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Franco Taroni

Showing results (161-170 of 204) with videos related to

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Brain : a Journal of Neurology|May 21, 2016
Multisystemic SYNE1 ataxia: confirming the high frequency and extending the mutational and phenotypic spectrumInès Mademan, Florian Harmuth, Ilaria Giordano, et al.
Annals of Neurology|June 29, 2010
Paraoxonase gene mutations in amyotrophic lateral sclerosisNicola Ticozzi, Ashley Lyn LeClerc, Pamela J Keagle, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 10, 2012
Ubiquilin 2 mutations in Italian patients with amyotrophic lateral sclerosis and frontotemporal dementiaCinzia Gellera, Cinzia Tiloca, Roberto Del Bo, et al.
Journal of Neurology|June 19, 2025
Exploring NEK1 genetic variability in Italian amyotrophic lateral sclerosis patientsViviana Pensato, Silvia Peverelli, Cinzia Tiloca, et al.
Epilepsy Research|April 16, 2019
HCN ion channels and accessory proteins in epilepsy: genetic analysis of a large cohort of patients and review of the literatureJacopo C DiFrancesco, Barbara Castellotti, Raffaella Milanesi, et al.
Journal of Neurology|May 12, 2023
Adult-onset leukodystrophy with vanishing white matter: a case series of 19 patientsChiara Benzoni, Marco Moscatelli, Laura Farina, et al.
Nature Genetics|March 9, 2010
Mutations in the mitochondrial protease gene AFG3L2 cause dominant hereditary ataxia SCA28Daniela Di Bella, Federico Lazzaro, Alfredo Brusco, et al.
Neurobiology of Aging|July 7, 2012
C9ORF72 repeat expansion in a large Italian ALS cohort: evidence of a founder effectAntonia Ratti, Lucia Corrado, Barbara Castellotti, et al.
Cell Death & Disease|September 27, 2024
Altered molecular and cellular mechanisms in KIF5A-associated neurodegenerative or neurodevelopmental disordersMarta Cozzi, Stefania Magri, Barbara Tedesco, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 5, 2024
Phenotypic spectrum of myelin protein zero-related neuropathies: a large cohort study from five mutation clusters across ItalyAlessandro Bertini, Luca Gentile, Tiziana Cavallaro, et al.
Pageof 21

Showing results (161-170 of 204) with videos related to

Sort By:
Pageof 21
Brain : a Journal of Neurology|May 21, 2016
Multisystemic SYNE1 ataxia: confirming the high frequency and extending the mutational and phenotypic spectrumInès Mademan, Florian Harmuth, Ilaria Giordano, et al.
Annals of Neurology|June 29, 2010
Paraoxonase gene mutations in amyotrophic lateral sclerosisNicola Ticozzi, Ashley Lyn LeClerc, Pamela J Keagle, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 10, 2012
Ubiquilin 2 mutations in Italian patients with amyotrophic lateral sclerosis and frontotemporal dementiaCinzia Gellera, Cinzia Tiloca, Roberto Del Bo, et al.
Journal of Neurology|June 19, 2025
Exploring NEK1 genetic variability in Italian amyotrophic lateral sclerosis patientsViviana Pensato, Silvia Peverelli, Cinzia Tiloca, et al.
Epilepsy Research|April 16, 2019
HCN ion channels and accessory proteins in epilepsy: genetic analysis of a large cohort of patients and review of the literatureJacopo C DiFrancesco, Barbara Castellotti, Raffaella Milanesi, et al.
Journal of Neurology|May 12, 2023
Adult-onset leukodystrophy with vanishing white matter: a case series of 19 patientsChiara Benzoni, Marco Moscatelli, Laura Farina, et al.
Nature Genetics|March 9, 2010
Mutations in the mitochondrial protease gene AFG3L2 cause dominant hereditary ataxia SCA28Daniela Di Bella, Federico Lazzaro, Alfredo Brusco, et al.
Neurobiology of Aging|July 7, 2012
C9ORF72 repeat expansion in a large Italian ALS cohort: evidence of a founder effectAntonia Ratti, Lucia Corrado, Barbara Castellotti, et al.
Cell Death & Disease|September 27, 2024
Altered molecular and cellular mechanisms in KIF5A-associated neurodegenerative or neurodevelopmental disordersMarta Cozzi, Stefania Magri, Barbara Tedesco, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 5, 2024
Phenotypic spectrum of myelin protein zero-related neuropathies: a large cohort study from five mutation clusters across ItalyAlessandro Bertini, Luca Gentile, Tiziana Cavallaro, et al.
Pageof 21