메뉴 건너뛰기




Volumn 93, Issue 3, 2005, Pages 549-553

Variability in clinical laboratory practice in testing for disorders of platelet function. Results of two surveys of the North American Specialized Coagulation Laboratory Association

Author keywords

Platelet disorders; Platelet function testing; Platelet secretion

Indexed keywords

ADENOSINE DIPHOSPHATE; ADRENALIN; ARACHIDONIC ACID; COLLAGEN; RISTOCETIN; THROMBOXANE DERIVATIVE;

EID: 15344344771     PISSN: 03406245     EISSN: None     Source Type: Journal    
DOI: 10.1160/TH04-10-0670     Document Type: Article
Times cited : (119)

References (24)
  • 1
    • 0041701487 scopus 로고    scopus 로고
    • Inherited platelet disorders
    • Hayward CPM. Inherited platelet disorders. Curr Opin Hematol 2003; 10: 362-8.
    • (2003) Curr. Opin. Hematol. , vol.10 , pp. 362-368
    • Hayward, C.P.M.1
  • 2
    • 0002764492 scopus 로고    scopus 로고
    • Congenital disorders of platelet secretion
    • Gresele P, Page C, Fuster V, Vermylen J, eds. Cambridge UK: The Press Syndicate of the University of Cambridge
    • Cattaneo M. Congenital disorders of platelet secretion. In: Gresele P, Page C, Fuster V, Vermylen J, eds. Platelets in thrombotic and non-thrombotic disorders. Pathophysiology, pharmacology and therapeutics. Cambridge UK: The Press Syndicate of the University of Cambridge; 2002; 655-73.
    • (2002) Platelets in Thrombotic and Non-thrombotic Disorders. Pathophysiology, Pharmacology and Therapeutics , pp. 655-673
    • Cattaneo, M.1
  • 3
    • 0142010841 scopus 로고    scopus 로고
    • Inherited Disorders of Platelet Function
    • Michelson AD (editor). San Diego, CA: Academic Press
    • Nurden AT, Nurden P. Inherited Disorders of Platelet Function. In: Michelson AD (editor). Platelets. San Diego, CA: Academic Press; 2002; 681-700.
    • (2002) Platelets , pp. 681-700
    • Nurden, A.T.1    Nurden, P.2
  • 4
    • 0002136770 scopus 로고    scopus 로고
    • Inherited abnormalities of the platelet membrane: Glanzmann thrombasthenia, Bernard-Soulier syndrome, and other disorders
    • Colman WR, Hirsh J, Marder VJ, Clowes AW, George JN (editors). 4th Ed. Philadelphia PA: Lippincott Williams and Wilkins
    • Nurden AT, George JN. Inherited abnormalities of the platelet membrane: Glanzmann thrombasthenia, Bernard-Soulier syndrome, and other disorders. In: Colman WR, Hirsh J, Marder VJ, Clowes AW, George JN (editors). Hemostasis and Thrombosis: Basic Principles and Clinical Practise. 4th Ed. Philadelphia PA: Lippincott Williams and Wilkins; 2001; 921-43.
    • (2001) Hemostasis and Thrombosis: Basic Principles and Clinical Practise , pp. 921-943
    • Nurden, A.T.1    George, J.N.2
  • 5
    • 0024259795 scopus 로고
    • Guidelines on platelet function testing
    • The British Society for Haematology, BCSH Haemostasis and Thrombosis Task Force
    • The British Society for Haematology, BCSH Haemostasis and Thrombosis Task Force. Guidelines on platelet function testing. J Clin Pathol 1988; 41: 1322-30.
    • (1988) J. Clin. Pathol. , vol.41 , pp. 1322-1330
  • 6
    • 0042859862 scopus 로고    scopus 로고
    • Adenosine diphosphate-induced platelet aggregation is associated with P2Y12 gene sequence variations in healthy subjects
    • Fontana P, Dupont A, Gandrille S, et al. Adenosine diphosphate-induced platelet aggregation is associated with P2Y12 gene sequence variations in healthy subjects. Circulation 2003; 108: 989-95.
    • (2003) Circulation , vol.108 , pp. 989-995
    • Fontana, P.1    Dupont, A.2    Gandrille, S.3
  • 7
    • 0030061416 scopus 로고    scopus 로고
    • Prevalence of impaired responsiveness to epinephrine in platelets among Japanese
    • Kambayashi J, Shinoki N, Nakamura T, et al. Prevalence of impaired responsiveness to epinephrine in platelets among Japanese. Thromb Res 1996; 81: 85-90.
    • (1996) Thromb. Res. , vol.81 , pp. 85-90
    • Kambayashi, J.1    Shinoki, N.2    Nakamura, T.3
  • 8
    • 0034323126 scopus 로고    scopus 로고
    • 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 P, et al. 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. Arterioscler Thromb Vasc Biol 2000; 20: e101-6.
    • (2000) Arterioscler. Thromb. Vasc. Biol. , vol.20
    • Cattaneo, M.1    Lecchi, A.2    Lombardi, P.3
  • 9
    • 0028942659 scopus 로고
    • An inherited bleeding disorder linked to a defective interaction between ADP and its receptor on platelets
    • Nurden P, Savi P, Heilmann E, et al. An inherited bleeding disorder linked to a defective interaction between ADP and its receptor on platelets. J Clin Invest 1995; 95: 1612-22.
    • (1995) J. Clin. Invest. , vol.95 , pp. 1612-1622
    • Nurden, P.1    Savi, P.2    Heilmann, E.3
  • 10
    • 0023907023 scopus 로고
    • Heterogeneous defects of platelet secretion and responses to weak agonists in patients with bleeding disorders
    • Lages B, Weiss HJ. Heterogeneous defects of platelet secretion and responses to weak agonists in patients with bleeding disorders. Br J Haematol 1988; 68: 53-62.
    • (1988) Br. J. Haematol. , vol.68 , pp. 53-62
    • Lages, B.1    Weiss, H.J.2
  • 11
    • 0034889515 scopus 로고    scopus 로고
    • The effect of human platelet alloantigen polymorphisms on the in vitro responsiveness to adrenaline and collagen
    • Theodoropoulos I, Christopoulos C, Metcalfe P, et al. The effect of human platelet alloantigen polymorphisms on the in vitro responsiveness to adrenaline and collagen. Br J Haematol 2001; 114: 387-93.
    • (2001) Br. J. Haematol. , vol.114 , pp. 387-393
    • Theodoropoulos, I.1    Christopoulos, C.2    Metcalfe, P.3
  • 12
    • 0022485174 scopus 로고
    • Laboratory investigation of platelet function: A review of methodology
    • Yardumian DA, Mackie IJ, Machin SJ. Laboratory investigation of platelet function: a review of methodology. J Clin Pathol 1986; 39: 701-12.
    • (1986) J. Clin. Pathol. , vol.39 , pp. 701-712
    • Yardumian, D.A.1    Mackie, I.J.2    Machin, S.J.3
  • 13
    • 0035990305 scopus 로고    scopus 로고
    • The laboratory evaluation of platelet dysfunction
    • Peerschke EIB. The laboratory evaluation of platelet dysfunction. Clin Lab Med 2002; 22: 405-20.
    • (2002) Clin. Lab. Med. , vol.22 , pp. 405-420
    • Peerschke, E.I.B.1
  • 14
    • 0030299974 scopus 로고    scopus 로고
    • Pathogenic analysis of five cases with a platelet disorder characterized by the absence of thromboxane A2 (TXA2)-induced platelet aggregation in spite of normal TXA2 binding activity
    • Fuse I, Hattori A, Mito M, et al. Pathogenic analysis of five cases with a platelet disorder characterized by the absence of thromboxane A2 (TXA2)-induced platelet aggregation in spite of normal TXA2 binding activity. Thromb Haemost 1996; 76: 1080-5.
    • (1996) Thromb. Haemost. , vol.76 , pp. 1080-1085
    • Fuse, I.1    Hattori, A.2    Mito, M.3
  • 15
    • 0018750661 scopus 로고
    • Inherited defective platelet aggregation with arachidonate as the main expression of a defective metabolism of arachidonic acid
    • Nyman D, Eriksson AW, Lehmann W, et al. Inherited defective platelet aggregation with arachidonate as the main expression of a defective metabolism of arachidonic acid. Thromb Res 1979; 14: 739-46.
    • (1979) Thromb. Res. , vol.14 , pp. 739-746
    • Nyman, D.1    Eriksson, A.W.2    Lehmann, W.3
  • 16
    • 0019781070 scopus 로고
    • Epinephrine potentiation of arachidonate-induced aggregation of cyclooxygenase-deficient platelets
    • Rao GHR, White JG. Epinephrine potentiation of arachidonate-induced aggregation of cyclooxygenase-deficient platelets. Am J Hematol 1981; 11: 355-66.
    • (1981) Am. J. Hematol. , vol.11 , pp. 355-366
    • Rao, G.H.R.1    White, J.G.2
  • 17
    • 0023858616 scopus 로고
    • Differential requirements for platelet aggregation and inhibition of adenylate cyclase by epinephrine. Studies of a familial platelet alpha2-adrenergic receptor defect
    • Rao AK, Willis J, Kowalska MA, et al. Differential requirements for platelet aggregation and inhibition of adenylate cyclase by epinephrine. Studies of a familial platelet alpha2-adrenergic receptor defect. Blood 1988; 71: 494-501.
    • (1988) Blood , vol.71 , pp. 494-501
    • Rao, A.K.1    Willis, J.2    Kowalska, M.A.3
  • 18
    • 0029952371 scopus 로고    scopus 로고
    • An autosomal dominant, qualitative platelet disorder associated with multimerin deficiency, abnormalities in platelet factor V, thrombospondin, von Willebrand factor, and fibrinogen and an epinephrine aggregation defect
    • Hayward CPM, Rivard GE, Kane WH, et al. An autosomal dominant, qualitative platelet disorder associated with multimerin deficiency, abnormalities in platelet factor V, thrombospondin, von Willebrand factor, and fibrinogen and an epinephrine aggregation defect. Blood 1996; 87: 4967-78.
    • (1996) Blood , vol.87 , pp. 4967-4978
    • Hayward, C.P.M.1    Rivard, G.E.2    Kane, W.H.3
  • 19
    • 0014664167 scopus 로고
    • A familial defect in platelet function associated with impaired release of adenosine diphosphate
    • Weiss HJ, Chervenick PA, Zalusky R, et al. A familial defect in platelet function associated with impaired release of adenosine diphosphate. N Engl J Med 1969; 281: 1264-70.
    • (1969) N. Engl. J. Med. , vol.281 , pp. 1264-1270
    • Weiss, H.J.1    Chervenick, P.A.2    Zalusky, R.3
  • 20
    • 0018673733 scopus 로고
    • Heterogeneity in storage pool deficiency: Studies on granule-bound substances in 18 patients including variants deficient in α-granules, platelet factor 4, β-thromboglobulin, and platelet-derived growth factor
    • Weiss HJ, Witte LD, Kaplan KL, et al. Heterogeneity in storage pool deficiency: studies on granule-bound substances in 18 patients including variants deficient in α-granules, platelet factor 4, β-thromboglobulin, and platelet-derived growth factor. Blood 1979; 54: 1296-319.
    • (1979) Blood , vol.54 , pp. 1296-1319
    • Weiss, H.J.1    Witte, L.D.2    Kaplan, K.L.3
  • 21
    • 0027411863 scopus 로고
    • Heterogeneous abnormalities of platelet dense granule ultrastructure in 20 patients with congenital storage pool deficiency
    • Weiss HJ, Lages B, Vicic W, et al. Heterogeneous abnormalities of platelet dense granule ultrastructure in 20 patients with congenital storage pool deficiency. Br J Haematol 1993; 83: 282-95.
    • (1993) Br. J. Haematol. , vol.83 , pp. 282-295
    • Weiss, H.J.1    Lages, B.2    Vicic, W.3
  • 22
    • 0028201807 scopus 로고
    • A revised classification of von Willebrand Disease
    • Sadler JE. A revised classification of von Willebrand Disease. Thromb Haemost 1994; 71: 520-5.
    • (1994) Thromb. Haemost. , vol.71 , pp. 520-525
    • Sadler, J.E.1
  • 23
    • 2342656365 scopus 로고    scopus 로고
    • The diagnosis of von Willebrand disease: A guideline from the UK haemophilia centre doctors' organization
    • Laffan M, Brown SA, Collins PW, et al. The diagnosis of von Willebrand disease: a guideline from the UK haemophilia centre doctors' organization. Haemophilia 2004; 10: 199-217.
    • (2004) Haemophilia , vol.10 , pp. 199-217
    • Laffan, M.1    Brown, S.A.2    Collins, P.W.3
  • 24
    • 0141609789 scopus 로고    scopus 로고
    • Inherited platelet-based bleeding disorders
    • Cattaneo M. Inherited platelet-based bleeding disorders. J Thromb Haemost 2003; 1: 1628-36.
    • (2003) J. Thromb. Haemost. , vol.1 , pp. 1628-1636
    • Cattaneo, M.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.