Search Results - "Jakab, David A."

  • Showing 1 - 2 results of 2
Refine Results
  1. 1

    Intersection of mechanisms of type 2A VWD through defects in VWF multimerization, secretion, ADAMTS-13 susceptibility, and regulated storage by Jacobi, Paula M., Gill, Joan Cox, Flood, Veronica H., Jakab, David A., Friedman, Kenneth D., Haberichter, Sandra L.

    Published in Blood (10-05-2012)
    “…Type 2A VWD is characterized by the absence of large VWF multimers and decreased platelet-binding function. Historically, type 2A variants are subdivided into…”
    Get full text
    Journal Article
  2. 2

    Upstream Mechanisms Causing Type 1C Von Willebrand Disease (VWD): Contribution Of Defective Von Willebrand Factor (VWF) Multimerization, Regulated Storage, and Secretion by Haberichter, Sandra L., Jakab, David A, Jacobi, Paula M.

    Published in Blood (15-11-2013)
    “…One mechanism causing type 1 VWD is the reduced survival of VWF in plasma (type 1C VWD), characterized by markedly decreased VWF:Ag and VWF half-life,…”
    Get full text
    Journal Article