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D Pareyson

Showing results (81-90 of 113) with videos related to

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Journal of Neurology|October 1, 1990
A multicentre follow-up study of 1152 patients with myasthenia gravis in ItalyR Mantegazza, E Beghi, D Pareyson, et al.
Annals of Neurology|June 14, 2000
Partial laminin alpha2 chain deficiency in a patient with myopathy resembling inclusion body myositisC Di Blasi, M Mora, D Pareyson, et al.
European Journal of Neurology|August 25, 2019
Treadmill training in patients affected by Charcot-Marie-Tooth neuropathy: results of a multicenter, prospective, randomized, single-blind, controlled studyL Mori, A Signori, V Prada, et al.
European Journal of Neurology|January 16, 2007
Quality of life is not impaired in patients with hereditary neuropathy with liability to pressure palsiesL Padua, C Pazzaglia, T Cavallaro, et al.
Gait & Posture|April 23, 2011
Reliability of instrumented movement analysis as outcome measure in Charcot-Marie-Tooth disease: results from a multitask locomotor protocolM Ferrarin, G Bovi, M Rabuffetti, et al.
Gait & Posture|September 28, 2011
Gait pattern classification in children with Charcot-Marie-Tooth disease type 1AM Ferrarin, G Bovi, M Rabuffetti, et al.
AJNR. American Journal of Neuroradiology|September 26, 2000
MR imaging and proton MR spectroscopy in adult Krabbe diseaseL Farina, A Bizzi, G Finocchiaro, et al.
Journal of Neurology|July 10, 1999
Clinical and molecular studies of 73 Italian families with autosomal dominant cerebellar ataxia type I: SCA1 and SCA2 are the most common genotypesD Pareyson, C Gellera, B Castellotti, et al.
Journal of Neurology|July 7, 2019
Mutation update for myelin protein zero-related neuropathies and the increasing role of variants causing a late-onset phenotypeIlaria Callegari, C Gemelli, A Geroldi, et al.
Neurology|November 17, 2010
Four novel cases of periaxin-related neuropathy and review of the literatureC Marchesi, M Milani, M Morbin, et al.
Pageof 12

Showing results (81-90 of 113) with videos related to

Sort By:
Pageof 12
Journal of Neurology|October 1, 1990
A multicentre follow-up study of 1152 patients with myasthenia gravis in ItalyR Mantegazza, E Beghi, D Pareyson, et al.
Annals of Neurology|June 14, 2000
Partial laminin alpha2 chain deficiency in a patient with myopathy resembling inclusion body myositisC Di Blasi, M Mora, D Pareyson, et al.
European Journal of Neurology|August 25, 2019
Treadmill training in patients affected by Charcot-Marie-Tooth neuropathy: results of a multicenter, prospective, randomized, single-blind, controlled studyL Mori, A Signori, V Prada, et al.
European Journal of Neurology|January 16, 2007
Quality of life is not impaired in patients with hereditary neuropathy with liability to pressure palsiesL Padua, C Pazzaglia, T Cavallaro, et al.
Gait & Posture|April 23, 2011
Reliability of instrumented movement analysis as outcome measure in Charcot-Marie-Tooth disease: results from a multitask locomotor protocolM Ferrarin, G Bovi, M Rabuffetti, et al.
Gait & Posture|September 28, 2011
Gait pattern classification in children with Charcot-Marie-Tooth disease type 1AM Ferrarin, G Bovi, M Rabuffetti, et al.
AJNR. American Journal of Neuroradiology|September 26, 2000
MR imaging and proton MR spectroscopy in adult Krabbe diseaseL Farina, A Bizzi, G Finocchiaro, et al.
Journal of Neurology|July 10, 1999
Clinical and molecular studies of 73 Italian families with autosomal dominant cerebellar ataxia type I: SCA1 and SCA2 are the most common genotypesD Pareyson, C Gellera, B Castellotti, et al.
Journal of Neurology|July 7, 2019
Mutation update for myelin protein zero-related neuropathies and the increasing role of variants causing a late-onset phenotypeIlaria Callegari, C Gemelli, A Geroldi, et al.
Neurology|November 17, 2010
Four novel cases of periaxin-related neuropathy and review of the literatureC Marchesi, M Milani, M Morbin, et al.
Pageof 12