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Journal Abstract Search

217 related items for PubMed ID: 3718874

  • 1. Platelet prothrombin converting activity in hereditary disorders of platelet function.
    Bevers EM, Comfurius P, Nieuwenhuis HK, Levy-Toledano S, Enouf J, Belluci S, Caen JP, Zwaal RF.
    Br J Haematol; 1986 Jun; 63(2):335-45. PubMed ID: 3718874
    [Abstract] [Full Text] [Related]

  • 2. Platelet prothrombinase activity and intracellular calcium responses in patients with storage pool deficiency, glycoprotein IIb-IIIa deficiency, or impaired platelet coagulant activity--a comparison with Scott syndrome.
    Weiss HJ, Lages B.
    Blood; 1997 Mar 01; 89(5):1599-611. PubMed ID: 9057642
    [Abstract] [Full Text] [Related]

  • 3. Congenital platelet function disorders: survey findings and pathophysiology.
    Yasunaga K.
    Nihon Ketsueki Gakkai Zasshi; 1986 Dec 01; 49(8):1499-508. PubMed ID: 3564845
    [No Abstract] [Full Text] [Related]

  • 4. [Congenital thrombocytopathies].
    Kirchmaier CM, Pillitteri D.
    Internist (Berl); 2010 Sep 01; 51(9):1109-14, 1116-7. PubMed ID: 20725709
    [Abstract] [Full Text] [Related]

  • 5. Responses of platelets to strains of streptococcus sanguis: findings in healthy subjects, Bernard-Soulier, Glanzmann's, and collagen-unresponsive patients.
    Soberay AH, Herzberg MC, Rudney JD, Nieuwenhuis HK, Sixma JJ, Seligsohn U.
    Thromb Haemost; 1987 Apr 07; 57(2):222-5. PubMed ID: 3603413
    [Abstract] [Full Text] [Related]

  • 6. Development of procoagulant binding sites on the platelet surface.
    Bevers EM, Rosing J, Zwaal RF.
    Adv Exp Med Biol; 1985 Apr 07; 192():359-71. PubMed ID: 3914834
    [Abstract] [Full Text] [Related]

  • 7. [Membrane glycoproteins of human platelets: structures, functions, and abnormalities in Glanzmann's thrombasthenia and Bernard-Soulier syndrome].
    Ando Y, Fusegawa H, Kawada T, Tanaka Y, Watanabe K, Kobayashi N.
    Rinsho Byori; 1989 Dec 07; 37(12):1344-52. PubMed ID: 2614964
    [Abstract] [Full Text] [Related]

  • 8. Analysis of platelet glycoproteins in thrombocytopathias using the lectin-avidin-biotin-peroxidase (LABP) technique.
    Kehrel B, Kokott R, Stenzinger W, Balleisen L.
    Folia Haematol Int Mag Klin Morphol Blutforsch; 1988 Dec 07; 115(4):425-9. PubMed ID: 2465945
    [Abstract] [Full Text] [Related]

  • 9. Inherited disorders of platelets and megakaryocytes.
    Nurden AT, Pico M, Heilmann E, Jallu V, Hourdillé P.
    Prog Clin Biol Res; 1990 Dec 07; 356():333-46. PubMed ID: 2217448
    [No Abstract] [Full Text] [Related]

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  • 11. Congenital disorders associated with platelet dysfunctions.
    Nurden P, Nurden AT.
    Thromb Haemost; 2008 Feb 07; 99(2):253-63. PubMed ID: 18278172
    [Abstract] [Full Text] [Related]

  • 12. Both the high affinity thrombin receptor (GPIb-IX-V) and GPIIb/IIIa are implicated in expression of thrombin-induced platelet procoagulant activity.
    Dicker IB, Pedicord DL, Seiffert DA, Jamieson GA, Greco NJ.
    Thromb Haemost; 2001 Oct 07; 86(4):1065-9. PubMed ID: 11686325
    [Abstract] [Full Text] [Related]

  • 13. Freeze-fracture cytochemistry of wheat germ agglutinin and concanavalin A receptors on the plasma membrane of normal, Bernard-Soulier, and thrombasthenic platelets.
    Chevalier J, Caen JP, Pinto da Silva P.
    Am J Pathol; 1986 Feb 07; 122(2):292-301. PubMed ID: 3753826
    [Abstract] [Full Text] [Related]

  • 14. Functional platelet defects and their laboratory evaluation.
    Bowie EJ, Owen CA.
    Southeast Asian J Trop Med Public Health; 1979 Jun 07; 10(2):234-40. PubMed ID: 524147
    [Abstract] [Full Text] [Related]

  • 15. [The immunodiagnosis of thrombocyte membrane glycoprotein deficiencies: Glanzmann's thrombasthenia, Bernard-Soulier syndrome and GMP-140 protein deficiency].
    Agafonova OG, Vinogradov DV, Khaspekova SG, Lagutina NIa, Labinskaia TA, Vasil'ev SA, Mazurov AV.
    Biull Eksp Biol Med; 1992 Dec 07; 114(12):635-7. PubMed ID: 1284039
    [Abstract] [Full Text] [Related]

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  • 17. The use of fluorescence flow cytometry in the characterization of Bernard-Soulier syndrome and Glanzmann's thrombasthenia.
    Fabris F, Casonato A, Randi ML, Luzzatto G, De Silvestro G, Ongaro G, Girolami A.
    Haematologica; 1989 Dec 07; 74(1):39-44. PubMed ID: 2498181
    [Abstract] [Full Text] [Related]

  • 18. Qualitative disorders of platelets and megakaryocytes.
    Nurden AT.
    J Thromb Haemost; 2005 Aug 07; 3(8):1773-82. PubMed ID: 16102044
    [Abstract] [Full Text] [Related]

  • 19. Inherited abnormalities of the platelet membrane and secretory granules.
    White JG.
    Hum Pathol; 1987 Feb 07; 18(2):123-39. PubMed ID: 3542800
    [Abstract] [Full Text] [Related]

  • 20. Platelet IgG Fc receptor.
    Kelton JG, Smith JW, Santos AV, Murphy WG, Horsewood P.
    Am J Hematol; 1987 Jul 07; 25(3):299-310. PubMed ID: 3605076
    [Abstract] [Full Text] [Related]

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