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D Pareyson

Showing results (71-80 of 113) 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|September 24, 2008
Late-onset sporadic ataxia, pontine lesion, and retroperitoneal fibrosis: a case of Erdheim-Chester diseaseE Salsano, M Savoiardo, S Nappini, et al.
Journal of Neurology|March 1, 1992
Efficacy of intranasal administration of neostigmine in myasthenic patientsA Sghirlanzoni, D Pareyson, C Benvenuti, et al.
European Neurology|January 1, 1994
17p11.2 duplication is a common finding in sporadic cases of Charcot-Marie-Tooth type 1G L Mancardi, A Uccelli, E Bellone, et al.
Annals of the New York Academy of Sciences|November 1, 2017
Heterozygous Null Mutation in the P<sub>0</sub> Gene Associated with Mild Charcot-Marie-Tooth DiseaseD Pareyson, D Menichella, S Botti, et al.
Annals of the New York Academy of Sciences|December 10, 1999
Heterozygous null mutation in the P0 gene associated with mild Charcot-Marie-Tooth diseaseD Pareyson, D Menichella, S Botti, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|December 18, 2009
Natural history of Charcot-Marie-Tooth 2: 2-year follow-up of muscle strength, walking ability and quality of lifeLuca Padua, D Pareyson, I Aprile, et al.
Journal of Medical Genetics|July 1, 1992
Charcot-Marie-Tooth (CMT) 1a duplication at 17p11.2 in Italian familiesE Bellone, P Mandich, G L Mancardi, et al.
Gait & Posture|August 2, 2014
Postural stabilization and balance assessment in Charcot-Marie-Tooth 1A subjectsT Lencioni, M Rabuffetti, G Piscosquito, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|July 10, 2008
Relationship between clinical examination, quality of life, disability and depression in CMT patients: Italian multicenter studyL Padua, I Aprile, T Cavallaro, et al.
American Journal of Human Genetics|January 1, 1995
A 1.5-Mb deletion in 17p11.2-p12 is frequently observed in Italian families with hereditary neuropathy with liability to pressure palsiesD Lorenzetti, D Pareyson, A Sghirlanzoni, et al.
Pageof 12

Showing results (71-80 of 113) with videos related to

Sort By:
Pageof 12
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|September 24, 2008
Late-onset sporadic ataxia, pontine lesion, and retroperitoneal fibrosis: a case of Erdheim-Chester diseaseE Salsano, M Savoiardo, S Nappini, et al.
Journal of Neurology|March 1, 1992
Efficacy of intranasal administration of neostigmine in myasthenic patientsA Sghirlanzoni, D Pareyson, C Benvenuti, et al.
European Neurology|January 1, 1994
17p11.2 duplication is a common finding in sporadic cases of Charcot-Marie-Tooth type 1G L Mancardi, A Uccelli, E Bellone, et al.
Annals of the New York Academy of Sciences|November 1, 2017
Heterozygous Null Mutation in the P<sub>0</sub> Gene Associated with Mild Charcot-Marie-Tooth DiseaseD Pareyson, D Menichella, S Botti, et al.
Annals of the New York Academy of Sciences|December 10, 1999
Heterozygous null mutation in the P0 gene associated with mild Charcot-Marie-Tooth diseaseD Pareyson, D Menichella, S Botti, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|December 18, 2009
Natural history of Charcot-Marie-Tooth 2: 2-year follow-up of muscle strength, walking ability and quality of lifeLuca Padua, D Pareyson, I Aprile, et al.
Journal of Medical Genetics|July 1, 1992
Charcot-Marie-Tooth (CMT) 1a duplication at 17p11.2 in Italian familiesE Bellone, P Mandich, G L Mancardi, et al.
Gait & Posture|August 2, 2014
Postural stabilization and balance assessment in Charcot-Marie-Tooth 1A subjectsT Lencioni, M Rabuffetti, G Piscosquito, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|July 10, 2008
Relationship between clinical examination, quality of life, disability and depression in CMT patients: Italian multicenter studyL Padua, I Aprile, T Cavallaro, et al.
American Journal of Human Genetics|January 1, 1995
A 1.5-Mb deletion in 17p11.2-p12 is frequently observed in Italian families with hereditary neuropathy with liability to pressure palsiesD Lorenzetti, D Pareyson, A Sghirlanzoni, et al.
Pageof 12