Abnormalities of platelet aggregation in sickle cell anemia presence of a plasma factor inhibiting aggregation by ristocetin
- 1 February 1979
- journal article
- research article
- Published by Elsevier in Thrombosis Research
- Vol. 14 (2-3) , 283-297
- https://doi.org/10.1016/0049-3848(79)90238-x
Abstract
No abstract availableThis publication has 12 references indexed in Scilit:
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- Platelet function in sickle cell anemiaThrombosis Research, 1977
- The in vivo increase of factor VIII activity by 2,3-diphosphoglycerateThrombosis Research, 1976
- ADP-induced inhibition of von Willebrand factor-mediated platelet agglutinationAmerican Journal of Physiology-Legacy Content, 1976
- Coagulation Changes during the Steady State in Homozygous Sickle‐Cell Disease in JamaicaBritish Journal of Haematology, 1975
- Willebrand Factor and Ristocetin II. RELATIONSHIP BETWEEN WILLEBRAND FACTOR, WILLEBRAND ANTIGEN AND FACTOR‐VIII ACTIVITYBritish Journal of Haematology, 1974
- Abnormalities of platelet aggregation in the vaso-occlusive crisis of sickle-cell anemiaThe Journal of Pediatrics, 1974
- Role of coagulation system in pathophysiology of sickle cell diseaseArchives of internal medicine (1960), 1974
- Factor-VIII (Antihaemophilic Factor) Activity in Sickle-Cell AnaemiaBritish Journal of Haematology, 1967
- Morphology and Enumeration of Human Blood PlateletsJournal of Applied Physiology, 1950