Analysis of von Willebrand Disease in the “Heart of Europe”

Background  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 making diagnosis difficult. Objectives  Complete laboratory analysis of VWD as an e...

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Detalles Bibliográficos
Autores principales: Vangenechten, Inge, Smejkal, Petr, Zavrelova, Jiri, Zapletal, Ondrej, Wild, Alexander, Michiels, Jan Jacques, Berneman, Zwi, Blatny, Jan, Batorova, Angelika, Prigancova, Tatiana, Penka, Miroslav, Gadisseur, Alain
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Georg Thieme Verlag KG 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9581583/
https://www.ncbi.nlm.nih.gov/pubmed/36299619
http://dx.doi.org/10.1055/s-0042-1757635

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9581583/
https://www.ncbi.nlm.nih.gov/pubmed/36299619
http://dx.doi.org/10.1055/s-0042-1757635

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