Molecular pathogenesis of spinocerebellar ataxias

The autosomal dominant spinocerebellar ataxias (SCAs) are a group of neurodegenerative diseases, clinically and genetically heterogeneous, characterized by loss of balance and motor coordination due to dysfunction of the cerebellum and its afferent and efferent connections. Despite a well-described...

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Veröffentlicht in:	Brain (London, England : 1878) England : 1878), 2006-06, Vol.129 (6), p.1357-1370
Hauptverfasser:	Dueñas, Antoni Matilla, Goold, Robert, Giunti, Paola
Format:	Artikel
Sprache:	eng
Schlagworte:	Animals Apoptosis Biological and medical sciences Calcium - metabolism cerebellum Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases Homeostasis - genetics Human viral diseases Humans Infectious diseases Medical sciences Mitochondria - physiology neurodegenerative disorders neurodegenerative mechanisms Neurology Peptides - genetics Peptides - physiology Signal Transduction - genetics spinocerebellar ataxias Spinocerebellar Ataxias - genetics Spinocerebellar Ataxias - metabolism Spinocerebellar Ataxias - therapy therapy Viral diseases Viral diseases of the lymphoid tissue and the blood. Aids
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