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Low VWF: insights into pathogenesis, diagnosis, and clinical management

von Willebrand disease (VWD) constitutes the most common inherited human bleeding disorder. Partial quantitative von Willebrand factor (VWF) deficiency is responsible for the majority of VWD cases. International guidelines recommend that patients with mild to moderate reductions in plasma VWF antige...

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Bibliografiska uppgifter
I publikationen:Blood Adv
Huvudupphovsman: O’Donnell, James S.
Materialtyp: Artigo
Språk:Inglês
Publicerad: American Society of Hematology 2020
Ämnen:
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC7362371/
https://ncbi.nlm.nih.gov/pubmed/32663299
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/bloodadvances.2020002038
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