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Franco Taroni

Showing results (171-180 of 204) with videos related to

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Pharmacological Research|June 19, 2023
Chronic cholesterol administration to the brain supports complete and long-lasting cognitive and motor amelioration in Huntington's diseaseGiulia Birolini, Marta Valenza, Ilaria Ottonelli, et al.
Pharmacological Research|October 22, 2025
Corrigendum to "Chronic cholesterol administration to the brain supports complete and long-lasting cognitive and motor amelioration in Huntington's disease" [Pharmacol. Res. 194 (2023) 106823]Giulia Birolini, Marta Valenza, Ilaria Ottonelli, et al.
Brain : a Journal of Neurology|April 19, 2016
SYNE1 ataxia is a common recessive ataxia with major non-cerebellar features: a large multi-centre studyMatthis Synofzik, Katrien Smets, Martial Mallaret, et al.
Journal of Neurology|April 21, 2015
TUBA4A gene analysis in sporadic amyotrophic lateral sclerosis: identification of novel mutationsViviana Pensato, Cinzia Tiloca, Lucia Corrado, et al.
Annals of Neurology|March 29, 2020
ATPase Domain AFG3L2 Mutations Alter OPA1 Processing and Cause Optic NeuropathyLeonardo Caporali, Stefania Magri, Andrea Legati, et al.
Neuropathology and Applied Neurobiology|July 29, 2022
The SPTLC1 p.S331 mutation bridges sensory neuropathy and motor neuron disease and has implications for treatmentChiara Fiorillo, Giovanna Capodivento, Alessandro Geroldi, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 7, 2019
Expanding the spectrum of genes responsible for hereditary motor neuropathiesStefano C Previtali, Edward Zhao, Dejan Lazarevic, et al.
European Journal of Neurology|May 12, 2023
Clinical spectrum and frequency of Charcot-Marie-Tooth disease in Italy: Data from the National CMT RegistryChiara Pisciotta, Alessandro Bertini, Irene Tramacere, et al.
Annals of Neurology|February 2, 2019
Variation in SIPA1L2 is correlated with phenotype modification in Charcot- Marie- Tooth disease type 1AFeifei Tao, Gary W Beecham, Adriana P Rebelo, et al.
Journal of Neuromuscular Diseases|April 9, 2019
Modifier Gene Candidates in Charcot-Marie-Tooth Disease Type 1A: A Case-Only Genome-Wide Association StudyFeifei Tao, Gary W Beecham, Adriana P Rebelo, et al.
Pageof 21

Showing results (171-180 of 204) with videos related to

Sort By:
Pageof 21
Pharmacological Research|June 19, 2023
Chronic cholesterol administration to the brain supports complete and long-lasting cognitive and motor amelioration in Huntington's diseaseGiulia Birolini, Marta Valenza, Ilaria Ottonelli, et al.
Pharmacological Research|October 22, 2025
Corrigendum to "Chronic cholesterol administration to the brain supports complete and long-lasting cognitive and motor amelioration in Huntington's disease" [Pharmacol. Res. 194 (2023) 106823]Giulia Birolini, Marta Valenza, Ilaria Ottonelli, et al.
Brain : a Journal of Neurology|April 19, 2016
SYNE1 ataxia is a common recessive ataxia with major non-cerebellar features: a large multi-centre studyMatthis Synofzik, Katrien Smets, Martial Mallaret, et al.
Journal of Neurology|April 21, 2015
TUBA4A gene analysis in sporadic amyotrophic lateral sclerosis: identification of novel mutationsViviana Pensato, Cinzia Tiloca, Lucia Corrado, et al.
Annals of Neurology|March 29, 2020
ATPase Domain AFG3L2 Mutations Alter OPA1 Processing and Cause Optic NeuropathyLeonardo Caporali, Stefania Magri, Andrea Legati, et al.
Neuropathology and Applied Neurobiology|July 29, 2022
The SPTLC1 p.S331 mutation bridges sensory neuropathy and motor neuron disease and has implications for treatmentChiara Fiorillo, Giovanna Capodivento, Alessandro Geroldi, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 7, 2019
Expanding the spectrum of genes responsible for hereditary motor neuropathiesStefano C Previtali, Edward Zhao, Dejan Lazarevic, et al.
European Journal of Neurology|May 12, 2023
Clinical spectrum and frequency of Charcot-Marie-Tooth disease in Italy: Data from the National CMT RegistryChiara Pisciotta, Alessandro Bertini, Irene Tramacere, et al.
Annals of Neurology|February 2, 2019
Variation in SIPA1L2 is correlated with phenotype modification in Charcot- Marie- Tooth disease type 1AFeifei Tao, Gary W Beecham, Adriana P Rebelo, et al.
Journal of Neuromuscular Diseases|April 9, 2019
Modifier Gene Candidates in Charcot-Marie-Tooth Disease Type 1A: A Case-Only Genome-Wide Association StudyFeifei Tao, Gary W Beecham, Adriana P Rebelo, et al.
Pageof 21