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Franco Taroni

Showing results (141-150 of 204) with videos related to

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Neurology|June 6, 2014
Frontal cortex BOLD signal changes in premanifest Huntington disease: a possible fMRI biomarkerStefania Ferraro, Lorenzo Nanetti, Sylvie Piacentini, et al.
Cells|January 17, 2020
Glutamine Synthetase 1 Increases Autophagy Lysosomal Degradation of Mutant Huntingtin Aggregates in Neurons, Ameliorating Motility in a <i>Drosophila</i> Model for Huntington's DiseaseLuisa Vernizzi, Chiara Paiardi, Giusimaria Licata, et al.
Parkinsonism & Related Disorders|March 3, 2018
Cortical thickness, stance control, and arithmetic skill: An exploratory study in premanifest Huntington diseaseLorenzo Nanetti, Valeria Elisa Contarino, Anna Castaldo, et al.
Neurogenetics|April 6, 2011
Ataxia with oculomotor apraxia type1 (AOA1): novel and recurrent aprataxin mutations, coenzyme Q10 analyses, and clinical findings in Italian patientsBarbara Castellotti, Caterina Mariotti, Marco Rimoldi, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2021
Digenic inheritance of STUB1 variants and TBP polyglutamine expansions explains the incomplete penetrance of SCA17 and SCA48Stefania Magri, Lorenzo Nanetti, Cinzia Gellera, et al.
Journal of Neurology|December 6, 2018
ANO10 mutational screening in recessive ataxia: genetic findings and refinement of the clinical phenotypeLorenzo Nanetti, Elisa Sarto, Anna Castaldo, et al.
Brain : a Journal of Neurology|May 17, 2014
Overlapping phenotypes in complex spastic paraplegias SPG11, SPG15, SPG35 and SPG48Viviana Pensato, Barbara Castellotti, Cinzia Gellera, et al.
European Journal of Neurology|November 15, 2020
Hypomyelinating leukodystrophies in adults: Clinical and genetic featuresDaniela Di Bella, Stefania Magri, Chiara Benzoni, et al.
Human Molecular Genetics|January 12, 2018
Effect of diazoxide on Friedreich ataxia modelsAntonella Santoro, Sara Anjomani Virmouni, Eleonora Paradies, et al.
Journal of the Neurological Sciences|April 17, 2016
The diagnostic challenge of Divry van Bogaert and Sneddon Syndrome: Report of three cases and literature reviewAnna Bersano, Michela Morbin, Elisa Ciceri, et al.
Pageof 21

Showing results (141-150 of 204) with videos related to

Sort By:
Pageof 21
Neurology|June 6, 2014
Frontal cortex BOLD signal changes in premanifest Huntington disease: a possible fMRI biomarkerStefania Ferraro, Lorenzo Nanetti, Sylvie Piacentini, et al.
Cells|January 17, 2020
Glutamine Synthetase 1 Increases Autophagy Lysosomal Degradation of Mutant Huntingtin Aggregates in Neurons, Ameliorating Motility in a <i>Drosophila</i> Model for Huntington's DiseaseLuisa Vernizzi, Chiara Paiardi, Giusimaria Licata, et al.
Parkinsonism & Related Disorders|March 3, 2018
Cortical thickness, stance control, and arithmetic skill: An exploratory study in premanifest Huntington diseaseLorenzo Nanetti, Valeria Elisa Contarino, Anna Castaldo, et al.
Neurogenetics|April 6, 2011
Ataxia with oculomotor apraxia type1 (AOA1): novel and recurrent aprataxin mutations, coenzyme Q10 analyses, and clinical findings in Italian patientsBarbara Castellotti, Caterina Mariotti, Marco Rimoldi, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2021
Digenic inheritance of STUB1 variants and TBP polyglutamine expansions explains the incomplete penetrance of SCA17 and SCA48Stefania Magri, Lorenzo Nanetti, Cinzia Gellera, et al.
Journal of Neurology|December 6, 2018
ANO10 mutational screening in recessive ataxia: genetic findings and refinement of the clinical phenotypeLorenzo Nanetti, Elisa Sarto, Anna Castaldo, et al.
Brain : a Journal of Neurology|May 17, 2014
Overlapping phenotypes in complex spastic paraplegias SPG11, SPG15, SPG35 and SPG48Viviana Pensato, Barbara Castellotti, Cinzia Gellera, et al.
European Journal of Neurology|November 15, 2020
Hypomyelinating leukodystrophies in adults: Clinical and genetic featuresDaniela Di Bella, Stefania Magri, Chiara Benzoni, et al.
Human Molecular Genetics|January 12, 2018
Effect of diazoxide on Friedreich ataxia modelsAntonella Santoro, Sara Anjomani Virmouni, Eleonora Paradies, et al.
Journal of the Neurological Sciences|April 17, 2016
The diagnostic challenge of Divry van Bogaert and Sneddon Syndrome: Report of three cases and literature reviewAnna Bersano, Michela Morbin, Elisa Ciceri, et al.
Pageof 21