Preliminary results of National Amyotrophic Lateral Sclerosis (ALS) Registry risk factor survey data

Affiliates Leah Bryan [1], Wendy Kaye [2], Vinicius Antao [3], Paul Mehta [3], Oleg Muravov [3], D. Kevin Horton [3]


[1] Carter Consulting Incorporated
[2] McKing Consutling Corportation
[3] Division of Toxicology and Human Health Sciences

Journal PLOS One
Summary The National ALS Registry web portal, to our knowledge, is the largest, most geographically diverse collection of risk factor data about adults living with ALS. Various characteristics were consistent with other published studies on ALS risk factors and will allow researchers to generate hypotheses for future research.
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