Participating in Ataxia Research
To learn about ongoing research projects at the University of Minnesota Ataxia Center please contact Diane Hutter at (612) 625-2350, e-mail: email@example.com.
CoRDS is a centralized international patient registry for all rare diseases based at Sanford Research. The goal of the CoRDS registry is to connect as many patients and researchers as possible to help advance treatments and cures for rare diseases. The CoRDS registry is free for patients to enroll and for researchers to access. They work with patient advocacy groups, individuals, and researchers to coordinate the advancement of research into the 7,000 rare diseases. To join the CoRDS registry, click here.
Episodic Ataxia Registry: Patients with Episodic Ataxia can register to participate in ongoing and future studies of Episodic Ataxia. Please visit the Episodic Ataxia Registry website.