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Davide Pareyson

Showing results (41-50 of 231) with videos related to

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Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|November 14, 2020
Hereditary transthyretin amyloidosis overviewFiore Manganelli, Gian Maria Fabrizi, Marco Luigetti, et al.
Neuromuscular Disorders : NMD|October 28, 2017
221st ENMC International Workshop:: Foot Surgery in Charcot-Marie-Tooth disease. 10-12 June 2016, Naarden, The NetherlandsMary M Reilly, Davide Pareyson, Joshua Burns, et al.
Journal of Neurophysiology|February 4, 2005
Lack of on-going adaptations in the soleus muscle activity during walking in patients affected by large-fiber neuropathyNazarena Mazzaro, Michael J Grey, Thomas Sinkjaer, et al.
Muscle & Nerve|August 20, 2004
Tubule and neurofilament immunoreactivity in human hairy skin: markers for intraepidermal nerve fibersGiuseppe Lauria, Monica Borgna, Michela Morbin, et al.
The Cochrane Database of Systematic Reviews|December 15, 2015
Ascorbic acid for the treatment of Charcot-Marie-Tooth diseaseBurkhard Gess, Jonathan Baets, Peter De Jonghe, et al.
Journal of the Peripheral Nervous System : JPNS|May 4, 2010
Slowly progressive sensory hemisyndrome: unusual presentation of paraneoplastic sensory neuronopathyLorenzo Nanetti, Giuseppe Lauria, Vidmer Scaioli, et al.
Journal of Neurology|April 21, 2020
Asymptomatic adrenoleukodystrophy in elderly malesChiara Benzoni, Silvia Fenu, Viviana Pensato, et al.
Journal of the Peripheral Nervous System : JPNS|March 8, 2006
Normal expression of myelin protein zero with frame-shift mutation correlates with mild phenotypeAndreas J Steck, Beat Erne, Davide Pareyson, et al.
Journal of the Peripheral Nervous System : JPNS|January 3, 2013
Myelin protein zero Arg36Gly mutation with very late onset and rapidly progressive painful neuropathyPatrizia Dacci, Franco Taroni, Eleonora Dalla Bella, et al.
Journal of Neurology|June 18, 2013
Selective theory of mind impairment and cerebellar atrophy: a case reportAnnalisa Parente, Valentina Manfredi, Anna Tarallo, et al.
Pageof 24

Showing results (41-50 of 231) with videos related to

Sort By:
Pageof 24
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|November 14, 2020
Hereditary transthyretin amyloidosis overviewFiore Manganelli, Gian Maria Fabrizi, Marco Luigetti, et al.
Neuromuscular Disorders : NMD|October 28, 2017
221st ENMC International Workshop:: Foot Surgery in Charcot-Marie-Tooth disease. 10-12 June 2016, Naarden, The NetherlandsMary M Reilly, Davide Pareyson, Joshua Burns, et al.
Journal of Neurophysiology|February 4, 2005
Lack of on-going adaptations in the soleus muscle activity during walking in patients affected by large-fiber neuropathyNazarena Mazzaro, Michael J Grey, Thomas Sinkjaer, et al.
Muscle & Nerve|August 20, 2004
Tubule and neurofilament immunoreactivity in human hairy skin: markers for intraepidermal nerve fibersGiuseppe Lauria, Monica Borgna, Michela Morbin, et al.
The Cochrane Database of Systematic Reviews|December 15, 2015
Ascorbic acid for the treatment of Charcot-Marie-Tooth diseaseBurkhard Gess, Jonathan Baets, Peter De Jonghe, et al.
Journal of the Peripheral Nervous System : JPNS|May 4, 2010
Slowly progressive sensory hemisyndrome: unusual presentation of paraneoplastic sensory neuronopathyLorenzo Nanetti, Giuseppe Lauria, Vidmer Scaioli, et al.
Journal of Neurology|April 21, 2020
Asymptomatic adrenoleukodystrophy in elderly malesChiara Benzoni, Silvia Fenu, Viviana Pensato, et al.
Journal of the Peripheral Nervous System : JPNS|March 8, 2006
Normal expression of myelin protein zero with frame-shift mutation correlates with mild phenotypeAndreas J Steck, Beat Erne, Davide Pareyson, et al.
Journal of the Peripheral Nervous System : JPNS|January 3, 2013
Myelin protein zero Arg36Gly mutation with very late onset and rapidly progressive painful neuropathyPatrizia Dacci, Franco Taroni, Eleonora Dalla Bella, et al.
Journal of Neurology|June 18, 2013
Selective theory of mind impairment and cerebellar atrophy: a case reportAnnalisa Parente, Valentina Manfredi, Anna Tarallo, et al.
Pageof 24