SARTORELLO, FRANCESCA
SARTORELLO, FRANCESCA
A new L1446P mutation is responsible for impaired von Willebrand factor synthesis, structure, and function.
2004 Casonato, Sandra; Cattini, Mg; Soldera, C; Marcato, Stefania; Sartorello, Francesca; Pontara, Elena; Pagnan, Antonio
A novel von Willebrand factor mutation (11372S) associated with type 2B-like von Willebrand disease: An elusive phenotype and a difficult diagnosis
2007 Casonato, Sandra; Sartorello, Francesca; Pontara, Elena; Gallinaro, Lisa; Bertomoro, Antonella; Cattini, Mg; Daidone, Viviana; Szukowska, M; Pagnan, Antonio
A shorter von Willebrand factor survival in O blood group subjects explains how ABO determinants influence plasma von Willebrand factor
2008 Gallinaro, Lisa; Cattini, Mg; Sztukowska, Maryta; Padrini, Roberto; Sartorello, Francesca; Pontara, Elena; Bertomoro, Antonella; Daidone, Viviana; Pagnan, Antonio; Casonato, Sandra
Abnormalities of von Willebrand factor are also part of the prothrombotic state of Cushing's syndrome.
1999 Casonato, Sandra; Pontara, Elena; Boscaro, Marco; Sonino, Nicoletta; Sartorello, Francesca; Ferasin, S.; Girolami, Antonio
Absence of hypercoagulability after nCoV-19 vaccination: An observational pilot study
2021 Campello, Elena; Simion, Chiara; Bulato, Cristiana; Radu, Claudia M; Gavasso, Sabrina; Sartorello, Francesca; Saggiorato, Graziella; Zerbinati, Patrizia; Fadin, Mariangela; Spiezia, Luca; Simioni, Paolo
An Arg760Cys mutation in the consensus sequence of the von Willebrand factor propeptide cleavage site is responsible for a new von Willebrand disease variant.
2003 Casonato, Sandra; Sartorello, Francesca; Cattini, Mg; Pontara, Elena; Soldera, C; Bertomoro, Antonella; Girolami, Antonio
Assessing Clinically Meaningful Hypercoagulability after COVID-19 Vaccination: A Longitudinal Study
2022 Campello, Elena; Bulato, Cristiana; Simion, Chiara; Spiezia, Luca; Radu, Claudia Maria; Gavasso, Sabrina; Sartorello, Francesca; Saggiorato, Graziella; Zerbinati, Patrizia; Fadin, Mariangela; Tormene, Daniela; Simioni, Paolo
Association between ABO blood group and bleeding phenotype in patients with mild rare bleeding disorders
2018 Spiezia, Luca; Campello, Elena; Turatti, Giacomo; Simion, Chiara; Fadin, Mariangela; Gavasso, Sabrina; Saggiorato, Graziella; Sartorello, Francesca; Zerbinati, Patrizia; Simioni, Paolo
Combined exon skipping and cryptic splice activation as a new molecular mechanism for recessive type 1 von Willebrand disease.
2006 Gallinaro, Lisa; Sartorello, Francesca; Pontara, Elena; Cattini, Mg; Bertomoro, Antonella; Bartoloni, L; Pagnan, Antonio; Casonato, Sandra
Combined hemophilia A and type 2 von Willebrand's disease: defect of both factor VIII level and factor VIII binding capacity of von Willebrand factor.
2001 Casonato, Sandra; Pontara, Elena; Sartorello, Francesca; Gemmati, D; Cattini, Mg; Girolami, Antonio
Combined partial exon skipping and cryptic splice site activation as a new molecular mechanism for recessive type 1 von Willebrand disease.
2006 Gallinaro, Lisa; Sartorello, Francesca; Pontara, Elena; Cattini, Mg; Bertomoro, Antonella; Bartoloni, L; Pagnan, Antonio; Casonato, Sandra
Endocytosis of exogenous factor V by ex-vivo differentiated megakaryocytes from patients with severe parahaemophilia
2016 Radu, Claudia M.; Spiezia, Luca; Bulato, Cristiana; Gavasso, Sabrina; Campello, Elena; Sartorello, Francesca; Castoldi, Elisabetta; Simioni, Paolo
Haplotypes of Von Willebrand factor promoter predict thrombotic risk in Cushing's syndrome
2006 Daidone, Viviana; Sartorello, Francesca; Albiger, NORA MARIA ELVIRA; Mantero, Franco; Pagnan, Antonio; Casonato, Sandra; Scaroni, Carla
Higher and lower active circulating VWF levels: different facets of von Willebrand disease
2015 Casonato, Sandra; Pontara, Elena; Morpurgo, Margherita; Sartorello, Francesca; De Groot, Pg; Daidone, Viviana; De Marco, L.
Identifying carriers of type 2N von Willebrand disease: procedures and significance.
2007 Casonato, Sandra; Pontara, Elena; Sartorello, Francesca; Cattini, Mg; Perutelli, P; Bertomoro, Antonella; Gallinaro, Lisa; Pagnan, Antonio
Microsatellite (GT)(n) repeats and SNPs in the von Willebrand factor gene promoter do not influence circulating von Willebrand factor levels under normal conditions.
2009 Daidone, Viviana; Cattini, Mg; Pontara, Elena; Sartorello, Francesca; Gallinaro, Lisa; Marotti, A; Scaroni, Carla; Pagnan, Antonio; Casonato, Sandra
Multiple von Willebrand factor mutations in patients with recessive type 1 von Willebrand disease.
2007 Casonato, Sandra; Gallinaro, Lisa; Pontara, Elena; Bernardo, L; Sartorello, Francesca; Daidone, Viviana; Pagnan, Antonio
Partial F8 gene duplication (Factor VIII Padua) associated with high factor VIII levels and familial thrombophilia
2021 Simioni, Paolo; Cagnin, Stefano; Sartorello, Francesca; Sales, Gabriele; Pagani, Luca; Bulato, Cristiana; Gavasso, Sabrina; Nuzzo, Francesca; Chemello, Francesco; Radu, Claudia Maria; Tormene, Daniela; Spiezia, Luca; Hackeng, Tilman M; Campello, Elena; Castoldi, Elisabetta
Plasma and platelet von Willebrand factor abnormalities in patients with uremia: lack of correlation with uremic bleeding.
2001 Casonato, Sandra; Pontara, Elena; Vertolli, Up; Steffan, A; Durante, C; De Marco, L; Sartorello, Francesca; Girolami, Antonio
Reduced von Willebrand factor survival in type Vicenza von Willebrand disease.
2002 Casonato, Sandra; Pontara, Elena; Sartorello, Francesca; Cattini, Mg; Sartori, Mt; Padrini, Roberto; Girolami, Antonio