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Franco Taroni

Showing results (111-120 of 204) with videos related to

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Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 16, 2020
Frequency and distribution of polyQ disease intermediate-length repeat alleles in healthy Italian populationAlessia Mongelli, Stefania Magri, Elena Salvatore, et al.
Journal of Neuropathology and Experimental Neurology|September 8, 2006
NMDA receptor composition differs among anatomically diverse malformations of cortical developmentAdele Finardi, Fabrizio Gardoni, Stefania Bassanini, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 15, 2024
Paroxysmal Non-Kinesigenic Dyskinesias Associated with Biallelic POLG Variants: A Case ReportBarbara Castellotti, Cinzia Gellera, Davide Caputo, et al.
Stem Cell Research|December 24, 2022
Generation of an iPSC line from a patient with spastic paraplegia type 10 carrying a novel mutation in KIF5A geneSerena Santangelo, Patrizia Bossolasco, Stefania Magri, et al.
Journal of Neurology|May 18, 2013
Adult-onset autosomal dominant leukodystrophy without early autonomic dysfunctions linked to lamin B1 duplication: a phenotypic variantAna Potic, Aleksandra M Pavlovic, Graziella Uziel, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 14, 2012
Erythropoietin in Friedreich ataxia: no effect on frataxin in a randomized controlled trialCaterina Mariotti, Roberto Fancellu, Serena Caldarazzo, et al.
Journal of Clinical Neurology (Seoul, Korea)|October 18, 2014
Somatosensory conduction pathway in spastic paraplegia type 5Alessandra Vanotti, Lorenzo Nanetti, Davide Rossi Sebastiano, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 30, 2025
Self-silencing <i>GFAP</i> missense alleles in familial subclinical Alexander disease: implications for therapyTiziana Bachetti, Stefania Magri, Francesca Balistreri, et al.
Journal of Clinical Medicine|February 8, 2020
Sorting Rare ALS Genetic Variants by Targeted Re-Sequencing Panel in Italian Patients: <i>OPTN</i>, <i>VCP</i>, and <i>SQSTM1</i> Variants Account for 3% of Rare Genetic FormsViviana Pensato, Stefania Magri, Eleonora Dalla Bella, et al.
Investigative Ophthalmology & Visual Science|May 20, 2016
MRI Evidence of Cerebellar and Extraocular Muscle Atrophy Differently Contributing to Eye Movement Abnormalities in SCA2 and SCA28 DiseasesLetterio Salvatore Politi, Stefania Bianchi Marzoli, Claudia Godi, et al.
Pageof 21

Showing results (111-120 of 204) with videos related to

Sort By:
Pageof 21
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 16, 2020
Frequency and distribution of polyQ disease intermediate-length repeat alleles in healthy Italian populationAlessia Mongelli, Stefania Magri, Elena Salvatore, et al.
Journal of Neuropathology and Experimental Neurology|September 8, 2006
NMDA receptor composition differs among anatomically diverse malformations of cortical developmentAdele Finardi, Fabrizio Gardoni, Stefania Bassanini, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 15, 2024
Paroxysmal Non-Kinesigenic Dyskinesias Associated with Biallelic POLG Variants: A Case ReportBarbara Castellotti, Cinzia Gellera, Davide Caputo, et al.
Stem Cell Research|December 24, 2022
Generation of an iPSC line from a patient with spastic paraplegia type 10 carrying a novel mutation in KIF5A geneSerena Santangelo, Patrizia Bossolasco, Stefania Magri, et al.
Journal of Neurology|May 18, 2013
Adult-onset autosomal dominant leukodystrophy without early autonomic dysfunctions linked to lamin B1 duplication: a phenotypic variantAna Potic, Aleksandra M Pavlovic, Graziella Uziel, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 14, 2012
Erythropoietin in Friedreich ataxia: no effect on frataxin in a randomized controlled trialCaterina Mariotti, Roberto Fancellu, Serena Caldarazzo, et al.
Journal of Clinical Neurology (Seoul, Korea)|October 18, 2014
Somatosensory conduction pathway in spastic paraplegia type 5Alessandra Vanotti, Lorenzo Nanetti, Davide Rossi Sebastiano, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 30, 2025
Self-silencing <i>GFAP</i> missense alleles in familial subclinical Alexander disease: implications for therapyTiziana Bachetti, Stefania Magri, Francesca Balistreri, et al.
Journal of Clinical Medicine|February 8, 2020
Sorting Rare ALS Genetic Variants by Targeted Re-Sequencing Panel in Italian Patients: <i>OPTN</i>, <i>VCP</i>, and <i>SQSTM1</i> Variants Account for 3% of Rare Genetic FormsViviana Pensato, Stefania Magri, Eleonora Dalla Bella, et al.
Investigative Ophthalmology & Visual Science|May 20, 2016
MRI Evidence of Cerebellar and Extraocular Muscle Atrophy Differently Contributing to Eye Movement Abnormalities in SCA2 and SCA28 DiseasesLetterio Salvatore Politi, Stefania Bianchi Marzoli, Claudia Godi, et al.
Pageof 21