von Willebrand Disease: Oral Health
In the Sunday afternoon joint Laboratory Sciences and VWD Professional Development Workshop, Alison Dougall discusses oral health in people with von Willebrand disease (VWD). This talk was part of the joint Laboratory Sciences and VWD Professional Development Workshop. See below for the other talks in this workshop:
Guide to Developing a National Patient Registry
Having a national patient registry means being able to answer fundamental questions about the hemophilia population within a given country. This step-by-step guide outlines the basic principles of data collection, maintenance, and analysis and compares different types of registries.