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Antonio Toscano

Showing results (91-100 of 223) with videos related to

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Neuromolecular Medicine|May 27, 2015
Clinical, Molecular, and Functional Characterization of CLCN1 Mutations in Three Families with Recessive Myotonia CongenitaSimona Portaro, Concetta Altamura, Norma Licata, et al.
Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences|July 19, 2016
Analysis of lipid profile in lipid storage myopathyM'hammed Aguennouz, Marco Beccaria, Giorgia Purcaro, et al.
Heliyon|July 5, 2021
Vascular pattern and radiological follow up in a case of pontine warning syndromeCarmelo Tiberio Currò, Isabella Francalanza, Masina Cotroneo, et al.
Medicine|September 21, 2017
Five years experience on 3,4-diaminopyridine phosphate in Lambert-Eaton syndrome: Case reportsSimona Portaro, Teresa Brizzi, Stefano Sinicropi, et al.
Journal of Anesthesia, Analgesia and Critical Care|November 17, 2023
Which ultrasound-guided parasternal intercostal nerve block for post-sternotomy pain? Results from a prospective observational studyAntonio Toscano, Paolo Capuano, Chiara Perrucci, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|December 31, 2014
Charcot-Marie-Tooth 2F: phenotypic presentation of the Arg136Leu HSP27 mutation in a multigenerational familyClaudia Stancanelli, Gian Maria Fabrizi, Moreno Ferrarini, et al.
Journal of Neurology|September 28, 2015
Variants in KIF1A gene in dominant and sporadic forms of hereditary spastic paraparesisAndrea Citterio, Alessia Arnoldi, Elena Panzeri, et al.
Frontiers in Neurology|February 23, 2019
Late and Severe Myopathy in a Patient With Glycogenosis VII Worsened by Cyclosporine and AmiodaroneMassimiliano Filosto, Stefano Cotti Piccinelli, Anna Pichiecchio, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|October 17, 2020
Intracranial aneurysm management in patients with late-onset Pompe disease (LOPD)Enricomaria Mormina, Olimpia Musumeci, Agostino Tessitore, et al.
Brain Sciences|April 30, 2021
Patisiran in hATTR Amyloidosis: Six-Month Latency Period before EfficacyLuca Gentile, Massimo Russo, Marco Luigetti, et al.
Pageof 23

Showing results (91-100 of 223) with videos related to

Sort By:
Pageof 23
Neuromolecular Medicine|May 27, 2015
Clinical, Molecular, and Functional Characterization of CLCN1 Mutations in Three Families with Recessive Myotonia CongenitaSimona Portaro, Concetta Altamura, Norma Licata, et al.
Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences|July 19, 2016
Analysis of lipid profile in lipid storage myopathyM'hammed Aguennouz, Marco Beccaria, Giorgia Purcaro, et al.
Heliyon|July 5, 2021
Vascular pattern and radiological follow up in a case of pontine warning syndromeCarmelo Tiberio Currò, Isabella Francalanza, Masina Cotroneo, et al.
Medicine|September 21, 2017
Five years experience on 3,4-diaminopyridine phosphate in Lambert-Eaton syndrome: Case reportsSimona Portaro, Teresa Brizzi, Stefano Sinicropi, et al.
Journal of Anesthesia, Analgesia and Critical Care|November 17, 2023
Which ultrasound-guided parasternal intercostal nerve block for post-sternotomy pain? Results from a prospective observational studyAntonio Toscano, Paolo Capuano, Chiara Perrucci, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|December 31, 2014
Charcot-Marie-Tooth 2F: phenotypic presentation of the Arg136Leu HSP27 mutation in a multigenerational familyClaudia Stancanelli, Gian Maria Fabrizi, Moreno Ferrarini, et al.
Journal of Neurology|September 28, 2015
Variants in KIF1A gene in dominant and sporadic forms of hereditary spastic paraparesisAndrea Citterio, Alessia Arnoldi, Elena Panzeri, et al.
Frontiers in Neurology|February 23, 2019
Late and Severe Myopathy in a Patient With Glycogenosis VII Worsened by Cyclosporine and AmiodaroneMassimiliano Filosto, Stefano Cotti Piccinelli, Anna Pichiecchio, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|October 17, 2020
Intracranial aneurysm management in patients with late-onset Pompe disease (LOPD)Enricomaria Mormina, Olimpia Musumeci, Agostino Tessitore, et al.
Brain Sciences|April 30, 2021
Patisiran in hATTR Amyloidosis: Six-Month Latency Period before EfficacyLuca Gentile, Massimo Russo, Marco Luigetti, et al.
Pageof 23