UCLA Health researchers say study findings uncover Huntington's disease mechanisms and pave new ways to develop treatments.

Huntington's disease is a rare genetic, autosomal dominant, neurodegenerative disease, caused by CAG repeat expansions in the HTT gene, that is polymorphic on the healthy allele and contains more than ...

This #HDGratitudeDay, we’re going beyond science & getting to the heart of what drives this community—the people. Learn how ...

Researchers have revealed for the first time how a key protein linked to Parkinson's mutates, leads to cell death in the ...

What initially seems like purely psychological trouble may indeed have roots in physical conditions that, once identified, ...

Federally funded research at Johns Hopkins offers new avenues for detecting brain disease long before it strikes ...

Biosciences presented data from the KINECT-HD study showcasing significant improvements in chorea across body regions with ...