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Non-invasive ventilation in amyotrophic lateral sclerosis: a 10 year population based study
Pathogenic VCP mutations induce mitochondrial uncoupling and reduced ATP levels
Regional spreading of symptoms at diagnosis as a prognostic marker in amyotrophic lateral sclerosis: a population-based study
Early weight loss in amyotrophic lateral sclerosis: outcome relevance and clinical correlates in a population-based cohort
Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis
Exome sequencing reveals VCP mutations as a cause of familial ALS
