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Consulte los últimos artículos sobre la enfermedad de von Willebrand

Última actualización: Viernes, 25 de noviembre de 2022

Ristocetin dependent cofactor activity in von Willebrand disease diagnosis: Limitations of relying on a single measure

Von Willebrand disease (VWD) is a common inherited bleeding disorder, however the diagnosis can be complicated by a subjective bleeding history and issues with some current von Willebrand factor (VWF)...
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Research and Practice in Thrombosis and Haemostasis, 05 October 2022
Pamela A. Christopherson BSc et al.

Analysis of von Willebrand Disease in the "Heart of Europe".

von Willebrand disease (VWD) is a genetic bleeding disorder caused by defects of von Willebrand factor (VWF), quantitative (type 1 and 3) or qualitative (type 2). The laboratory phenotyping is heterogenic...
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TH open : companion journal to thrombosis and haemostasis 2022 Oct; 6(4): e335-e346
Vangenechten Inge et al.

"I thought everybody bled like that": a patient's experience with von Willebrand disease.

As a kid, I had frequent nosebleeds and bruising. Sometimes, I’d have nosebleeds daily and need to apply pressure for 20–30 minutes. That’s what I was known for. As I got older, I’d get bruises on my legs...
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CMAJ : Canadian Medical Association journal = journal de l'Association medicale canadienne 2022 Aug; 194(33): E1137
Laupacis Andreas.

Von Willebrand Disease-Specific Aspects in Women.

Von Willebrand disease (VWD) is the most common inherited bleeding disorder, which results from a deficiency or dysfunction of von Willebrand factor (VWF). The major symptoms of patients affected by VWD include mucocutaneous and gastrointestinal bleeding, easy bruising, and prolonged provoked bleeding due to injury or surgery. Although women and men are equally likely to be affected by VWD, women continue to be disproportionately affected by the bleeding...
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Hamostaseologie 2022 Oct; 42(5): 330-336

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