Links

European Commission

 

Other related European Research Programmes

  • Neurostemcellrepair 
    European stem cell consortium for neural cell replacement, reprogramming and functional brain repair

  

  • Eurostemcell
    The Eurostemcell website provides reliable, independent information and educational resources on stem cells and their impact on society. Information available in six languages (EN, FR, DE, IT, ES, PL).

 

  

Information on Huntington's disease and patient associations  

  

  • IHA - The International Huntington Association
    The IHA is a federation of national voluntary health agencies that share common concern for individuals with Huntington's Disease (HD) and their families. Each agency promotes lay and professional education; individual and family support; psycho-social, clinical and biomedical research; and ethical and legal considerations related to Huntington's Disease in its respective country. IHA lists patient support groups and Huntington's Disease organisations worldwide 

  

  

  

  • ORPHANET
    Orphanet is dedicated to provide exhaustive and regularly updated information on rare diseases, including HUNTINGTON, and orphan drugs. ORPHANET offers services adapted to the needs of patients and their families, health professionals and researchers, support groups and industry. Information is available in 7 languages (EN, FR, DE, ES, IT, PT, NL).

 

  • EURORDIS - European Organisation for Rare Diseases
    EURORDIS is a patient-driven alliance of patient organisations and individuals active in the field of rare diseases. It's mission is to build a strong pan-European community of patient organisations and people living with rare diseases, to be their voice at the European level, and - directly or indirectly - to fight against the impact of rare diseases on their lives. The site is available in 7 languages (EN, FR, DE, ES, IT, PT, RU).

  

  • Huntington Study Group
    Clinical researchers worldwide make up the Huntington Study Group (HSG). HSG members care for Huntington disease (HD) patients and families and work diligently to combat this disease.
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