Genetic Creutzfeldt-Jakob disease with R208H mutation presenting as progressive supranuclear palsy

Movement Disorders

Volumn 27, Issue 4, 2012, Pages 476-479

  Matěj, Radoslav ^a,b,c   Kovacs, Gabor G ^c   Johanidesová, Silvie ^a   Keller, Jiří ^b,d   Matějčková, Milada ^a   Nováková, Jana ^a   Šigut, Vladimír ^e   Keller, Otakar ^a   Rusina, Robert ^a  

^a Thomayer Teaching Hospital   (Czech Republic)

^b CHARLES UNIVERSITY   (Czech Republic)

^c MEDICAL UNIVERSITY OF VIENNA   (Austria)

^d NA HOMOLCE HOSPITAL   (Czech Republic)

^e District Hospital   (Czech Republic)

Author keywords

[No Author keywords available]

Indexed keywords

LEVODOPA;

ADULT; AGITATION; AKINESIA; APATHY; CASE REPORT; CONFUSION; CREUTZFELDT JAKOB DISEASE; DEPRESSION; DRUG DOSE TITRATION; FALLING; FEMALE; HUMAN; LOW BACK PAIN; MYOCLONUS; NOTE; PRIORITY JOURNAL; PROGRESSIVE SUPRANUCLEAR PALSY; SENSORIMOTOR NEUROPATHY; SEPTICEMIA; WALKING DIFFICULTY;

ARGININE; CREUTZFELDT-JAKOB SYNDROME; DNA MUTATIONAL ANALYSIS; FEMALE; HISTIDINE; HUMANS; MAGNETIC RESONANCE IMAGING; MIDDLE AGED; MUTATION; PRIONS; SUPRANUCLEAR PALSY, PROGRESSIVE;

EID: 84859341110     PISSN: 08853185     EISSN: 15318257     Source Type: Journal    
DOI: 10.1002/mds.24002     Document Type: Note

References (13)

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