MM2 subtype of sporadic Creutzfeldt-Jakob disease may underlie the clinical presentation of progressive supranuclear palsy

Journal of Neurology

Volumn 260, Issue 4, 2013, Pages 1031-1036

  Petrovic, Igor N ^a,b   Martin Bastida, Antonio ^c   Massey, Luke ^a,d   Ling, Helen ^a   O'Sullivan, Sean S ^a   Williams, David R ^e   Holton, Janice L ^d   Revesz, Tamas ^d   Ironside, James W ^f   Lees, Andrew J ^a,d   Silveira Moriyama, Laura ^a,g  

^a UNIVERSITY COLLEGE LONDON   (United Kingdom)

^b CCS   (Serbia)

^c HOSPITAL UNIVERSITARIO VIRGEN MACARENA   (Spain)

^d UNIVERSITY COLLEGE LONDON   (United Kingdom)

^e MONASH UNIVERSITY   (Australia)

^f UNIVERSITY OF EDINBURGH   (United Kingdom)

^g UNIVERSITY OF CAMPINAS   (Brazil)

Author keywords

Creutzfeldt Jakob disease; MM2; Neuropathology; Prion; Progressive supranuclear palsy

Indexed keywords

ADULT; AGED; AKINESIA; APATHY; APRAXIA; ARTICLE; BRADYKINESIA; CLINICAL FEATURE; CREUTZFELDT JAKOB DISEASE; DEMENTIA; DISEASE COURSE; DISEASE DURATION; DYSARTHRIA; FALLING; FEMALE; FRONTOTEMPORAL DEMENTIA; GAZE PARALYSIS; HUMAN; MAJOR CLINICAL STUDY; MALE; MORTALITY; MOTOR NEURON DISEASE; MUSCLE RIGIDITY; PARKINSONISM; PRIORITY JOURNAL; PROGRESSIVE SUPRANUCLEAR PALSY; SACCADIC EYE MOVEMENT;

14-3-3 PROTEINS; AGED; BRAIN; CREUTZFELDT-JAKOB SYNDROME; ELECTROENCEPHALOGRAPHY; FEMALE; HUMANS; MALE; MIDDLE AGED; PRIONS; SUPRANUCLEAR PALSY, PROGRESSIVE;

EID: 84876464088     PISSN: 03405354     EISSN: 14321459     Source Type: Journal    
DOI: 10.1007/s00415-012-6752-7     Document Type: Article

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