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Viviana Pensato

Showing results (1-10 of 40) with videos related to

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Journal of Neurology|April 21, 2020
Asymptomatic adrenoleukodystrophy in elderly malesChiara Benzoni, Silvia Fenu, Viviana Pensato, et al.
The Neurologist|November 6, 2019
Leukoencephalopathy With Predominant Infratentorial Involvement Caused by a Novel ABCD1 Mutation: Does the Spinocerebellar Variant of Adrenoleukodystrophy Exist?Chiara Benzoni, Laura Farina, Viviana Pensato, et al.
Neurology|August 19, 2022
Behavioral and Cognitive Phenotypes of Patients With Amyotrophic Lateral Sclerosis Carrying SOD1 VariantsEleonora Dalla Bella, Enrica Bersano, Maria Grazia Bruzzone, et al.
Journal of Clinical Neurology (Seoul, Korea)|April 9, 2015
PEX7 Mutations Cause Congenital Cataract Retinopathy and Late-Onset Ataxia and Cognitive Impairment: Report of Two Siblings and Review of the LiteratureLorenzo Nanetti, Viviana Pensato, Valerio Leoni, et al.
Neurobiology of Aging|June 29, 2022
G507D mutation in FUS gene causes familial amyotrophic lateral sclerosis with a specific genotype-phenotype correlationIlaria Martinelli, Elisabetta Zucchi, Viviana Pensato, et al.
Pain and Therapy|February 20, 2021
Pain Study in X-Linked Adrenoleukodystrophy in Males and FemalesValeria Bachiocco, Marco Cappa, Anna Petroni, et al.
Neuroimage. Clinical|July 20, 2018
Cortical markers of cognitive syndromes in amyotrophic lateral sclerosisMonica Consonni, Valeria E Contarino, Eleonora Catricalà, et al.
Neurobiology of Aging|March 20, 2012
ATAXIN2 CAG-repeat length in Italian patients with amyotrophic lateral sclerosis: risk factor or variant phenotype? Implication for genetic testing and counselingCinzia Gellera, Nicola Ticozzi, Viviana Pensato, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|October 19, 2021
Duplication of exons 15 and 16 in Matrin-3: a phenotype bridging amyotrophic lateral sclerosis and immune-mediated disordersMaria Caputo, Elisabetta Zucchi, Ilaria Martinelli, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|June 22, 2022
Missense mutation in ATXN2 gene (c.2860C > T) in an amyotrophic lateral sclerosis patient with aggressive disease phenotypeAndrea Ghezzi, Ilaria Martinelli, Serena Carra, et al.
Pageof 4

Showing results (1-10 of 40) with videos related to

Sort By:
Pageof 4
Journal of Neurology|April 21, 2020
Asymptomatic adrenoleukodystrophy in elderly malesChiara Benzoni, Silvia Fenu, Viviana Pensato, et al.
The Neurologist|November 6, 2019
Leukoencephalopathy With Predominant Infratentorial Involvement Caused by a Novel ABCD1 Mutation: Does the Spinocerebellar Variant of Adrenoleukodystrophy Exist?Chiara Benzoni, Laura Farina, Viviana Pensato, et al.
Neurology|August 19, 2022
Behavioral and Cognitive Phenotypes of Patients With Amyotrophic Lateral Sclerosis Carrying SOD1 VariantsEleonora Dalla Bella, Enrica Bersano, Maria Grazia Bruzzone, et al.
Journal of Clinical Neurology (Seoul, Korea)|April 9, 2015
PEX7 Mutations Cause Congenital Cataract Retinopathy and Late-Onset Ataxia and Cognitive Impairment: Report of Two Siblings and Review of the LiteratureLorenzo Nanetti, Viviana Pensato, Valerio Leoni, et al.
Neurobiology of Aging|June 29, 2022
G507D mutation in FUS gene causes familial amyotrophic lateral sclerosis with a specific genotype-phenotype correlationIlaria Martinelli, Elisabetta Zucchi, Viviana Pensato, et al.
Pain and Therapy|February 20, 2021
Pain Study in X-Linked Adrenoleukodystrophy in Males and FemalesValeria Bachiocco, Marco Cappa, Anna Petroni, et al.
Neuroimage. Clinical|July 20, 2018
Cortical markers of cognitive syndromes in amyotrophic lateral sclerosisMonica Consonni, Valeria E Contarino, Eleonora Catricalà, et al.
Neurobiology of Aging|March 20, 2012
ATAXIN2 CAG-repeat length in Italian patients with amyotrophic lateral sclerosis: risk factor or variant phenotype? Implication for genetic testing and counselingCinzia Gellera, Nicola Ticozzi, Viviana Pensato, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|October 19, 2021
Duplication of exons 15 and 16 in Matrin-3: a phenotype bridging amyotrophic lateral sclerosis and immune-mediated disordersMaria Caputo, Elisabetta Zucchi, Ilaria Martinelli, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|June 22, 2022
Missense mutation in ATXN2 gene (c.2860C > T) in an amyotrophic lateral sclerosis patient with aggressive disease phenotypeAndrea Ghezzi, Ilaria Martinelli, Serena Carra, et al.
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