SPREAFICO, MARTA
SPREAFICO, MARTA
Universita' degli Studi di MILANO
Prevalence and 9-year incidence of hepatitis E virus infection among north italian blood donors: Estimated transfusion risk
2020 M. Spreafico, L. Raffaele, I. Guarnori, B. Foglieni, A. Berzuini, L. Valenti, A. Gerosa, A. Colli, D. Prati
Lack of Siglec-7 expression identifies a dysfunctional natural killer cell subset associated with liver inflammation and fibrosis in chronic HCV infection
2016 S. Varchetta, D. Mele, A. Lombardi, B. Oliviero, S. Mantovani, C. Tinelli, M. Spreafico, D. Prati, S. Ludovisi, G. Ferraioli, C. Filice, A. Aghemo, P. Lampertico, F. Facchetti, F. Bernuzzi, P. Invernizzi, M.U. Mondelli
High serum levels of HDV RNA are predictors of cirrhosis and liver cancer in patients with chronic hepatitis delta
2014 R. Romeo, B. Foglieni, G. Casazza, M. Spreafico, M. Colombo, D. Prati
Bayesian inference analyses of the polygenic architecture of rheumatoid arthritis
2012 E.A. Stahl, D. Wegmann, G. Trynka, J. Gutierrez Achury, B.F. Do R, Voight, P. Kraft, R. Chen, H.J. Kallberg, F.A. Kurreeman, S. Kathiresan, C. Wijmenga, P.K. Gregersen, L. Alfredsson, K.A. Siminovitch, J. Worthington, P.I. de Bakker, S. Raychaudhuri, R.M. Plenge, B.F. Voight, L.J. Scott, V. Steinthorsdottir, A.P. Morris, C. Dina, R.P. Welch, E. Zeggini, C. Huth, Y.S. Aulchenko, G. Thorleifsson, L.J. Mcculloch, T. Ferreira, H. Grallert, N. Amin, G. Wu, C.J. Willer, S. Raychaudhuri, S.A. Mccarroll, C. Langenberg, O.M. Hofmann, J. Dupuis, L. Qi, A.V. Segrè, M. van Hoek, P. Navarro, K. Ardlie, B. Balkau, R. Benediktsson, A.J. Bennett, R. Blagieva, E. Boerwinkle, L.L. Bonnycastle, K.B. Boström, B. Bravenboer, S. Bumpstead, N.P. Burtt, G. Charpentier, P.S. Chines, M. Cornelis, D.J. Couper, G. Crawford, A.S. Doney, K.S. Elliott, A.L. Elliott, M.R. Erdos, C.S. Fox, C.S. Franklin, M. Ganser, C. Gieger, N. Grarup, T. Green, S. Griffin, C.J. Groves, C. Guiducci, S. Hadjadj, N. Hassanali, C. Herder, B. Isomaa, A.U. Jackson, P.R. Johnson, T. Jørgensen, W.H. Kao, N. Klopp, A. Kong, P. Kraft, J. Kuusisto, T. Lauritzen, M. Li, A. Lieverse, C.M. Lindgren, V. Lyssenko, M. Marre, T. Meitinger, K. Midthjell, M.A. Morken, N. Narisu, P. Nilsson, K.R. Owen, F. Payne, J.R. Perry, A.K. Petersen, C. Platou, C. Proença, I. Prokopenko, W. Rathmann, N.W. Rayner, N.R. Robertson, G. Rocheleau, M. Roden, M.J. Sampson, R. Saxena, B.M. Shields, P. Shrader, G. Sigurdsson, T. Sparsø, K. Strassburger, H.M. Stringham, Q. Sun, A.J. Swift, B. Thorand, J. Tichet, T. Tuomi, R.M. van Dam, T.W. van Haeften, T. van Herpt, J.V. van Vliet Ostaptchouk, G.B. Walters, M.N. Weedon, C. Wijmenga, J. Witteman, R.N. Bergman, S. Cauchi, F.S. Collins, A.L. Gloyn, U. Gyllensten, T. Hansen, W.A. Hide, G.A. Hitman, A. Hofman, D.J. Hunter, K. Hveem, M. Laakso, K.L. Mohlke, A.D. Morris, C.N. Palmer, P.P. Pramstaller, I. Rudan, E. Sijbrands, L.D. Stein, J. Tuomilehto, A. Uitterlinden, M. Walker, N.J. Wareham, R.M. Watanabe, G.R. Abecasis, B.O. Boehm, H. Campbell, M.J. Daly, A.T. Hattersley, F.B. Hu, J.B. Meigs, J.S. Pankow, O. Pedersen, H.E. Wichmann, I. Barroso, J.C. Florez, T.M. Frayling, L. Groop, R. Sladek, U. Thorsteinsdottir, J.F. Wilson, T. Illig, P. Froguel, C.M. van Duijn, K. Stefansson, D. Altshuler, M. Boehnke, M.I. Mccarthy, S. Kathiresan, J.B. Meigs, G. Williams, D.M. Nathan, C.A. Macrae, C.J. O'Donnell, D. Ardissino, P.A. Merlini, C. Berzuini, L. Bernardinelli, F. Peyvandi, M. Tubaro, P. Celli, M. Ferrario, R. Fetiveau, N. Marziliano, G. Casari, M. Galli, F. Ribichini, M. Rossi, F. Bernardi, P. Zonzin, A. Piazza, P.M. Mannucci, S.M. Schwartz, D.S. Siscovick, J. Yee, Y. Friedlander, R. Elosua, J. Marrugat, G. Lucas, I. Subirana, J. Sala, R. Ramos, V. Salomaa, A.S. Havulinna, L. Peltonen, O. Melander, G. Berglund, B.F. Voight, S. Kathiresan, J.N. Hirschhorn, R. Asselta, S. Duga, M. Spreafico, K. Musunuru, M.J. Daly, S. Purcell, S.M. Schwartz, J. Yee, S. Kathiresan, G. Lucas, I. Subirana, R. Elosua, A. Surti, C. Guiducci, L. Gianniny, D. Mirel, M. Parkin, N. Burtt, S.B. Gabriel
Influence of 9p21.3 genetic variants on clinical and angiographic outcomes in early-onset myocardial infarction
2011 D. Ardissino, C. Berzuini, P.A. Merlini, P.M. Mannucci, A. Surti, N. Burtt, B. Voight, M. Tubaro, F. Peyvandi, M. Spreafico, P. Celli, D. Lina, M.F. Notarangelo, M. Ferrario, R. Fetiveau, G. Casari, M. Galli, F. Ribichini, M.L. Rossi, F. Bernardi, N. Marziliano, P. Zonzin, F. Mauri, A. Piazza, L. Foco, L. Bernardinelli, D. Altshuler, S. Kathiresan, I. Atherosclerosis Thrombosis, V. Biology Investigators
Evaluation of assay methods to measure plasma ADAMTS13 activity in thrombotic microangiopathies
2011 R. Palla, C. Valsecchi, M. Bajetta, M. Spreafico, R. De Cristofaro, F. Peyvandi
Factor V and combined Factor V and VIII deficiencies
2010 F. Peyvandi, M. Spreafico
The association of factor V Leiden with myocardial infarction is replicated in 1880 patients with premature disease
2010 P.M. Mannucci, R. Asselta, S. Duga, I. Guella, M. Spreafico, L.A. Lotta, P.A. Merlini, F. Peyvandi, S. Kathiresan, D. Ardissino
Gynaecological and obstetrical problems in women with different bleeding disorders
2009 S.M. Siboni, M. Spreafico, L. Calò, A. Maino, E. Santagostino, A.B. Federici, F. Peyvandi
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants
2009 S. Kathiresan, B.F. Voight, S. Purcell, K. Musunuru, D. Ardissino, P.M. Mannucci, S. Anand, J.C. Engert, N.J. Samani, H. Schunkert, J. Erdmann, M.P. Reilly, D.J. Rader, T. Morgan, J.A. Spertus, M. Stoll, D. Girelli, P.P. McKeown, C.C. Patterson, D.S. Siscovick, C.J. O'Donnell, R. Elosua, L. Peltonen, V. Salomaa, S.M. Schwartz, O. Melander, D. Altshuler, D. Ardissino, P.A. Merlini, C. Berzuini, L. Bernardinelli, F. Peyvandi, M. Tubaro, P. Celli, M. Ferrario, R. Fetiveau, N. Marziliano, G. Casari, M. Galli, F. Ribichini, M. Rossi, F. Bernardi, P. Zonzin, A. Piazza, P.M. Mannucci, S.M. Schwartz, D.S. Siscovick, J. Yee, Y. Friedlander, R. Elosua,J. Marrugat, G. Lucas, I. Subirana, J. Sala, R. Ramos, S. Kathiresan, J.B. Meigs, G. Williams, D.M. Nathan, C.A. MacRae, C.J. O'Donnell, V. Salomaa, A.S. Havulinna, L. Peltonen, O. Melander, G. Berglund, B.F. Voight, S. Kathiresan, J.N. Hirschhorn, R. Asselta, S. Duga, M. Spreafico, K. Musunuru, M.J Daly, S. Purcell, B.F. Voight, S. Purcell, J. Nemesh, J.M. Korn, S.A. McCarroll, S.M. Schwartz, J. Yee, S. Kathiresan, G. Lucas, I. Subirana, R. Elosua, A. Surti, C. Guiducci, L. Gianniny, D. Mirel, M. Parkin, N. Burtt, S.B. Gabriel, N.J. Samani, J.R. Thompson, P.S. Braund, B.J. Wright, A.J Balmforth, S.G. Ball, A.S. Hall; Wellcome Trust Case Control Consortium, H. Schunkert, J. Erdmann, P. Linsel-Nitschke, W. Lieb, A. Ziegler, I. König, C. Hengstenberg, M. Fischer, K. Stark, A. Grosshennig, M. Preuss, H.E. Wichmann, S. Schreiber, H. Schunkert, N.J. Samani, J. Erdmann, W. Ouwehand, C. Hengstenberg, P. Deloukas, M. Scholz, F. Cambien, M.P. Reilly, M. Li, Z. Chen, R. Wilensky, W. Matthai, A. Qasim, H.H. Hakonarson, J. Devaney, M.S. Burnett, A.D. Pichard, K.M. Kent, L. Satler, J.M. Lindsay, W.R. Waksman, C.W. Knouff, D.M. Waterworth, M.C. Walker, V. Mooser, S.E. Epstein, D.J. Rader, T. Scheffold, K. Berger, M. Stoll, A. Huge, D. Girelli, N. Martinelli, O. Olivieri, R. Corrocher, T. Morgan, J.A. Spertus, P. McKeown, C.C. Patterson, H. Schunkert, E. Erdmann, P. Linsel-Nitschke, W. Lieb, A. Ziegler, I.R. König, C. Hengstenberg, M. Fischer, K. Stark, A. Grosshennig, M. Preuss, H.E. Wichmann, S. Schreiber, H. Hólm, G. Thorleifsson, U. Thorsteinsdottir, K. Stefansson, J.C. Engert, R. Do, C. Xie, S. Anand, S. Kathiresan, D. Ardissino, P.M. Mannucci, D. Siscovick, C.J. O'Donnell, N.J. Samani, O. Melander, R. Elosua, L. Peltonen, V. Salomaa, S.M. Schwartz, D. Altshuler
Combined factor V and factor VIII deficiency
2009 M. Spreafico, F. Peyvandi
Women with rare bleeding disorders
2008 F. Peyvandi, M. Spreafico, S.M. Siboni, C. Mistretta, L. Calò, E. Biguzzi, F.R. Rosendaal, A.H. James, R. Kadir, C. Lee, M. El Ekiaby, P. Kouides, G. Castaman, M. Lak, M. Karimi, S. Halimeh, D. Mikovic
Establishment of a European network of Rare Bleeding Disorders (RBDs)
2008 F. Peyvandi, M. Spreafico, M. Menegatti, R. Palla, A. Rocino, A. Iorio, P.M. Mannucci
Recurrent mutations identified on LMAN1 and coagulation factors VII, X, XIII genes
2008 A. Cairo, M. Spreafico, M. Menegatti, I.M. Garagiola, F. Peyvandi
Comparison of assays to evaluate ADAMTS13 activity in patients’ plasma
2008 R. Palla, M. Spreafico, C. Valsecchi, L. Beretta, P.M. Mannucci, F. Peyvandi
National and international registries of rare bleeding disorders
2008 F. Peyvandi, M. Spreafico
State of the art of rare bleeding disorders database (RBDD)
2008 M. Spreafico, M. Menegatti, R. Palla, I. Garagiola, L. Tagliabue, A. Cairo, S. Lavoretano, R. Asselta, S. Duga, P.M. Mannucci, F. Peyvandi
Effects of CYP2C9 and VKORC1 on INR variations and dose requirements during initial phase of anticoagulant therapy
2008 M. Spreafico, C. Lodigiani, Y. van Leeuven, D. Pizzotti, L.L. Rota, F. Rosendaal, P.M. Mannucci, F. Peyvandi
Rare bleeding disorders
2008 F. Peyvandi, M. Cattaneo, A. Inbal, P. De Moerloose, M. Spreafico
Dosing anticoagulant therapy with coumarin drugs : is genotyping clinically useful? No
2008 P.M. Mannucci, M. Spreafico, F. Peyvandi