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 |
| 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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Page last reviewed: July 14, 2021
Content source: Agency for Toxic Substances and Disease Registry