Categories: Amyotrophic lateral sclerosis
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Issue Information
Acta Neurologica Scandinavica, Volume 143, Issue 6, Page 575-576, June 2021. Read article at journal’s website
De novo mutations in SOD1 are a cause of ALS
Objective The only identified cause of amyotrophic lateral sclerosis (ALS) are mutations in a number of genes found in familial cases but also in sporadic…
Phenotyping of the thoracic-onset variant of amyotrophic lateral sclerosis
Introduction Thoracic-onset amyotrophic lateral sclerosis (T-ALS) is a rare subform, affecting only 3% of all patients with amyotrophic lateral sclerosis (ALS).1 In order to facilitate…
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