Sfoglia per Autore
Molecular characterization of a multiethnic group of 21 patients with type 3 von Willebrand disease
2000 L. Baronciani, G. Cozzi, M.T. Canciani, F. Peyvandi, A. Srivastava, A.B. Federici
Molecular defects in type 3 von Willebrand disease: updated results from 40 multiethnic patients
2003 L. Baronciani, G. Cozzi, M.T. Canciani, F. Peyvandi, A. Srivastava, A.B. Federici, P.M. Mannucci
A new candidate mutation, G1629R, in a patient with type 2A von Willebrand's disease: basic mechanisms and clinical implications
2004 L. Hilbert, A. Federici, L. Baronciani, S. Dallagiovanna, C. Mazurier
An association of candidate gene haplotypes and bleeding severity in von Willebrand disease (VWD) type 1 pedigrees
2004 T.J. Kunicki, A.B. Federici, D.R. Salomon, J.A. Koziol, S.R. Head, T.S. Mondala, J.D. Chismar, L. Baronciani, M.T. Canciani, I.R. Peake
von Willebrand disease type 2B must be always considered in the differential diagnosis of genetic thrombocytopenias with giant platelets
2006 G. Loffredo, L. Baronciani, P. Noris, F. Menna, A.B. Federici, C.L. Balduini
An association of candidate gene haplotypes and bleeding severity in von Willebrand disease type 2A, 2B, and 2M pedigrees
2006 T.J. Kunicki, L. Baronciani, M.T. Canciani, F. Gianniello, S.R. Head, T.S. Mondala, D.R. Salomon, A.B. Federici
Molecular mapping of chloride binding site in VWF : energetics and conformational effects on the VWF/ADAMTS-13 interaction
2006 R. De Cristofaro, F. Peyvandi, L. Baronciani, R. Palla, S. Lavoretano, E. Di Stasio, A.B. Federici, P.M. Mannucci
The natural VWF mutant P.R1306W, causing a type 2B VWD, binds, chloride ions with lower affinity than WT VWD and is cleaved more efficently by ADAMTS-13
2006 R. De Cristofaro, F. Peyvandi, L. Baronciani, R. Palla, S. Lavoretano, E. Di Stasio, A.B. Federici, P.M. Mannucci
Molecular mapping of the chloride binding site in von Willebrand factor (VWF): energetics and conformational effects on the VWF/ADAMTS1-13
2006 R. De Cristofaro, F. Peyvandi, L. Baronciani, R. Palla, S. Lavoretano, R. Lombardi, E. Di Stasio, A.B. Federici, P.M. Mannucci
Molecular mapping of the chloride binding site in von Willebrand factor (VWF) : energetics and conformational effects on the ADAMTS-13 interaction with wild type and type 2B R1306W VWF forms
2006 R. De Cristofaro, F. Peyvandi, L. Baronciani, R. Palla, S. Lavoretano, R. Lombardi, E. Di Stasio, A.B. Federici, P.M. Mannucci
Biochemical characterization of a recombinant von Willebrand factor (VWF) with combined type 2B and type 1 defects in the VWF gene in two patients with a type 2A phenotype of von Willebrand disease
2007 L. Baronciani, A.B. Federici, G. Cozzi, M.T. Canciani, P.M. Mannucci
Phenotype and genotype of a cohort of families historically diagnosed with type 1 von Willebrand disease in the European study, Molecular and Clinical Markers for the Diagnosis and Management of Type 1 von Willebrand Disease (MCMDM-1VWD)
2007 A. Goodeve, J. Eikenboom, G. Castaman, F. Rodeghiero, A.B. Federici, J. Batlle, D. Meyer, C. Mazurier, J. Goudemand, R. Schneppenheim, U. Budde, J. Ingerslev, D. Habart, Z. Vorlova, L. Holmberg, S. Lethagen, J. Pasi, F. Hill, M.H. Soteh, L. Baronciani, C. Hallden, A. Guilliatt, W. Lester, I. Peake
Alterata morfologia piastrinica nei pazienti con malattia di von Willebrand tipo 2B e 3 : i dati della microscopia elettronica
2007 M. Punzo, S. La Marca, L. Baronciani, A.B. Federici, A. Nurden, P. Nurden
Mutations leading to premature termination codons in the Von Willebrand factor gene are associated with the decay of the mutant mRNAs
2008 M. Platè, S. Duga, L. Baronciani, A.B. Federici, R. Asselta
Role of von Willebrand factor in the haemostasis
2011 F. Peyvandi, I.M. Garagiola, L. Baronciani
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
The type 2B p.R1306W natural mutation of von Willebrand factor dramatically enhances the multimer sensitivity to shear stress
2013 G.L. Scaglione, S. Lancellotti, M. Papi, M. De Spirito, A. Maiorana, L. Baronciani, M.T. Pagliari, A. Arcovito, E. Di Stasio, F. Peyvandi, R. De Cristofaro
A two-step approach (Enzyme-linked immunosorbent assay and confirmation assay) to detect antibodies against von Willebrand factor in patients with Acquired von Willebrand Syndrome
2014 F. Franchi, E. Biguzzi, F. Stufano, S.M. Siboni, L. Baronciani, F. Peyvandi
Predictors of von Willebrand disease diagnosis in individuals with borderline von Willebrand factor plasma levels
2015 P. Bucciarelli, S.M. Siboni, F. Stufano, E. Biguzzi, M.T. Canciani, L. Baronciani, M.T. Pagliari, S. La Marca, C. Mistretta, F.R. Rosendaal, F. Peyvandi
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