Speakers: Wendy E. Kaye, PhD, McKing Consulting Corporation and Paul Mehta, MD, National ALS Registry
The National ALS Registry does more than just count ALS cases. Learn how the Registry promotes and advances ALS research by connecting patients with researchers for clinical trials and studies, funding etiological research, and facilitating the availability of biological specimens collected by the newly launched National ALS Biorepository where patients can donate their specimens to advance ALS research.
