Factor VIII/von Willebrand factor (VIII/vWf) related properties were studied in twenty six patients with thrombocytopenia. Fifteen patients were affected by idiopathic thrombocytopenic purpura (ITP) and 11 patients by thrombocytopenia of a different nature or non-ITP (n-ITP). All patients showed an
✦ LIBER ✦
The possible value of platelet aggregation studies in patients with increased platelet number
✍ Scribed by Fabris, F. ;Randi, M. ;Sbrojavacca, R. ;Casonato, A. ;Girolami, A.
- Publisher
- Springer-Verlag
- Year
- 1981
- Weight
- 427 KB
- Volume
- 43
- Category
- Article
- ISSN
- 1432-0584
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## Abstract Because of the high prevalence of thrombotic complications in patients with sickle cell anemia (SCA), we investigated platelet function in patients with sickle hemoglobinopathies. Platelet aggregation induced by epinephrine, ADP, and collagen, except for absent secondary wave in 3 of 10