This Guideline addresses a number of medical issues which neurologists and other medical doctors who are involved in the medical management of patients with dementia are confronted with on a regular basis.
The urgent need for coordination of research efforts and strong EU leadership in health research embedded in a European Council for Health Research have been identified as key policy topics during the BioMed Alliance Spring meeting.
The European Academy of Neurology has launched a taskforce on Gender and Diversity in Neurology, with the overall mission to increase awareness and improve knowledge about sex, gender, ethnic and racial differences and disparities in neurological disorders with the aim to improve the outcome of care of neurological patients.
The European Reference Networks for Rare Neurological Diseases (ERN-RND) and for Rare Neuromuscular Diseases (ERN EURO-NMD) organise joint webinars throughout the year in collaboration with EAN.
As the CoVID-19 pandemic spreads across Europe and the world, in response the European Academy of Neurology is launching EANcore CoVID-19. This resource aims to help neurologists in Europe and beyond prepare for and manage the challenges this global crisis is bringing.
Rare Disease Day was launched in 2008 by EURORDIS, an alliance of patient organisations, and its Council of National Alliances, starting as a European event. It is now a major international event celebrated by rare disease organizations across the globe with… Continue Reading
EAN signed a Memorandum of Understanding withISNA – International Society for Neuro-Immunology joining forces to promote optimal cooperation in Europe between both societies.
EAN signed a Memorandum of Understanding with EPA – European Psychiatric Association joining forces to promote optimal cooperation in Europe between both societies.
29 February 2020, a rare day, will be the thirteenth international Rare Disease Day.
Many activities are organized in more than 100 countries to raise awareness amongst the general public and decision-makers about Rare Diseases and their impact on patients’… Continue Reading