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Volumn 22, Issue 6, 2007, Pages 898-899
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MV2 subtype of sporadic Creutzfeldt-Jakob disease presenting as corticobasal syndrome [1]
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Author keywords
[No Author keywords available]
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Indexed keywords
PRION PROTEIN;
ADULT;
CASE REPORT;
CEREBROSPINAL FLUID ANALYSIS;
CLINICAL FEATURE;
CORTICOBASAL DEGENERATION;
CREUTZFELDT JAKOB DISEASE;
DISEASE DURATION;
GENE MUTATION;
GLIOSIS;
HISTOPATHOLOGY;
HUMAN;
HUMAN TISSUE;
IMMUNOREACTIVITY;
LETTER;
MALE;
MOLECULAR GENETICS;
NEUROLOGIC EXAMINATION;
PRIORITY JOURNAL;
CEREBELLUM;
CEREBRAL CORTEX;
CREUTZFELDT-JAKOB SYNDROME;
HUMANS;
MALE;
MIDDLE AGED;
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EID: 34249008982
PISSN: 08853185
EISSN: 15318257
Source Type: Journal
DOI: 10.1002/mds.21426 Document Type: Letter |
Times cited : (7)
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References (8)
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