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European Study Reviews Importance of Population-based Registers of ALS Patients

A recent review highlights the importance of population-based registers of amyotrophic lateral sclerosis (ALS) in Europe, which for more than 20 years have helped scientists understand the disease’s incidence, prevalence, characterization and genetics, as well as the outcome assessment of clinical trials. The review, “The changing picture of amyotrophic lateral sclerosis: lessons from…

Psychological Factors, Experiences Affect ALS Caregivers’ Self-Reported Burden, Study Shows

Psychological factors and subjective experiences play a central role in the burdens felt by people who care for patients with amyotrophic lateral sclerosis (ALS), a new study says. The study, titled “Caregivers of Patients With Amyotrophic Lateral Sclerosis: Investigating Quality of Life, Caregiver Burden, Service Engagement and Patient Survival,“ appeared in the…