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Get the free National Amyotrophic Lateral Sclerosis (ALS) Registry Application Form: - wwwn cdc

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Remember the average high school graduate reads at the 8th grade level so use simple declarative sentences and avoid scientific jargon. ATSDR kindly requests that researchers include the following acknowledgement in any publications deriving from the study Recruitment for this study was in part made possible by ATSDR s National ALS Registry Research Notification Mechanism http //wwwn.cdc.gov/ALS/ALSClinicalResearch. All materials received by the Agency for Toxic Substances and Disease...
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Who needs national amyotrophic lateral sclerosis?

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National amyotrophic lateral sclerosis is a progressive neurodegenerative disease that affects nerve cells in the brain and spinal cord.
Healthcare providers, researchers, and organizations involved in the study or treatment of amyotrophic lateral sclerosis may be required to file national Amyotrophic Lateral Sclerosis (ALS) data.
National Amyotrophic Lateral Sclerosis (ALS) data can be filled out by providing accurate information about ALS cases, research findings, and treatment options.
The purpose of national Amyotrophic Lateral Sclerosis (ALS) data collection is to track and monitor the incidence and prevalence of ALS, identify trends, and improve patient care and outcomes.
Information that must be reported on national Amyotrophic Lateral Sclerosis (ALS) includes demographics of ALS patients, disease progression, treatments received, and outcomes.
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