Year: 2005
Language: English
This resource is also available in: Arabic French Russian Spanish Simplified Chinese
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.
The WFH Guidelines for the Management of Hemophilia: AAV Gene Therapy provide the first comprehensive, evidence-based recommendations to support the
The 3rd edition has also been translated into the following languages, with permission from the WFH, by NMOs/Other Organizations: Georgian,
A 3ª edição do Manual de Laboratório da WFH é o guia definitivo para o diagnóstico preciso da hemofilia e
People with bleeding disorders continue to face significant challenges in diagnosis, access to treatment and care around the world. To
The global bleeding disorders community reached a major milestone in 2025, as the World Health Organization updated both its Essential
The 3rd edition of the WFH laboratory Manual is the definitive how-to guide for the accurate diagnosis of hemophilia and
