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Mario Sabatelli

Showing results (101-110 of 179) with videos related to

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Internal Medicine (Tokyo, Japan)|September 18, 2013
MRI neurography findings in patients with idiopathic brachial plexopathy: correlations with clinical-neurophysiological data in eight consecutive casesMarco Luigetti, Emanuele Pravatà, Cesare Colosimo, et al.
Brain : a Journal of Neurology|September 29, 2014
Mutations in the CHCHD10 gene are a common cause of familial amyotrophic lateral sclerosisJanel O Johnson, Shannon M Glynn, J Raphael Gibbs, et al.
Clinical Epigenetics|November 18, 2020
Epigenetic profiling of Italian patients identified methylation sites associated with hereditary transthyretin amyloidosisAntonella De Lillo, Gita A Pathak, Flavio De Angelis, et al.
Neurobiology of Aging|December 29, 2016
Matrin 3 variants are frequent in Italian ALS patientsGiuseppe Marangi, Serena Lattante, Paolo Niccolò Doronzio, et al.
Neuromuscular Disorders : NMD|July 30, 2013
Influence of comorbidities on the phenotype of patients affected by Charcot-Marie-Tooth neuropathy type 1AGiulia Ursino, M Antonia Alberti, Marina Grandis, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|November 8, 2023
Early detection of nerve involvement in presymptomatic TTR mutation carriers: exploring potential markers of disease onsetAngela Romano, Valeria Guglielmino, Giulia Bisogni, et al.
Muscle & Nerve|September 9, 2024
Ultrasound assisted versus landmark based intrathecal administration of nusinersen in adults with spinal muscular atrophy disease: A randomized trialBruno Antonio Zanfini, Stefano Catarci, Agata Katia Patanella, et al.
Australasian Journal of Ultrasound in Medicine|December 30, 2024
Ultrasound-assisted and landmark-based nusinersen delivery in spinal muscular atrophy adults: A retrospective analysisBruno Antonio Zanfini, Agata Katia Patanella, Francesco Vassalli, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|September 6, 2022
Pupillometric findings in ATTRv patients and carriers: results from a single-centre experienceAngela Romano, Valeria Guglielmino, Andrea Di Paolantonio, et al.
Neurobiology of Aging|December 25, 2017
ATXN1 intermediate-length polyglutamine expansions are associated with amyotrophic lateral sclerosisSerena Lattante, Maria Grazia Pomponi, Amelia Conte, et al.
Pageof 18

Showing results (101-110 of 179) with videos related to

Sort By:
Pageof 18
Internal Medicine (Tokyo, Japan)|September 18, 2013
MRI neurography findings in patients with idiopathic brachial plexopathy: correlations with clinical-neurophysiological data in eight consecutive casesMarco Luigetti, Emanuele Pravatà, Cesare Colosimo, et al.
Brain : a Journal of Neurology|September 29, 2014
Mutations in the CHCHD10 gene are a common cause of familial amyotrophic lateral sclerosisJanel O Johnson, Shannon M Glynn, J Raphael Gibbs, et al.
Clinical Epigenetics|November 18, 2020
Epigenetic profiling of Italian patients identified methylation sites associated with hereditary transthyretin amyloidosisAntonella De Lillo, Gita A Pathak, Flavio De Angelis, et al.
Neurobiology of Aging|December 29, 2016
Matrin 3 variants are frequent in Italian ALS patientsGiuseppe Marangi, Serena Lattante, Paolo Niccolò Doronzio, et al.
Neuromuscular Disorders : NMD|July 30, 2013
Influence of comorbidities on the phenotype of patients affected by Charcot-Marie-Tooth neuropathy type 1AGiulia Ursino, M Antonia Alberti, Marina Grandis, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|November 8, 2023
Early detection of nerve involvement in presymptomatic TTR mutation carriers: exploring potential markers of disease onsetAngela Romano, Valeria Guglielmino, Giulia Bisogni, et al.
Muscle & Nerve|September 9, 2024
Ultrasound assisted versus landmark based intrathecal administration of nusinersen in adults with spinal muscular atrophy disease: A randomized trialBruno Antonio Zanfini, Stefano Catarci, Agata Katia Patanella, et al.
Australasian Journal of Ultrasound in Medicine|December 30, 2024
Ultrasound-assisted and landmark-based nusinersen delivery in spinal muscular atrophy adults: A retrospective analysisBruno Antonio Zanfini, Agata Katia Patanella, Francesco Vassalli, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|September 6, 2022
Pupillometric findings in ATTRv patients and carriers: results from a single-centre experienceAngela Romano, Valeria Guglielmino, Andrea Di Paolantonio, et al.
Neurobiology of Aging|December 25, 2017
ATXN1 intermediate-length polyglutamine expansions are associated with amyotrophic lateral sclerosisSerena Lattante, Maria Grazia Pomponi, Amelia Conte, et al.
Pageof 18