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Journal Abstract Search

132 related items for PubMed ID: 7196771

  • 1. Haemorrhagic thrombocytopathy associated with dilatation of the platelet--membrane complex.
    Green D, Ts'ao CH, Cohen I, Rossi EC.
    Br J Haematol; 1981 Aug; 48(4):595-600. PubMed ID: 7196771
    [Abstract] [Full Text] [Related]

  • 2. Hereditary thrombocytopathy: a familial bleeding disorder due to impaired platelet coagulant activity.
    Ardlie NG, Coupland WW, Schoefl GI.
    Aust N Z J Med; 1976 Feb; 6(1):37-45. PubMed ID: 1065298
    [Abstract] [Full Text] [Related]

  • 3. Thrombocytopathy due to a defect of the platelet membrane complex.
    Canizares C, Vivar N, Grijalva J.
    Acta Haematol; 1990 Feb; 83(2):99-104. PubMed ID: 2106203
    [Abstract] [Full Text] [Related]

  • 4. [Aspirin-like defect - a hereditary thrombocytopathy due to impaired release of platelet adenosine diphosphate].
    Elezović I, Mijović A, Rolović Z.
    Bilt Hematol Transfuz; 1979 Feb; 7(2-3):165-74. PubMed ID: 263623
    [Abstract] [Full Text] [Related]

  • 5. Characterization of platelet abnormalities of Tester Moriyama (TM) rats with storage pool deficiency.
    Fujimori H, Ozaki K, Nomura S, Nishikawa T, Pan-Hou H, Nishimura M, Narama I.
    Lab Anim Sci; 1998 Oct; 48(5):490-5. PubMed ID: 10090063
    [Abstract] [Full Text] [Related]

  • 6. Preliminary studies of a platelet function disorder in Simmental cattle.
    Searcy GP, Sheridan D, Dobson KA.
    Can J Vet Res; 1990 Jun; 54(3):394-6. PubMed ID: 2379119
    [Abstract] [Full Text] [Related]

  • 7. Electron microscopic and functional studies on platelets in gray platelet syndrome.
    Mori K, Suzuki S, Sugai K.
    Tohoku J Exp Med; 1984 Jul; 143(3):261-87. PubMed ID: 6484975
    [Abstract] [Full Text] [Related]

  • 8. Ultrastructural findings in storage pool disease and aspirin-like defects of platelets.
    Weiss HJ, Ames RP.
    Am J Pathol; 1973 Jun; 71(3):447-66. PubMed ID: 4715955
    [Abstract] [Full Text] [Related]

  • 9. Hereditary bleeding disorder due to a primary defect in platelet release reaction.
    Wu KK, Minkoff IM, Rossi EC, Chen YC.
    Br J Haematol; 1981 Feb; 47(2):241-9. PubMed ID: 7470394
    [Abstract] [Full Text] [Related]

  • 10. A platelet defect in a patient with eosinophilic leukaemia: absent ristocetin-induced platelet aggregation associated with a reduced platelet sialic acid content.
    Wautier JL, Souchon H, Dupuis D, Caen JP, Nurden AT.
    Scand J Haematol; 1979 Mar; 22(3):267-76. PubMed ID: 451458
    [Abstract] [Full Text] [Related]

  • 11. Platelets from bleeding Simmental cattle mobilize calcium, phosphorylate myosin light chain and bind normal numbers of fibrinogen molecules but have abnormal cytoskeletal assembly and aggregation in response to ADP.
    Searcy GP, Frojmovic MM, McNicol A, Robertson C, Wong T, Gerrard JM.
    Thromb Haemost; 1994 Feb; 71(2):240-6. PubMed ID: 8191406
    [Abstract] [Full Text] [Related]

  • 12. Failure to mobilize intracellular calcium in response to thrombin in a patient with familial thrombocytopathy characterized by macrothrombocytopenia and abnormal platelet membrane complexes.
    Parker RI, Bray GL, McKeown LP, White JG.
    J Lab Clin Med; 1993 Oct; 122(4):441-9. PubMed ID: 8228559
    [Abstract] [Full Text] [Related]

  • 13. Deficiency of intact thrombospondin and membrane glycoprotein Ia in platelets with defective collagen-induced aggregation and spontaneous loss of disorder.
    Kehrel B, Balleisen L, Kokott R, Mesters R, Stenzinger W, Clemetson KJ, van de Loo J.
    Blood; 1988 Apr; 71(4):1074-8. PubMed ID: 3355888
    [Abstract] [Full Text] [Related]

  • 14. Familial bleeding disorder associated with deficiencies in platelet signal processing and glycoproteins.
    Holmsen H, Walsh PN, Koike K, Murphy S, Holme S, Johnson MM, Dangelmaier CA, Egan JJ, Benzel JE, Tuszynski GP.
    Br J Haematol; 1987 Nov; 67(3):335-44. PubMed ID: 3689696
    [Abstract] [Full Text] [Related]

  • 15. Inherited platelet delta-storage pool disease in dogs causing severe bleeding: an animal model for a specific ADP deficiency.
    Callan MB, Bennett JS, Phillips DK, Haskins ME, Hayden JE, Anderson JG, Giger U.
    Thromb Haemost; 1995 Sep; 74(3):949-53. PubMed ID: 8571327
    [Abstract] [Full Text] [Related]

  • 16. Identification of an intrinsic platelet function defect in Spitz dogs.
    Boudreaux MK, Crager C, Dillon AR, Stanz K, Toivio-Kinnucan M.
    J Vet Intern Med; 1994 Sep; 8(2):93-8. PubMed ID: 8046682
    [Abstract] [Full Text] [Related]

  • 17. Studies of platelet 5-hydroxytryptamine (serotonin) in storage pool disease and albinism.
    Weiss HJ, Tschopp TB, Rogers J, Brand H.
    J Clin Invest; 1974 Aug; 54(2):421-33. PubMed ID: 4847252
    [Abstract] [Full Text] [Related]

  • 18. Abnormalities of cytoplasmic Ca2+ in platelets from patients with uremia.
    Ware JA, Clark BA, Smith M, Salzman EW.
    Blood; 1989 Jan; 73(1):172-6. PubMed ID: 2910357
    [Abstract] [Full Text] [Related]

  • 19. Platelets from a patient heterozygous for the defect of P2CYC receptors for ADP have a secretion defect despite normal thromboxane A2 production and normal granule stores: further evidence that some cases of platelet 'primary secretion defect' are heterozygous for a defect of P2CYC receptors.
    Cattaneo M, Lecchi A, Lombardi R, Gachet C, Zighetti ML.
    Arterioscler Thromb Vasc Biol; 2000 Nov; 20(11):E101-6. PubMed ID: 11073862
    [Abstract] [Full Text] [Related]

  • 20. Deficiency of P-selectin in a patient with grey platelet syndrome.
    Mazurov AV, Vinogradov DV, Khaspekova SG, Krushinsky AV, Gerdeva LV, Vasiliev SA.
    Eur J Haematol; 1996 Jul; 57(1):38-41. PubMed ID: 8698129
    [Abstract] [Full Text] [Related]

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