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Thromb Haemost 2011; 105(05): 921-924
DOI: 10.1160/TH10-08-0517
Letters to the Editor
Schattauer GmbH

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

Silvia Giannini
1   Division of Internal and Cardiovascular Medicine, Department of Internal Medicine, University of Perugia, Perugia, Italy
,
Maria Solimando
2   Angelo Bianchi Bonomi Hemophilia and Thrombosis Center, Department of Internal Medicine and Medical Specialties, IRCCS Maggiore Hospital and University of Milan, Milan, Italy
,
Tiziana Fierro
1   Division of Internal and Cardiovascular Medicine, Department of Internal Medicine, University of Perugia, Perugia, Italy
,
Luciano Baronciani
2   Angelo Bianchi Bonomi Hemophilia and Thrombosis Center, Department of Internal Medicine and Medical Specialties, IRCCS Maggiore Hospital and University of Milan, Milan, Italy
,
Augusto B. Federici
2   Angelo Bianchi Bonomi Hemophilia and Thrombosis Center, Department of Internal Medicine and Medical Specialties, IRCCS Maggiore Hospital and University of Milan, Milan, Italy
3   Division of Hematology and Transfusion Medicine, L. Sacco University Hospital, Milan, Italy
,
Paolo Gresele
1   Division of Internal and Cardiovascular Medicine, Department of Internal Medicine, University of Perugia, Perugia, Italy
› Author Affiliations
Further Information

Publication History

Received: 10 August 2011

Accepted after major revision: 13 January 2011

Publication Date:
28 November 2017 (online)

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