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1. An integrated multi-omic analysis of iPSC-derived motor neurons from C9ORF72 ALS patients

2. Postmortem Cortex Samples Identify Distinct Molecular Subtypes of ALS: Retrotransposon Activation, Oxidative Stress, and Activated Glia

3. Pathogenic huntingtin repeat expansions in patients with frontotemporal dementia and amyotrophic lateral sclerosis

4. Rehabilitation of motor neuron disease

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