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Journal Abstract Search

98 related items for PubMed ID: 229560

  • 1. [Hereditary dysfibrinogenaemia. Study of a family (author's transl)].
    Voinnesson A, Salaün M.
    Sem Hop; ; 55(33-34):1507-12. PubMed ID: 229560
    [Abstract] [Full Text] [Related]

  • 2. Hereditary dysfibrinogenaemia (fibrinogen Jena)--report of a family study.
    Maak B.
    Folia Haematol Int Mag Klin Morphol Blutforsch; 1988; 115(4):519-22. PubMed ID: 2465965
    [Abstract] [Full Text] [Related]

  • 3. Fibrinogen Kiel: a congenital dysfibrinogenaemia with (A alpha-16 Arg----His) substitution characterized by HPLC without prior isolation of fibrinogen.
    Seydewitz HH, Gram J, Bruhn HD, Witt I.
    Blood Coagul Fibrinolysis; 1991 Aug; 2(4):501-6. PubMed ID: 1768762
    [Abstract] [Full Text] [Related]

  • 4. [Congenital dysfibrinogenaemia. Two new cases (author's transl)].
    Amsellem M, Samama M, Conard J, Levyne S, Ohlgiesser C.
    Nouv Presse Med; 1978 Nov 25; 7(41):3745-8. PubMed ID: 733523
    [Abstract] [Full Text] [Related]

  • 5. Fibrinogen Milano II: a congenital dysfibrinogenaemia associated with juvenile arterial and venous thrombosis.
    Haverkate F, Koopman J, Kluft C, D'Angelo A, Cattaneo M, Mannucci PM.
    Thromb Haemost; 1986 Feb 28; 55(1):131-5. PubMed ID: 3705000
    [Abstract] [Full Text] [Related]

  • 6. An abnormal fibrinogen with delayed fibrinopeptide A release.
    Lane DA, VanRoss M, Kakkar VV, Bottomley KJ, Dhir K, Holt LP, MacIver JE.
    Br J Haematol; 1980 Sep 28; 46(1):89-98. PubMed ID: 7426452
    [Abstract] [Full Text] [Related]

  • 7. An abnormal inherited fibrinogen (fibrinogen Genova) with delayed fibrin aggregation.
    Hassan HJ, Orlando M, Tonini GP, Casalbore P, Sarti A, Boeri E, Giacchino R, Tentori L, Mori PG.
    Scand J Haematol; 1982 Oct 28; 29(4):287-94. PubMed ID: 7178834
    [Abstract] [Full Text] [Related]

  • 8. [Association of dysfibrinogenemia and thrombosis. Apropos of a family (Fibrinogen Melun) and review of the literature].
    Bentolila S, Samama MM, Conard J, Horellou MH, Ffrench P.
    Ann Med Interne (Paris); 1995 Oct 28; 146(8):575-80. PubMed ID: 8734083
    [Abstract] [Full Text] [Related]

  • 9. [Hereditary haemorrhagic telanglectasia in a large Saharan familly. 87 cases in the same family (author's transl)].
    Muller JY, Michailov T, Izrael V, Bernard J.
    Nouv Presse Med; 1978 May 20; 7(20):1723-5. PubMed ID: 673716
    [Abstract] [Full Text] [Related]

  • 10. [Abnormalities of fibrin formation in benign viral hepatitis (author's transl)].
    Thabaut A, Laverdant C, Durosoir JL, Cristau P, Essioux J, Molinié C.
    Ann Med Interne (Paris); 1979 May 20; 130(1):35-8. PubMed ID: 434713
    [Abstract] [Full Text] [Related]

  • 11. Hereditary dysfibrinogenaemia: structural and functional studies on three fibrinogen variants.
    Meyer M, Vogel G, Gromnica-Ihle E, Schellenberg I, Ostermann G.
    Folia Haematol Int Mag Klin Morphol Blutforsch; 1988 May 20; 115(4):499-502. PubMed ID: 2465961
    [Abstract] [Full Text] [Related]

  • 12. [The rapid determination of fibrin and fibrinogen split products with a bedside thrombin coagulase time test in obstetric coagulopathies (author's transl)].
    Kastendieck E, Barthels M.
    Geburtshilfe Frauenheilkd; 1974 Sep 20; 34(9):758-62. PubMed ID: 4437565
    [No Abstract] [Full Text] [Related]

  • 13. [Familial dysfibrinogenemia with abnormal nonomer aggregation. Paris III fibrinogen].
    Soria J, Soria C.
    Pathol Biol (Paris); 1974 Nov 20; 22 suppl():72-9. PubMed ID: 4620099
    [No Abstract] [Full Text] [Related]

  • 14. Dysfibrinogenaemia associated with a defect in the aggregation of the fibrin monomers (Almeria I fibrinogen). A preliminary study.
    Vila V, Regañon E, Fernandez-Pavon A, Aznar J.
    Scand J Haematol; 1984 Nov 20; 33(5):460-5. PubMed ID: 6515329
    [Abstract] [Full Text] [Related]

  • 15. Association of inherited dysfibrinogenaemia and protein C deficiency in two unrelated families.
    Gandrille S, Priollet P, Capron L, Roncato M, Fiessinger JN, Aiach M.
    Br J Haematol; 1988 Mar 20; 68(3):329-37. PubMed ID: 3355791
    [Abstract] [Full Text] [Related]

  • 16. "Fibrinogen Tokyo II". An abnormal fibrinogen with an impaired polymerization site on the aligned DD domain of fibrin molecules.
    Matsuda M, Baba M, Morimoto K, Nakamikawa C.
    J Clin Invest; 1983 Sep 20; 72(3):1034-41. PubMed ID: 6886002
    [Abstract] [Full Text] [Related]

  • 17. [A functional assay of fibrinoformation in the newborn (author's transl)].
    Merino J, García-Conde J, Benet I.
    Sangre (Barc); 1977 Sep 20; 22(4):439-52. PubMed ID: 897954
    [No Abstract] [Full Text] [Related]

  • 18. Blood coagulation abnormalities associated with envenoming by Trimeresurus albolabris in Hong Kong.
    Chan JC, Kwok MM, Cockram CS, Prematilleke MN, Tomlinson B, Critchley JA.
    Singapore Med J; 1993 Apr 20; 34(2):145-7. PubMed ID: 8266156
    [Abstract] [Full Text] [Related]

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