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Thromb Haemost 1975; 34(03): 890
DOI: 10.1055/s-0039-1689499
DOI: 10.1055/s-0039-1689499
Abstracts
Platelet Function in Various Haemorrhagic Disorders
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Publikationsverlauf
Publikationsdatum:
22. Mai 2019 (online)
Platelet aggregation by ADP, collagen, thrombin and ristocetin was studied systematically both in citrate platelet rich plasma and isolated platelets by density gradient using albumine (according to Nicholls and Hampton) in various cases of congenital haemorrhagic diathesis, namely v. Willebrand disease, Glanzmann disease (thrombasthenia), Thrombopathy (PF3, defect), Factor XIII deficiency and in unclassified hereditary haemorrhagic disorders as well as in acquired bleeding tendency. According to the platelet abnormalities found during this study a classification of “Thrombopathies” observed in Greece is attempted.