Sfoglia per Rivista
Central nervous system bleeding in patients with rare bleeding disorders
2012 S. M. Siboni, E. Zanon, G. Sottilotta, D. Consonni, G. Castaman, D. Mikovic, F. Biondo, A. Tagliaferri, A. Iorio, P. M. Mannucci, F. Peyvandi
Changes in factor XIII level during pregnancy
2014 L.T. Sharief, A.S. Lawrie, I.J. Mackie, C. Smith, F. Peyvandi, R.A. Kadir
Characterization of the genetic basis of FXI deficiency in two Turkish patients
2010 E. Berber, V. Rimoldi, S. Usluer, S. Aksu, Y. Pekçelen, S.H. Çağlayan, S. Duga
Choices of factor VIII products in previously untreated patients with haemophilia A: A global survey
2018 F. Payvandi, R. Palla, C. Franchi, A. Nobili, F.R. Rosendaal, P.M. Mannucci
Clinical advances in gene therapy updates on clinical trials of gene therapy in haemophilia
2019 F. Peyvandi, I. Garagiola
Clinical diagnosis of von Willebrand disease
2004 A. Federici
Clinical efficacy of highly purified, doubly virus-inactivated factor VIII/von Willebrand factor concentrate (Fanhdi) in the treatment of von Willebrand disease: a retrospective clinical study.
2002 A. Federici, F. Baudo, C. Caracciolo, G. Mancuso, M. Mazzucconi, R. Musso, P. Schinco, R. Targhetta, P. Mannuccio Mannucci
Clinical manifestations in 28 Italian and Iranian patients with severe factor VII deficiency
1997 F. Peyvandi, P.M. Mannucci, D. Asti, M. Abdoullahi, N. Di Rocco, R. Sharifian
Clinical outcomes and resource utilization associated with haemophilia care in Europe
2002 W. Schramm, S. Royal, B. Kroner, E. Berntorp, P. Giangrande, C. Ludlam, A. Gringeri, K. Berger, T. Szucs, T. European Hemophilia Economic Study Group
Clinical trials and haemophilia : does the Bayesian approach make the ideal and desirable good friends?
2009 A. Iorio, M. Marcucci
Combined FV and FVIII deficiency
2008 M. Spreafico, F. Peyvandi
A comparative evaluation of a new automated assay for von Willebrand factor activity
2013 A.S. Lawrie, F. Stufano, M.T. Canciani, I.J. Mackie, S.J. Machin, F. Peyvandi
A comparative evaluation of a new fully automated assay for von Willebrand factor collagen binding activity to an established method
2018 F. Stufano, L. Baronciani, D. Mane-Padros, G. Cozzi, S. Faraudo, F. Peyvandi
A comparison between two semi-quantitative bleeding scales for the diagnosis and assessment of bleeding severity in type 1 von Willebrand disease
2011 A. Tosetto, F. Rodeghiero, G. Castaman, A. Goodeve, A.B. Federici, J. Batlle, D. Meyer, J. Goudemand, J. Eikenboom, R. Schneppenheim, U. Budde, J. Ingerslev, S. Lethagen, F. G. Hill, I. Peake
Comparison of attitudes towards prenatal diagnosis and termination of pregnancy for haemophilia in Iran and Italy
2004 M. Karimi, F. Peyvandi, S.M. Siboni, R. Ardeshiri, A. Gringeri, P.M. Mannucci
Congenital factor XIII deficiency in Pakistan : characterization of seven families and identification of four novel mutations
2014 M. Borhany, H. Handrkova, A. Cairo, V. Schroeder, N. Fatima, A. Naz, S. Amanat, T. Shamsi, F. Peyvandi, H.P. Kohler
Congenital hypofibrinogenemia associated with novel heterozygous fibrinogen Bbeta and gamma chain mutations
2008 G. Castaman, S.H. Giacomelli, S. Duga, F. Rodeghiero
Congenital platelet disorders : overview of their mechanisms, diagnostic evaluation and treatment
2006 C.P.M. Hayward, A.K. Rao, M. Cattaneo
Consensus perspectives on prophylactic therapy for haemophilia : summary statement
2003 E. Berntorp, J. Astermark, S. Björkman, V. S. Blanchette, K. Fischer, P. L. F. Giangrande, A. Gringeri, R. C. Ljung, M. J. Manco-Johnson, M. Morfini, R. F. Kilcoyne, P. Petrini, E. C. Rodriguez-Merchan, W. Schramm, A. Shapiro, H. M. van Den Berg, C. Hart
Consensus perspectives on surgery in haemophilia patients with inhibitors: summary statement
2004 E.C. Rodriguez Merchan, A. Rocino, B. Ewenstein, L. Bartha, A. Batorova, J. Goudemand, A. Gringeri, M. Joao Diniz, S. Lopaciuk, C. Negrier, M. Quintana, G. Tagariello, G.E. Tjonnfjord, V.A. Villar, Z. Vorlova
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