The show is a joint project by artists Bert and Elise Holland, Charlotte, Clair, Evie, Kate, Spencer James and Steven Hart.
The past four years have brought disappointment for the Huntington’s community, but optimism is growing as companies ...
A fatal, highly hereditary illness with no disease-modifying treatments, Huntington’s is long overdue for a therapeutic win.
Salim Syed’s rating is based on the positive regulatory feedback from the FDA regarding Wave Life Sciences’ lead candidate, WVE-003, for Huntington’s disease. The FDA’s openness to a pathway for ...
Bayer has become the latest in a long line of drug developers to give up on Huntington’s disease after the German pharma ...
A polymer has been developed to optimize the use of a peptide to treat Huntington’s disease in mice.
Engineered polymers interfere with protein interactions to protect cell health in a mouse study. Researchers at Northwestern University and Case Western Reserve University have developed the first ...
The event was put on by a family in Tyler who has dealt with the disease in their family and wants to raise awareness and ...
The findings revealed that the consistent efficacy of Ingrezza in reducing chorea across various subgroups and its potential positive impact on emotional health in patients. Currently, Neurocrine's ...
The familial trend, it turned out, was linked to a genetic mutation. That meant Bill might also be at risk for the disease.
In addition to its lead GeneTACâ„¢ small molecule, DT-216, in development for patients with Friedreich ataxia, the company is advancing programs in Fuchs endothelial corneal dystrophy, Huntington's ...
Neurons have been reprogrammed from the skin cells of a patient with Huntington's disease. (Image: Yoo lab/WashU Medicine) ...