NINDS News Articles

NIH-funded twin study finds occupational chemical exposure may be linked to Parkinson’s risk Monday, Nov 14, 2011
New research in twins contributes to the increasing evidence that repeated occupational exposure to certain chemical solvents
raises the risk for Parkinson’s disease. Of the six chemicals investigated, researchers concluded that two common chemical
solvents, trichloroethylene (TCE) and perchloroethylene (PERC), are significantly linked to development of this disease.

Ultrathin flexible brain implant offers unique look at seizures in NIH-funded researchSunday, Nov 13, 2011
NIH-funded researchers have developed a flexible brain implant that could one day be used to treat epileptic seizures. In
animal studies, the researchers used the device – a type of electrode array – to take an unprecedented look at brain activity
during seizures. Someday, these arrays could be used to pinpoint where seizures start in the brain and perhaps to shut them
down, the researchers say.

NIH study finds stroke risk factors may lead to cognitive problemsTuesday, Nov 8, 2011
Having common risk factors for stroke can lead to cognitive problems without causing a full-blown stroke. The new findings
come from the REGARDS study, an effort to track stroke risk and cognitive health in Americans 45 and older. One of the strongest
predictors of cognitive decline was high systolic blood pressure, with each 10 mm Hg increase bumping up the risk by 4 percent.

NINDS Lab Helps Track a Viral Brain DiseaseFriday, Oct 28, 2011
NINDS intramural scientists led by Eugene Major have developed a sensitive laboratory assay to detect JC virus. The test has
become an important resource for diagnosing cases of progressive multifocal leukoencephalopathy or PML, a brain disease that
is a rare side effect associated with some monoclonal antibody therapies used to treat multiple sclerosis (MS) and other autoimmune
disorders.

Genetic mutation linked to inherited forms of ALS, dementiaWednesday, Sep 28, 2011
Researchers have identified the most common genetic cause known to date for two neurological diseases, amyotrophic lateral
sclerosis (ALS) and frontotemporal dementia (FTD). A mutation in a single gene on chromosome 9 accounts for nearly 50 percent
of familial ALS and FTD in Finland, and more than a third of familial ALS in other groups of European ancestry.
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