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Impact of the National Amyotrophic Lateral Sclerosis Registry: Analysis of Registry-funded Research.

Lindsay RechtmanStephan BrennerMarcienne WrightMaggie RitsickFarhana RahmanMoon HanJaime RaymondTheodore LarsonD Kevin HortonPaul Mehta
Published in: Annals of clinical and translational neurology (2022)
The National ALS Registry is a multifaceted research platform, one component of which is funded research. This Registry-funded research fills an essential gap in the overall ALS scientific community as it is difficult to prevent and treat a disease without a deeper understanding of its causes.
Keyphrases
  • amyotrophic lateral sclerosis
  • quality improvement
  • mental health