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Franco Taroni

Showing results (131-140 of 204) with videos related to

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Frontiers in Neurology|January 1, 2021
Progression of Cerebellar Atrophy in Spinocerebellar Ataxia Type 2 Gene Carriers: A Longitudinal MRI Study in Preclinical and Early Disease StagesAnna Nigri, Lidia Sarro, Alessia Mongelli, et al.
Frontiers in Genetics|March 16, 2026
Functional validation of the novel KIF5A p.R17Q VUS reveals defective axonal transport in iPSC-motoneurons from a SPG10 patientSerena Santangelo, Valeria Casiraghi, Claudia Fallini, et al.
Journal of Neurology|January 27, 2016
Early-onset progressive spastic paraplegia caused by a novel TUBB4A mutation: brain MRI and FDG-PET findingsAnna Sagnelli, Stefania Magri, Laura Farina, et al.
Annals of Clinical and Translational Neurology|May 4, 2021
Charcot-Marie-Tooth disease type 2F associated with biallelic HSPB1 mutationsElena Abati, Stefania Magri, Megi Meneri, et al.
Cerebellum (London, England)|June 9, 2021
Spinocerebellar Ataxia Type 1: One-Year Longitudinal Study to Identify Clinical and MRI Measures of Disease Progression in Patients and Presymptomatic CarriersAnna Nigri, Lidia Sarro, Alessia Mongelli, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 17, 2023
Complex Ataxia-Dementia Phenotype in Patients with Digenic TBP/STUB1 Spinocerebellar AtaxiaLorenzo Nanetti, Stefania Magri, Mario Fichera, et al.
Frontiers in Neurology|January 24, 2022
Multifaceted and Age-Dependent Phenotypes Associated With Biallelic <i>PNPLA6</i> Gene Variants: Eight Novel Cases and Review of the LiteratureLorenzo Nanetti, Daniela Di Bella, Stefania Magri, et al.
Annals of Neurology|August 13, 2014
Deferiprone in Friedreich ataxia: a 6-month randomized controlled trialMassimo Pandolfo, Javier Arpa, Martin B Delatycki, et al.
Brain : a Journal of Neurology|May 11, 2021
SREBP2 gene therapy targeting striatal astrocytes ameliorates Huntington's disease phenotypesGiulia Birolini, Gianluca Verlengia, Francesca Talpo, et al.
Human Mutation|September 15, 2004
Molecular and functional analysis of SLC25A20 mutations causing carnitine-acylcarnitine translocase deficiencyVito Iacobazzi, Federica Invernizzi, Silvia Baratta, et al.
Pageof 21

Showing results (131-140 of 204) with videos related to

Sort By:
Pageof 21
Frontiers in Neurology|January 1, 2021
Progression of Cerebellar Atrophy in Spinocerebellar Ataxia Type 2 Gene Carriers: A Longitudinal MRI Study in Preclinical and Early Disease StagesAnna Nigri, Lidia Sarro, Alessia Mongelli, et al.
Frontiers in Genetics|March 16, 2026
Functional validation of the novel KIF5A p.R17Q VUS reveals defective axonal transport in iPSC-motoneurons from a SPG10 patientSerena Santangelo, Valeria Casiraghi, Claudia Fallini, et al.
Journal of Neurology|January 27, 2016
Early-onset progressive spastic paraplegia caused by a novel TUBB4A mutation: brain MRI and FDG-PET findingsAnna Sagnelli, Stefania Magri, Laura Farina, et al.
Annals of Clinical and Translational Neurology|May 4, 2021
Charcot-Marie-Tooth disease type 2F associated with biallelic HSPB1 mutationsElena Abati, Stefania Magri, Megi Meneri, et al.
Cerebellum (London, England)|June 9, 2021
Spinocerebellar Ataxia Type 1: One-Year Longitudinal Study to Identify Clinical and MRI Measures of Disease Progression in Patients and Presymptomatic CarriersAnna Nigri, Lidia Sarro, Alessia Mongelli, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 17, 2023
Complex Ataxia-Dementia Phenotype in Patients with Digenic TBP/STUB1 Spinocerebellar AtaxiaLorenzo Nanetti, Stefania Magri, Mario Fichera, et al.
Frontiers in Neurology|January 24, 2022
Multifaceted and Age-Dependent Phenotypes Associated With Biallelic <i>PNPLA6</i> Gene Variants: Eight Novel Cases and Review of the LiteratureLorenzo Nanetti, Daniela Di Bella, Stefania Magri, et al.
Annals of Neurology|August 13, 2014
Deferiprone in Friedreich ataxia: a 6-month randomized controlled trialMassimo Pandolfo, Javier Arpa, Martin B Delatycki, et al.
Brain : a Journal of Neurology|May 11, 2021
SREBP2 gene therapy targeting striatal astrocytes ameliorates Huntington's disease phenotypesGiulia Birolini, Gianluca Verlengia, Francesca Talpo, et al.
Human Mutation|September 15, 2004
Molecular and functional analysis of SLC25A20 mutations causing carnitine-acylcarnitine translocase deficiencyVito Iacobazzi, Federica Invernizzi, Silvia Baratta, et al.
Pageof 21