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  • ALS Registry

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ALS Registry

The ALS registry will collect and examine data from thousands of people with Lou Gehrig's Disease. Its data will be used to help determine risk factors for ALS, as well as interventions that are beneficial and which educational approaches are best.

Icyou | December 21, 2007Watch more videos from Icyou

Tags:. .Healthcare. .educ. .collect. .thousand. .risk











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