Les patients SLA ont une espérance de vie de 3 à 5 ans. Pour arriver à identifier la base génétique de la SLA et trouver enfin un médicament pour cette maladie, nous voulons récolter des profils ADN d’au moins 15000 patients SLA et 7 500 profils ADN d’autres personnes.
Aidez-nous à collecter plus de fonds en lançant votre propre campagne. Besoin d'inspiration ? Consultez les campagnes actuelles.
Last year there were more than 2,000 participants in this great swim that raises for ALS research.
Team up for 4 times 500m. For information and registration
International Project MinE research partners and ALS foundations meet at the Project MinE interim meeting Dec 6th in Boston, USA.
On Dec 7th the researchers will meet and discuss their progress on data mining activities in Project MinE with the genomes so far.
The 28th International Symposium on ALS/MND. Researchers and clinicians from all over the world gather to discuss the best research and treatment. The aim is to find effective treatments for ALS/ MND as quickly as possible!
This International Symposium is the largest medical and scientific conference on MND/ALS. It is the premier event in the MND research calendar, attracting over 800 delegates, representing the energy and dynamism of the global MND research community.
Researchers meet and discuss their progress on data mining activities in Project MinE with the genomes so far.
First get-together for researchers to challenge their big-data calculation skills on the Project MinE database located in Amsterdam Science Park
International Project MinE research partners and ALS foundations meet at the Project MinE interim meeting in Oxford, UK
2 km swim for MND in the Royal Victoria Docks.
More info: www.londoncityswim.com
The 29th International ALS symposium is from 7-9 December 2018 in Glasgow, United Kingdom.
Researchers from al over the world meet to discuss their latest results, share ideas and start up more collaborations.
More information: www.mndassociation.org/symposium