The EuroWilson website contains information about Wilson disease that we
believe might be of interest to patients, family members and health care
professionals. We strive to ensure that the contents are correct and up-to-date.
The website is under the responsibility of a scientific committee whose members all have expertise in Wilson disease. Its object is to disseminate information, but not to be a substitute for consultation with healthcare professionals.
It must be emphasized that each patient is unique, and that only a patient's
physician can provide appropriate and individual information and care.
www.eurowilson.org
Presentation
Presentation
Living with Wilson's
LIVING WITH WILSON'S DISEASE
For medical professionals
FOR MEDICAL PROFESSIONALS
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Report a new case
Headlines
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Results of the 2012 Patient Survey03/01/2013
See details
Results of the 2012 Patient Survey
Questionnaire for WD patients on healthcare needs, specially dedicated to diagnosis and treatment.
Newsletter
Coming soon
EuroWilson is a European Reference Network for Wilson’s disease. EuroWilson is governed by a group of academic doctors with support from the European patient groups. Eurowilson was funded from 2004-2008 through the European Commission Six Framework Programme (LSHM-CT2004 503430). In 2011 EuroWilson received funding from the European Commission Directorate General for Health and Consumers Operating Grant. It is currently hosted by the Assisstance Publique Hopitaux de Paris (APHP)
