Diffusion-weighted MRI in familial Creutzfeldt-Jakob disease with the codon 200 mutation in the prion protein gene

Journal of the Neurological Sciences

Volumn 232, Issue 1-2, 2005, Pages 45-49

  Tsuboi, Yoshio ^a   Baba, Yasuhiko ^b   Doh Ura, Katsumi ^c   Imamura, Akiko ^a   Fujioka, Shinsuke ^a   Yamada, Tatsuo ^a  

^a FUKUOKA UNIVERSITY   (Japan)

^b MAYO CLINIC   (United States)

^c TOHOKU UNIVERSITY   (Japan)

Author keywords

Creutzfeldt Jakob disease; Diagnostic methods; Diffusion weighted imaging; Familial; Magnetic resonance imaging; Prion disease; Prion gene mutation

Indexed keywords

MEPACRINE; PRION PROTEIN;

ADULT; ANAMNESIS; ARTICLE; BASAL GANGLION; BRAIN CORTEX; CASE REPORT; CLINICAL EXAMINATION; CLINICAL FEATURE; CODON; CREUTZFELDT JAKOB DISEASE; DIFFUSION WEIGHTED IMAGING; DNA EXTRACTION; FEMALE; GENE MUTATION; GENETIC ANALYSIS; GLOBUS PALLIDUS; HUMAN; IMAGE ANALYSIS; LABORATORY TEST; MINI MENTAL STATE EXAMINATION; NEUROIMAGING; PHYSICAL EXAMINATION; PRIORITY JOURNAL; PROTEIN LOCALIZATION; SIGNAL TRANSDUCTION;

EID: 17844400287     PISSN: 0022510X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jns.2005.01.006     Document Type: Article

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