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Mario Sabatelli

Showing results (61-70 of 179) with videos related to

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Brain Communications|February 8, 2023
Allele-specific silencing as therapy for familial amyotrophic lateral sclerosis caused by the p.G376D <i>TARDBP</i> mutationRoberta Romano, Maria De Luca, Victoria Stefania Del Fiore, et al.
Muscle & Nerve|August 16, 2021
Ultrasound assisted lumbar intrathecal administration of nusinersen in adult patients with spinal muscular atrophy: A case seriesBruno Antonio Zanfini, Stefano Catarci, Agata Katia Patanella, et al.
Journal of Neurology|August 22, 2016
Start codon mutation of GYG1 causing late-onset polyglucosan body myopathy with nemaline rodsGiorgio Tasca, Fabiana Fattori, Mauro Monforte, et al.
Journal of Neurology|April 23, 2011
Progressive ascending myelopathy: atypical forms of multiple sclerosis or what else?Viviana Nociti, Anna Paola Batocchi, Marco Luigetti, et al.
Journal of the Neurological Sciences|April 15, 2014
Clinical, neurophysiological and pathological findings of HNPP patients with 17p12 deletion: a single-centre experienceMarco Luigetti, Alessandra Del Grande, Amelia Conte, et al.
Stem Cell Research|July 24, 2021
Generation of an induced pluripotent stem cell line (UCSCi001-A) from a patient with early-onset amyotrophic lateral sclerosis carrying a FUS variantFrancesco Martello, Serena Lattante, Paolo Niccolò Doronzio, et al.
Journal of the Neurological Sciences|August 11, 2014
Clinical, electrophysiological and pathological findings in a patient with Charcot-Marie-Tooth disease 4D caused by the NDRG1 Lom mutationMarco Luigetti, Franco Taroni, Micaela Milani, et al.
Journal of Clinical Sleep Medicine : JCSM : Official Publication of the American Academy of Sleep Medicine|September 3, 2013
Restless leg syndrome in different types of demyelinating neuropathies: a single-center pilot studyMarco Luigetti, Alessandra Del Grande, Elisa Testani, et al.
Stem Cell Research|June 5, 2021
Generation of an induced pluripotent stem cell line (CSS012-A (7672)) carrying the p.G376D heterozygous mutation in the TARDBP proteinAngela D'Anzi, Filomena Altieri, Elisa Perciballi, et al.
Brain and Behavior|October 30, 2021
Prevalence of amyotrophic lateral sclerosis in Latium region, ItalyMaria Puopolo, Ilaria Bacigalupo, Paola Piscopo, et al.
Pageof 18

Showing results (61-70 of 179) with videos related to

Sort By:
Pageof 18
Brain Communications|February 8, 2023
Allele-specific silencing as therapy for familial amyotrophic lateral sclerosis caused by the p.G376D <i>TARDBP</i> mutationRoberta Romano, Maria De Luca, Victoria Stefania Del Fiore, et al.
Muscle & Nerve|August 16, 2021
Ultrasound assisted lumbar intrathecal administration of nusinersen in adult patients with spinal muscular atrophy: A case seriesBruno Antonio Zanfini, Stefano Catarci, Agata Katia Patanella, et al.
Journal of Neurology|August 22, 2016
Start codon mutation of GYG1 causing late-onset polyglucosan body myopathy with nemaline rodsGiorgio Tasca, Fabiana Fattori, Mauro Monforte, et al.
Journal of Neurology|April 23, 2011
Progressive ascending myelopathy: atypical forms of multiple sclerosis or what else?Viviana Nociti, Anna Paola Batocchi, Marco Luigetti, et al.
Journal of the Neurological Sciences|April 15, 2014
Clinical, neurophysiological and pathological findings of HNPP patients with 17p12 deletion: a single-centre experienceMarco Luigetti, Alessandra Del Grande, Amelia Conte, et al.
Stem Cell Research|July 24, 2021
Generation of an induced pluripotent stem cell line (UCSCi001-A) from a patient with early-onset amyotrophic lateral sclerosis carrying a FUS variantFrancesco Martello, Serena Lattante, Paolo Niccolò Doronzio, et al.
Journal of the Neurological Sciences|August 11, 2014
Clinical, electrophysiological and pathological findings in a patient with Charcot-Marie-Tooth disease 4D caused by the NDRG1 Lom mutationMarco Luigetti, Franco Taroni, Micaela Milani, et al.
Journal of Clinical Sleep Medicine : JCSM : Official Publication of the American Academy of Sleep Medicine|September 3, 2013
Restless leg syndrome in different types of demyelinating neuropathies: a single-center pilot studyMarco Luigetti, Alessandra Del Grande, Elisa Testani, et al.
Stem Cell Research|June 5, 2021
Generation of an induced pluripotent stem cell line (CSS012-A (7672)) carrying the p.G376D heterozygous mutation in the TARDBP proteinAngela D'Anzi, Filomena Altieri, Elisa Perciballi, et al.
Brain and Behavior|October 30, 2021
Prevalence of amyotrophic lateral sclerosis in Latium region, ItalyMaria Puopolo, Ilaria Bacigalupo, Paola Piscopo, et al.
Pageof 18