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What is a Randomized Controlled Trial (RCT)? Before a new drug or therapy can reach patients, researchers and regulatory agencies need evidence that it is safe and effective. One of Read More…
Written by Jamie Hyde Edited by Marija Cvetanovic, PhD “A new matched stem cell model gives SCA1 researchers a clearer way to study disease mechanisms and test potential treatments.” Using Read More…
Spastic Paraplegia Type 4 (SPG4) A collection of resources for individuals and families affected by Spastic paraplegia type 4 (SPG4). WEBINARS RESEARCH INFORMATION RESEARCH NEWS BECOME A MEMBER >> Spastic paraplegia type 4 (SPG4) is caused by Read More…
SCA17 A collection of resources for individuals and families affected by SCA17. WEBINARS RESEARCH INFORMATION RESEARCH NEWS BECOME A MEMBER >> Spinocerebellar Ataxia type 17 (SCA17) is caused by a genetic mutation Read More…
SCA35 A collection of resources for individuals and families affected by Spinocerebellar Ataxia Type 35 (SCA35). WEBINARS RESEARCH INFORMATION RESEARCH NEWS BECOME A MEMBER >> Spinocerebellar Ataxia type 35 (SCA35) is caused Read More…
Unknown Ataxia with Family History A collection of resources for individuals and families affected by Unknown Ataxia with Family History. WEBINARS RESEARCH INFORMATION RESEARCH NEWS BECOME A MEMBER >> People affected by Read More…
SCAR20 A collection of resources for individuals and families affected by Autosomal Recessive Spinocerebellar Ataxia 20 (SCAR20). WEBINARS RESEARCH INFORMATION RESEARCH NEWS BECOME A MEMBER >> Autosomal Recessive Spinocerebellar Ataxia 20 (SCAR20) is Read More…
SCA28 A collection of resources for individuals and families affected by Spinocerebellar Ataxia type 28. WEBINARS RESEARCH INFORMATION RESEARCH NEWS BECOME A MEMBER >> Spinocerebellar Ataxia type 28 (SCA28) and Read More…
SPAX5 A collection of resources for individuals and families affected by Autosomal Recessive Spastic Ataxia type 5 (SPAX5). WEBINARS RESEARCH INFORMATION RESEARCH NEWS BECOME A MEMBER >> Autosomal Recessive Spastic Read More…
It has been more than 30 years since the discovery of the first gene for Spinocerebellar Ataxia (SCA), a group of rare, progressively debilitating neurodegenerative diseases. It has been even Read More…
