Episodic ataxias

Handbook of Clinical Neurology
Joanna C Jen, Jijun Wan

Abstract

The familial episodic ataxias (EAs) are prototypical channelopathies in the central nervous system clinically characterized by attacks of imbalance and incoordination variably associated with progressive ataxia and variable interictal features. EA1, EA2, and EA6 are caused by mutations in ion channel- and transporter-encoding genes that regulate neuronal excitability and neurotransmission.

Citations

Feb 9, 2019·Journal of Movement Disorders·Ileok Jung, Ji-Soo Kim
Sep 10, 2020·International Journal of Molecular Sciences·Paola GiuntiMarina Frontali
May 7, 2020·Movement Disorders Clinical Practice·Simone Gana, Enza Maria Valente

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