Sfoglia per Rivista HAEMOPHILIA
Laboratory issues in bleeding disorders
2006 D. Lillicrap, S.C. Nair, A. Srivastava, F. Rodeghiero, I. Pabinger, A.B. Federici
Long-term prophylaxis in severe factor VII deficiency
2015 S.M. Siboni, E. Biguzzi, C. Mistretta, I. Garagiola, F. Peyvandi
Low thrombin generation during major orthopaedic surgery fails to predict the bleeding risk in inhibitor patients treated with bypassing agents
2016 M.E. Mancuso, V. Chantarangkul, M. Clerici, M.R. Fasulo, L. Padovan, E. Scalambrino, F. Peyvandi, A. Tripodi, E. Santagostino
Low-rate of complications after a long-term use of ateriovenous fistula (AVF) in hemophilic children
2008 E. Santagostino, M.E. Mancuso, A. Gringeri, S.M. Siboni, P.M. Mannucci
Management of bleeding disorders in adults
2012 F. Peyvandi, R. Klamoroth, M. Carcao, A.B. Federici, G. Di Minno, V. Jimenez-Yuste, E.C. Rodriguez Merchan
Management of orthopaedic surgery in rare bleeding disorders
2014 S.M. Siboni, E. Biguzzi, G. Pasta, P.M. Mannucci, C. Mistretta, N.N. Fantini, L.P. Solimeno, F. Peyvandi
Management of pregnancy in type 2B von Willebrand disease: case report and literature review
2015 E. Biguzzi, S.M. Siboni, M.W. Ossola, B. Zaina, A.C. Migliorini, F. Peyvandi
Minimal residual FXIII coagulant activity to prevent spontaneous major bleeding, on behalf of the PRO-RBDD group
2016 F. Peyvandi, R. Palla, M. Menegatti, P. Bucciarelli, M. Boscarino, L. Muszbek
Molecular diagnosis of von Willebrand disease
2017 L. Baronciani, A. Goodeve, F. Peyvandi
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 investigation of 41 patients affected by coagulation factor XI deficiency
2018 V. Rimoldi, E.M. Paraboschi, M. Menegatti, F. Peyvandi, O. Salomon, S. Duga, R. Asselta
Mortality and causes of death in Italian persons with haemophilia, 1990-2007
2010 A. Tagliaferri, G.F. Rivolta, A. Iorio, E. Oliovecchio, M.E. Mancuso, M. Morfini, A. Rocino, M.G. Mazzucconi, M. Franchini, N. Ciavarella, A. Scaraggi, L. Valdrè, G. Tagariello, P. Radossi, G. Muleo, P.G. Iannaccaro, C. Biasoli, D. Vincenzi, M.L. Serino, S. Linari, C. Molinari, E. Boeri, M. La Pecorella, M.T. Carloni, E. Santagostino, G. Di Minno, A. Coppola, A. Rocino, E. Zanon, L. Spiezia, C. Di Perna, M. Marchesini, M. Marcucci, A. Dragani, S. Macchi, P. Albertini, M. D'Incà, C. Santoro, F. Biondo, G. Piseddu, G. Rossetti, G. Barillari, G. Gandini, A.C. Giuffrida, G. Castaman
Mutations in the MCFD2 gene are predominant among patients with hereditary combined FV and FVIII deficiency (F5F8D) in India
2007 G. Jayandharan, M. Spreafico, A. Viswabandya, M. Chandy, A. Srivastava, F. Peyvandi
The natural history of occult or angiodysplastic gastrointestinal bleeding in von Willebrand disease
2015 M. Makris, A.B. Federici, P. Mannucci, P. Bolton Maggs, T. Yee, T. Abshire, E. Berntorp
New approaches for measuring coagulation
2006 T. W. Barrowcliffe, M. Cattaneo, G. M. Podda, P. Bucciarelli, F. Lussana, A. Lecchi, C. H. Toh, H. C. Hemker, S. Beguin, J. Ingerslev, B. Soerensen
New findings on inhibitor development: from registries to clinical studies
2017 F. Peyvandi, C.E. Ettingshausen, J. Goudemand, V. Jiménez-Yuste, E. Santagostino, M. Makris
Non-genetic risk factors and the development of inhibitors in haemophilia : a comprehensive review and consensus report
2010 J. Astermark, C. Altisen, A. Batorova, M. J. Diniz, A. Gringeri, P. A. Holme, A. Karafoulidou, M. F. Lopez-Fernández, B. M. Reipert, A. Rocino, M. Schiavoni, M. von Depka, J. Windyga, K. Fijnvandraat
Non-invasive tool for foetal sex determination in early gestational age
2011 M. Mortarino, I.M. Garagiola, L.A. Lotta, S.M. Siboni, A.E. Semprini, F. Peyvandi
Occurrence of inhibitors in previously untreated or minimally treated patients with haemophilia A after exposure to a plasma-derived solvent-detergent factor VIII concentrate
2006 A. Gringeri, M. Monzini, G. Tagariello, F.A. Scaraggi, P.M. Mannucci, C. Biasoli, G. Delios, A. Iorio, G. Mancuso, R. Musso, M. Perja, L. Perugini, A. Borchiellini, R. Santi, F.A. Scaraggi, M. Schiavoni, A. Spigariol, R. Targhetta, E. Zanon
Orthopaedic surgery in patients with von Willebrand disease
2013 S.M. Siboni, E. Biguzzi, L.P. Solimeno, G. Pasta, C. Mistretta, P.M. Mannucci, F. Peyvandi
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