For Researchers: Online Resources
Below are online resources and websites with additional information regarding ALS that might be of help to Researchers.
The ALS Association (ALSA)
The mission of The ALS Association is to discover treatments and a cure for ALS, and to serve, advocate for, and empower people affected by ALS to live their lives to the fullest.
Answer ALS
Building the most comprehensive clinical, genetic, molecular & biochemical assessment of ALS, while openly sharing the results with the global research community.
ClinicalTrials.gov
ClinicalTrials.gov is a database of privately and publicly funded clinical studies conducted around the world.
Northeast Amyotrophic Lateral Sclerosis Consortium® (NEALS)
The mission of The ALS Association is to discover treatments and a cure for ALS, and to serve, advocate for, and empower people affected by ALS to live their lives to the fullest.
NeuroBANK®
NeuroBANK® is the flagship platform for collecting data on research volunteers who participate in natural history studies or in multiple projects within a disease consortium.
Target ALS
Target ALS is a 501(c)(3) medical research foundation committed to the search for effective treatments for Amyotrophic Lateral Sclerosis (ALS), also known as Lou Gehrig’s disease.