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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> mutation
Roberta 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 series
Bruno 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 rods
Giorgio 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 experience
Marco 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 variant
Francesco 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 mutation
Marco 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 study
Marco 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 protein
Angela D'Anzi, Filomena Altieri, Elisa Perciballi, et al.
Brain and Behavior
|
October 30, 2021
Prevalence of amyotrophic lateral sclerosis in Latium region, Italy
Maria Puopolo, Ilaria Bacigalupo, Paola Piscopo, et al.
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Search research articles
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Showing results (61-70 of 179) with videos related to
Sort By:
Page
of 18
Brain Communications
|
February 8, 2023
Allele-specific silencing as therapy for familial amyotrophic lateral sclerosis caused by the p.G376D <i>TARDBP</i> mutation
Roberta 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 series
Bruno 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 rods
Giorgio 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 experience
Marco 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 variant
Francesco 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 mutation
Marco 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 study
Marco 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 protein
Angela D'Anzi, Filomena Altieri, Elisa Perciballi, et al.
Brain and Behavior
|
October 30, 2021
Prevalence of amyotrophic lateral sclerosis in Latium region, Italy
Maria Puopolo, Ilaria Bacigalupo, Paola Piscopo, et al.
Page
of 18