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1. Pathogenic Huntingtin Repeat Expansions in Patients with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis

2. Analysis of shared common genetic risk between amyotrophic lateral sclerosis and epilepsy

3. Humanized mutant FUS drives progressive motor neuron degeneration without aggregation in 'FUSDelta14' knockin mice.

4. Improving the knowledge of amyotrophic lateral sclerosis genetics: novel SOD1 and FUS variants.

5. Safety and efficacy of edaravone compared to historical controls in patients with amyotrophic lateral sclerosis from North-Eastern Italy.

6. Association of Variants in the SPTLC1 Gene with Juvenile Amyotrophic Lateral Sclerosis

7. Analysis of hnRNPA1, A2/B1, and A3 genes in patients with amyotrophic lateral sclerosis.

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