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  1. 29. sij

    Are you interested in research? A research grant on identifying risk factors for ALS is accepting applications! Deadline to apply is March 4. Learn more: .

  2. 24. sij

    The National Registry is working to ensure that with research, our future generations may have a different outlook. Learn more about enrolling in the : .

  3. patients fight many battles and earn the title warriors. We should not have to battle too. However, we are more than prepared given that it’s much easier than what we’ve already battled.

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  4. The National is working toward a better future for people living with by funding research, collecting meaningful data, and more. To see how you can help future generations, click here:

  5. 14. sij

    The National ALS Registry collects and analyzes information from people living with in the United States, helping researchers understand who gets and why. By joining the , you can help us answer these important questions. Visit: .

  6. 29. stu 2019.

    The National Registry is linking people with ALS with researchers. A new study, Psychosocial Impact of Genetic Testing in ALS, is currently recruiting eligible persons who are enrolled in the . Learn more: .

  7. 21. stu 2019.

    When people living with join the National ALS Registry, they can make a difference. Together, we can better understand ALS, one person at a time. Learn about the : .

  8. 25. lis 2019.

    Are you living with ? Do you want to make a difference for future generations? Take part by joining the National ALS Registry: .

  9. 18. lis 2019.

    The National Registry provides hope for patients and data for researchers. Learn why this is so important.

  10. About 16,000 people in the US are living with . The National ALS Registry is the only population-based registry in the U.S. that collects information to help scientists learn more about who gets ALS and its causes. Learn more:

  11. 10. lis 2019.

    Every person’s story counts in the fight against . Share your story by joining the National ALS Registry. Learn more at:

  12. 2. lis 2019.

    The National Registry doesn't just track prevalence, it also connects people to research. Learn more: .

  13. 14. kol 2019.

    Learn how the National ALS Registry is studying the disease and how you can join. Visit: .

  14. 5. kol 2019.

    Researchers are using the National ALS Registry to recruit persons with who are enrolled in the Registry for participation in a new study, Symptoms of Greatest Importance in Motor Neuron Disease (MND). Learn more: .

  15. 18. srp 2019.

    Each year brings together persons with , neurologists, researchers, ALS advocates, and other ALS experts at the National ALS Registry Annual Meeting. The meeting will be live streamed on July 23 from 8:30 a.m. to 4:00 p.m. ET at .

  16. 4. tra 2019.

    The ALS Association Tennessee Chapter thanks you for signing the FY2020 Appropriations “Dear Colleague” letter to support .

  17. 27. ožu 2019.

    As your constituent & someone impacted by , I urge you to sign on to the FY2020 ALS Appropriations “Dear Colleague” letter to support by contacting & .

  18. 13. ožu 2019.

    We make progress in the fight against through research. Learn more about the :

  19. 14. pro 2018.

    The Nat’l is helping gather important info needed to learn more about the causes of .

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