Abstract
Immune-mediated cerebellar ataxias (IMCAs) have diverse etiologies. Paraneoplastic cerebellar degeneration, gluten ataxia, and primary autoimmune cerebellar ataxia are discussed in separate chapters. This chapter will discuss the clinical characteristics and pathoimmunological mechanisms of two other IMCAs: (1) postinfectious cerebellitis and Miller Fisher syndrome in which the autoimmunity is triggered by infection, and (2) anti-GAD, anti-VGCC, anti-mGluR1, anti-GluR delta, anti-Caspr2, and anti-DPPX ataxias, in which autoantibodies target synaptic machinery proteins or ion channels/ion channel-related proteins.
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Hadjivassiliou, M., Mitoma, H. (2023). Immune-Mediated Cerebellar Ataxias. In: Gruol, D.L., Koibuchi, N., Manto, M., Molinari, M., Schmahmann, J.D., Shen, Y. (eds) Essentials of Cerebellum and Cerebellar Disorders. Springer, Cham. https://doi.org/10.1007/978-3-031-15070-8_87
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