Amyotrophic lateral sclerosis - The Lancet
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Frontiers | Protein Homeostasis in Amyotrophic Lateral Sclerosis: Therapeutic Opportunities? | Frontiers in Molecular Neuroscience
CUG initiation and frameshifting enable production of dipeptide repeat proteins from ALS/FTD C9ORF72 transcripts | Nature Communications
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Microglia-mediated recovery from ALS-relevant motor neuron degeneration in a mouse model of TDP-43 proteinopathy | Nature Neuroscience
Amyotrophic Lateral Sclerosis | NEJM
Modelling amyotrophic lateral sclerosis: progress and possibilities | Disease Models & Mechanisms
Amyotrophic Lateral Sclerosis | NEJM
Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis | Nature Genetics
ALS-specific cognitive and behavior changes associated with advancing disease stage in ALS | Neurology
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Amyotrophic lateral sclerosis - ScienceDirect
Amyotrophic lateral sclerosis | Nature Reviews Disease Primers
ALS Genes in the Genomic Era and their Implications for FTD: Trends in Genetics
Safety and efficacy of edaravone in well defined patients with amyotrophic lateral sclerosis: a randomised, double-blind, placebo-controlled trial - The Lancet Neurology
What Is ALS - ALS Symptoms | ALS Pathways
Retromer stabilization results in neuroprotection in a model of Amyotrophic Lateral Sclerosis | Nature Communications
Pathophysiological and diagnostic implications of cortical dysfunction in ALS | Nature Reviews Neurology
Amyotrophic Lateral Sclerosis | NEJM
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
