Sfoglia per Rivista HAEMOPHILIA
Factor VIII products and inhibitor development : the SIPPET study (survey of inhibitors in plasma-product exposed toddlers)
2007 P.M. Mannucci, A. Gringeri, F. Peyvandi, E. Santagostino
Factors influencing illness representations and perceived adherence in haemophilic patients : a pilot study
2015 G. Lamiani, I. Strada, M.E. Mancuso, A. Coppola, E. Vegni, E.A. Moja
Fifth Åland Island conference on von Willebrand disease
2018 E. Berntorp, A. Agren, L. Aledort, M. Blomback, M.H. Cnossen, S.E. Croteau, M. von Depka, A.B. Federici, A. Goodeve, J. Goudemand, P.M. Mannucci, M. Mourik, P.T. Onundarson, F. Rodeghiero, T. Szanto, J. Windyga
First-year results of an expanded humanitarian aid programme for haemophilia in resource-constrained countries
2018 G.F. Pierce, A. Haffar, G. Ampartzidis, F. Payvandi, S. Diop, M. El-Ekiaby, H.M. van den Berg
Functional characterization of a novel missense mutation identified in a Turkish patient affected by severe coagulation factor V deficiency
2012 E.M. Paraboschi, S.M. Kayiran, N. Ozbek, B. Gürakan, F. Peyvandi, I. Guella, S. Duga, R. Asselta
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
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
FVIII inhibitor development according to concentrate : data from the EUHASS registry excluding overlap with other studies
2016 K. Fischer, A. Iorio, R. Hollingsworth, M. Makris, H. Watson, J. Rae, H. Platokouki, H. Pergantou, O. Katsarou, G. Theodossiades, F. Nomikou, R. Parra, S. Alonso, R. Klamroth, C. Kubicek, J. Wilde, T. Dunkley, J. Oldenburg, D. Schmickler, S. Ackroyd, L. Mirza, A. Batorova, D. Jankovicova, G. Auerswald, M. Buehrlen, M. Penka, P. Smejkal, J. Blatny, O. Zapletal, C. Hermans, C. Lambert, G. Tagariello, P. Radossi, B. Nolan, B. Brady, J. O'Donnell, F. Singleton, A. Thomas, I. Shea, M. Morfini, S. Linari, P. de Moerloose, F. Boehlen, R. Campbell Tait, N. Brodie, F. Chalmers, A. Gibson, K. Meijer, R. Tamminga, R. Lassila, E. Armstrong, B. Zulfikar, N. Ozdemir, K. Kavakli, C. Balkan, R. Jurgutis, N. Gailiute, K. Peerlinck, C.V. Geet, J. Goudemand, B. Wibaut, M.J. Diniz, M. Antunes, R. Liesner, K. Khair, M. Laffan, S. Patel, T. Thynn Yee, C. Harrington, J. Pasi, L. Bowles, D. Bevan, B. Madan, C. Negrier, S. Ringenbach, M.E. Mingot Castellano, J. Astermark, K. Lindvall, A. Gatt, C.R.M. Hay, P. Grey, A. Will, A. Hague, F. Peyvandi, M.E. Mancuso, J.F. Schved, F. Rousseau, K. Kurnik, C. Bidlingmaier, A. Rocino, J. Hanley, K. Talks, M. Antoniades, E. Zanon, E.D. Bon, T. Lambert, C. Rothschild, M. Matingou, A. Tagliaferri, G.F. Rivolta, A. Iorio, E. Marchesini, C. Fraga, L. Cunha Ribeiro, M. Carvalho, V. Komrska, E. Pindurova, S. Lejniece, G. Kluce, F. Leebeek, M. Cnossen, M. Makris, C. Lockley, J. Payne, V. Vidler, T. Lissitchkov, P. Raia, M. Holmstre om, V. Garipidou, S. Vakalopoulou, M. Serban, M.D. Mihailov, P. Schinco, F. Valeri, R. Schutgens, S. Bonanad, A.R. Cid, G. Castaman, I. Pabinger, S.E. Reitter, C. Male, K. Thom, J. Windyga, M. Piorowski, M. Schmugge, M. Albisetti
Genetic aspects and research development in haemostasis
2008 E.G. Tuddenham, J. Ingerslev, L.N. Sorensen, K. Christiansen, G. Mariani, F. Peyvandi, S.N. Waddington, S.M. Buckley, S. Kochanek, M.K. Chuah, T. Vandendriessche, E. Berntorp
Genetic background and risk of postpartum haemorrhage : results from an Italian cohort of 3219 women
2014 E. Biguzzi, F. Franchi, B. Acaia, W. Ossola, U. Nava, E.M. Paraboschi, R. Asselta, F. Peyvandi
Genetic diagnosis of haemophilia and other inherited bleeding disorders
2006 F. Peyvandi, G. Jayandharan, M. Chandy, A. Srivastava, S.M. Nakaya, M.J. Johnson, A.R. Thompson, A. Goodeve, I. Garagiola, S. Lavoretano, M. Menegatti, R. Palla, M. Spreafico, L. Tagliabue, R. Asselta, S. Duga, P.M. Mannucci
Genetic variants at the chromosomal region 2q21.3 underlying inhibitor development in patients with severe haemophilia A
2022 S. Spena, A. Cairo, E. Pappalardo, M.M. Gorski, I. Garagiola, S. Hassan, R. Gualtierotti, F. Peyvandi
Genomic approaches to bleeding disorders
2016 F. Peyvandi, C.P.M. Hayward
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
Guidelines for the diagnosis and management of von Willebrand disease in Italy
2002 A.B. Federici, G. Castaman, P.M. Mannucci, Italian Association of Hemophilia Centers (AICE)
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
Haemophilia prophylaxis : how can we justify the costs?
2012 B.M. Feldman, K. Berger, R. Bohn, M. Carcao, K. Fischer, A. Gringeri, K. Hoots, L. Mantovani, A.R. Willian, W. Schramm
Health status and health-related quality of life of children with haemophilia from six West European countries
2004 A. Gringeri, S. Von Mackensen, G. Auerswald, M. Bullinger, R. Perez Garrido, E. Kellermann, K. Khair, H. Lenk, M. Vicariot, A. Villar, C. Wermes
Health status in elderly persons with haemophilia
2008 S.M. Siboni, S. von Mackensen, M. Franchini, A. Tagliaferri, A. Gringeri, P.M. Mannucci
Health-related quality of life and health status in adolescent and adult people with haemophilia A without factor VIII inhibitors : A non-interventional study
2021 J. Oldenburg, H. Tran, F. Peyvandi, R. Nunez, P. Trask, S. Chebon, J.N. Mahlangu, M. Lehle, V. Jimenez-Yuste, S. von Mackensen
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