The National Amyotrophic Lateral Sclerosis (ALS) Registry patient guide

Details

• Corporate Authors:
  United States. Agency for Toxic Substances and Disease Registry.
• Description:
  The National ALS Registry is a program to collect, manage, and analyze data about people with ALS. It is important to include as many people with the disease as pos- sible to get the most accurate information. ; Because learning more about ALS is an important step in the battle to defeat it, the Agency for Toxic Substances and Disease Registry (ATSDR) has developed a national registry to gather information from people who are living with ALS. This information can help doctors and scientists learn more as they work toward a cure. ; CS216408-A ; Publication date from document properties.
• Subjects:
  • Amyotrophic Lateral Sclerosis/Epidemiology
  • National ALS Registry
  • Registries
• Document Type:
  Pamphlet (or booklet)
• Genre:
  Fact Sheet
• Pages in Document:
  2 unnumbered pages which, when folded, make a 6 page brochure
• Download URL:
  https://stacks.cdc.gov/view/cdc/36645/cdc_36645_DS1.pdf
• File Type:
  [PDF - 3.05 MB]
• Collection(s):
  Stephen B. Thacker CDC Library
• Main Document Checksum:
  urn:sha256:6cdc1c77b7e4f2f5c7f47dafa5579f9ee281145887b8f06a88543dcf5ddb1bc6