Genetic mutations in many forms of ALS lead to early problems with the transport and function of mitochondria, a study found.

Some patients with a rare form of ALS benefited from an experimental therapy, with biomarker evidence of reduced injury to neurons and even limited functional recovery.

but also the community of ALS patients." Data from 12 patients—all treated with the novel therapy for a rare form of ALS caused by a genetic mutation in a gene called FUS—were presented in a ...

An experimental drug could help young people with a rare form of ALS, researchers at New York’s Columbia University Irving Medical Center announced on Thursday. Known as “ulefnersen,” the ...

For patients with ALS, REM inhibition via receipt of antidepressant medication is associated with a trend toward survival benefit.

(MENAFN- IANS) New Delhi, May 23 (IANS) Treatment with an experimental drug has shown significant improvements in young patients with a rare form of Amyotrophic Lateral Sclerosis (ALS ...

but also the community of ALS patients.” Data from 12 patients—all treated with the novel therapy for a rare form of ALS caused by a genetic mutation in a gene called FUS—were presented in a case ...

He highlighted the FDA's clearance to initiate the trial as "a significant milestone, bringing us closer to commencing patient enrollment ... from "numerous renowned ALS clinicians and researchers ...

An experimental drug could help young people with a rare form of ALS, researchers at New York’s Columbia University Irving Medical Center announced on Thursday. Known as “ulefnersen,” the therapy ...