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Laura Orsi

Showing results (11-20 of 26) with videos related to

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Neurocase|July 17, 2009
Neuropsychological and functional study in a case of partial cerebellar agenesisPaola Caroppo, Laura Orsi, Federico D'Agata, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 21, 2008
A previously undiagnosed case of Gerstmann-Sträussler-Scheinker disease revealed by PRNP gene analysis in patients with adult-onset ataxiaClaudia Cagnoli, Alessandro Brussino, Luca Sbaiz, et al.
Neuropsychological Rehabilitation|October 23, 2015
The rehabilitative effects on written language of a combined language and parietal dual-tDCS treatment in a stroke caseBarbara De Tommaso, Alessandro Piedimonte, Marcella M Caglio, et al.
Cerebellum (London, England)|January 19, 2010
Two Italian families with ITPR1 gene deletion presenting a broader phenotype of SCA15Eleonora Di Gregorio, Laura Orsi, Massimiliano Godani, et al.
Parkinsonism & Related Disorders|May 5, 2016
Clinical and neuroradiological features of spinocerebellar ataxia 38 (SCA38)Barbara Borroni, Eleonora Di Gregorio, Laura Orsi, et al.
Brain Structure & Function|April 5, 2011
Linking coordinative and executive dysfunctions to atrophy in spinocerebellar ataxia 2 patientsFederico D'Agata, Paola Caroppo, Andrea Boghi, et al.
Neurobiology of Aging|October 22, 2018
ATXN2 intermediate repeat expansions influence the clinical phenotype in frontotemporal dementiaElisa Rubino, Cecilia Mancini, Silvia Boschi, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 23, 2019
The largest caucasian kindred with dentatorubral-pallidoluysian atrophy: A founder mutation in italySilvia Grimaldi, Chiara Cupidi, Nicoletta Smirne, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 15, 2010
Spinocerebellar ataxia type 12 identified in two Italian families may mimic sporadic ataxiaAlessandro Brussino, Claudio Graziano, Dario Giobbe, et al.
Parkinsonism & Related Disorders|March 14, 2019
Long-term efficacy of docosahexaenoic acid (DHA) for Spinocerebellar Ataxia 38 (SCA38) treatment: An open label extension studyMarta Manes, Antonella Alberici, Eleonora Di Gregorio, et al.
Pageof 3

Showing results (11-20 of 26) with videos related to

Sort By:
Pageof 3
Neurocase|July 17, 2009
Neuropsychological and functional study in a case of partial cerebellar agenesisPaola Caroppo, Laura Orsi, Federico D'Agata, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 21, 2008
A previously undiagnosed case of Gerstmann-Sträussler-Scheinker disease revealed by PRNP gene analysis in patients with adult-onset ataxiaClaudia Cagnoli, Alessandro Brussino, Luca Sbaiz, et al.
Neuropsychological Rehabilitation|October 23, 2015
The rehabilitative effects on written language of a combined language and parietal dual-tDCS treatment in a stroke caseBarbara De Tommaso, Alessandro Piedimonte, Marcella M Caglio, et al.
Cerebellum (London, England)|January 19, 2010
Two Italian families with ITPR1 gene deletion presenting a broader phenotype of SCA15Eleonora Di Gregorio, Laura Orsi, Massimiliano Godani, et al.
Parkinsonism & Related Disorders|May 5, 2016
Clinical and neuroradiological features of spinocerebellar ataxia 38 (SCA38)Barbara Borroni, Eleonora Di Gregorio, Laura Orsi, et al.
Brain Structure & Function|April 5, 2011
Linking coordinative and executive dysfunctions to atrophy in spinocerebellar ataxia 2 patientsFederico D'Agata, Paola Caroppo, Andrea Boghi, et al.
Neurobiology of Aging|October 22, 2018
ATXN2 intermediate repeat expansions influence the clinical phenotype in frontotemporal dementiaElisa Rubino, Cecilia Mancini, Silvia Boschi, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 23, 2019
The largest caucasian kindred with dentatorubral-pallidoluysian atrophy: A founder mutation in italySilvia Grimaldi, Chiara Cupidi, Nicoletta Smirne, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 15, 2010
Spinocerebellar ataxia type 12 identified in two Italian families may mimic sporadic ataxiaAlessandro Brussino, Claudio Graziano, Dario Giobbe, et al.
Parkinsonism & Related Disorders|March 14, 2019
Long-term efficacy of docosahexaenoic acid (DHA) for Spinocerebellar Ataxia 38 (SCA38) treatment: An open label extension studyMarta Manes, Antonella Alberici, Eleonora Di Gregorio, et al.
Pageof 3