Search Trials
Rare Disease Patient Registry & Natural History Study – Coordination of Rare Diseases at Sanford
Status:
Recruiting
Last Changed:
Dec 15, 2021
First Changed:
Feb 15, 2013
Disease(s):
Rare Disorders
Natural History, Genetic Bases and Phenotype-genotype Correlations in Autosomal Dominant Spinocerebellar Degenerations
Status:
Completed
Last Changed:
Aug 25, 2021
First Changed:
Aug 29, 2005
Disease(s):
Spinocerebellar Ataxias
Biomarkers in Autosomal Dominant Cerebellar Ataxia
Status:
Completed
Last Changed:
Sep 6, 2019
First Changed:
Nov 11, 2011
Disease(s):
Spinocerebellar Ataxia Type 1
Intervention(s):
metabolic and imaging biomarkers in SCA1,2,3 and 7 patients
Rare Disease Patient Registry & Natural History Study – Coordination of Rare Diseases at Sanford
Status:
Recruiting
Last Changed:
Dec 10, 2020
First Changed:
Feb 15, 2013
Disease(s):
Rare Disorders

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