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Volumn 86, Issue 11, 2015, Pages 1279-1280
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Variant Creutzfeldt-Jakob disease in older patients
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Author keywords
[No Author keywords available]
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Indexed keywords
PRION PROTEIN;
PRION;
PRNP PROTEIN, HUMAN;
ADULT;
AGE DISTRIBUTION;
ATAXIA;
BLOOD TRANSFUSION;
BOVINE SPONGIFORM ENCEPHALOPATHY;
CLINICAL ARTICLE;
CLINICAL FEATURE;
COGNITIVE DEFECT;
DEMENTIA;
DETERIORATION;
DISEASE COURSE;
FEMALE;
FRONTOTEMPORAL DEMENTIA;
HISTOPATHOLOGY;
HUMAN;
INFECTION RISK;
INVOLUNTARY MOVEMENT;
LETTER;
MALE;
MULTIINFARCT DEMENTIA;
NEUROIMAGING;
NEUROLOGIC DISEASE;
NUCLEAR MAGNETIC RESONANCE IMAGING;
PRIORITY JOURNAL;
SENSITIVITY AND SPECIFICITY;
SURGICAL TECHNIQUE;
VARIANT CREUTZFELDT JAKOB DISEASE;
WERNICKE ENCEPHALOPATHY;
ZOONOSIS;
AGED;
CREUTZFELDT-JAKOB SYNDROME;
DIFFERENTIAL DIAGNOSIS;
GENETICS;
MIDDLE AGED;
ONSET AGE;
PATHOLOGY;
PRION;
VERY ELDERLY;
AGE OF ONSET;
AGED;
AGED, 80 AND OVER;
CREUTZFELDT-JAKOB SYNDROME;
DEMENTIA;
DIAGNOSIS, DIFFERENTIAL;
FEMALE;
HUMANS;
MALE;
MIDDLE AGED;
PRION PROTEINS;
PRIONS;
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EID: 84947032049
PISSN: 00223050
EISSN: 1468330X
Source Type: Journal
DOI: 10.1136/jnnp-2014-309397 Document Type: Letter |
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Times cited : (9)
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References (5)
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