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.
نویسندگان
چکیده
Silvia Giannini1; Maria Solimando2; Tiziana Fierro1; Luciano Baronciani2; Augusto B. Federici2,3; Paolo Gresele1 1Division of Internal and Cardiovascular Medicine, Department of Internal Medicine, University of Perugia, Perugia, Italy; 2Angelo Bianchi Bonomi Hemophilia and Thrombosis Center, Department of Internal Medicine and Medical Specialties, IRCCS Maggiore Hospital and University of Milan, Milan, Italy; 3Division of Hematology and Transfusion Medicine, L. Sacco University Hospital, Milan, Italy
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ورودعنوان ژورنال:
- Thrombosis and haemostasis
دوره 105 5 شماره
صفحات -
تاریخ انتشار 2011