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  1. Friedreich’s ataxia is an autosomal recessive, severely incapacitating disorder. There is little objective evidence regarding FRDA management. Abnormalities in the insulin/insulin-like growth factor 1 (IGF-1) ...

    Authors: Irene Sanz-Gallego, Ignacio Torres-Aleman and Javier Arpa

    Citation: Cerebellum & Ataxias 2014 1:10

    Content type: Research

    Published on:

  2. Two affected and one unaffected siblings from a French-Canadian family were evaluated in our neurogenetic clinic. The oldest brother had intentional and postural hand tremor while his youngest sister presented...

    Authors: Anne Noreau, Philippe Beauchemin, Alexandre Dionne-Laporte, Patrick A Dion, Guy A Rouleau and Nicolas Dupré

    Citation: Cerebellum & Ataxias 2014 1:8

    Content type: Case report

    Published on:

  3. 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

    Content type: Review

    Published on:

  4. 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

    Content type: Research

    Published on:

  5. 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

    Content type: Research

    Published on: