For Researchers: Online Resources
Below are online resources and websites with additional information regarding ALS that might be of help to Researchers.
![ALS_Association_logo_transparent](https://www.alsfindingacure.org/wp-content/uploads/2021/06/ALS_Association_logo_transparent-1024x600.png)
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.
![answerals](https://www.alsfindingacure.org/wp-content/uploads/2022/01/answerals.png)
Answer ALS
Building the most comprehensive clinical, genetic, molecular & biochemical assessment of ALS, while openly sharing the results with the global research community.
![ct.gov-nlm-nih-logo](https://www.alsfindingacure.org/wp-content/uploads/2022/01/ct.gov-nlm-nih-logo.png)
ClinicalTrials.gov
ClinicalTrials.gov is a database of privately and publicly funded clinical studies conducted around the world.
![logo](https://www.alsfindingacure.org/wp-content/uploads/2021/06/logo.png)
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](https://www.alsfindingacure.org/wp-content/uploads/2022/01/neurobank.png)
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-logo-scaled-1](https://www.alsfindingacure.org/wp-content/uploads/2021/07/target-als-logo-scaled-1.jpg)
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.