Natural History, Genetic Bases and Phenotype-Genotype Correlations in Autosomal Dominant Spinocerebellar Degenerations - Related Studies

Natural History, Genetic Bases and Phenotype-Genotype Correlations in Autosomal Dominant Spinocerebellar Degenerations

This study is currently recruiting participants.

Study NCT00136630. Last updated on October 16, 2007. Information provided by Institut National de la Santé Et de la Recherche Médicale, France

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1	Conditions listed in this trial
		Spinocerebellar Ataxias
		Spastic Paraplegias

2	Additional conditions recognized in this trial
		Paraplegia
		Spinocerebellar Degenerations

3	More general conditions related to this trial
		Ataxia
		Brain Diseases
		Central Nervous System Diseases
		Cerebellar Ataxia
		Cerebellar Diseases
		Dyskinesias
		Genetic Diseases, Inborn
		Heredodegenerative Disorders, Nervous System
		Nervous System Diseases
		Neurodegenerative Diseases
		Neurologic Manifestations
		Paralysis
		Signs and Symptoms
		Spinal Cord Diseases

4	Sponsors listed in this trial
		Institut National de la Santé Et de la Recherche Médicale, France
		Assistance Publique - Hôpitaux de Paris