Preliminary Results of National Amyotrophic Lateral Sclerosis (ALS) Registry Risk Factor Survey Data.

by Leah Bryan, Wendy Kaye, Vinicius Antao, Paul Mehta, Oleg Muravov, D Kevin Horton
Published 2016-01-01

Increasing Patient Self-Enrollment in the National Amyotrophic Lateral Sclerosis Registry: Lessons Learned From a Direct to Provider Campaign

by Lindsay Rechtman DrPH, Heather Jordan MPH, Wendy Kaye PhD, Maggie Ritsick MPH, Paul Mehta MD
Published 2020-02-01