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PUBMED FOR HANDHELDS

Journal Abstract Search


436 related items for PubMed ID: 23607876

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  • 2. Factor XIII deficiency: an update.
    Schroeder V, Kohler HP.
    Semin Thromb Hemost; 2013 Sep; 39(6):632-41. PubMed ID: 23929307
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  • 4. Factor XIII: congenital deficiency factor XIII, acquired deficiency, factor XIII A-subunit, and factor XIII B-subunit.
    Tahlan A, Ahluwalia J.
    Arch Pathol Lab Med; 2014 Feb; 138(2):278-81. PubMed ID: 24476525
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  • 5. Alloantibodies against the B subunit of plasma factor XIII developed in its congenital deficiency.
    Wada H, Souri M, Matsumoto R, Sugihara T, Ichinose A.
    Thromb Haemost; 2013 Apr; 109(4):661-8. PubMed ID: 23407795
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  • 6. Biology of Factor XIII and clinical manifestations of Factor XIII deficiency.
    Levy JH, Greenberg C.
    Transfusion; 2013 May; 53(5):1120-31. PubMed ID: 22928875
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  • 7. Corifact™/Fibrogammin® P in the prophylactic treatment of hereditary factor XIII deficiency: results of a prospective, multicenter, open-label study.
    Nugent D.
    Thromb Res; 2012 Dec; 130 Suppl 2():S12-4. PubMed ID: 23439001
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  • 8. Developing the First Recombinant Factor XIII for Congenital Factor XIII Deficiency: Clinical Challenges and Successes.
    Carcao M, Fukutake K, Inbal A, Kerlin B, Lassila R, Oldenburg J, Garly ML, Nugent D.
    Semin Thromb Hemost; 2017 Feb; 43(1):59-68. PubMed ID: 27556350
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  • 11. Aggressive fatal case of autoimmune hemorrhaphilia resulting from anti-Factor XIII antibodies.
    Sugiyama H, Uesugi H, Suzuki S, Tanaka K, Souri M, Ichinose A.
    Blood Coagul Fibrinolysis; 2013 Jan; 24(1):85-9. PubMed ID: 23183237
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  • 14. Factor XIII deficiency: complete phenotypic characterization of two cases with novel causative mutations.
    Katona É, Muszbek L, Devreese K, Kovács KB, Bereczky Z, Jonkers M, Shemirani AH, Mondelaers V, Ermens AA.
    Haemophilia; 2014 Jan; 20(1):114-20. PubMed ID: 24118344
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  • 15. Factor XIII Deficiency.
    Karimi M, Bereczky Z, Cohan N, Muszbek L.
    Semin Thromb Hemost; 2009 Jun; 35(4):426-38. PubMed ID: 19598071
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  • 20. Coagulation factor XIII deficiency. Diagnosis, prevalence and management of inherited and acquired forms.
    Biswas A, Ivaskevicius V, Thomas A, Oldenburg J.
    Hamostaseologie; 2014 Jun; 34(2):160-6. PubMed ID: 24503678
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