Characterization of movement disorders in patients with familial creutzfeldt-jakob disease carrying the E200K mutation

Israel Medical Association Journal

Volumn 14, Issue 3, 2012, Pages 162-165

  Cohen, Oren S ^a,b   Prohovnik, Isak ^e   Korczyn, Amos D ^b   Inzelberg, Rivka ^a,b   Nitsan, Zeev ^a   Appel, Shmuel ^a   Kahana, Ester ^c   Rosenmann, Hanna ^d   Chapman, Joab ^a,b  

^a SHEBA MEDICAL CENTER   (Israel)

^b TEL AVIV UNIVERSITY   (Israel)

^c BARZILAI MEDICAL CENTER   (Israel)

^d HADASSAH HEBREW UNIVERSITY MEDICAL CENTER   (Israel)

^e MOUNT SINAI MEDICAL CENTER   (United States)

Author keywords

Creutzfeld jakob disease (CJD); Extrapyramidal signs; Movement disorders; Myoclonus; Prion diseases

Indexed keywords

GLUTAMIC ACID; LYSINE; PRION PROTEIN;

ADULT; AGED; ARTICLE; ATAXIA; BRADYKINESIA; CLINICAL ARTICLE; EXTRAPYRAMIDAL SYMPTOM; FAMILIAL CREUTZFELDT JAKOB DISEASE; FEMALE; GENE; GENE MUTATION; HUMAN; MALE; MOTOR DYSFUNCTION; MYOCLONUS; NEUROLOGIC EXAMINATION; PREVALENCE; PRION PROTEIN GENE; RIGIDITY; TREMOR;

ADULT; AGED; BASAL GANGLIA DISEASES; CREUTZFELDT-JAKOB SYNDROME; FEMALE; HUMANS; ISRAEL; JEWS; LIBYA; MALE; MIDDLE AGED; MOVEMENT DISORDERS; MUTATION; MYOCLONUS; PREVALENCE; PRIONS; PROSPECTIVE STUDIES;

EID: 84859061213     PISSN: 15651088     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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