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Research

Welcome to our research page to learn more about our latest findings

Take part in a study to improve Google…

A team of researchers is currently looking for people with…

Registration for our online Research Information Day and…

Please note, registration for our online Research Information Day and…

Research identifies genetic variant which determines speed of…

New research has identified a genetic variant which determines how…

Participants wanted for study looking into mechanisms of…

Participants are being sort for a research study looking into the…

New report to bring rare diseases ‘Out of…

Following nine months of consultation, the rare neurological disease report,…

Research shows neuroinflammation and tau co-localise in PSP

New research at the University of Cambridge with PSPA funding…

Durham University study into use of prism glasses

Researchers at Durham University are looking for people living with…

PSPA Funded Research Update

Since the lockdown began, many medical researchers who also usually…

Nominate PSPA for a £1000 donation

Help PSPA be in with a chance of receiving a…

Join the #TwoPointSixChallenge to support PSPA

On 26 April the nation is coming together for an…

Message from the CEO

The developing Coronavirus pandemic is currently at the forefront of…

#JointheFight to help raise awareness of PSP &…

Could you #JointheFight against the misdiagnosis of PSP & CBD…

OxQuip – Oxford study of Quantification in Parkinsonism

OxQuip are looking for patients with Progressive Supranuclear Palsy to…

Initial findings from the PROSPECT Study

Research estimates that up to 10,000 people may be living…

PASSPORT Study Discontinued

At the end of last week pharmaceutical company Biogen announced…

Help us identify the priority research questions for…

This month PSPA launched its first study to identify the…

New online interactive resource

We are thrilled to launch our new online interactive resource…

Exploring physical activity in people with rare neurological…

The PARC (Physical Activity for people with Rare Neurological Conditions)…

25 years of PSPA – interview with our…

“We were so upset that no one seemed to know…

The Neurological Alliance Patient Experience Survey

This questionnaire is about your care and treatment for your…