All-in-one wearable drug efficacy assessment systems for bulbar muscle function using amyotrophic lateral sclerosis animal models
Author:
Funder
U.S. Department of Health & Human Services | National Institutes of Health
Publisher
Springer Science and Business Media LLC
Link
https://www.nature.com/articles/s41467-024-51300-1.pdf
Reference40 articles.
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2. Zarei, S. et al. A comprehensive review of amyotrophic lateral sclerosis. Surgical Neurol. Int. 6, 171 (2015).
3. Tapia, R. Cellular and molecular mechanisms of motor neuron death in amyotrophic lateral sclerosis: a perspective. Front. Cell. Neurosci. 8, 1–3 (2014).
4. Haverkamp, L. J., Appel, V. & Appel, S. H. Natural history of amyotrophic lateral sclerosis in a database population Validation of a scoring system and a model for survival prediction. Brain 118, 707–719 (1995).
5. Armon, C. & Moses, D. Linear estimates of rates of disease progression as predictors of survival in patients with ALS entering clinical trials. J. Neurol. Sci. 160, S37–S41 (1998).
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