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Volumn 70, Issue 13 PART 2, 2008, Pages 1155-1156
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TNFRSF1A R92Q mutation in association with a multiple sclerosis-like demyelinating syndrome
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Author keywords
[No Author keywords available]
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Indexed keywords
IMMUNOGLOBULIN G;
MITOXANTRONE;
NATALIZUMAB;
ADOLESCENT;
ARTICLE;
CASE REPORT;
DIFFUSION WEIGHTED IMAGING;
DISEASE COURSE;
DRUG WITHDRAWAL;
FACIAL NERVE PARALYSIS;
FAMILY HISTORY;
FEMALE;
GENE;
GENE MUTATION;
GENETIC ANALYSIS;
HUMAN;
INFECTION COMPLICATION;
MANIA;
MOOD CHANGE;
NUCLEAR MAGNETIC RESONANCE IMAGING;
OPTIC NEURITIS;
PERSONALITY DISORDER;
PRIORITY JOURNAL;
PSYCHOPATHY;
TNFRSF1A GENE;
TUMOR NECROSIS FACTOR RECEPTOR ASSOCIATED PERIODIC SYNDROME;
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EID: 41549156916
PISSN: 00283878
EISSN: None
Source Type: Journal
DOI: 10.1212/01.wnl.0000296279.98236.8a Document Type: Article |
Times cited : (17)
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References (5)
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