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  1. Content type: Review

    Ataxic mutant mice can be used to represent models of cerebellar degenerative disorders. They serve for investigation of cerebellar function, pathogenesis of degenerative processes as well as of therapeutic ap...

    Authors: Jan Cendelin

    Citation: Cerebellum & Ataxias 2014 1:4

    Published on:

  2. Content type: Research

    Rapid uptake of glutamate by neuronal and glial glutamate transporters (EAATs, a family of excitatory amino acid transporters) is critical for shaping synaptic responses and for preventing excitotoxicity. Two ...

    Authors: Emmet M Power and Ruth M Empson

    Citation: Cerebellum & Ataxias 2014 1:3

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  3. Content type: Research

    Spinocerebellar ataxia type 7 (SCA7) is a genetic disorder characterized by degeneration of the motor and visual systems. Besides neural deterioration, these patients also show functional connectivity changes ...

    Authors: Carlos R Hernandez-Castillo, Víctor Galvez, Consuelo Morgado-Valle and Juan Fernandez-Ruiz

    Citation: Cerebellum & Ataxias 2014 1:2

    Published on: