Sfoglia per Autore
Effect of adenosine derivatives on in vitro thrombus formation induced by shear stress
1999 M. Menegatti, G. Cristalli, L. Gallo, P.M. Mannucci, F.I. Pareti
Identification of four novel polymorphisms in the Aα and γ fibrinogen genes and analysis of association with plasma levels of the protein
2001 M. Menegatti, R. Asselta, S. Duga, M. Malcovati, P. Bucciarelli, P.M. Mannucci, M.L. Tenchini
Gene mutations and three-dimensional structural analysis in 13 families with severe factor X deficiency
2002 F. Peyvandi, M. Menegatti, E. Santagostino, S. Akhavan, J. Uprichard, D.J. Perry, S.J. Perkins, P.M. Mannucci
Relatively poor performance of clinical laboratories for DNA analyses in the detection of two thrombophilic mutations : a cause for concern
2002 A. Tripodi, F. Peyvandi, V. Chantarangkul, M. Menegatti, P.M. Mannucci
No evidence of association between prothrombotic gene polymorphisms and the development of acute myocardial infarction at a young age
2003 P.M. Mannucci, P.A. Merlini, D. Ardissino, C. Barzuini, F. Bernardi, L. Bernardinelli, C. Cavallini, P. Celli, G. Corsini, M. Ferrario, R. Fetiveau, M. Galli, F. Peyvandi, A. Piazza, F. Ribichini, E. Sacchi, M. Tubaro, P. Zonzin, L. Foco, L. Tagliabue, M. Menegatti, A. Repetto, U. Canosi, V. Cucci, S. Buratti, M. Galli, M. Ferrario, M. Ponzetta, M. Rinuncini, M. Spolverato, A. Vetrano, M. Lamponi, L. Cacciavillani, G. Russo, C. Castelli, A. Colizzi, N. Pagnoni, E. Colombi, D. Covini, G. Fantini, C. Dodi, P. Paoloni, I. Maoddi, G. Bardelli, M. Azzarito, M. Beciani, F. Tettamanti, M.E. Caccia, P. Massoli, R. Pozzi, F. Pecchio, P. Barberis, M. Giudice, R. Di Giovanbattista, B. Mazzocco, G. Gaeta, M. Margaglione, P. Diotallevi, A. Salvioni, S. Biancoli, A. Rosi, E. Milanesi, S. Span, A.C. Maugeri Saccà, D. Scorzoni, M. Maffi, G.A. Dei Tos, P.P. Cannarozzo, R. Vandelli, M. Fici, A. Tempesta, G. Ricci Lucchi, D. Baragli, D. Laiso, L. Garzaro, R. Vaninetti, G. Cattadori, A. Picozzi, R. Petacchi, C. Berardi, V. Guiducci, O. Gaddi, N. Franco, E. Buia, F. Fedeli, F. Barillà, L. Irace, S. Sarracino, N. De Giorgio, G. Scalera, M. Elia, P. Sabella, A. Previtera, G. Di Tano, B. Francaviglia, G. Contini, F. Del Nevo, N. Gandolfo, P. Agricola, V. Cutaia, G. Susco, P. Musso, G. Falsini, S. Baldassarre, S. Meloni, G. Piccinni, C. Tolardo, S. Morelloni, L. Sartorelli, M. Ragazzo, E. Violi, G. Zobbi, M. Milli, C. Luciani, N. Cosentino, S. Gubelli, M. Traina, R. Glenzer, M. Negrini, F. Alitto, M. Pretolani, S. Amidei, G. Molle, L. Giamundo, M. Manetta, G. Milanese, R. Martignano, F. Fusco, M. Bielli, P. Zanini, C. Pasotti, B. Scardovi, S. Calcagno, A. Rossi, F.D. Tucci, L. Massironi, S. Lucreziotti, B.M. Fadin, D. Carbone, S. Bongioanni, C. Nicastro, L. Rusconi, L. Caravita, R. Scioli
Phenotype-genotype characterization of 10 families with severe a subunit factor XIII deficiency
2004 F. Peyvandi, L. Tagliabue, M. Menegatti, M. Karimi, I. Komáromi, E. Katona, L. Muszbek, P.M. Mannucci
A rare inherited coagulation disorder : combined homozygous factor VII and factor X deficiency
2004 M. Menegatti, M. Karimi, I.M. Garagiola, P.M. Mannucci, F. Peyvandi
Genotype analysis of rare coagulation factor deficiency cases from India
2004 D. Mohanty, K. Goshi, S. Shetty, M. Menegatti, S. Duga, F. Peyvandi, P.M. Mannucci
International Registry of rare bleeding disorders (RBD)
2004 F. Peyvandi, M. Spreafico, M. Menegatti, I.M. Garagiola, L. Tagliabue, P.M. Mannucci
Molecular evaluation of a naturally occuring mutation on Factor X gene (Gly222Asp) causing severe FX deficiency
2004 F. Peyvandi, M. Menegatti, K. Kavakli, M. Karimi, P.M. Mannucci
Molecular characterization in an Italian patient with plasminogen deficiency and ligneous conjunctivitis
2005 S.M. Siboni, M. Spreafico, M. Menegatti, I. Martinelli, F. Peyvandi
In vitro expression studies and immunofluorescence microscopy analysis of two naturally occuring mutations on Factor X (FX) gene (G94R and D95E)
2005 M. Menegatti, M. Karimi, P.M. Mannucci, F. Peyvandi
Italian experience in the assessment of performance of clinical laboratories for DNA analyses to detect three thrombophilic mutations
2005 V. Chantarangkul, M. Menegatti, L. Tagliabue, F. Peyvandi, A. Tripodi
In Vitro Expression Studies And Immunofluorescence Microscopy Analysis Of Two Naturally Occurring Mutations On Factor X (FX) Gene (G94R And D95E)
2005 M. Menegatti, M. Karimi, P.M. Mannucci, F. Peyvandi
International Rare Bleeding Disorders Database
2005 F. Peyvandi, R. Palla, M. Menegatti, I. Garagiola, S.M. Siboni, P.M. Mannucci, M. Spreafico, L. Tagliabue, S. Lavoretano, A. Cairo
Performance of clinical laboratories for DNA analyses to detect thrombophilia mutations
2005 A. Tripodi, V. Chantarangkul, M. Menegatti, L. Tagliabue, F. Peyvandi
Molecular characterization in an Italian patient with plasminogen deficiency and ligneous conjunctivitis
2005 S.M. Siboni, M. Spreafico, M. Menegatti, I. Martinelli, F. Peyvandi
Future perspective of international registry on rare inherited bleeding disorder
2006 F. Peyvandi, M. Spreafico, M. Menegatti, R. Palla, S.M. Siboni, P.M. Mannucci
Rare bleeding disorders
2006 F. Peyvandi, R.J. Kaufman, U. Seligsohn, O. Salomon, P.H. Bolton-Maggs, M. Spreafico, M. Menegatti, R. Palla, S. Siboni, P.M. Mannucci
Genetics of rare bleeding disorders
2006 F. Peyvandi, I.M. Garagiola, S. Lavoretano, M. Menegatti, R. Palla, M. Spreafico, L. Tagliabue, S. Duga, P.M. Mannucci
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