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Isabelle Le Ber

Showing results (91-100 of 211) with videos related to

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Movement Disorders : Official Journal of the Movement Disorder Society|February 3, 2011
Quantitative assessment of the evolution of cerebellar signs in spinocerebellar ataxiasEllis Chan, Perrine Charles, Pascale Ribai, et al.
Neurobiology of Aging|September 21, 2019
A unique common ancestor introduced P301L mutation in MAPT gene in frontotemporal dementia patients from Barcelona (Baix Llobregat, Spain)Leire Palencia-Madrid, Raquel Sánchez-Valle, Ierai Fernández de Retana, et al.
Brain : a Journal of Neurology|April 2, 2008
Composite cerebellar functional severity score: validation of a quantitative score of cerebellar impairmentSophie Tezenas du Montcel, Perrine Charles, Pascale Ribai, et al.
Neurology|December 21, 2012
Mutation of the PDGFRB gene as a cause of idiopathic basal ganglia calcificationGaël Nicolas, Cyril Pottier, David Maltête, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|December 7, 2021
Conceptual framework for the definition of preclinical and prodromal frontotemporal dementiaAlberto Benussi, Antonella Alberici, Kiran Samra, et al.
Cortex; a Journal Devoted to the Study of the Nervous System and Behavior|October 30, 2021
Primary progressive aphasias associated with C9orf72 expansions: Another side of the storyDario Saracino, Amandine Géraudie, Anne M Remes, et al.
Neurology|August 8, 2014
Contribution of ATXN2 intermediary polyQ expansions in a spectrum of neurodegenerative disordersSerena Lattante, Stéphanie Millecamps, Giovanni Stevanin, et al.
European Journal of Neurology|September 20, 2021
Evaluation of CSF1R-related adult onset leukoencephalopathy with axonal spheroids and pigmented glia diagnostic criteriaXavier Ayrignac, Clarisse Carra-Dallière, Pekes Codjia, et al.
BMC Medical Genomics|June 20, 2013
Genome-wide expression profiling and functional characterization of SCA28 lymphoblastoid cell lines reveal impairment in cell growth and activation of apoptotic pathwaysCecilia Mancini, Paola Roncaglia, Alessandro Brussino, et al.
Neurology|October 18, 2022
Brain Metabolic Profile in Presymptomatic <i>GRN</i> Carriers Throughout a 5-Year Follow-upDario Saracino, Leila Sellami, Hugo Boniface, et al.
Pageof 22

Showing results (91-100 of 211) with videos related to

Sort By:
Pageof 22
Movement Disorders : Official Journal of the Movement Disorder Society|February 3, 2011
Quantitative assessment of the evolution of cerebellar signs in spinocerebellar ataxiasEllis Chan, Perrine Charles, Pascale Ribai, et al.
Neurobiology of Aging|September 21, 2019
A unique common ancestor introduced P301L mutation in MAPT gene in frontotemporal dementia patients from Barcelona (Baix Llobregat, Spain)Leire Palencia-Madrid, Raquel Sánchez-Valle, Ierai Fernández de Retana, et al.
Brain : a Journal of Neurology|April 2, 2008
Composite cerebellar functional severity score: validation of a quantitative score of cerebellar impairmentSophie Tezenas du Montcel, Perrine Charles, Pascale Ribai, et al.
Neurology|December 21, 2012
Mutation of the PDGFRB gene as a cause of idiopathic basal ganglia calcificationGaël Nicolas, Cyril Pottier, David Maltête, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|December 7, 2021
Conceptual framework for the definition of preclinical and prodromal frontotemporal dementiaAlberto Benussi, Antonella Alberici, Kiran Samra, et al.
Cortex; a Journal Devoted to the Study of the Nervous System and Behavior|October 30, 2021
Primary progressive aphasias associated with C9orf72 expansions: Another side of the storyDario Saracino, Amandine Géraudie, Anne M Remes, et al.
Neurology|August 8, 2014
Contribution of ATXN2 intermediary polyQ expansions in a spectrum of neurodegenerative disordersSerena Lattante, Stéphanie Millecamps, Giovanni Stevanin, et al.
European Journal of Neurology|September 20, 2021
Evaluation of CSF1R-related adult onset leukoencephalopathy with axonal spheroids and pigmented glia diagnostic criteriaXavier Ayrignac, Clarisse Carra-Dallière, Pekes Codjia, et al.
BMC Medical Genomics|June 20, 2013
Genome-wide expression profiling and functional characterization of SCA28 lymphoblastoid cell lines reveal impairment in cell growth and activation of apoptotic pathwaysCecilia Mancini, Paola Roncaglia, Alessandro Brussino, et al.
Neurology|October 18, 2022
Brain Metabolic Profile in Presymptomatic <i>GRN</i> Carriers Throughout a 5-Year Follow-upDario Saracino, Leila Sellami, Hugo Boniface, et al.
Pageof 22