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Journal Abstract Search

153 related items for PubMed ID: 110893

  • 1. Molecular heterogeneity of Hageman trait (factor XII deficiency): evidence that two of 49 subjects are cross-reacting material positive (CRM+).
    Saito H, Scott JG, Movat HZ, Scialla SJ.
    J Lab Clin Med; 1979 Aug; 94(2):256-65. PubMed ID: 110893
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  • 2. Heterogeneity of human prekallikrein deficiency (Fletcher trait): evidence that five of 18 cases are positive for cross-reacting material.
    Saito H, Goodnough LT, Soria J, Soria C, Aznar J, España F.
    N Engl J Med; 1981 Oct 15; 305(16):910-4. PubMed ID: 6792540
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  • 3. [The genetics of factor XII deficiency].
    Kempter B, Rüth S, Epple I, Lohse P.
    Beitr Infusionsther; 1993 Oct 15; 31():174-8. PubMed ID: 7693250
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  • 5. Relationship between kallikrein release and factor XII in normal persons and carriers of the Hageman trait.
    Torres M, Ercoreca L, Lucia JF, Giralt M, Raichs A.
    Thromb Haemost; 1979 Dec 21; 42(4):1286-8. PubMed ID: 261563
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  • 8. Radioimmunoassay of human Hageman factor (factor XII).
    Saito H, Ratnoff OD, Pensky J.
    J Lab Clin Med; 1976 Sep 21; 88(3):506-14. PubMed ID: 956701
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  • 9. Functional characterization of a variant factor XII (F XII Locarno) in a cross reacting material positive F XII deficient plasma.
    Wuillemin WA, Furlan M, Stricker H, Lämmle B.
    Thromb Haemost; 1992 Feb 03; 67(2):219-25. PubMed ID: 1621242
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  • 10. Immunoquantitation of Hageman factor in urine and plasma of children with nephrotic syndrome.
    Hruby MA, Honig GR, Shapira E.
    J Lab Clin Med; 1980 Sep 03; 96(3):501-10. PubMed ID: 6772722
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  • 11. Genetic study in patients with factor XII deficiency: a report of three new mutations exon 13 (Q501STOP), exon 14 (P547L) and -13C>T promoter region in three compound heterozygotes.
    Lombardi AM, Bortoletto E, Scarparo P, Scapin M, Santarossa L, Girolami A.
    Blood Coagul Fibrinolysis; 2008 Oct 03; 19(7):639-43. PubMed ID: 18832903
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  • 12. 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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  • 13. Urinary excretion of Hageman factor (factor XII) and the presence of nonfunctional Hageman factor in the nephrotic syndrome.
    Saito H, Goodnough LT, Makker SP, Kallen RJ.
    Am J Med; 1981 Mar 12; 70(3):531-4. PubMed ID: 7211894
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  • 16. The interaction of Hageman factor and immune complexes.
    Cochrane CG, Wuepper KD, Aiken BS, Revak SD, Spiegelberg HL.
    J Clin Invest; 1972 Oct 12; 51(10):2736-45. PubMed ID: 5056666
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  • 19. A rapid purification with high recovery of factor XII (Hageman factor) on immunoaffinity column: application to an abnormal clotting factor XII (factor XIITORONTO).
    Takahashi I, Saito H.
    J Biochem; 1988 Apr 12; 103(4):641-3. PubMed ID: 3139646
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  • 20. Classic gout in Hageman factor (Factor XII) deficiency.
    Green D, Arsever CL, Grumet KA, Ratnoff OD.
    Arch Intern Med; 1982 Aug 12; 142(8):1556-7. PubMed ID: 7103639
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