Year: 2005
Language: Arabic
Author(s): Bruce Evatt
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.
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VWD Diagnosis Guidelines Executive Summary VWD Management Guidelines Executive Summary These clinical practice guidelines for the diagnosis and management of
