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ALS Registry

Added: October 24, 2007 | Time 04:31 | Views: 1,164

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.

Topics: ALS (Lou Gehrig's Disease)

Tags: ALS, Dr. Mona, lou gehrig's disease, registry

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chicagogal says:44 weeks ago | Reply

I'm surprised a registry didn't already exist for people with ALS

jbauer says:45 weeks ago | Reply

"Science is data". I like that!

thesundog says:45 weeks ago | Reply

She does a very good job of explaining difficult medical issues.

Healthnut26 says:45 weeks ago | Reply

Glad to hear something is being done to find a cure for ALS! The ALS registry is a step in the right direction.

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