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Von Willebrand's disease with spontaneous platelet aggregation induced by an abnormal plasma von Willebrand factor.

We have investigated and characterized the abnormalities in four unrelated patients with von Willebrand's disease (vWd) who have (a) enhanced ristocetin-induced platelet aggregation (RIPA) at low ristocetin concentrations, (b) absence of the largest plasma von Willebrand factor (vWf) multimers, and...

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Bibliografiske detaljer
Udgivet i:J Clin Invest
Principais autores: Grainick, H R, Williams, S B, McKeown, L P, Rick, M E, Maisonneuve, P, Jenneau, C, Sultan, Y
Format: Artigo
Sprog:Inglês
Udgivet: American Society for Clinical Investigation 1985
Fag:
Online adgang:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC424119/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/2932469/
https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI112132
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