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0819 The role of SPECT with 123I-IMP in the diagnosis of Creutzfeldt-Jakob disease


Book ID
123585693
Publisher
Elsevier Science
Year
2005
Tongue
English
Weight
122 KB
Volume
238
Category
Article
ISSN
0022-510X

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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