A shorter von Willebrand factor survival in O blood group subjects explains how ABO determinants influence plasma von Willebrand factorGALLINARO, Lisa; GRAZIA CATTINI, Maria; SZTUKOWSKA, Maryta et al.Blood. 2008, Vol 111, Num 7, pp 3540-3545, issn 0006-4971, 6 p.Article

Combined partial exon skipping and cryptic splice site activation as a new molecular mechanism for recessive type I von Willebrand diseaseGALLINARO, Lisa; SARTORELLO, Francesca; PONTARA, Elena et al.Thrombosis and haemostasis. 2006, Vol 96, Num 6, pp 711-716, issn 0340-6245, 6 p.Article

An Arg760Cys mutation in the consensus sequence of the von Willebrand factor propeptide cleavage site is responsible for a new von Willebrand disease variantCASONATO, Alessandra; SARTORELLO, Francesca; CATTINI, Maria Grazia et al.Blood. 2003, Vol 101, Num 1, pp 151-156, issn 0006-4971, 6 p.Article

An apparently silent nucleotide substitution (c.7056C>T) in the von Willebrand factor gene is responsible for type 1 von Willebrand diseaseDAIDONE, Viviana; GALLINARO, Lisa; GRAZIA CATTINI, Maria et al.Haematologica (Roma). 2011, Vol 96, Num 6, pp 881-887, issn 0390-6078, 7 p.Article

A novel von Willebrand factor mutation (11372S) associated with type 2B-like von Willebrand disease : An elusive phenotype and a difficult diagnosisCASONATO, Alessandra; SARTORELLO, Francesca; PONTARA, Elena et al.Thrombosis and haemostasis. 2007, Vol 98, Num 6, pp 1182-1187, issn 0340-6245, 6 p.Article