Von Willebrand disease (VWD) is the most common inherithed bleeding disorder and it is caused by a deficiencies of von Willebrand factor (VWF), which is a glycoprotein fundamental in the coagulation process. Type 1 is the most common VWD variant; through the clinical data and a pharmacokinetic model, an algorithmic approach supporting the diagnosis of type 1 VWD is proposed.

Development of a model-based approach to the characterization and diagnosis of type 1 von Willebrand disease

Bicego, Matteo
2018/2019

Abstract

Von Willebrand disease (VWD) is the most common inherithed bleeding disorder and it is caused by a deficiencies of von Willebrand factor (VWF), which is a glycoprotein fundamental in the coagulation process. Type 1 is the most common VWD variant; through the clinical data and a pharmacokinetic model, an algorithmic approach supporting the diagnosis of type 1 VWD is proposed.
2018-10-12
VWD, tipo 1, model-based, diagnosis
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.12608/23892