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| Found 28 studies with search of: | Open Studies | "Ataxia" |
| Rank | Status | Study | ||||
|---|---|---|---|---|---|---|
| 1 | Not yet recruiting |
Natural History Study of and Genetic Modifiers in Spinocerebellar Ataxias
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| 2 | Recruiting |
Status of Growth Hormone/ Insulin-like Growth Factor-1 (GH/IGF-1) Axis and Growth Failure in Ataxia Telangiectasia (AT)
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| 3 | Recruiting |
Lithium Treatment for Patients With Spinocerebellar Ataxia Type I
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| 4 | Recruiting |
Clinical and Molecular Correlations in Spinocerebellar Ataxia Type 10 (SCA10)
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| 5 | Recruiting |
Amantadine for Improving Neurologic Symptoms in Ataxia-Telangiectasia
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| 6 | Recruiting |
Characteristics of Episodic Ataxia Syndrome
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| 7 | Recruiting |
A Study Investigating the Long-term Safety and Efficacy of Deferiprone in Patients With Friedreich's Ataxia
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| 8 | Not yet recruiting |
Safety and Tolerability of Lithium in Spinocerebellar Ataxia 2 (SCA2)
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| 9 | Recruiting |
Safety Study of Carbamylated Erythropoietin to Treat Patients With the Neurodegenerative Disorder Friedreich's Ataxia
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| 10 | Recruiting |
Study to Determine the Safety and Tolerability of Varenicline (Chantix®) in Treating Spinocerebellar Ataxia Type 3
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| 11 | Recruiting |
Effect of Pioglitazone Administered to Patients With Friedreich's Ataxia: Proof of Concept
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| 12 | Recruiting |
Baclofen Treatment of Ataxia Telangiectasia
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| 13 | Recruiting |
Efficacy of EGb761 in Patients Suffering From Friedreich Ataxia
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| 14 | Recruiting |
Pilot Study of Varenicline (Chantix®) in the Treatment of Friedreich's Ataxia
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| 15 | Recruiting |
Safety and Efficacy Study of A0001 in Subjects With Friedreich's Ataxia
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| 16 | Recruiting |
SPATAX: Clinical and Genetic Analysis of Cerebellar Ataxias and Spastic Paraplegias
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| 17 | Recruiting |
RISCA : Prospective Study of Individuals at Risk for SCA1, SCA2, SCA3, SCA6, SCA7
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| 18 | Recruiting |
Memantine Treatment in Fragile X-Associated Tremor/Ataxia Syndrome
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| 19 | Recruiting |
Autoimmunity in Neurologic Complications of Celiac Disease
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| 20 | Recruiting |
Natural History, Genetic Bases and Phenotype-genotype Correlations in Autosomal Dominant Spinocerebellar Degenerations
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