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Journal Abstract Search

193 related items for PubMed ID: 2414173

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  • 4. Thromboembolism and bleeding tendency in congenital factor XII deficiency--a study on 74 subjects from 14 Swiss families.
    Lämmle B, Wuillemin WA, Huber I, Krauskopf M, Zürcher C, Pflugshaupt R, Furlan M.
    Thromb Haemost; 1991 Feb 12; 65(2):117-21. PubMed ID: 1905067
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  • 5. Factor-XII congenital deficiency. A new family study.
    Lucia JF, Ercoreca L, Torres M, Giralt M, Raichs A.
    Thromb Haemost; 1979 Oct 31; 42(3):1009-17. PubMed ID: 505391
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  • 6. Report 2 cases of congenital factor XII deficiency: a rare coagulation disorder.
    Kanjanapongkul S.
    J Med Assoc Thai; 2011 Aug 31; 94 Suppl 3():S231-2. PubMed ID: 22043782
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  • 7. Thrombosis in subjects with homozygous and heterozygous factor XII deficiency.
    Rodeghiero F, Castaman G, Ruggeri M, Tosetto A.
    Thromb Haemost; 1992 May 04; 67(5):590-1. PubMed ID: 1519222
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  • 8. Symptomatic combined homozygous factor XII deficiency and heterozygous factor V Leiden. luscaber@tin.it.
    Girolami A, Simioni P, Scarano L, Girolami B, Zerbinati P.
    J Thromb Thrombolysis; 2000 Apr 04; 9(3):271-5. PubMed ID: 10728027
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  • 9. [Factor XII (Hageman factor) deficiency: a risk factor for development of thromboembolism. Incidence of factor XII deficiency in patients after recurrent venous or arterial thromboembolism and myocardial infarction].
    Halbmayer WM, Mannhalter C, Feichtinger C, Rubi K, Fischer M.
    Wien Med Wochenschr; 1993 Apr 04; 143(2):43-50. PubMed ID: 8488686
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  • 15. [Familial study in congenital Hageman factor deficiency (blood coagulation factor XII)].
    Baumann R, Straub PW.
    Schweiz Med Wochenschr; 1968 Oct 19; 98(42):1653-5. PubMed ID: 5698343
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  • 19. Hereditary Hageman factor (factor XII) deficiency: report of three families and review of the literature published in Japan.
    Sano M, Saito H, Sugihara T, Suzuki H, Kojima T, Shirakawa M, Kamiya T, Ohya I.
    Nihon Ketsueki Gakkai Zasshi; 1986 Sep 19; 49(6):1275-81. PubMed ID: 3811790
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