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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

276 related items for PubMed ID: 3596361

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  • 5. Fibrinogen Oviedo I. A new Spanish dysfibrinogenaemia.
    Fernández FJ, Rodríguez Pinto C, Páramo J, Cuesta B, Collado M, Rocha E.
    Blood Coagul Fibrinolysis; 1990 Oct; 1(4-5):571-5. PubMed ID: 2133236
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  • 10. Dysfibrinogenaemia characterized by abnormal fibrin monomer polymerization and normal fibrinopeptide A release.
    Lane DA, Cuddigan B, VanRoss M, Kakkar VV.
    Br J Haematol; 1980 Mar; 44(3):483-94. PubMed ID: 6769460
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  • 11. Fibrinogen Vicenza and Genova II: two new cases of congenital dysfibrinogenemia with isolated defect of fibrin monomer polymerization and inhibitory activity on normal coagulation.
    Rodeghiero F, Castaman GC, Dal Belin Peruffo A, Dini E, Galletti A, Barone E, Gastaldi G.
    Thromb Haemost; 1987 Jun 03; 57(3):252-8. PubMed ID: 2958952
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  • 13. Fibrinogen Šumperk II: dysfibrinogenemia in an individual with two coding mutations.
    Kotlín R, Suttnar J, Cápová I, Hrachovinová I, Urbánková M, Dyr JE.
    Am J Hematol; 2012 May 03; 87(5):555-7. PubMed ID: 22407772
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  • 14. Fibrinogen Troyes--fibrinogen Metz. Two new cases of congenital dysfibrinogenemia.
    Soria J, Soria C, Samama M, Poirot E, Kling C.
    Thromb Diath Haemorrh; 1972 Jul 31; 27(3):619-33. PubMed ID: 4662617
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  • 15. Fibrinogen Alès: a homozygous case of dysfibrinogenemia (gamma-Asp(330)-->Val) characterized by a defective fibrin polymerization site "a".
    Lounes KC, Soria C, Mirshahi SS, Desvignes P, Mirshahi M, Bertrand O, Bonnet P, Koopman J, Soria J.
    Blood; 2000 Nov 15; 96(10):3473-9. PubMed ID: 11071644
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  • 16. Fibrinogen Marburg: a homozygous case of dysfibrinogenemia, lacking amino acids A alpha 461-610 (Lys 461 AAA-->stop TAA).
    Koopman J, Haverkate F, Grimbergen J, Egbring R, Lord ST.
    Blood; 1992 Oct 15; 80(8):1972-9. PubMed ID: 1391954
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