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Article

[The genetics of movement disorders--spinocerebellar degenerations].

Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke - 9 Sept 2004

Tallaksen Chantal M E, Dietrichs Espen

Abstract excerpt

BACKGROUND: Hereditary movement disorders include spinocerebellar disorders, a large and heterogeneous group of syndromes with ataxia or spasticity as the prominent symptom. In spite of the vast clinical and genetic heterogeneity, patterns of pathogenesis slowly emerge and help us understand these disorders. MATERIAL AND METHODS: This review is based on personal experience and recent literature. RESULTS: More...

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PMID: 15356686

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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