Spinocerebellar Ataxia Type 23 Overview

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Learn About Spinocerebellar Ataxia Type 23

Condition 101 content is not available at this time, but we are continually updating the site. Please check back.

However, there may be experts who have treated this or similar conditions in our Find a Doctor section and research may be available in our Latest Advances section.

Who are the top Spinocerebellar Ataxia Type 23 Local Doctors?
Elite in Spinocerebellar Ataxia Type 23
Elite in Spinocerebellar Ataxia Type 23
Uppsala, C, SE 

Georgy Bakalkin practices in Uppsala, Sweden. Ms. Bakalkin is rated as an Elite expert by MediFind in the treatment of Spinocerebellar Ataxia Type 23. Her top areas of expertise are Spinocerebellar Ataxia Type 23, Traumatic Brain Injury, Alternating Hemiplegia of Childhood, Hemiplegia, and Rhizotomy.

Elite in Spinocerebellar Ataxia Type 23
Elite in Spinocerebellar Ataxia Type 23
Nagoya, JP 

Hirohisa Watanabe practices in Nagoya, Japan. Watanabe is rated as an Elite expert by MediFind in the treatment of Spinocerebellar Ataxia Type 23. Their top areas of expertise are Multiple System Atrophy, Familial Dysautonomia, Spinocerebellar Ataxia Type 23, Deep Brain Stimulation, and Thalamotomy.

 
 
 
 
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Elite in Spinocerebellar Ataxia Type 23
Elite in Spinocerebellar Ataxia Type 23
Nijmegen, GE, NL 

Cleo Smeets practices in Nijmegen, Netherlands. Ms. Smeets is rated as an Elite expert by MediFind in the treatment of Spinocerebellar Ataxia Type 23. Her top areas of expertise are Spinocerebellar Ataxia Type 23, Hereditary Ataxia, Spinocerebellar Ataxia, and Drug Induced Dyskinesia.

What are the latest Spinocerebellar Ataxia Type 23 Clinical Trials?
Coordination of Rare Diseases at Sanford

Summary: CoRDS, or the Coordination of Rare Diseases at Sanford, is based at Sanford Research in Sioux Falls, South Dakota. It provides researchers with a centralized, international patient registry for all rare diseases. This program allows patients and researchers to connect as easily as possible to help advance treatments and cures for rare diseases. The CoRDS team works with patient advocacy groups, in...

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