FAIONI, ELENA MARIA
FAIONI, ELENA MARIA
Dipartimento di Scienze della Salute
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
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
A novel G-to-A mutation in intron-N of the protein S gene leading to abnormal RNA splicing in a patient with protein S deficiency
2003 G. D'Andrea, P. Di Perna, V. Brancaccio, E. Faioni, G. Castaman, G. Cibelli, G. Di Minno, M. Margaglione
A novel G-to-A mutation in the intron-N of the protein S gene leading to abnormal RNA splicing in a patient with protein S deficiency
2003 G. D'Andrea, P. Di Perna, V. Brancaccio, E.M. Faioni, G. Castaman, G. Cibelli, G. Di Minno, M. Margaglione
A proteomic analysis of changes in prothrombin and plasma proteins associated with the G20210A mutation
2004 C. Gelfi, A. Viganò, M. Ripamonti, R. Wait, S. Begum, E. Biguzzi, G. Castaman, E.M. Faioni
Abnormalities of homocysteine and B vitamins in the nephrotic syndrome
2007 G.M. Podda, F. Lussana, G. Moroni, E.M. Faioni, R. Lombardi, G. Fontana, C. Ponticelli, C. Maioli, M. Cattaneo
Activation of protein C in human trophoblasts in culture and downregulation of trophoblast endothelial protein C receptor by TNF-α
2015 E.M. Faioni, G. Fontana, C. Razzari, L. Avagliano, G. Bulfamante, E. Calvi, P. Doi, A.M. Marconi
ACTIVATION OF THE COAGULATION CASCADE AFTER INFUSION OF A FACTOR-XI CONCENTRATE IN CONGENITALLY DEFICIENT PATIENTS
1994 P. MANNUCCI, K. BAUER, E. SANTAGOSTINO, E. FAIONI, S. BARZEGAR, R. COPPOLA, R. ROSENBERG
Activation of the protein C pathway in hereditary thrombophilia
1998 E. Faioni, F. Franchi, D. Asti, P. Mannucci
ANOTHER PROTEIN-S FUNCTIONAL ASSAY IS SENSITIVE TO RESISTANCE TO ACTIVATED PROTEIN-C
1994 E. FAIONI, C. BOYERNEUMANN, F. FRANCHI, M. WOLF, D. MEYER, P. MANNUCCI
Association of estrogen receptor-alpha gene polymorphisms with venous thrombosis
2006 F. Lussana, E.M. Faioni, C. Mavilia, P. Bucciarelli, L. Brandi, M. Cattaneo
Association of factor V deficiency with factor V HR2
2004 E.M. Faioni, G. Castaman, D. Asti, F. Lussana, F. Rodeghiero
Association of protein S p.Pro667Pro dimorphism with plasma protein S levels in normal individuals and patients with inherited protein S deficiency
2007 G. Castaman, E. Biguzzi, C. Razzari, A. Tosetto, G. Fontana, D. Asti, V. Brancaccio, D. Castori, D.A. Lane, E.M. Faioni
Atrial fibrillation and psychological factors : a systematic review
2017 F. Galli, L. Borghi, S. Carugo, M. Cavicchioli, E.M. Faioni, M.S. Negroni, E. Vegni
Autoimmune protein S deficiency and deep vein thrombosis after chickenpox
1996 F. Peyvandi, E. Faioni, G.A. Moroni, A. Rosti, L. Leo, M. Moia
Bleeding diathesis and gastro-duodenal ulcers in inherited cytosolic phospholipase-A2 alpha deficiency
2014 E.M. Faioni, C. Razzari, E.A. Femia, L. Fenu, M. Trinchera, G.M. Podda, M. Pugliano, F. Marongiu, M. Cattaneo, A. Zulueta
c.301C > T (p.Arg101Cys): a novel mutation in the thrombin-sensitive region of protein S associated with a dysfunctional protein
2006 F. FANCHI, Y. VISCARDI, C. RAZZARI, E.M. FAIONI, P. BONARA, E. BIGUZZI, P.M. 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
Complement proteins C5b-9 cause release of membrane vesicles from the platelet surface that are enriched in the membrane receptor for coagulation factor Va and express prothrombinase activity.
1988 P.J. Sims, E.M. Faioni, T. Weidmer, S.J. Shattil
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