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TNFRSF1A R92Q mutation in association with a multiple sclerosis-like demyelinating syndrome.

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  • Authors+Show Affiliations

    ,

    Institute of Clinical Neuroimmunology, Ludwig-Maximilians-University, Munich, Germany.

    , , , ,

    Source

    Neurology 70:13 Pt 2 2008 Mar 25 pg 1155-6

    MeSH

    Adolescent
    Amino Acid Substitution
    Brain
    Chemotaxis, Leukocyte
    Chromosome Disorders
    DNA Mutational Analysis
    Diagnosis, Differential
    Female
    Genes, Dominant
    Genetic Markers
    Genetic Predisposition to Disease
    Genotype
    Hereditary Central Nervous System Demyelinating Diseases
    Humans
    Leukocytes
    Magnetic Resonance Imaging
    Multiple Sclerosis
    Mutation
    Receptors, Tumor Necrosis Factor, Type I
    Syndrome
    Tumor Necrosis Factor-alpha

    Pub Type(s)

    Case Reports
    Journal Article

    Language

    eng

    PubMed ID

    18287568

    Citation

    Hoffmann, L A., et al. "TNFRSF1A R92Q Mutation in Association With a Multiple Sclerosis-like Demyelinating Syndrome." Neurology, vol. 70, no. 13 Pt 2, 2008, pp. 1155-6.
    Hoffmann LA, Lohse P, König FB, et al. TNFRSF1A R92Q mutation in association with a multiple sclerosis-like demyelinating syndrome. Neurology. 2008;70(13 Pt 2):1155-6.
    Hoffmann, L. A., Lohse, P., König, F. B., Feneberg, W., Hohlfeld, R., & Kümpfel, T. (2008). TNFRSF1A R92Q mutation in association with a multiple sclerosis-like demyelinating syndrome. Neurology, 70(13 Pt 2), pp. 1155-6. doi:10.1212/01.wnl.0000296279.98236.8a.
    Hoffmann LA, et al. TNFRSF1A R92Q Mutation in Association With a Multiple Sclerosis-like Demyelinating Syndrome. Neurology. 2008 Mar 25;70(13 Pt 2):1155-6. PubMed PMID: 18287568.
    * Article titles in AMA citation format should be in sentence-case
    TY - JOUR T1 - TNFRSF1A R92Q mutation in association with a multiple sclerosis-like demyelinating syndrome. AU - Hoffmann,L A, AU - Lohse,P, AU - König,F B, AU - Feneberg,W, AU - Hohlfeld,R, AU - Kümpfel,T, Y1 - 2008/02/20/ PY - 2008/2/22/pubmed PY - 2008/6/20/medline PY - 2008/2/22/entrez SP - 1155 EP - 6 JF - Neurology JO - Neurology VL - 70 IS - 13 Pt 2 SN - 1526-632X UR - https://www.unboundmedicine.com/medline/citation/18287568/TNFRSF1A_R92Q_mutation_in_association_with_a_multiple_sclerosis_like_demyelinating_syndrome_ L2 - http://www.neurology.org/cgi/pmidlookup?view=long&pmid=18287568 DB - PRIME DP - Unbound Medicine ER -