Published: Jul 8, 2013 2:00:00 PM
Published: Jun 13, 2013 1:18:00 PM
Published: May 15, 2013 4:45:54 PM
Published: May 13, 2013 3:05:00 PM
New gene identified for Dominant Congenital Spinal Muscular Atrophy and Hereditary Spastic Paraparesis
Publication date: 16 May 2013
Researchers at the UCL Institute of Neurology together with international collaborators have identified a new gene, BICD2, which causes both dominant Congenital Spinal Muscular Atrophy and Hereditary Spastic Paraparesis.
Teaching Awards 2013
Publication date: 10 May 2013
TRACK-HD study identifies early predictors of disease progression in Huntington’s disease
Publication date: 9 May 2013
An international team led by researchers at the UCL Institute of Neurology has identified a set of tests that could help identify whether - and how - Huntington’s disease (HD) is progressing in groups of people who are not yet showing symptoms.