Frequent genetic cause of late-onset ataxia uncovered by a Quebec-led international collaboration

Published: 15 December 2022

Discovery will improve diagnosis and open treatment possibilities for thousands of people with this debilitating neurodegenerative condition worldwide...

Exercise may be key to developing treatments for rare movement disorder

Published: 16 September 2022

Spinal cerebellar ataxia 6 (SCA6) is an inherited neurological condition which has a debilitating impact on motor coordination. Affecting around 1 in 100,000 people, the rarity of SCA6 has seen it...

The Neuro and Thermo Fisher Scientific Partner to Fight Neurodegenerative Disease

Published: 5 March 2018

Industry and academia to share expertise in effort to develop improved methods to produce and characterize antibodies and reagents for neurological research

Recognizing rare diseases

Published: 28 February 2017

Research and clinical care complement each other at The Neuro...

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