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Mario Sabatelli

Showing results (31-40 of 179) with videos related to

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Clinical Neurology and Neurosurgery|May 24, 2015
Admission neurophysiological abnormalities in Guillain-Barré syndrome: A single-center experienceMarco Luigetti, Serenella Servidei, Anna Modoni, et al.
Neurological Research|May 17, 2022
Guillain-Barré syndrome from an emergency department view: how to better predict the outcome?Marcello Covino, Marina Romozzi, Benedetta Simeoni, et al.
Neurobiology of Aging|May 31, 2011
SOD1 G93D sporadic amyotrophic lateral sclerosis (SALS) patient with rapid progression and concomitant novel ANG variantMarco Luigetti, Serena Lattante, Marcella Zollino, et al.
Genes|September 29, 2020
High-Throughput Genetic Testing in ALS: The Challenging Path of Variant Classification Considering the ACMG GuidelinesSerena Lattante, Giuseppe Marangi, Paolo Niccolò Doronzio, et al.
Brain Sciences|August 27, 2021
Renal Involvement in Hereditary Transthyretin Amyloidosis: An Italian Single-Centre ExperiencePietro Manuel Ferraro, Viola D'Ambrosio, Andrea Di Paolantonio, et al.
Neurological Research|March 15, 2003
Multinevritis of cranial nerves following inhalation of toxinsIrene Aprile, Luca Padua, Pietro Caliandro, et al.
Stem Cell Research|October 27, 2018
Generation and characterization of a human iPSC line from an ALS patient carrying the Q66K-MATR3 mutationDaniele Pollini, Rosa Loffredo, Marina Cardano, et al.
Muscle & Nerve|September 17, 2011
A novel GJB1 mutation in an Italian patient with Charcot-Marie-Tooth disease and pyramidal signsMarco Luigetti, Gian Maria Fabrizi, Federico Ranieri, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|May 12, 2004
Motor cortex stimulation for amyotrophic lateral sclerosis. Time for a therapeutic trial?Vincenzo Di Lazzaro, Antonio Oliviero, Eleonora Saturno, et al.
Journal of the Neurological Sciences|May 12, 2009
Progressive multifocal leukoencephalopathy in a patient with Franklin disease and hypogammaglobulinemiaGiorgio Tasca, Raffaele Iorio, Umberto Basile, et al.
Pageof 18

Showing results (31-40 of 179) with videos related to

Sort By:
Pageof 18
Clinical Neurology and Neurosurgery|May 24, 2015
Admission neurophysiological abnormalities in Guillain-Barré syndrome: A single-center experienceMarco Luigetti, Serenella Servidei, Anna Modoni, et al.
Neurological Research|May 17, 2022
Guillain-Barré syndrome from an emergency department view: how to better predict the outcome?Marcello Covino, Marina Romozzi, Benedetta Simeoni, et al.
Neurobiology of Aging|May 31, 2011
SOD1 G93D sporadic amyotrophic lateral sclerosis (SALS) patient with rapid progression and concomitant novel ANG variantMarco Luigetti, Serena Lattante, Marcella Zollino, et al.
Genes|September 29, 2020
High-Throughput Genetic Testing in ALS: The Challenging Path of Variant Classification Considering the ACMG GuidelinesSerena Lattante, Giuseppe Marangi, Paolo Niccolò Doronzio, et al.
Brain Sciences|August 27, 2021
Renal Involvement in Hereditary Transthyretin Amyloidosis: An Italian Single-Centre ExperiencePietro Manuel Ferraro, Viola D'Ambrosio, Andrea Di Paolantonio, et al.
Neurological Research|March 15, 2003
Multinevritis of cranial nerves following inhalation of toxinsIrene Aprile, Luca Padua, Pietro Caliandro, et al.
Stem Cell Research|October 27, 2018
Generation and characterization of a human iPSC line from an ALS patient carrying the Q66K-MATR3 mutationDaniele Pollini, Rosa Loffredo, Marina Cardano, et al.
Muscle & Nerve|September 17, 2011
A novel GJB1 mutation in an Italian patient with Charcot-Marie-Tooth disease and pyramidal signsMarco Luigetti, Gian Maria Fabrizi, Federico Ranieri, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|May 12, 2004
Motor cortex stimulation for amyotrophic lateral sclerosis. Time for a therapeutic trial?Vincenzo Di Lazzaro, Antonio Oliviero, Eleonora Saturno, et al.
Journal of the Neurological Sciences|May 12, 2009
Progressive multifocal leukoencephalopathy in a patient with Franklin disease and hypogammaglobulinemiaGiorgio Tasca, Raffaele Iorio, Umberto Basile, et al.
Pageof 18