Movement disturbances in the differential diagnosis of Creutzfeldt-Jakob disease

Movement Disorders

Volumn 24, Issue 3, 2009, Pages 350-356

  Edler, Jan ^a   Mollenhauer, Brit ^b   Heinemann, Uta ^a   Varges, Daniela ^a   Werner, Carola ^a   Zerr, Inga ^a   Schulz Schaeffer, Walter J ^a  

^a UNIVERSITY MEDICAL CENTER GÖTTINGEN   (Germany)

^b MASSACHUSETTS GENERAL HOSPITAL   (United States)

Author keywords

Alzheimer's disease; Ataxia; Cogwheel rigidity; Dysmetria; Hypokinesia; Prion disease

Indexed keywords

METHIONINE; PRION PROTEIN; VALINE; PRNP PROTEIN, HUMAN;

ADULT; AGED; AMINO ACID SUBSTITUTION; ARTICLE; ATAXIA; ATHETOSIS; CHOREA; CLINICAL FEATURE; CONTROLLED STUDY; CREUTZFELDT JAKOB DISEASE; DIFFERENTIAL DIAGNOSIS; DIFFUSE LEWY BODY DISEASE; DISEASE DURATION; DYSMETRIA; DYSTONIA; FEMALE; GAIT DISORDER; GENETIC ASSOCIATION; GENETIC POLYMORPHISM; HOMOZYGOSITY; HUMAN; HYPOKINESIA; MAJOR CLINICAL STUDY; MALE; MORBIDITY; MOTOR DYSFUNCTION; MUSCLE RIGIDITY; MUSCLE TONE; MYOCLONUS; NEUROPATHOLOGY; NYSTAGMUS; ONSET AGE; PRIORITY JOURNAL; PYRAMIDAL SIGN; SEX DIFFERENCE; SPASTICITY; TREMOR; ALZHEIMER DISEASE; CODON; GENETICS; MIDDLE AGED; PHENOTYPE; PREVALENCE; PRION;

ADULT; AGED; AGED, 80 AND OVER; ALZHEIMER DISEASE; ATAXIA; CODON; CREUTZFELDT-JAKOB SYNDROME; DIAGNOSIS, DIFFERENTIAL; FEMALE; HUMANS; HYPOKINESIA; MALE; MIDDLE AGED; MOVEMENT DISORDERS; MUSCLE RIGIDITY; PHENOTYPE; POLYMORPHISM, GENETIC; PREVALENCE; PRIONS;

EID: 67651090104     PISSN: 08853185     EISSN: 15318257     Source Type: Journal    
DOI: 10.1002/mds.22253     Document Type: Article

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