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Cerebellum and Emotion Recognition

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  1. Article

    Open Access

    O056. Migraine as presenting symptom of SLC20A2gene mutations

    Elisa Rubino, Elisa Giorgio, Innocenzo Rainero… in The Journal of Headache and Pain (2015)

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  2. Article

    Open Access

    An atypical form of AOA2 with myoclonus associated with mutations in SETX and AFG3L2

    Hereditary ataxias are a heterogeneous group of neurodegenerative disorders, where exome sequencing may become an important diagnostic tool to solve clinically or genetically complex cases.

    Cecilia Mancini, Laura Orsi, Yiran Guo, Jiankang Li, Yulan Chen… in BMC Medical Genetics (2015)

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