EU FIFTH FRAMEWORK
Quality of Life & Management of Living Resources
Molecular & Clinical Markers for Diagnosis & Management of Type I Von Willebrands Disease

LINKS TO OTHER WEB SITES

 

VWF Mutation and Polymorphism Website. Up-to-date databases of point mutations, insertions, deletions, and polymorphisms found in the gene for human von Willebrand Factor.
The Haemophilia Society. The Society was established in 1950 and is the national charity in the UK of and for people with haemophilia, von Willebrand’s and related bleeding disorders. There is a head office in central London with a full-time staff of 11 and 3 volunteers and an office in Glasgow with one full-time staff member. The Society has over 2000 members and a network of 20 local groups throughout the UK.
The World Federation of Hemophilia is an international organization working to introduce, improve, and maintain care for people with hemophilia and related bleeding disorders around the world. Through its various partnerships, health care development programs and publications, WFH continues to grow and succeed in realizing its mission.
European Union Community Research and Development Information Service (CORDIS) - is a free service provided by the European Commission's Innovation/SMEs programme. CORDIS offers access to a wide range of information on EU research and innovation development activities.
The ISTH is a non-profit organization with over 2,000 members from more than 50 countries.