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Franco Taroni

Showing results (71-80 of 204) with videos related to

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Current Treatment Options in Neurology|July 26, 2017
CADASIL: Treatment and Management OptionsAnna Bersano, Gloria Bedini, Joshua Oskam, et al.
Journal of the Peripheral Nervous System : JPNS|January 3, 2013
Myelin protein zero Arg36Gly mutation with very late onset and rapidly progressive painful neuropathyPatrizia Dacci, Franco Taroni, Eleonora Dalla Bella, et al.
Journal of Neurogenetics|November 27, 2024
A familial form of Charcot-Marie-Tooth disease (type 2d) caused by a previously unreported variant in <i>GARS1</i>Dora Varvara, Serena Lattante, Stefania Magri, et al.
Experimental Neurology|September 24, 2008
Alpha-lipoic acid prevents mitochondrial damage and neurotoxicity in experimental chemotherapy neuropathyGiorgia Melli, Michela Taiana, Francesca Camozzi, et al.
Journal of Clinical Neurology (Seoul, Korea)|April 9, 2015
PEX7 Mutations Cause Congenital Cataract Retinopathy and Late-Onset Ataxia and Cognitive Impairment: Report of Two Siblings and Review of the LiteratureLorenzo Nanetti, Viviana Pensato, Valerio Leoni, et al.
Free Radical Biology & Medicine|December 13, 2006
Mitochondrial DNA deletions inhibit proteasomal activity and stimulate an autophagic transcriptMansour Alemi, Alessandro Prigione, Alice Wong, 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.
Neurogenetics|December 19, 2007
Identification of new ANG gene mutations in a large cohort of Italian patients with amyotrophic lateral sclerosisCinzia Gellera, Claudia Colombrita, Nicola Ticozzi, et al.
Neurology. Genetics|September 12, 2022
3-Methylglutaconic Aciduria Type I: A Rare Cause of Late-Onset LeukoencephalopathyChiara Benzoni, Stefania Magri, Marco Moscatelli, et al.
Journal of the Peripheral Nervous System : JPNS|August 21, 2020
Expanding the phenotypic spectrum of TRIM2-associated Charcot-Marie-Tooth diseaseStefania Magri, Federica Rachele Danti, Francesca Balistreri, et al.
Pageof 21

Showing results (71-80 of 204) with videos related to

Sort By:
Pageof 21
Current Treatment Options in Neurology|July 26, 2017
CADASIL: Treatment and Management OptionsAnna Bersano, Gloria Bedini, Joshua Oskam, et al.
Journal of the Peripheral Nervous System : JPNS|January 3, 2013
Myelin protein zero Arg36Gly mutation with very late onset and rapidly progressive painful neuropathyPatrizia Dacci, Franco Taroni, Eleonora Dalla Bella, et al.
Journal of Neurogenetics|November 27, 2024
A familial form of Charcot-Marie-Tooth disease (type 2d) caused by a previously unreported variant in <i>GARS1</i>Dora Varvara, Serena Lattante, Stefania Magri, et al.
Experimental Neurology|September 24, 2008
Alpha-lipoic acid prevents mitochondrial damage and neurotoxicity in experimental chemotherapy neuropathyGiorgia Melli, Michela Taiana, Francesca Camozzi, et al.
Journal of Clinical Neurology (Seoul, Korea)|April 9, 2015
PEX7 Mutations Cause Congenital Cataract Retinopathy and Late-Onset Ataxia and Cognitive Impairment: Report of Two Siblings and Review of the LiteratureLorenzo Nanetti, Viviana Pensato, Valerio Leoni, et al.
Free Radical Biology & Medicine|December 13, 2006
Mitochondrial DNA deletions inhibit proteasomal activity and stimulate an autophagic transcriptMansour Alemi, Alessandro Prigione, Alice Wong, 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.
Neurogenetics|December 19, 2007
Identification of new ANG gene mutations in a large cohort of Italian patients with amyotrophic lateral sclerosisCinzia Gellera, Claudia Colombrita, Nicola Ticozzi, et al.
Neurology. Genetics|September 12, 2022
3-Methylglutaconic Aciduria Type I: A Rare Cause of Late-Onset LeukoencephalopathyChiara Benzoni, Stefania Magri, Marco Moscatelli, et al.
Journal of the Peripheral Nervous System : JPNS|August 21, 2020
Expanding the phenotypic spectrum of TRIM2-associated Charcot-Marie-Tooth diseaseStefania Magri, Federica Rachele Danti, Francesca Balistreri, et al.
Pageof 21