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Novel approaches in diagnosis and therapy of Creutzfeldt–Jakob disease

✍ Scribed by Werner E.G Müller; Jean-Louis Laplanche; Hiroshi Ushijima; Heinz C Schröder

Book ID
114095855
Publisher
Elsevier Science
Year
2000
Tongue
English
Weight
221 KB
Volume
116
Category
Article
ISSN
0047-6374

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## Abstract Movement disturbances are common in dementia disorders and are a central feature of the clinical classification criteria of Creutzfeldt‐Jakob disease (CJD). Polymorphism at codon 129 of the prion protein gene is known to determine the clinical picture of CJD. The frequency and character