Concurrent TNFRSF1A R92Q and pyrin E230K mutations in a child with multiple sclerosis

Multiple Sclerosis

Volumn 16, Issue 12, 2010, Pages 1517-1520

  Blaschek, A ^a   Lohse, P ^a   Huss, K ^a   Borggraefe, I ^a   Mueller Felber, W ^a   Heinen, F ^a   Hohlfeld, R ^b   Kumpfel T ^b  

^a LUDWIG MAXIMILIANS UNIVERSITY   (Germany)

^b UNIVERSITY OF MUNICH   (Germany)

Author keywords

childhood; demyelinating autoimmune diseases; Familial Mediterranean Fever; genetics; multiple sclerosis; receptors; tumor necrosis factor; type 1

Indexed keywords

BETA INTERFERON; GADOLINIUM; GLATIRAMER; TUMOR NECROSIS FACTOR RECEPTOR;

ADOLESCENT; ARTICLE; AUTOINFLAMMATORY DISEASE; BALANCE DISORDER; BRAIN STEM; CASE REPORT; CEREBROSPINAL FLUID ANALYSIS; CLINICAL FEATURE; CONTRAST ENHANCEMENT; DIPLOPIA; DRUG DOSE INCREASE; DRUG SUBSTITUTION; DRUG WITHDRAWAL; FAMILIAL MEDITERRANEAN FEVER; FAMILY HISTORY; FEMALE; FLU LIKE SYNDROME; GENE MUTATION; GENETIC DISORDER; HEADACHE; HEARING IMPAIRMENT; HUMAN; IMMUNOMODULATION; MIGRAINE; MULTIPLE SCLEROSIS; MYALGIA; NUCLEAR MAGNETIC RESONANCE IMAGING; NYSTAGMUS; ONSET AGE; PARESTHESIA; PEDIGREE ANALYSIS; PERICARDIAL EFFUSION; POINT MUTATION; SYMPTOM; THORAX PAIN; TREATMENT OUTCOME; TUMOR NECROSIS FACTOR RECEPTOR ASSOCIATED PERIODIC SYNDROME;

ADOLESCENT; CYTOSKELETAL PROTEINS; FEMALE; HUMANS; MALE; MULTIPLE SCLEROSIS; MUTATION; PEDIGREE; RECEPTORS, TUMOR NECROSIS FACTOR, TYPE I;

EID: 78650158607     PISSN: 13524585     EISSN: None     Source Type: Journal    
DOI: 10.1177/1352458510382933     Document Type: Article

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