Sfoglia per Rivista
A systematic approach to controlling problem bleeds in patients with severe congenital haemophilia A and high-titre inhibitors
2007 J. Teitel, E. Berntorp, P. Collins, R. D'Oiron, B. Ewenstein, E. Gomperts, J. Goudemand, A. Gringeri, N. Key, C. Leissinger, P. Monahan, G. Young
Acquired Von Willebrand syndrome and response to desmopressin
2018 E. Biguzzi, S.M. Siboni, F. Peyvandi
Addressing current challenges in haemophilia care: consensus recommendations of a European Interdisciplinary Working Group
2005 C.A. Ludlam, P.M. Mannucci, W.G. Powderly
Adoption of emicizumab (Hemlibra®) for hemophilia A in Europe: Data from the 2020 European Association for Haemophilia and Allied Disorders survey
2021 E. Krumb, K. Fijnvandraat, M. Makris, F. Peyvandi, A. Ryan, A. Athanasopoulos, C. Hermans
Ageing successfully with haemophilia : A multidisciplinary programme
2018 E. Boccalandro, M.E. Mancuso, S. Riva, D.M. Pisaniello, F. Ronchetti, E. Santagostino, F. Peyvandi, L.P. Solimeno, P.M. Mannucci, G. Pasta
Arteriovenous fistula as stable venous access in children with severe haemophilia
2010 M.E. Mancuso, L. Berardinelli
Assaying FVIII activity : one method is not enough, and never was
2014 M. Makris, F. Peyvandi
Assessing joint health in haemophilia patients: The combined value of physical examination and ultrasound imaging
2024 R. Gualtierotti, A. Giachi, A. Truma, S. Arcudi, A. Ciavarella, P. Bucciarelli, D. Consonni, E. Boccalandro, V. Begnozzi, L.P. Solimeno, S.M. Siboni, F. Peyvandi
Back to the future : a recent history of haemophilia treatment
2008 P.M. Mannucci
Baseline factor VIII plasma levels and age at first bleeding in patients with severe forms of von Willebrand disease
2016 S.M. Siboni, E. Biguzzi, V. Caiani, C. Mistretta, P. Bucciarelli, F. Peyvandi
Burden of mild haemophilia A: Systematic literature review
2019 F. Peyvandi, F. Tavakkoli, D. Frame, J. Quinn, B. Kim, A. Lawal, M.C. Lee, W.Y. Wong
Bypassing agent regimens and costs for prophylaxis in patients with inhibitors
2009 A. Gringeri
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
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