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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

87 related items for PubMed ID: 234603

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  • 3. Congenital deficiency of factor 13: report of a family from Newfoundland with associated mild deficiency of factor XII.
    Hanna M.
    Pediatrics; 1970 Oct; 46(4):611-9. PubMed ID: 5503696
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  • 5. Congenital deficiency of Hageman factor (clotting factor XII). Report on the first two families found in Switzerland.
    Baumann R, Straub PW.
    Helv Med Acta; 1968 Nov; 34(4):313-26. PubMed ID: 5704616
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  • 6. [Hemorrhagic diathesis associated with partial factor XII deficiency].
    Zywicka-Lopaciuk H, Lopaciuk S.
    Acta Haematol Pol; 1972 Nov; 3(3):257-63. PubMed ID: 4649309
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  • 8. New families with factor XII deficiency.
    Egeberg O.
    Thromb Diath Haemorrh; 1970 Jun 30; 23(3):441-8. PubMed ID: 5432189
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  • 9. 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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  • 10. [The combined deficiency of factor VIII and factor XII in a family. (preliminary report) (author's transl)].
    Hosokawa Y, Yachi A, Wada T, Kurokawa I.
    Rinsho Ketsueki; 1974 Aug 31; 15(8):923-7. PubMed ID: 4475154
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  • 12. A new family with congenital factor XII deficiency.
    Barbui T, Dini E.
    Acta Haematol; 1975 Aug 31; 54(6):345-9. PubMed ID: 812321
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  • 16. New families with hereditary hemorrhagic trait due to deficiency of fibrin stabilizing factor (F. 13).
    Egeberg O.
    Thromb Diath Haemorrh; 1968 Dec 31; 20(3):534-41. PubMed ID: 5710470
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  • 17. [Hageman factor deficiency. Apropos of a case].
    Aznar J, Mayans J, Aznar JA, Fernández-Pavón A, Calabuig R.
    Sangre (Barc); 1973 Dec 31; 18(3):356-64. PubMed ID: 4757644
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  • 18. Hageman trait (factor XII deficiency): a probably second genotype inherited as an autosomal dominant characteristic.
    Bennett B, Ratnoff OD, Holt JB, Roberts HR.
    Blood; 1972 Sep 31; 40(3):412-5. PubMed ID: 4626869
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  • 19. Inhibitor of human blood coagulation elicited by thrombin.
    Marciniak E.
    J Lab Clin Med; 1972 Jun 31; 79(6):924-34. PubMed ID: 5025460
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  • 20. Detection of the carrier state in hereditary coagulation disorders. II.
    Veltkamp JJ, Drion EF, Loeliger EA.
    Thromb Diath Haemorrh; 1968 Jul 31; 19(3):403-22. PubMed ID: 4884702
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