A study of β-thromboglobulin and platelet factor-4 plasma levels in steady state sickle cell patients

Author:

Adamides S.,Konstantopoulos K.,Toumbis M.,Douratsos D.,Travlou A.,Kasfiki A.

Publisher

Springer Science and Business Media LLC

Subject

Hematology,General Medicine,Hematology

Reference11 articles.

1. Billet HB, Nagel RL, Farby ME (1988) Evolution of laboratory parameters during sickle cell painful crisis: Evidence compatible with dense red cell sequestration without thrombosis. Am J Med Sci 296: 293–298

2. Buchanan GR, Holtcamp CA (1983) Evidence against enhanced platelet activity in sickle cell anaemia. Br J Haematol 54: 595–603

3. Chaplin H, Alkjaersig N, Fletcher AP, Michael JM, Joist JH (1980) Aspirin-dipyridamole prophylaxis of sickle cell disease pain crises. Thromb Hemostas 44: 218–221

4. Greenberg J, Ohene-Frempong K, Halus J, Schwartz E (1981) Aspirin as anti-platelet therapy in patients with sickle cell disease. Blood 58 [Suppl 1]:59a

5. Kaplan KL, Owen J (1981) Plasma levels of β-thromboglobulin and platelet factor 4 as indices of platelet activation in vivo. Blood 57: 199–202

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