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Paola Saveri

Showing results (1-10 of 36) with videos related to

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Current Opinion in Neurology|July 6, 2017
New developments in Charcot-Marie-Tooth neuropathy and related diseasesDavide Pareyson, Paola Saveri, Chiara Pisciotta
Brain Sciences|November 27, 2021
Challenges in Treating Charcot-Marie-Tooth Disease and Related Neuropathies: Current Management and Future PerspectivesChiara Pisciotta, Paola Saveri, Davide Pareyson
Expert Review of Neurotherapeutics|May 25, 2021
Updated review of therapeutic strategies for Charcot-Marie-Tooth disease and related neuropathiesChiara Pisciotta, Paola Saveri, Davide Pareyson
Neuroscience Letters|April 8, 2015
Mitochondrial dynamics and inherited peripheral nerve diseasesDavide Pareyson, Paola Saveri, Anna Sagnelli, et al.
Expert Review of Neurotherapeutics|February 27, 2025
Charcot-Marie-Tooth disease: a review of clinical developments and its management - What's new in 2025?Amedeo De Grado, Marina Serio, Paola Saveri, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 28, 2019
Late-onset and fast progressive neuropathy and cardiomyopathy in Val32Ala transthyretin gene mutationDaniele Cazzato, Eleonora Dalla Bella, Paola Saveri, et al.
Journal of the Peripheral Nervous System : JPNS|December 17, 2016
A novel NDRG1 mutation in a non-Romani patient with CMT4D/HMSN-LomGiuseppe Piscosquito, Stefania Magri, Paola Saveri, et al.
Journal of the Peripheral Nervous System : JPNS|August 27, 2015
Mutational mechanisms in MFN2-related neuropathy: compound heterozygosity for recessive and semidominant mutationsGiuseppe Piscosquito, Paola Saveri, Stefania Magri, et al.
Journal of the Peripheral Nervous System : JPNS|May 28, 2014
X-linked Charcot-Marie-Tooth type 1: stroke-like presentation of a novel GJB1 mutationAnna Sagnelli, Giuseppe Piscosquito, Luisa Chiapparini, et al.
Cells|February 15, 2022
Autophagy and Lysosomal Functionality in CMT2B Fibroblasts Carrying the RAB7<sup>K126R</sup> MutationRoberta Romano, Victoria Stefania Del Fiore, Paola Saveri, et al.
Pageof 4

Showing results (1-10 of 36) with videos related to

Sort By:
Pageof 4
Current Opinion in Neurology|July 6, 2017
New developments in Charcot-Marie-Tooth neuropathy and related diseasesDavide Pareyson, Paola Saveri, Chiara Pisciotta
Brain Sciences|November 27, 2021
Challenges in Treating Charcot-Marie-Tooth Disease and Related Neuropathies: Current Management and Future PerspectivesChiara Pisciotta, Paola Saveri, Davide Pareyson
Expert Review of Neurotherapeutics|May 25, 2021
Updated review of therapeutic strategies for Charcot-Marie-Tooth disease and related neuropathiesChiara Pisciotta, Paola Saveri, Davide Pareyson
Neuroscience Letters|April 8, 2015
Mitochondrial dynamics and inherited peripheral nerve diseasesDavide Pareyson, Paola Saveri, Anna Sagnelli, et al.
Expert Review of Neurotherapeutics|February 27, 2025
Charcot-Marie-Tooth disease: a review of clinical developments and its management - What's new in 2025?Amedeo De Grado, Marina Serio, Paola Saveri, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 28, 2019
Late-onset and fast progressive neuropathy and cardiomyopathy in Val32Ala transthyretin gene mutationDaniele Cazzato, Eleonora Dalla Bella, Paola Saveri, et al.
Journal of the Peripheral Nervous System : JPNS|December 17, 2016
A novel NDRG1 mutation in a non-Romani patient with CMT4D/HMSN-LomGiuseppe Piscosquito, Stefania Magri, Paola Saveri, et al.
Journal of the Peripheral Nervous System : JPNS|August 27, 2015
Mutational mechanisms in MFN2-related neuropathy: compound heterozygosity for recessive and semidominant mutationsGiuseppe Piscosquito, Paola Saveri, Stefania Magri, et al.
Journal of the Peripheral Nervous System : JPNS|May 28, 2014
X-linked Charcot-Marie-Tooth type 1: stroke-like presentation of a novel GJB1 mutationAnna Sagnelli, Giuseppe Piscosquito, Luisa Chiapparini, et al.
Cells|February 15, 2022
Autophagy and Lysosomal Functionality in CMT2B Fibroblasts Carrying the RAB7<sup>K126R</sup> MutationRoberta Romano, Victoria Stefania Del Fiore, Paola Saveri, et al.
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