Microglia-mediated recovery from ALS-relevant motor neuron degeneration in a mouse model of TDP-43 proteinopathy | Nature Neuroscience
Neurogenic Treatment of ALS w/ MSC+ Stem Cells
Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis | Nature Genetics
Abnormal RNA stability in amyotrophic lateral sclerosis | Nature Communications
Frontiers | Protein Homeostasis in Amyotrophic Lateral Sclerosis: Therapeutic Opportunities? | Frontiers in Molecular Neuroscience
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High-dose pharmaceutical grade biotin (MD1003) in amyotrophic lateral sclerosis: A pilot study - EClinicalMedicine
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Amyotrophic Lateral Sclerosis | NEJM
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Targeting the Sigma-1 Receptor via Pridopidine Ameliorates Central Features of ALS Pathology in a SOD1 G93A Model | Cell Death & Disease
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Retromer stabilization results in neuroprotection in a model of Amyotrophic Lateral Sclerosis | Nature Communications
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CUG initiation and frameshifting enable production of dipeptide repeat proteins from ALS/FTD C9ORF72 transcripts | Nature Communications
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Pathophysiological and diagnostic implications of cortical dysfunction in ALS | Nature Reviews Neurology