Characterising the uncommon corticobasal syndrome presentation of sporadic Creutzfeldt-Jakob disease

Parkinsonism and Related Disorders

Volumn 19, Issue 1, 2013, Pages 81-85

  Lee, Will ^a,d   Simpson, Marion ^a,b   Ling, Helen ^c   McLean, Catriona ^a   Collins, Steven ^b   Williams, David R ^a,d  

^a ALFRED HOSPITAL   (Australia)

^b UNIVERSITY OF MELBOURNE   (Australia)

^c UNIVERSITY COLLEGE LONDON   (United Kingdom)

^d MONASH UNIVERSITY   (Australia)

Author keywords

Alien limb; Corticobasal; Dystonia; Myoclonus; Prion disease

Indexed keywords

PROTEIN 14 3 3;

ADULT; AGED; ALIEN HAND SYNDROME; ARTICLE; AUSTRALIA; CLINICAL ARTICLE; CLINICAL FEATURE; COMPARATIVE STUDY; CORTICOBASAL DEGENERATION; CORTICOBASAL SYNDROME; DEATH; DIAGNOSTIC APPROACH ROUTE; DIFFERENTIAL DIAGNOSIS; DIFFUSION WEIGHTED IMAGING; DISEASE ASSOCIATION; DISEASE COURSE; DISEASE DURATION; DISEASE REGISTRY; ELECTROENCEPHALOGRAM; FEMALE; HISTOPATHOLOGY; HUMAN; MALE; MYOCLONUS; PATIENT IDENTIFICATION; PRIORITY JOURNAL; PROTEIN CEREBROSPINAL FLUID LEVEL; SENSORY DYSFUNCTION; SPORADIC CREUTZFELDT JAKOB DISEASE;

AGED; AUSTRALIA; BRAIN; CREUTZFELDT-JAKOB SYNDROME; DIAGNOSIS, DIFFERENTIAL; DYSTONIA; ELECTROENCEPHALOGRAPHY; FEMALE; HUMANS; IMAGE PROCESSING, COMPUTER-ASSISTED; MAGNETIC RESONANCE IMAGING; MALE; MIDDLE AGED; MYOCLONUS;

EID: 84871497023     PISSN: 13538020     EISSN: 18735126     Source Type: Journal    
DOI: 10.1016/j.parkreldis.2012.07.010     Document Type: Article

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