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The Journal of Clinical Investigation|April 1, 1986
von Willebrand factor interaction with the glycoprotein IIb/IIa complex. Its role in platelet function as demonstrated in patients with congenital afibrinogenemiaL De Marco, A Girolami, T S Zimmerman, et al.
Acta Haematologica|January 1, 1987
The significance of thrombocytosis in old ageM L Randi, A Casonato, F Fabris, et al.
Clinical and Applied Thrombosis/Hemostasis : Official Journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis|March 22, 2000
Aspirin seems as effective as myelosuppressive agents in the prevention of rethrombosis in essential thrombocythemiaM L Randi, C Rossi, F Fabris, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|October 1, 1990
Hereditary heparin cofactor II deficiency and thrombosis: report of six patients belonging to two separate kindredsP Simioni, A R Lazzaro, E Coser, et al.
Acta Haematologica|January 1, 1990
Heterozygous protein-S deficiency: a study of a large kindredA Girolami, P Simioni, A R Lazzaro, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|October 1, 1995
Heterozygous factor VII deficiency and severe hemophilia A in the same kindredA Girolami, M T Sartori, C Rossi, et al.
Haematologica|January 1, 1992
Long-term treatment of refractory HIV-related immune thrombocytopenia in a patient with haemophilia AF Fabris, M Mares, M T Sartori, et al.
Folia Haematologica (Leipzig, Germany : 1928)|January 1, 1980
Normal platelet adhesiveness and aggregation in congenital PTA or Hageman factor deficiencyA Girolami, A Casonato, M Randi, et al.
Acta Haematologica|July 8, 2016
Thrombotic Events in Asymptomatic FXII Deficiency versus Symptomatic FXI Deficiency: Surprising ObservationsA Girolami, E Cosi, C Santarossa, et al.
Hematology (Amsterdam, Netherlands)|July 14, 2016
Thrombocytosis in Malignancy: A Paraneoplastic Syndrome?C Rossi, M L Randi, P Zerbinati, et al.
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