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Disturbed post-movement beta synchronization in Wilson's disease with neurological manifestation

✍ Scribed by Gertrúd Tamás; Jan Raethjen; Muthuraman Muthuraman; Anikó Folhoffer; Günther Deuschl; Ferenc Szalay; Annamária Takáts; Anita Kamondi

Book ID
116773060
Publisher
Elsevier Science
Year
2011
Tongue
English
Weight
346 KB
Volume
494
Category
Article
ISSN
0304-3940

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## Abstract Wilson's disease (WD) is a rare autosomal‐recessive disorder of copper metabolism with predominantly hepatic and extrapyramidal motor symptoms. Copper chelating therapy has proven to be an effective treatment for WD. Yet, if conservative treatment fails, liver transplantation (LT) often