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D. Gemmati

Department of Biomedical Sciences and Advanced Therapies

Centre for the Study of Haemostasis and Thrombosis

University of Ferrara

Ferrara

Italy

[email]@unife.it

Name/email consistency: low

 
 
 
 
 
 
 

Affiliations

  • Department of Biomedical Sciences and Advanced Therapies, Centre for the Study of Haemostasis and Thrombosis, University of Ferrara, Ferrara, Italy. 2001
  • Centre for the Study of Haemostasis and Thrombosis, University of Ferrara, Italy. 2001

References

  1. A common mutation in the gene for coagulation factor XIII-A (VAL34Leu): a risk factor for primary intracerebral hemorrhage is protective against atherothrombotic diseases. Gemmati, D., Serino, M.L., Ongaro, A., Tognazzo, S., Moratelli, S., Resca, R., Moretti, M., Scapoli, G.L. Am. J. Hematol. (2001) [Pubmed]
  2. Coexistence of factor V G1691A and factor II G20210A gene mutations in a thrombotic family is associated with recurrence and early onset of venous thrombosis. Gemmati, D., Serino, M.L., Moratelli, S., Tognazzo, S., Ongaro, A., Scapoli, G.L. Haemostasis (2001) [Pubmed]
  3. The reduced sensitivity of the ProC Global test in protein S deficient subjects reflects a reduction in the associated thrombotic risk. Gemmati, D., Serino, M.L., Tognazzo, S., Ongaro, A., Moratelli, S., Gilli, G., Forini, E., De Mattei, M., Scapoli, G.L. Blood Coagul. Fibrinolysis (2001) [Pubmed]
 
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