How we can work together
Platform Residras includes data from tens of hospitals and clinics all over Europe, collected from hundreds of registered patients with Dravet Syndrome.
These projects target to improve the quality of life of patients and their family caregivers by promoting and developing medical/social initiatives.
One of the aims of DSEF is to stimulate research and development into treatments by specialist physicians and researchers.
You can easier understand Dravet Syndrome or even start to look for better treatments and a cure by using a mouse model carrying the a mutation in the Scn1a gene.
This body works to operate and advise with regard to medical and clinical aspects or for those related to the research.
Other projects of DSEF aim to raise funds for medical and social research, and also to raise awareness of Dravet Syndrome among the public and the medical/social community.