An autopsied case of V180I Creutzfeldt-Jakob disease presenting with panencephalopathic-type pathology and a characteristic prion protein type

Neuropathology

Volumn 31, Issue 5, 2011, Pages 540-548

  Iwasaki, Yasushi ^a   Mori, Keiko ^a   Ito, Masumi ^a   Nagaoka, Masamitsu ^a   Ieda, Toshiaki ^b   Kitamoto, Tetsuyuki ^c   Yoshida, Mari ^d   Hashizume, Yoshio ^d  

^a Oyamada Memorial Spa Hospital   (Japan)

^b Yokkaichi Municipal Hospital   (Japan)

^c TOHOKU UNIVERSITY GRADUATE SCHOOL OF MEDICINE   (Japan)

^d AICHI MEDICAL UNIVERSITY   (Japan)

Author keywords

Akinetic mutism state; Creutzfeldt Jakob disease; Panencephalopathic type; Prion protein type; V180I

Indexed keywords

PRION PROTEIN;

AGED; AKINETIC MUTISM; AMINO ACID SUBSTITUTION; APHASIA; APRAXIA; ARTICLE; ASTROCYTOSIS; AUTOPSY; BIOACCUMULATION; BRAIN CORTEX; BRAIN SPONGIOSIS; CASE REPORT; CELL LOSS; CLINICAL FEATURE; CREUTZFELDT JAKOB DISEASE; DEMENTIA; DIFFUSION WEIGHTED IMAGING; DISEASE COURSE; ELECTROENCEPHALOGRAPHY; FEMALE; GENETIC DISORDER; HISTOPATHOLOGY; HOMOZYGOSITY; HUMAN; HUMAN TISSUE; MYOCLONUS; NUCLEAR MAGNETIC RESONANCE IMAGING; PARKINSONISM; POINT MUTATION; PRIORITY JOURNAL; PURKINJE CELL; WESTERN BLOTTING;

AGED; AUTOPSY; CREUTZFELDT-JAKOB SYNDROME; DIAGNOSIS, DIFFERENTIAL; FATAL OUTCOME; FEMALE; HUMANS; ISOLEUCINE; PRION DISEASES; SUBACUTE SCLEROSING PANENCEPHALITIS; VALINE;

EID: 80053126198     PISSN: 09196544     EISSN: 14401789     Source Type: Journal    
DOI: 10.1111/j.1440-1789.2010.01192.x     Document Type: Article

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