Gene therapy for disorders such as amyotrophic lateral sclerosis, Parkinson’s disease and Batten disease has seen success in animal models.
Browsing: Amyotrophic lateral sclerosis
Researchers have revealed that RNA-binding proteins accumulate in the brains of people with non-heritable amyotrophic lateral sclerosis and frontotemporal dementia.
A potential new therapeutic for inherited amyotrophic lateral sclerosis, which extended survival and reversed fatal neuromuscular damage in rodents, has entered Phase I/II clinical trials.
After careful evaluation of the ‘Right to Try ‘Act, BrainStorm have announced that it will not make NurOwn® available under this legislation at this time.
Researchers have identified genes in the human genome that could modify the severity of amyotrophic lateral sclerosis and frontotemporal dementia.
Disturbance to nuclear transport caused by protein aggregation has been implicated in the pathology of ALS and FTD.
As we begin a new year on Neuro Central, we’re taking this opportunity to look back at some of the highlights across neuroscience and neurology in 2017.
Discover more about how advances in amyotrophic lateral sclerosis research are influencing approaches to patient care in this review from Neurodegenerative Disease Management
Researchers from the University of Missouri have discovered an enzyme pathway that may present a potential therapeutic target for ALS and, possibly, other neurological diseases including stroke.
The California Institute for Regenerative Medicine (CIRM) announces that it is investing $15.9 million in a therapy to tackle ALS.