...A. Girolami; A. Brunetti; D. Fioretti; E. Gravina A case of platelet factor 3 deficiency (thrombocytopathy) is presented. The coagulation study showed a normal plasmatic pattern but a defective prothrombin consumption. The thromboplastin generation was defective too and was corrected...

...Meir Djaldetti; Pnina Fishman; Draga Creter; Izhar Zahavi; Dina Zevin; Joseph Levi The platelet element content was determined by semiquantitative X-ray microanalysis in 6 patients with chronic renal failure. The patients showed a different degree of thrombocytopathy expressed by impaired...

...I. Melamed; M. Djaldetti; H. Joshua; U. Seligsohn Associations of hereditary abnormalities of the factor VIII complex and hereditary platelet disorders have previously been reported in 12 families. Another family is reported in which 6 members had a bleeding tendency and thrombocytopathy...

... cases whereas PF 4 was markedly elevated in one. Platelet dysfunction was not reversed by clinical remission. These studies confirm that megakaryoblastic leukemia is associated with a thrombocytopathy which may play a role in hemorrhagic diathesis and should be taken into account in the management...

...C. Canizares; N. Vivar; J. Grijalva A new type of primary thrombocytopathy is described. Three main alterations were found: (1) a defect of the aggregation reaction with ADP, epinephrine and collagen and a normal response to ristocetin and arachidonic acid; (2) a moderate deficiency of platelet...