PubMed ID: 23439004
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  • 7. Inherited abnormalities of fibrinogen: 10-year clinical experience of an Italian group.
    Santacroce R, Cappucci F, Pisanelli D, Perricone F, Papa ML, Santoro R, Grandone E, Margaglione M.
    Blood Coagul Fibrinolysis; 2006 Jun; 17(4):235-40. PubMed ID: 16651864
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  • 8. Diagnosis of congenital fibrinogen disorders.
    Lebreton A, Casini A.
    Ann Biol Clin (Paris); 2016 Aug 01; 74(4):405-12. PubMed ID: 27492693
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  • 9. Congenital hypofibrinogenemia and recurrent placental abruption.
    Ness PM, Budzynski AZ, Olexa SA, Rodvien R.
    Obstet Gynecol; 1983 Apr 01; 61(4):519-23. PubMed ID: 6828283
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  • 10. [Life-long hemorrhagic diathesis in a young man with unclottable global coagulation tests--congenital afibrinogenemia].
    Peter K, Furlan M, Lämmle B.
    Ther Umsch; 1999 Sep 01; 56(9):516-8. PubMed ID: 10517123
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  • 11. Cryoprecipitate: no longer the best therapeutic choice in congenital fibrinogen disorders?
    Bevan DH.
    Thromb Res; 2009 Dec 01; 124 Suppl 2():S12-6. PubMed ID: 20109651
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  • 12. Treatment of patients with dysfibrinogenemia and a history of abortions during pregnancy.
    Miesbach W, Galanakis D, Scharrer I.
    Blood Coagul Fibrinolysis; 2009 Jul 01; 20(5):366-70. PubMed ID: 19357502
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  • 14. Guideline for the diagnosis and management of the rare coagulation disorders: a United Kingdom Haemophilia Centre Doctors' Organization guideline on behalf of the British Committee for Standards in Haematology.
    Mumford AD, Ackroyd S, Alikhan R, Bowles L, Chowdary P, Grainger J, Mainwaring J, Mathias M, O'Connell N, BCSH Committee.
    Br J Haematol; 2014 Nov 01; 167(3):304-26. PubMed ID: 25100430
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  • 15. Diagnosis, clinical features and molecular assessment of the dysfibrinogenaemias.
    Hill M, Dolan G.
    Haemophilia; 2008 Sep 01; 14(5):889-97. PubMed ID: 18564189
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  • 16. Fibrinogen and the risk of thrombosis.
    de Moerloose P, Boehlen F, Neerman-Arbez M.
    Semin Thromb Hemost; 2010 Feb 01; 36(1):7-17. PubMed ID: 20391292
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  • 17. Genetics, diagnosis and clinical features of congenital hypodysfibrinogenemia: a systematic literature review and report of a novel mutation.
    Casini A, Brungs T, Lavenu-Bombled C, Vilar R, Neerman-Arbez M, de Moerloose P.
    J Thromb Haemost; 2017 May 01; 15(5):876-888. PubMed ID: 28211264
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  • 18. [Obstetrical management in dysfibrinogenemia].
    Heidegger H, Spannagel M, Schramm W.
    Geburtshilfe Frauenheilkd; 1990 May 01; 50(5):365-7. PubMed ID: 2373333
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  • 19. Mutational screening of six afibrinogenemic patients: identification and characterization of four novel molecular defects.
    Monaldini L, Asselta R, Duga S, Peyvandi F, Karimi M, Malcovati M, Tenchini ML.
    Thromb Haemost; 2007 Apr 01; 97(4):546-51. PubMed ID: 17393016
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