Sfoglia per Autore
Resistance to activated protein C in unselected patients with arterial and venous thrombosis
1997 E. Faioni, C. Razzari, I. Martinelli, D. Panzeri, F. Franchi, P. Mannucci
Free protein S deficiency is a risk factor for venous thrombosis
1997 E. Faioni, C. Valsecchi, A. Palla, E. Taioli, C. Razzari, P. Mannucci
Venocclusive disease of the liver after bone marrow transplantation: The role of hemostasis
1997 E. Faioni, P. Mannucci
A factor V genetic component differing from factor V R506Q contributes to the activated protein C resistance phenotype
1997 F. Bernardi, E. Faioni, E. Castoldi, B. Lunghi, G. Castaman, E. Sacchi, P. Mannucci
The G1456 to T mutation in the thrombomodulin gene is not frequent in patients with venous thrombosis
1997 E.M. Faioni, G. Merati, F. Peyvandi, P. Bettini, P.M. Mannucci
Activation of the protein C pathway in hereditary thrombophilia
1998 E. Faioni, F. Franchi, D. Asti, P. Mannucci
Different risks of thrombosis in four coagulation defects associated with inherited thrombophilia: A study of 150 families
1998 I. Martinelli, P. Mannucci, V. De Stefano, E. Taioli, V. Rossi, F. Crosti, K. Paciaroni, G. Leone, E. Faioni
Laboratory screening of thrombophilia. Evaluation of the diagnostic efficacy of a global test to detect congenital deficiencies of the protein C anticoagulant pathway
1998 A. Tripodi, S. Akhavan, D. Asti, E. Faioni, P. Mannucci
Coinheritance of the HR2 haplotype in the factor V gene confers an increased risk of venous thromboembolism to carriers of factor V R506Q (Factor V leiden)
1999 E. Faioni, F. Franchi, P. Bucciarelli, M. Margaglione, V. De Stefano, G. Castaman, G. Finazzi, P. Mannucci
Poor relationship between phenotypes of protein S deficiency and mutations in the protein S alpha gene
1999 J. Hermida, E. Faioni, P. Mannucci
Consumption of C4b-binding protein (C4BP) during in vivo activation of the classical complement pathway
1999 L. Bergamaschini, A. Miedico, M. Cicardi, R. Coppola, E.N. Faioni, A. Agostoni
Factor VHR2: An ancient haplotype out of Africa - reasons for being interested
2000 E. Faioni
Type II protein C deficiency: identification and molecular modelling of two natural mutants with low anticoagulant and normal amidolytic activity
2000 E. Faioni, J. Hermida, E. Rovida, C. Razzari, D. Asti, S. Zeinali, P. Mannucci
A 23bp insertion in the endothelial protein C receptor (EPCR) gene impairs EPCR function
2001 E. Biguzzi, G. Merati, P. Liaw, P. Bucciarelli, N. Oganesyan, D. Qu, J. Gu, R. Fetiveau, C. Esmon, P. Mannucci, E. Faioni
Mutations in the thrombomodulin and endothelial protein C receptor genes in women with late fetal loss
2001 F. Franchi, E. Biguzzi, I. Cetin, F. Facchetti, T. Radaelli, M. Bozzo, G. Pardi, E. Faioni
The HR2 haplotype of coagulation factor V: Biochemistry, epidemiology, and clinical relevance = Der HR2-haplotyp des gerinnungsfaktors V: Biochemie, epidemiologie und klinische bedeutung
2001 E.M. Faioni
Reduced free protein S levels in patients with inflammatory bowel disease - Prevalence, clinical relevance, and role of anti-protein S antibodies
2001 S. Saibeni, M. Vecchi, C. Valsecchi, E. Faioni, C. Razzari, R. De Franchis
Reliable estimates of plasma protein S levels: Are we getting any closer?
2001 E. Faioni
Mutations in the thrombomodulin gene are rare in patients with severe thrombophilia
2002 E. Faioni, F. Franchi, G. Castaman, E. Biguzzi, F. Rodeghiero
Identification of differentially expressed genes in coronary atherosclerotic plaques from patients with stable or unstable angina by cDNA array analysis
2003 A.M. Randi, E. Biguzzi, F. Falciani, P. Merlini, S. Blakemore, E. Bramucci, S. Lucreziotti, M. Lennon, E.M. Faioni, D. Ardissino, P.M. Mannucci
Legenda icone
- file ad accesso aperto
- file disponibili sulla rete interna
- file disponibili agli utenti autorizzati
- file disponibili solo agli amministratori
- file sotto embargo
- nessun file disponibile