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  1. No Access

    Chapter

    Cerebellum and Emotion Recognition

    In this chapter, after having clarified which definition of emotion we followed, starting from Darwin and evolutionary psychology, we tried to examine the main mechanisms of emotional recognition from a behavi...

    Federico D’Agata, Laura Orsi in The Emotional Cerebellum (2022)

  2. 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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  3. 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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  4. No Access

    Article

    Novel mutation of SLC20A2 in an Italian patient presenting with migraine

    Elisa Rubino, Elisa Giorgio, Salvatore Gallone, Lorenzo Pinessi… in Journal of Neurology (2014)

  5. No Access

    Article

    Linking coordinative and executive dysfunctions to atrophy in spinocerebellar ataxia 2 patients

    Spinocerebellar ataxias type 2 (SCA2) is a rare genetic disorder characterised by the degeneration of the Cerebellum, its connections and many Brainstem areas. A voxel-based morphometry (VBM) analysis was perf...

    Federico D’Agata, Paola Caroppo, Andrea Boghi… in Brain Structure and Function (2011)

  6. No Access

    Article

    The Recognition of Facial Emotions in Spinocerebellar Ataxia Patients

    Patients with cerebellar lesions present some affective and cognitive disorders, defining a peculiar pattern of cognitive impairment, so-called cerebellar cognitive affective syndrome. This pattern has been co...

    Federico D’Agata, Paola Caroppo, Bruno Baudino, Marcella Caglio… in The Cerebellum (2011)

  7. No Access

    Article

    Two Italian Families with ITPR1 Gene Deletion Presenting a Broader Phenotype of SCA15

    Spinocerebellar ataxia type15 (SCA15) is a pure ataxia characterized by very slow progression. Only seven families have been identified worldwide, in which partial deletions and a missense mutation of the inos...

    Eleonora Di Gregorio, Laura Orsi, Massimiliano Godani, Giovanna Vaula… in The Cerebellum (2010)

  8. No Access

    Article

    Analysis of SCA8 and SCA12 loci in 134 Italian ataxic patients negative for SCA1–3, 6 and 7 CAG expansions

    Spinocerebellar ataxias (SCA) are a heterogeneous group of neurodegenerative disorders, six of which are caused by expansion of a polyglutamine-coding CAG repeats (SCA1- 3, 6, 7 and 17). In addition, expansions ...

    Alfredo Brusco, Claudia Cagnoli, Alessandra Franco, Elisa Dragone… in Journal of Neurology (2002)

  9. No Access

    Article

    Glycosaminoglycan changes in human gliomas. A biochemical study

    Glycosaminoglycans (GAGs) were isolated, separated by electrophoresis and quantified in 36 neurosurgical specimens of human gliomas and in 8 samples of normal white and gray matter. Gliomas of various degrees ...

    Antonio Bertolotto MD, Maria Luisa Magrassi, Laura Orsi… in Journal of Neuro-Oncology (1986)