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Differential diagnosis of 201 possible Creutzfeldt-Jakob disease patients

✍ Scribed by Bart Everbroeck; Itte Dobbeleir; Michele Waele; Peter Deyn; Jean-Jacques Martin; Patrick Cras


Book ID
106092380
Publisher
Springer
Year
2004
Tongue
English
Weight
309 KB
Volume
251
Category
Article
ISSN
0340-5354

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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