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Journal Abstract Search

99 related items for PubMed ID: 5432189

  • 1. New families with factor XII deficiency.
    Egeberg O.
    Thromb Diath Haemorrh; 1970 Jun 30; 23(3):441-8. PubMed ID: 5432189
    [No Abstract] [Full Text] [Related]

  • 2. Factor XII defect and hemorrhage. Evidence for a new type of hereditary hemostatic disorder.
    Egeberg O.
    Thromb Diath Haemorrh; 1970 Jun 30; 23(3):432-40. PubMed ID: 5432188
    [No Abstract] [Full Text] [Related]

  • 3. 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 30; 34(4):313-26. PubMed ID: 5704616
    [No Abstract] [Full Text] [Related]

  • 4.
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  • 5. [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
    [No Abstract] [Full Text] [Related]

  • 6. Congenital deficiency of factor 13: report of a family from Newfoundland with associated mild deficiency of factor XII.
    Hanna M.
    Pediatrics; 1970 Oct 19; 46(4):611-9. PubMed ID: 5503696
    [No Abstract] [Full Text] [Related]

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    ; . PubMed ID:
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  • 8. Prothrombin utilization in congenital coagulation deficiency states.
    Owen CA, Thompson JH.
    Thromb Diath Haemorrh; 1971 Jun 30; 25(2):297-311. PubMed ID: 5568049
    [No Abstract] [Full Text] [Related]

  • 9. [Study of a family with factor XII deficiency].
    Licenziati M, Lazzari R, Falsina A.
    Minerva Med; 1975 Feb 14; 66(11):511-3. PubMed ID: 234603
    [No Abstract] [Full Text] [Related]

  • 10. Proceedings: Kininogen deficiency and defective surface activation of blood coagulation and fibrinolysis in a kindred with Fitzgerald trait.
    Donaldson VH, Glueck HI, Miller MA.
    Thromb Diath Haemorrh; 1975 Sep 30; 34(1):352-3. PubMed ID: 1188801
    [No Abstract] [Full Text] [Related]

  • 11. [Is factor XII deficiency a contraindication to surgery?].
    Neidhardt B, Eckhoff UP, Schricker KT.
    Fortschr Med; 1975 Oct 16; 93(29):1388-94. PubMed ID: 1228095
    [Abstract] [Full Text] [Related]

  • 12. Hypercoagulability associated with chronic ulcerative colitis: changes in blood coagulation factors.
    Lee LC, Spittell JA, Sauer WG, Owen CA, Thompson JH.
    Gastroenterology; 1968 Jan 16; 54(1):76-85. PubMed ID: 5638294
    [No Abstract] [Full Text] [Related]

  • 13. [Spontaneous intracerebral hematoma in a familial congenital coagulation disorder (factor XIII deficiency)].
    Fiaschi A, Ferrari G.
    Riv Patol Nerv Ment; 1969 Jan 16; 90(1):31-40. PubMed ID: 5406277
    [No Abstract] [Full Text] [Related]

  • 14. Report of the fifth homozygous patient with factor VII Padua defect.
    Girolami A, Dal Bo Zanon R, Caenazzo A, Scattolo N.
    Folia Haematol Int Mag Klin Morphol Blutforsch; 1983 Jan 16; 110(3):447-54. PubMed ID: 6194079
    [Abstract] [Full Text] [Related]

  • 15. Factor XII and other hemostatic protein abnormalities in nephrotic syndrome patients.
    Thompson AR.
    Thromb Haemost; 1982 Aug 24; 48(1):27-32. PubMed ID: 6813992
    [Abstract] [Full Text] [Related]

  • 16. Disseminated intravascular coagulation associated with low factor VII. Evidence for a new type of hemostatic disorder.
    Egeberg O.
    Thromb Diath Haemorrh; 1970 Dec 31; 24(3):559-61. PubMed ID: 5511869
    [No Abstract] [Full Text] [Related]

  • 17. [Factor XII deficiency in two brothers].
    Müller G, Hilgard P, Hiemeyer V.
    Dtsch Med Wochenschr; 1973 Feb 09; 98(6):267-9. PubMed ID: 4684650
    [No Abstract] [Full Text] [Related]

  • 18. Coagulation studies in patients with trisomy 8 syndrome.
    Stenbjerg S, Husted S, Bernsen A, Jacobsen P, Nielsen J, Rasmussen K.
    Ann Genet; 1975 Dec 09; 18(4):241-2. PubMed ID: 1083193
    [Abstract] [Full Text] [Related]

  • 19. Rare congenital coagulation factor defects in Finland.
    Ikkala E, Myllylä G, Nevanlinna HR.
    Scand J Haematol; 1971 Dec 09; 8(3):210-5. PubMed ID: 5093998
    [No Abstract] [Full Text] [Related]

  • 20. [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 Dec 09; 143(2):43-50. PubMed ID: 8488686
    [Abstract] [Full Text] [Related]

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