Acquired von Willebrand syndrome type 2A in a JAK2-positive essential thrombocythaemia -affected member of a large von Willebrand disease family with a novel autosomal dominant A1716P mutation - Giannini, Silvia; Solimando, Maria; Fierro, Tiziana; Baronciani, Luciano; Federici, Augusto B.; Gresele, Paolo (Thrombosis and Haemostasis, 2011)