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Immunological Assessment in Sporadic Amyotrophic Lateral Sclerosis (ALS)

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Part of the book series: Advances in Experimental Medicine and Biology ((AEMB,volume 209))

Abstract

The immune system may be able to contribute to the pathogenesis of ALS as it has to other neurological diseases such as experimental allergic encephalomyelitis, multiple sclerosis and lymphocytic choriomeningitis. The selective damage to upper and lower motor neurons in ALS might be regarded as a feature of a brain-confined, organ-specific autoimmune disease. The greater frequency of some histocompatibility antigens (HLA3, HLB12, HLBW35) may suggest the possible predisposition to autoimmune and infectious diseases [1-3].

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© 1987 Plenum Press, New York

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Provinciali, L., Giovagnoli, A.R., Battucci, S., Bartocci, C., Montroni, M. (1987). Immunological Assessment in Sporadic Amyotrophic Lateral Sclerosis (ALS). In: Cosi, V., Kato, A.C., Parlette, W., Pinelli, P., Poloni, M. (eds) Amyotrophic Lateral Sclerosis. Advances in Experimental Medicine and Biology, vol 209. Springer, Boston, MA. https://doi.org/10.1007/978-1-4684-5302-7_25

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  • DOI: https://doi.org/10.1007/978-1-4684-5302-7_25

  • Publisher Name: Springer, Boston, MA

  • Print ISBN: 978-1-4684-5304-1

  • Online ISBN: 978-1-4684-5302-7

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