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British Journal of Haematology|March 22, 2001
Von Willebrand factor collagen binding activity in the diagnosis of von Willebrand disease: an alternative to ristocetin co-factor activity?A Casonato, E Pontara, A Bertomoro, et al.
Haematologia|January 1, 1993
Combined haemophilia A and type I von Willebrand's disease: a family study including an evaluation of the effects of DDAVP infusionA Casonato, E Pontara, M Boscaro, et al.
Biochimica Et Biophysica Acta|March 20, 1993
The dysfunction of coagulation factor VIIPadua results from substitution of arginine-304 by glutamineH L James, A Girolami, J G Hubbard, et al.
Haematologia|January 1, 1994
A new variant of von Willebrand's disease (type I Padua): doublet-organized plasma von Willebrand factor oligomers in the presence of all size multimersA Casonato, E Pontara, D Dannhäuser, et al.
Folia Haematologica (Leipzig, Germany : 1928)|January 1, 1983
Failure of sulphinpyrazone to affect platelet survival in patients with rheumatic heart valvular disease: a double blind study using 75Se-methionine labeled plateletsF Fabris, A Casonato, M L Randi, et al.
Acta Haematologica|January 1, 1984
Antithrombin III Trento. A 'new' congenital AT III abnormality with a peculiar crossed-immunoelectrophoretic pattern in the absence of heparinA Girolami, F Marafioti, M Rubertelli, et al.
Folia Haematologica (Leipzig, Germany : 1928)|January 1, 1990
Haematological complications in polycythaemia vera and thrombocythaemia patients treated with radiophosphorus (32P)M L Randi, F Fabris, L Varotto, et al.
Journal of Medicine|January 1, 1996
Essential thrombocythemia following polycythemia vera: an unusual sequenceM L Randi, E Barbone, P Zerbinati, et al.
Thrombosis and Haemostasis|August 30, 1985
Further studies on the hypercoagulable state of patients with Cushing's syndromeG M Patrassi, R Dal Bo Zanon, M Boscaro, et al.
Haemostasis|January 1, 1977
Clotting factors and platelets. Immunofluorescence evidence that fibrinogen and factor VIII are present in human washed platelets, whereas prothrombin complex factors and factor XIII are lackingC Betterle, F Fabris, L de Marco, et al.
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