Elisabetta Castoldi
Department of Biochemistry
Maastricht University P.O. Box 616
6200 Maastricht
Netherlands
Name/email consistency: high
- Similar hypercoagulable state and thrombosis risk in type I and type III protein S-deficient individuals from families with mixed type I/III protein S deficiency. Castoldi, E., Maurissen, L.F., Tormene, D., Spiezia, L., Gavasso, S., Radu, C., Hackeng, T.M., Rosing, J., Simioni, P. Haematologica (2010)
- Hereditary and acquired protein S deficiencies are associated with low TFPI levels in plasma. Castoldi, E., Simioni, P., Tormene, D., Rosing, J., Hackeng, T.M. J. Thromb. Haemost. (2010)
- Similar hypercoagulable state and thrombosis risk in type I and type III protein S-deficient individuals from mixed type I/III families. Castoldi, E., Maurissen, L.F., Tormene, D., Spiezia, L., Gavasso, S., Radu, C., Hackeng, T.M., Rosing, J., Simioni, P. Haematologica (2010)
- Differential effects of high prothrombin levels on thrombin generation depending on the cause of the hyperprothrombinemia. Castoldi, E., Simioni, P., Tormene, D., Thomassen, M.C., Spiezia, L., Gavasso, S., Rosing, J. J. Thromb. Haemost. (2007)
- Impaired APC cofactor activity of factor V plays a major role in the APC resistance associated with the factor V Leiden (R506Q) and R2 (H1299R) mutations. Castoldi, E., Brugge, J.M., Nicolaes, G.A., Girelli, D., Tans, G., Rosing, J. Blood (2004)
- Coinheritance of Factor V (FV) Leiden enhances thrombin formation and is associated with a mild bleeding phenotype in patients homozygous for the FVII 9726+5G>A (FVII Lazio) mutation. Castoldi, E., Govers-Riemslag, J.W., Pinotti, M., Bindini, D., Tans, G., Berrettini, M., Mazzucconi, M.G., Bernardi, F., Rosing, J. Blood (2003)
