PAYVANDI, FLORA
PAYVANDI, FLORA
Dipartimento di Fisiopatologia Medico-Chirurgica e dei Trapianti
A case of ceftazidime-related myoclonus
2020 E. Pagliaro, P. Agosti, E.R. Bregani, 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 critical appraisal of one-stage and chromogenic assays of factor VIII activity
2016 F. Peyvandi, J. Oldenburg, K.D. Friedman
A critical role for Gly25 in the B chain of human thrombin
2005 S. Akhavan, M.A. Miteva, B.O. Villoutreix, L. Venisse, F. Peyvandi, P.M. Mannucci, M.C. Guillin, A. Bezeaud
A fatal case of COVID-19 pneumonia occurring in a patient with severe acute ulcerative colitis
2020 S. Mazza, A. Sorce, F. Peyvandi, M. Vecchi, F. Caprioli
A homozygous duplication of the FGG exon 8-intron 8 junction causes congenital afibrinogenemia. Lessons learned from the study of a large consanguineous Turkish family
2021 M. Guipponi, F. Masclaux, F. Sloan-Béna, C. Di Sanza, N. Özbek, F. Peyvandi, M. Menegatti, A. Casini, B. Malbora, M. Neerman-Arbez
A homozygous is bp insertion in the human factor vu gene results in modification of a calcium binding site and reduced secretion/function
2000 F. Peyvandi
A natural prothrombin mutant reveals an unexpected influence of the A-chain's structure on the activity of human α-thrombin
2004 R. De Cristofaro, S. Akhavan, C. Altomare, A. Carotti, F. Peyvandi, P.M. Mannucci
A new hemophilia carrier nomenclature to define hemophilia in women and girls: Communication from the SSC of the ISTH
2021 K.P.M. van Galen, R. D'Oiron, P. James, R. Abdul-Kadir, P.A. Kouides, R. Kulkarni, J.N. Mahlangu, M. Othman, F. Peyvandi, D. Rotellini, R. Winikoff, R.F. Sidonio
A novel CD46 mutation in a patient with microangiopathy clinically resembling thrombotic thrombocytopenic purpura and normal ADAMTS13 activity
2015 R. Rossio, L.A. Lotta, S. Pontiggia, N. Borsa Ghiringhelli, I. Garagiola, G. Ardissino, D. Mikovic, M. Cugno, F. Peyvandi
A novel mutation of alpha2-plasmin inhibitor gene causes an inherited deficiency and a bleeding tendency
2008 A. Maino, I. Garagiola, A. Artoni, S. Al-Humood, F. Peyvandi
A novel polymorphism in intron 1a of the human factor VII gene (G73A): study of a healthy Italian population and of 190 young survivors of myocardial infarction
2000 F. Peyvandi, P.M. Mannucci, P. Bucciarelli, S. Zeinali, S. Akhavan, E. Sacchi, P.A. Merlini, D.J. Perry
A Randomized Trial of Factor VIII and Neutralizing Antibodies in Hemophilia A
2016 F. Peyvandi, P.M. Mannucci, I. Garagiola, A. El Beshlawy, M. Elalfy, V. Ramanan, P. Eshghi, S. Hanagavadi, R. Varadarajan, M. Karimi, M.V. Manglani, C. Ross, G. Young, T. Seth, S. Apte, D.M. Nayak, E. Santagostino, M.E. Mancuso, A.C. Sandoval Gonzalez, J.N. Mahlangu, S. Bonanad Boix, M. Cerqueira, N.P. Ewing, C. Male, T. Owaidah, V. Soto Arellano, N.L. Kobrinsky, S. Majumdar, R. Perez Garrido, A. Sachdeva, M. Simpson, M. Thomas, E. Zanon, B. Antmen, K. Kavakli, M.J. Manco Johnson, M. Martinez, E. Marzouka, M.G. Mazzucconi, D. Neme, A. Palomo Bravo, R. Paredes Aguilera, A. Prezotti, K. Schmitt, B.M. Wicklund, B. Zulfikar, F.R. Rosendaal
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
A recurrent F8 mutation (c.6046C>T) causing hemophilia A in 8% of northern Italian patients : evidence for a founder effect
2016 I. Garagiola, S. Seregni, M. Mortarino, M.E. Mancuso, M.R. Fasulo, L.D. Notarangelo, F. Peyvandi
A recurrent Gly43Asp substitution in coagulation Factor X rigidifies its catalytic pocket and impairs catalytic activity and intracellular trafficking
2014 M. Menegatti, A. Vangone, R. Palla, G. Milano, L. Cavallo, R. Oliva, R. De Cristofaro, F. Peyvandi
A recurrent Gly43Asp substitution of coagulation Factor X rigidifies its catalytic pocket and impairs catalytic activity and intracellular trafficking
2013 M. Menegatti, R. De Cristofaro, A. Vangone, R. Palla, G. Milano, L. Cavallo, R. Oliva, F. Peyvandi
A synonymous (c.3390C>T) or a splice-site (c.3380-2A>G) mutation causes exon 26 skipping in four patients with von Willebrand disease (2A/IIE)
2013 M.T. Pagliari, L. Baronciani, I. Garcìa Oya, M. Solimando, S. La Marca, G. Cozzi, F. Stufano, M.T. Canciani, F. Peyvandi
A two-centre comparative evaluation of new automated assays for von Willebrand factor ristocetin cofactor activity and antigen
2013 F. Stufano, A.S. Lawrie, S. La Marca, P.E.C. Berbenni, L. Baronciani, F. Peyvandi