Hemophilia

Researchers at Medical University of Vienna target hemophilia

Published in Blood Weekly, June 25th, 2009

According to recent research from Vienna, Austria, "Patient registries are databases essential for identifying and tracking individuals with a particular disease and for collecting epidemiological information. The data obtained are necessary for quality control and quality assurance in treatment and for studying the impact of new developments on prevention, diagnosis and treatment."

"The Austrian Hemophilia Registry is a joint initiative between Austrian hemophilia treaters, represented by the Austrian Hemophilia Society's scientific advisory board, and the Austrian Hemophilia Society (A-HG). The registry's main objective is to record information on patients with...

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Source: Blood Weekly (2009-06-25)

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